Department of Education Child Development Program 3214 Austin Street, Houston, TX 77004 713-718-6303 phone 713-718-6235 fax TECA 1354 Child Growth and Development Case Study Key Assessment NAEYC Standard 1: Promoting Child Development and Learning a. Students know and understand young children’s characteristics and needs. b. Students know and understand the multiple influences on development and learning. c. Students use developmental knowledge to create healthy, respectful, supportive, and challenging learning environments. NAEYC Supportive Skills SS3 Written and Verbal Communication: Well-prepared associate degree graduates have strong skills in written and verbal communication. Students are technologically literate. Required Component This assignment (key assessment) is required for completion of this course. If this assignment is not completed with 70% of possible points, (at least 70 points of the 100 possible on each case study), you will not receive a passing grade in this class. If you do not earn at least 70 points, you will be allowed one revision on each case study. The maximum grade a student can earn on a revised assignment is 70 % of the possible points (which is 70 points). See syllabus for more details. Case Study Description The purpose of this case study is to give the reader a detailed description of a child as viewed by you, the writer, with respect to the developmental domains specified below. You will select and report on a child in each of the four case studies: 1.) infant or toddler (ages 0-2), 2.) Preschool (ages 3-5), 3.) Middle childhood (ages 6-11), and 4.) Adolescence (ages 12-18). Be sure to report the child’s current level in each domain. You may choose any child EXCEPT your own, for example, extended family members, neighbors, or friends. If you have any questions or concerns regarding selection of children, contact your professor. Your report should be written in formal academic language. Your report should be an objective evaluation using information gathered from direct observation. You may supplement this information with facts provided by the family or caregiver. Examples of objective reporting are: “The mother reports Jason feels more secure when he sleeps with his teddy bear,” or “The caregiver stated that Gina shares her crayons at the art table with any child who needs crayons.” The case study should NOT include subjective (opinion) statements such as: “Jason seems like a secure child,” or “Gina is the nicest girl in the room.” Be as thorough as possible with the data available to you. Include as much factual data as you can to "paint" a comprehensive picture of the child Case Study Outline Use the following headings, prompts, and rubric to guide you as you write each section of the case study. Type the headings for each section. Provide plenty of descriptions and details. Use only the summary section to include any re.

1. Department of Education
Child Development Program
3214 Austin Street, Houston, TX 77004
713-718-6303 phone 713-718-6235 fax
TECA 1354 Child Growth and Development
Case Study
Key Assessment
NAEYC Standard 1: Promoting Child Development and
Learning
a. Students know and understand young children’s
characteristics and needs.
b. Students know and understand the multiple influences on
development and learning.
c. Students use developmental knowledge to create healthy,
respectful, supportive, and challenging learning environments.
NAEYC Supportive Skills
SS3 Written and Verbal Communication: Well-prepared
associate degree graduates have strong skills in written and
verbal
communication. Students are technologically literate.

2. Required Component
This assignment (key assessment) is required for completion of
this course. If this assignment is not completed with 70% of
possible
points, (at least 70 points of the 100 possible on each case
study), you will not receive a passing grade in this class. If you
do not earn
at least 70 points, you will be allowed one revision on each case
study. The maximum grade a student can earn on a revised
assignment is 70 % of the possible points (which is 70 points).
See syllabus for more details.
Case Study Description
The purpose of this case study is to give the reader a detailed
description of a child as viewed by you, the writer, with respect
to the
developmental domains specified below. You will select and
report on a child in each of the four case studies: 1.) infant or
toddler (ages
0-2), 2.) Preschool (ages 3-5), 3.) Middle childhood (ages 6-
11), and 4.) Adolescence (ages 12-18). Be sure to report the
child’s
current level in each domain. You may choose any child
EXCEPT your own, for example, extended family members,
neighbors, or
friends. If you have any questions or concerns regarding
selection of children, contact your professor.
Your report should be written in formal academic language.
Your report should be an objective evaluation using information
gathered
from direct observation. You may supplement this information
with facts provided by the family or caregiver. Examples of
objective
reporting are: “The mother reports Jason feels more secure
when he sleeps with his teddy bear,” or “The caregiver stated

3. that Gina
shares her crayons at the art table with any child who needs
crayons.” The case study should NOT include subjective
(opinion)
statements such as: “Jason seems like a secure child,” or “Gina
is the nicest girl in the room.” Be as thorough as possible with
the data
available to you. Include as much factual data as you can to
"paint" a comprehensive picture of the child
Case Study Outline
Use the following headings, prompts, and rubric to guide you as
you write each section of the case study. Type the headings for
each
section. Provide plenty of descriptions and details. Use only
the summary section to include any relevant personal
interpretations,
opinions, or conclusions. Case study requirements include
college level writing (1000 words, double-spaced). Use the
following format
for each of the four case studies.
Introduction
Include the following descriptors:
Give the child's name, age, family make up, and a brief
description of physical appearance.
Describe the child's environment at home, childcare and/or
school.
Describe characteristics that identify the socioeconomic status
of the child’s family. Instead of reporting income, report items
such as
parents’ education level, housing and neighborhood, current
job, etc. Please do not ask the family any personal income
questions!
Tell why you have chosen this child.

4. Physical Development NAEYC STANDARD 1a
Specifically describe the child’s small (fine) skills
Specifically describe the child’s large (gross) motor skills.
Include examples and direct observations for small motor skills.
Include examples and direct observations for large motor skills.
TECA 1354 – Case Study
2
Give any background about the child's health, nutrition, and rest
habits.
*Compare the child to the norms for children this age, using in-
text citations (Manis, 2017).
Cognitive Development NAEYC STANDARD 1a
Describe evidence of learning from your observations and other
sources, parents, teachers, grades, etc.
Identify specific areas of strength and areas that need
improvement (memory, attention, etc.)
Give examples of the child's language development. What
evidence do you see that indicates the child understands spoken
language?
How does she express herself? As applicable, discuss the
child’s literacy skills (reading, composition, math, technology).
*Compare the child to the norms for children this age, using in-
text citations (Manis, 2017).
Social and Emotional Development NAEYC STANDARD 1a
Describe the child’s social interactions with other children,

5. family, relatives, siblings, classmates, etc. (sharing, solving
problems, playing
and working cooperatively).
What evidence do you see that would indicate a positive or
negative self-esteem? Include observations and examples that
might
indicate whether the child is generally happy or unhappy, secure
or insecure, stressed or relaxed.
What signs do you see that would indicate appropriate or poor
emotional adjustment?
As applicable, find out how the child describes him or herself
(self-concept).
*Compare the child to the norms for children this age, using in-
text citations (Manis, 2017).
Family and Home Factors NAEYC STANDARD 1b
Describe family conditions that may affect the child’s
development.
Identify the size of the family, what family members are present
in the home, the marital status of parents or guardians, etc.
Information may be obtained from the caregiver and/or parent.
Based on the research presented in your textbook, describe how
each factor may influence the child’s development and learning.
*Include in-text citations to support your descriptions.
Reminder: no opinions are allowed in this section of the paper.
Summary
The summary should include two parts (two different
paragraphs).
Part I: On the basis of facts and your observations, summarize
the most important factors influencing the child and his/her
behavior?
You may offer your interpretations, opinions, and conclusions
in this section of the paper. You should include at least 5
factors.

6. Part II: NAEYC STANDARD 1c In the second part of the
summary, use your knowledge of child development to describe
an ideal
learning environment for this child (home and/or school). If
you believe the child is already in an ideal learning
environment, describe
this environment. Include at least one idea for each of the
following: healthy, respectful, supportive, and challenging
learning
environment. Paint a picture of this environment with your
narrative.
NOTE: You must include in-text citations from your text to
support your observations in each section: Physical
Development, Cognitive
Development, Social and Emotional Development, and Family
or Home Factors. Be sure your in-text citations clearly relate to
your
observations and explain how they are related. You may also
include brief quotes from the text, with appropriate in-text
citations.
Consult APA resources for correct formatting of in-text
citations. You are also required to have a references page (APA
format) at the
end of the case study.
Example of a case study in-text citation:
After reviewing worksheets and homework that Alex completed
in pre-k, it is evident that his handwriting has become more
legible. His
ability to print the alphabet, write his first and last name, and
copy a square, triangle, and circle, demonstrate that he is on
track
compared to other children his age. By the time children
complete kindergarten, they can accurately copy many two-
dimensional shapes
and they can integrate these into their drawings (Manis, 2017).

7. .
APA Guidelines
The following APA Guidelines are required for TECA 1354 and
are included on the grading rubric for the Case Study. This list
is adapted
from the APA Quick Reference Guide, University of North
Carolina School of Social Work
(https://ssw.unc.edu/files/web/pdf/APA_Quick_Reference_Guid
e.pdf)
This is not intended to be a complete list of APA formatting
requirements; rather, these are the requirements for the Case
Study. Please
consult Purdue OWL
(https://owl.english.purdue.edu/owl/section/2/10/) for the
complete formatting guide.
https://ssw.unc.edu/files/web/pdf/APA_Quick_Reference_Guide
.pdf
https://owl.english.purdue.edu/owl/section/2/10/
TECA 1354 – Case Study
3
APA Guidelines required for the Case Study Assignment
Margins Minimum of 1” margin on all sides
Flush left (ragged right edge)

8. Font New Times Roman
Font size 12 pt. for text and headings
Spacing Double-spaced throughout, including references
Paragraphs Indent the beginning of a new paragraph 0.5”
Avoid one-sentence paragraphs.
Avoid full-page paragraphs.
Pagination and
header
Page numbers begin with the title page (i.e., page 1), but the
number is not shown on the title page.
Beginning with page 2, numbers are placed in the upper right-
hand corner.
Allow 5 spaces between the end of the header and the page
number.
Title page Title : Centered Headline: Not Boldface
Student Name
Institution’s Name
Example:
Case Study I: Infants Through Age Two
Elizabeth L. Cruz

9. Houston Community College
In-text citations APA format followed. See examples provided,
above, and consult
https://ssw.unc.edu/files/web/pdf/APA_Quick_Reference_Guide
.pdf
https://owl.english.purdue.edu/owl/section/2/10/)
References page APA format followed.
See
https://ssw.unc.edu/files/web/pdf/APA_Quick_Reference_Guide
.pdf
https://ssw.unc.edu/files/web/pdf/APA_Quick_Reference_Guide
.pdf
https://owl.english.purdue.edu/owl/section/2/10/
https://ssw.unc.edu/files/web/pdf/APA_Quick_Reference_Guide
.pdf
TECA 1354 – Case Study
4
Revision – Dec. 2017
TECA 1354 Child Growth and Development Case Study Rubric
Student Name:
Case Study #

10. Criteria Meets Expectations
12
Approaches Expectation
8
Falls Below
Expectations
5
Does Not Meet
Criteria
0
Points
Introduction Introduction provided a
complete picture of the
child and included all 7
descriptors listed.
Introduction provided a
complete picture of the
child and included only 4-6
of the descriptors listed.
Introduction provided an
incomplete picture of the
child and included only
1-3 of the descriptors
listed.
Introduction not
included.

11. Standard 1a. Know and
understand young children’s
characteristics and needs
Demonstrates all 3
elements:
-Clearly identify
appropriate characteristics
for all 3 developmental
domains.
- Provide examples of
appropriate characteristics
and needs in all 3
developmental domains.
-Compared the child to the
norms for children this
age, using in-text citations
Demonstrates the ability to:
- Clearly identify
appropriate characteristics
for 2 developmental
domains.
-Provided examples of
appropriate characteristics
and needs for 2
developmental domains.
-Compared the child to the
norms for children this age,
using in-text citations
Demonstrates the ability
to:

12. - Clearly identify
appropriate
characteristics for 1
developmental domain.
-Provided examples of
appropriate
characteristics and
needs for 1
developmental domain1.
-Compared the child to
the norms for children
this age, using in-text
citations.
Characteristics for
developmental
domains not identified.
Examples of
appropriate
characteristics and
needs for
developmental
domains not provided.
Standard 1b. Know and
understand the multiple
influences on development and
learning
Provided at least 3
factors pertaining to
family and home and how
each may influence the
child’s development and
learning.

13. Provided at least 2 factors
pertaining to family and
home and how each may
influence the child’s
development and learning.
Provided at least 1
factor pertaining to
family and home and
how it may influence the
child’s development and
learning.
Factors pertaining to
family and home and
their influence not
provided.
Summary Part 1 The summary includes at
least 5 of the most
important factors
influencing the child and
his/her behavior.
The summary includes at
least 3-4 of the most
important factors
influencing the child and
his/her behavior.
The summary includes at
least 1-2 of the most
important factors
influencing the child and

14. his/her behavior.
Factors influencing the
child and his/her
behavior not provided
Summary Part 2
Standard 1c. Use
developmental knowledge to
create healthy, respectful,
supportive, and challenging
learning environments
Uses developmental
knowledge in the
summary by providing at
least one idea for each of
the following categories: a
healthy, supportive, and
challenging learning
environment for this child.
Uses developmental
knowledge in the summary
by providing at least 1 idea
for 2 of the following
categories: a healthy,
supportive, and challenging
learning environment for
this child.
Uses developmental
knowledge in the
summary by providing at
least 1 idea for only 1 of
the following categories:

15. a healthy, supportive,
and challenging learning
environment for this
child.
Ideas demonstrating
developmental
knowledge not
provided in any of the
categories.
Criteria Meets Expectations
10
Approaches Expectation
7
Falls Below
Expectations
5
Does Not Meet
Criteria
0
Points
Textbook Application Applied and connected
textbook citations to the
case study in each of the
required sections:
physical, cognitive,
Applied and connected

16. textbook citations to the
case study in 2-3 of the
required sections.
Applied and connected
textbook citations to the
case study in only 1 of
the required sections.
Did not apply or
connect textbook
citations to the case
study.
TECA 1354 – Case Study
5
social/emotional, and
family/home factors.
Used Factual Information Gave only facts in the
first 5 sections and saved
opinions for the summary.
Gave facts for at least 2-4
of the first five sections and
saved most opinions for the
summary.
Gave facts in only 1 of

17. the first five sections.
Factual information
missing; only opinion
provided.
Written Communication
Criteria
Meets Expectations
10
Approaches Expectation
7
Falls Below
Expectations
5
Does Not Meet
Criteria
0
Points
SS3 Written & verbal
communication
(punctuation, capitalization,
grammar, spelling)
All elements present:
-1000 word minimum
-Double-spaced
-All section headings

18. -0-3 English mechanics
errors
-formal, academic
language
At least 3 elements
present:
- 1000 word minimum
- Double spaced
-All section headings
-4-6 English mechanics
errors
-formal, academic language
At least 2 elements
present:
- 1000 word minimum
- Double spaced
-All section headings
-7-10 English mechanics
errors
-formal, academic
language
At least 0-1 elements
present:
- 1000 word minimum
- Double spaced
-All section headings
-More than 10 English
mechanics errors
-formal, academic
language

19. APA Documentation Criteria Meets Expectations
10
Approaches Expectation
7
Falls Below
Expectations
5
Does Not Meet
Criteria
0
Followed APA Guidelines ( see
above)
All 9 APA Guidelines
followed
At least 6-8 APA Guidelines
followed.
At least 3-4 APA
Guidelines followed.
No APA Guidelines
followed.

20. Annual Report to the Nation on the Status of Cancer,
Part I: National Cancer Statistics
Kathleen A. Cronin, PhD, MPH1; Andrew J. Lake, BS2; Susan
Scott, MPH 1; Recinda L. Sherman, MPH, PhD, CTR3;
Anne-Michelle Noone, MS1; Nadia Howlader, MS, PhD1; S.
Jane Henley, MSPH4; Robert N. Anderson, PhD5;
Albert U. Firth, BS2; Jiemin Ma, PhD, MHS6; Betsy A. Kohler,
MPH, CTR3; and Ahmedin Jemal, DVM, PhD 6
BACKGROUND: The American Cancer Society (ACS), the
Centers for Disease Control and Prevention (CDC), the National
Cancer
Institute (NCI), and the North American Association of Central
Cancer Registries (NAACCR) collaborate to provide annual
updates
on cancer occurrence and trends in the United States.
METHODS: Incidence data were obtained from the CDC-funded
and NCI-
funded population-based cancer registry programs and compiled
by NAACCR. Data on cancer deaths were obtained from the
National Center for Health Statistics National Vital Statistics
System. Trends in age-standardized incidence and death rates
for all can-

21. cers combined and for the leading cancer types by sex, race, and
ethnicity were estimated by joinpoint analysis and expressed as
the
annual percent change. Stage distribution and 5-year survival by
stage at diagnosis were calculated for breast cancer, colon and
rec-
tum (colorectal) cancer, lung and bronchus cancer, and
melanoma of the skin. RESULTS: Overall cancer incidence
rates from 2008 to
2014 decreased by 2.2% per year among men but were stable
among women. Overall cancer death rates from 1999 to 2015
decreased by 1.8% per year among men and by 1.4% per year
among women. Among men, incidence rates during the most
recent 5-
year period (2010-2014) decreased for 7 of the 17 most common
cancer types, and death rates (2011-2015) decreased for 11 of
the 18
most common types. Among women, incidence rates declined
for 7 of the 18 most common cancers, and death rates declined
for 14
of the 20 most common cancers. Death rates decreased for
cancer sites, including lung and bronchus (men and women),
colorectal
(men and women), female breast, and prostate. Death rates
increased for cancers of the liver (men and women); pancreas
(men and

22. women); brain and other nervous system (men and women); oral
cavity and pharynx (men only); soft tissue, including heart (men
only); nonmelanoma skin (men only); and uterus. Incidence and
death rates were higher among men than among women for all
racial
and ethnic groups. For all cancer sites combined, black men and
white women had the highest incidence rates compared with
other
racial groups, and black men and black women had the highest
death rates compared with other racial groups. Non-Hispanic
men
and women had higher incidence and mortality rates than those
of Hispanic ethnicity. Five-year survival for cases diagnosed
from
2007 through 2013 ranged from 100% (stage I) to 26.5% (stage
IV) for female breast cancer, from 88.1% (stage I) to 12.6%
(stage IV)
for colorectal cancer, from 55.1% (stage I) to 4.2% (stage IV)
for lung and bronchus cancer, and from 99.5% (stage I) to 16%
(stage IV)
for melanoma of the skin. Among children, overall cancer
incidence rates increased by 0.8% per year from 2010 to 2014,
and overall
cancer death rates decreased by 1.5% per year from 2011 to
2015. CONCLUSIONS: For all cancer sites combined, cancer
incidence
rates decreased among men but were stable among women.

23. Overall, there continue to be significant declines in cancer
death rates
among both men and women. Differences in rates and trends by
race and ethnic group remain. Progress in reducing cancer
mortality
has not occurred for all sites. Examining stage distribution and
5-year survival by stage highlights the potential benefits
associated
with early detection and treatment. Cancer 2018;124:2785-800.
VC 2018 The Authors. Cancer published by Wiley Periodicals,
Inc. on
behalf of American Cancer Society. This is an open access
article under the terms of the Creative Commons Attribution-
NonCommercial
License, which permits use, distribution and reproduction in any
medium, provided the original work is properly cited and is not
used
for commercial purposes.
KEYWORDS: Annual Report to the Nation, cancer, incidence,
mortality, National Program of Cancer Registries (NPCR),
National Vital
Statistics System (NVSS), North American Association of
Central Cancer Registries (NAACCR), Surveillance,
Epidemiology, and End
Results (SEER), survival, trends.
Corresponding author: Kathleen A. Cronin, PhD, MPH, Division

24. of Cancer Control and Population Sciences, National Cancer
Institute, 9609 Medical Center Drive,
Room 4E454, Bethesda, MD 20892-9765; [email protected]
1
Division of Cancer Control and Population Sciences, National
Cancer Institute, Bethesda, Maryland;
2
Information Management Services, Inc., Rockville, Maryland;
3
North American Association of Central Cancer Registries,
Springfield, Illinois;
4
Division of Cancer Prevention and Control, National Center for
Chronic Disease Pre-
vention and Health Promotion, Centers for Disease Control and
Prevention, Atlanta, Georgia; 5National Center for Health
Statistics, Centers for Disease Control
and Prevention, Hyattsville, Maryland;
6
Surveillance and Health Services Research, American Cancer
Society, Atlanta, Georgia
See companion article on pages 2801-14, this issue.
This article has been contributed to by US Government
employees, and their work is in the public domain in the United
States.
We gratefully acknowledge the contributions of the state and
regional cancer registry staff for their work in collecting the
data used in this report. In addition,

25. we thank Daniel Miller, Joe Zou, and Steve Scoppa of
Information Management Services, Inc., for assistance in
compiling the data used in this report. We thank
Alyssa Wang, MPH, for assistance with preparation of the
graphics and Trish Murphy, MS, for editorial assistance.
The findings and conclusions in this article are those of the
authors and do not necessarily represent the official positions of
the author’s agencies (the Centers
for Disease Control and Prevention, the National Cancer
Institute, the American Cancer Society, or the North American
Association of Central Cancer Registries).
DOI: 10.1002/cncr.31551, Received: March 22, 2018; Revised:
April 23, 2018; Accepted: April 26, 2018, Published online May
22, 2018 in Wiley Online Library
(wileyonlinelibrary.com)
Cancer July 1, 2018 2785
Original Article
http://orcid.org/0000-0001-5881-8313
http://orcid.org/0000-0002-0000-4111
http://crossmark.crossref.org/dialog/?doi=10.1002%2Fcncr.3155
1&domain=pdf&date_stamp=2018-05-22
INTRODUCTION
The American Cancer Society (ACS), Centers for Disease
Control and Prevention (CDC), National Cancer Insti-
tute (NCI), and North American Association of Central
Cancer Registries (NAACCR) have collaborated annually

26. since 1998 to provide updates on cancer incidence and
mortality patterns in the United States.1-19 This report
uses a single database to estimate delay-adjusted incidence
to monitor population-based cancer trends. In addition to
reporting on incidence and mortality trends overall and
for common cancer sites, this year’s report highlights 4
cancer sites (female breast, colon and rectum [colorectal],
lung and bronchus, and melanoma of the skin) by pre-
senting the percentage of cases by stage at diagnosis and 5-
year survival estimates by stage at diagnosis.
MATERIALS AND METHODS
Data Sources
Cancer incidence data
Population-based cancer incidence data by age, sex, and
race/ethnicity were obtained from 42 state registries that
participate in the CDC’s National Program of Cancer
Registries (NPCR) and/or the NCI’s Surveillance, Epi-
demiology, and End Results (SEER) Program. The data
satisfied the NAACCR’s data quality criteria and repre-
sented cases diagnosed from 1999 through 2014,20 cover-
ing 89% of the US population. Information on incident
cases came primarily from the abstracts of inpatient and
outpatient medical records but also from a variety of other
sources, including pathology reports and death certifi-
cates. This database of 42 registries was used to derive all
incidence statistics presented in this report.
Anatomic site and histology were coded according
to the International Classification of Diseases for Oncol-
ogy (ICD-O) edition in use at the time of diagnosis and
were converted to the third edition (ICD-O-3) coding21
and categorized according to SEER site groups.22 Only

27. cases defined as malignant under ICD-O-2 and ICD-O-3
were included in this report, with the exception of bladder
cancer. In situ and malignant cancers were combined
when reporting bladder cancer incidence rates. All case
counts and rates were adjusted for delay in reporting.23
After adjusting for reporting delay, the 5-year fixed inter-
val incidence rates are based on 3.6 million male cases and
3.5 million female cases diagnosed between 2010 and
2014.
Cancer mortality data
Although cancer incidence data were available through
2014, an additional year of data was available for analysis
of mortality. Cause of death by age, sex, and race/ethnicity
(1999-2015) came from the National Vital Statistics Sys-
tem and was based on death certificate information
reported to state vital statistics offices and compiled into a
national file covering all states in the United States by the
National Center for Health Statistics (NCHS).24 Catego-
rization methods for cause of death have been described in
previous reports.19
Race/ethnicity data
In this report, information on race and ethnicity was
based on medical records for incidence or death certifi-
cates from the NCHS for mortality. Race was categorized
as white, black, Asian/Pacific Islander (API), and Ameri-
can Indian/Alaska Native (AI/AN). Race information for
AI/AN, however, was considered reliable only for geo-
graphic areas covered by the Indian Health Service Con-
tract Health Service Delivery Areas (CHSDA)10,25,26;
therefore, incidence and mortality data for AI/AN were

28. based only on these areas. Overall, 83% of the AI/AN
population lived in CHSDA areas between the years 2010
and 2014. This percentage varied by geographic area,
with 100% or close to 100% of the AI/AN population liv-
ing in CHSDA areas in Alaska, the Pacific Coast, the
Southern Plains, and the East; 67% living in the Northern
Plains; and 60% living in the Southwest. Hispanic ethnic-
ity included individuals from all races identified as His-
panic. Although the accuracy of race and ethnicity
reporting has improved over time, recent studies have
demonstrated that reporting of race in medical records
remains less accurate for API, Hispanic, and AIs/ANs
than for whites and blacks.27,28 We present incidence and
mortality data separately by race and by Hispanic ethnic-
ity. The number of cases included in the 5-year incidence
rate calculation ranged from 12,000 male and 13,500
female AIs/ANs residing in CHSDA areas to almost 3
million white men and women.
Population data
The population estimates used as the denominators to cal-
culate incidence and death rates were a modification of
the intercensal and Vintage 2015 annual times series of
July 1, county population estimates by age, sex, race, and
Hispanic origin produced by the US Census Bureau’s
Population Estimates Program in collaboration with the
NCHS and with support from the NCI.29 The estimates
incorporate intercensal (for July 1, 2000-2009) and Vin-
tage 2015 (for July 1, 2010-2015) bridged, single-race
estimates that are derived from the original multiple-race
categories in the 2000 and 2010 Censuses, as specified in
Original Article
2786 Cancer July 1, 2018

29. the 1997 Office of Management and Budget standards for
the collection of data on race and ethnicity.30,31 Some
additional adjustments were made to refine the July 1
population estimates, as with previous reports.19
Survival data
Estimates for 5-year relative survival were calculated for
cases diagnosed from 2007 through 2013. We used 34
central cancer registries (33 states and 1 metropolitan
area, referenced hereafter as states) compiled by the
NAACCR (covering 70% of the US population) to
examine survival differences by sex and cancer stage at
diagnosis for cancers of the lung and bronchus, breast,
colon and rectum, and melanoma of the skin.32 These
34 states were considered to have sufficient vital status
follow-up to conduct survival analyses, because they
either conducted recent National Death Index linkages
or they routinely conduct active vital status follow-up of
all cases.33 Cancers that were identified by death certifi-
cate or autopsy only were excluded from the survival
analysis, as were patients who died so soon after diagno-
sis that their survival time was not measurable. The first
site-specific cancer of the analysis period (2007-2013)
was used in the analysis. Patients were followed for vital
status through December 31, 2013, because not all regis-
tries had complete information on vital status through

30. December 31, 2014.
Statistical Methods
Cancer incidence and death rates and trends
Cross-sectional incidence (2010-2014) and death (2011-
2015) rates for all ages combined were calculated for all
cancer sites combined and for the most common cancer
sites by sex, race, and ethnicity. These rates were calcu-
lated with their 95% confidence intervals using SEER*-
Stat software, version 8.3.4.34,35 Incidence rates were
adjusted for delay in reporting.36 Similarly, we calculated
overall cancer incidence and death rates for children (ages
0-14 years). All rates were age-standardized to the 2000
US standard population and were expressed per 100,000
persons.34 Rates based on fewer than 16 cases were
deemed to be statistically unstable and were suppressed.
Temporal trends in age-standardized, delay-adjusted
cancer incidence (1999-2014) and death (1999-2015)
rates were estimated using joinpoint regression,37,38 with
a maximum of 2 joinpoints (3 line segments) allowed in
each model for incidence and 3 joinpoints (4 line seg-
ments) allowed in each model for mortality. The maxi-
mum number of joinpoints is based on the number of
data points in the series.39 The resultant trends were
described by the annual percent change (APC). The 5-
year average APCs (AAPCs) for 2010 through 2014 (inci-
dence) and for 2011 through 2015 (mortality) were calcu-
lated using a weighted average of the slope coefficients of
the underlying joinpoint regression line, with the weights
equal to the length of each segment over the interval. The

31. AAPC was equal to the APC when the AAPC was entirely
within the last joinpoint segment.40 Two-sided statistical
significance (P < .05) for the APC and the AAPC was
determined using a t test for the APC and for the AAPC
when it lay entirely within the last joinpoint segment; and
a Z test was used when the AAPC extended beyond the
last joinpoint segment.39
In describing trends, the terms increase and decrease
are used when the slope of the trend (APC or AAPC) was
statistically significant; otherwise, the term stable is used.
Trends based on fewer than 10 cases in any of the data
years (1999-2014 for incidence and 1999-2015 for mor-
tality) were considered statistically unstable and were
suppressed.
RESULTS
Cancer Incidence Rates for All Sites Combined
and for the Most Common Cancers
Figure 1 illustrates trends from 1999 to 2014 in age-
standardized, delay-adjusted incidence rates for all cancer
sites combined among men and among women. Incidence
rates among men decreased throughout the study period,
with the decrease accelerating from 0.6% (on average) per
year during 1999 to 2008 to 2.2% (on average) per year
during 2008 to 2014. In contrast, over the same 15-year
period, incidence rates among women were stable.
Figure 2 presents average annual incidence rates and
5-year AAPCs (2010-2014) for the 17 most common can-
cers among men and the 18 most common cancers among
women. Among men, incidence rates decreased for 7 of
the 17 most common cancers: prostate (5-year AAPC,
27.6%), lung and bronchus (22.4%), colon and rec-

32. tum (colorectal) (21.9%), urinary bladder (bladder)
(20.8%), esophagus (21.6%), brain and other nervous
system (20.2%), and larynx (22.3%) (Table 1 and Fig.
2). In contrast, incidence rates among men increased for
8 cancers: melanoma of the skin (5-year AAPC, 2.3%),
kidney and renal pelvis (kidney) (1.1%), leukemia
(1.6%), oral cavity and pharynx (1.3%), pancreas (1.0%),
liver and intrahepatic bile duct (liver) (2.8%), myeloma
(2.5%), and thyroid (2.4%). Incidence rates were stable
for non-Hodgkin lymphoma (NHL) and stomach cancer.
Among women, incidence rates decreased for 7 of
the 18 most common cancers: lung and bronchus (5-year
Annual Report National Cancer Statistics/Cronin et al
Cancer July 1, 2018 2787
AAPC, 21.2%), colorectal (21.7%), NHL (20.4%),
ovary (21.6%), bladder (20.8%), cervix uteri (cervix)
(21.0%), and brain and other nervous system (20.7%).
However, incidence rates increased for 10 cancers: breast
(0.4%), corpus and uterus not otherwise specified (uterus)
(1.2%), thyroid (1.9%), melanoma of the skin (1.2%),
leukemia (1.4%), kidney (0.4%), pancreas (1.1%), oral
cavity and pharynx (0.8%), myeloma (1.6%), and liver
(3.8%). Incidence rates remained unchanged for stomach
cancer (Table 1 and Fig. 2). Liver cancer replaced thyroid
cancer as the most rapidly increasing incident cancer
among women. For most cancer sites, the increasing or
decreasing trends from 2010 to 2014 among men and
among women were continuations of past trends (Sup-
porting Table 1).

33. At the end of this Results section, incidence and
mortality trends for female breast cancer, colorectal can-
cer, lung and bronchus cancer, and melanoma of the
skin are discussed in greater detail—along with stage at
diagnosis and survival by stage. Prostate cancer inci-
dence and mortality are examined in detail in Part II of
this report.
Cancer Death Rates for All Sites Combined
and for the Most Common Cancers
Figure 1 illustrates trends in death rates from 1999 to
2015 for all cancer sites combined, by sex. Death rates
decreased during this period by 1.8% on average per year
among men and by 1.4% on average per year among
women.
Figure 3 presents average annual death rates and 5-
year AAPCs (2011-2015) for the 18 most common can-
cers among men and the 20 most common cancers among
women. Among men, death rates during this period
decreased for 11 of the 18 cancers: lung and bronchus (5-
year AAPC, 23.8%), prostate (22.2%), colorectal
(22.5%), leukemia (22.2%), NHL (22.0%), esophagus
(21.1%), kidney (20.5%), stomach (21.6%), myeloma

34. (20.9%), melanoma of the skin (23.0%), and larynx
(22.5%). In contrast, death rates among men increased
for cancers of the pancreas (0.2%), liver (1.6%), brain and
other nervous system (0.5%), oral cavity and pharynx
(1.0%), nonmelanoma skin (2.8%), and soft tissue
(including heart) (0.8%). The death rate among men was
stable for bladder cancer (Fig. 3 and Table 2).
Figure 1. Trends in age-standardized incidence (1999-2014) and
mortality rates (1999-2015) are illustrated for all cancer sites
combined, all races/ethnicities combined, and by sex. An
asterisk indicates that the annual percent change (APC) or the
average
APC (AAPC) is statistically significantly different from zero
(2-sided t test; P <.05). UNK indicates unknown. Rates were
age-
standardized to the 2000 US standard population (19 age
groups; Bureau of the Census. Current Population Reports,
Publication
25-1130. Washington, DC: US Government Printing Office;
2000 [Census 25-1130]). Scattered points indicate observed
rates, and
lines are fitted rates according to joinpoint regression.
Incidence rates were delay-adjusted and covered 89% of the US
popula-
tion, and mortality covered the entire United States. The
following registries were included for incidence: Alabama,
Alaska, Ari-
zona, Arkansas, California, Colorado, Connecticut, Delaware,
Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa,

35. Kentucky,
Louisiana, Maine, Maryland, Massachusetts, Michigan,
Missouri, Montana, Nebraska, New Hampshire, New Jersey,
New York, North
Carolina, North Dakota, Ohio, Oklahoma, Oregon,
Pennsylvania, Rhode Island, South Carolina, Texas, Utah,
Vermont, Washington,
West Virginia, Wisconsin, and Wyoming. The AAPC is a
weighted average of the APCs over the fixed interval (2010-
2014 for inci-
dence; 2011-2015 for mortality) using the underlying Joinpoint
model for the period from 1999 to 2014 for incidence and the
period from 1999 to 2015 for mortality. Joinpoint models with
up to 2 joinpoints for incidence and up to 3 joinpoints for
mortality
are based on rates per 100,000 persons age standardized to the
2000 US standard population (19 age groups; Census P25-
1130). For joinpoint analysis, the Joinpoint Regression Program
was used (version 4.5.01; Bethesda, MD: Statistical Research
and
Applications Branch, National Cancer Institute; June 2017).
Original Article
2788 Cancer July 1, 2018
Among women, during the same time period, death
rates decreased for 14 of the 20 most common cancer
types: lung and bronchus (5-year AAPC, 22.4%), breast
(21.6%), colorectal (22.7%), ovary (22.3%), leukemia
(22.3%), NHL (22.7%), kidney (21.4%), stomach
(21.8%), cervix (20.7%), bladder (20.5%), melanoma
of the skin (22.6%), esophagus (21.6%), oral cavity and

36. pharynx (21.3%), and gallbladder (21.3%) (Fig. 3 and
Table 2). In contrast, death rates among women increased
for cancers of the pancreas (0.2%), uterus (1.9%), liver
(2.7%), and brain and other nervous system (0.5%).
Death rates among women were stable for myeloma and
soft tissue (including heart). Like the incidence trends,
increases or decreases in death rates for most cancers
among men and women were continuations of past trends
(Supporting Table 2).
Current Cancer Incidence Rates and Trends
by Sex, Race, and Ethnicity
Table 1 lists average annual age-standardized, delay-
adjusted incidence rates and trends for the most recent 5-
year period (2010-2014) by cancer site, sex, race, and eth-
nicity. For all cancer sites combined, rates were higher
among men than among women overall (all races/ethnici-
ties combined; 502.0 vs 420.6 per 100,000 persons) and
among persons in every racial/ethnic group. Black men
and white women had higher overall cancer incidence
rates than other racial groups. Non-Hispanic men and
women had higher incidence rates than those of Hispanic
ethnicity. API men and API women had the lowest rates
relative to other racial and ethnic groups. In every racial
and ethnic group, prostate cancer among men and breast
cancer among women were the most frequent incident
cancers, followed by lung and bronchus cancer, and colo-
rectal cancer, except among Hispanics. Among Hispanic
men and Hispanic women, colorectal cancer was more
frequent than lung and bronchus cancer. Rankings for
several other cancers varied substantially by race and eth-
nicity among both men and women. Among men, for
example, melanoma of the skin ranked fifth in whites and
19th in blacks; and liver cancer ranked 11th in whites,
sixth in blacks, and fourth in APIs.

37. Among men in each racial/ethnic group, incidence
trends during 2010 to 2014 for all cancer sites combined
and for each of the 17 most common cancers were gener-
ally similar in direction (decrease or increase) to those for
all races/ethnicities combined (Table 1). Incidence rates
among men in each racial and ethnic group decreased for
all cancers combined and for each of the 3 most common
cancers (prostate, lung and bronchus, colorectal), except
that the rate was stable for lung and bronchus cancer
among AIs/ANs. Rates also decreased among men in each
racial/ethnic group for cancers of the bladder, stomach,
Figure 2. Age-standardized, delay-adjusted incidence rates
and recent trends (2010-2014) are illustrated for the 17 most
common cancers in men and the 18 most common cancers in
women for all races/ethnicities combined and by sex. The 5-
year average annual percent change (AAPC) is based on the
joinpoint trend from 1999 to 2014. An asterisk indicates that
the AAPC is statistically significantly different from zero (2-
sided t test or Z test; P <.05). Rates were age-standardized to
the 2000 US standard population (19 age groups; Census P25-
1130), were delay-adjusted, and covered 89% of the US popula-
tion. The following registries were included in the analyses:
Ala-
bama, Alaska, Arizona, Arkansas, California, Colorado,
Connecticut, Delaware, Florida, Georgia, Hawaii, Idaho,
Illinois,
Indiana, Iowa, Kentucky, Louisiana, Maine, Maryland,
Massachu-
setts, Michigan, Missouri, Montana, Nebraska, New Hampshire,
New Jersey, New York, North Carolina, North Dakota, Ohio,
Oklahoma, Oregon, Pennsylvania, Rhode Island, South Caro-
lina, Texas, Utah, Vermont, Washington, West Virginia,
Wiscon-
sin, and Wyoming. The AAPC is a weighted average of the

38. annual percent changes (APCs) over the fixed interval (2010-
2014) using the underlying joinpoint model for the period from
1999 to 2014. Joinpoint models with up to 2 joinpoints are
based on rates per 100,000 persons age standardized to the
2000 US standard population (19 age groups; Census P25-
1130). For joinpoint analysis, the Joinpoint Regression Program
was used (version 4.5.0.1; Bethesda, MD: Statistical Research
and Applications Branch, National Cancer Institute; June 2017).
Annual Report National Cancer Statistics/Cronin et al
Cancer July 1, 2018 2789
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Original Article
2790 Cancer July 1, 2018
T
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164. u
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;
A
I/
A
N
,
A
m
e
ri

188. c
a
n
In
d
ia
n
/A
la
s
k
a
N
a
ti
v
e
;
A
P
C
,
a
n
n
u
a
l

189. p
e
rc
e
n
t
c
h
a
n
g
e
;
A
P
I,
A
s
ia
n
/P
a
c
if
ic
Is
la

190. n
d
e
r;
C
H
S
D
A
,
In
d
ia
n
H
e
a
lt
h
S
e
rv
ic
e
C

191. o
n
tr
a
c
t
H
e
a
lt
h
S
e
rv
ic
e
s
D
e
liv
e
ry
A
re
a
;

192. N
O
S
,
n
o
t
o
th
e
rw
is
e
s
p
e
c
if
ie
d
.
a
S
o
u
rc

193. e
:
N
a
ti
o
n
a
l
P
ro
g
ra
m
o
f
C
a
n
c
e
r
R
e
g
is

194. tr
ie
s
a
n
d
S
u
rv
e
ill
a
n
c
e
,
E
p
id
e
m
io
lo
g
y,
a

195. n
d
E
n
d
R
e
s
u
lt
s
a
re
a
s
re
p
o
rt
e
d
b
y
th
e
N

196. o
rt
h
A
m
e
ri
c
a
n
A
s
s
o
c
ia
ti
o
n
o
f
C
e
n
tr
a

197. l
C
a
n
c
e
r
R
e
g
is
tr
ie
s
a
s
m
e
e
ti
n
g
h
ig
h
-q
u

198. a
lit
y
in
c
i-
d
e
n
c
e
d
a
ta
s
ta
n
d
a
rd
s
fo
r
th
e
s

199. p
e
c
if
ie
d
ti
m
e
p
e
ri
o
d
s
.
b
T
h
e
fo
llo
w
in
g
re

200. g
is
tr
ie
s
w
e
re
in
c
lu
d
e
d
in
th
e
in
c
id
e
n
c
e
ra

201. te
s
(2
0
1
0
-2
0
1
4
)
a
n
d
J
o
in
p
o
in
t
m
o
d
e
ls

202. (1
9
9
9
-2
0
1
4
)
fo
r
a
ll
ra
c
e
s
/e
th
n
ic
it
ie
s
,
w
h

203. it
e
,
b
la
c
k
,
A
I/
A
N
,
A
P
I,
H
is
p
a
n
ic
,
a
n
d

204. n
o
n
-H
is
p
a
n
ic
(4
2
s
ta
te
s
):
A
la
b
a
m
a
,
A
la

205. s
k
a
,
A
ri
z
o
n
a
,
A
rk
a
n
s
a
s
,
C
a
lif
o
rn
ia
,
C
o

206. lo
ra
d
o
,
C
o
n
n
e
c
ti
c
u
t,
D
e
la
w
a
re
,
F
lo
ri
d
a

207. ,
G
e
o
rg
ia
,
H
a
w
a
ii,
Id
a
h
o
,
Il
lin
o
is
,
In
d
ia

208. n
a
,
Io
w
a
,
K
e
n
tu
c
k
y,
L
o
u
is
ia
n
a
,
M
a
in
e
,

209. M
a
ry
la
n
d
,
M
a
s
s
a
c
h
u
s
e
tt
s
,
M
ic
h
ig
a
n
,

210. M
is
s
o
u
ri
,
M
o
n
-
ta
n
a
,
N
e
b
ra
s
k
a
,
N
e
w
H

211. a
m
p
s
h
ir
e
,
N
e
w
J
e
rs
e
y,
N
e
w
Y
o
rk
,
N
o
rt
h

212. C
a
ro
lin
a
,
N
o
rt
h
D
a
k
o
ta
,
O
h
io
,
O
k
la
h
o

213. m
a
,
O
re
g
o
n
,
P
e
n
n
s
y
lv
a
n
ia
,
R
h
o
d
e
Is
la

214. n
d
,
S
o
u
th
C
a
ro
lin
a
,
T
e
x
a
s
,
U
ta
h
,
V
e
rm

215. o
n
t,
W
a
s
h
in
g
to
n
,
W
e
s
t
V
ir
g
in
ia
,
W
is
c
o

216. n
s
in
,
a
n
d
W
y
o
m
in
g
.
c
W
h
it
e
,
b
la
c
k
,
A
P

217. I,
a
n
d
A
I/
A
N
(C
H
S
D
A
2
0
1
2
c
o
u
n
ti
e
s
)
in
c

218. lu
d
e
H
is
p
a
n
ic
a
n
d
n
o
n
-H
is
p
a
n
ic
;
th
e
ra

219. c
e
a
n
d
e
th
n
ic
it
y
c
a
te
g
o
ri
e
s
a
re
n
o
t
m

220. u
tu
a
lly
e
x
c
lu
s
iv
e
.
A
I/
A
N
(C
H
S
D
A
2
0
1
2
)

221. s
ta
ti
s
ti
c
s
e
x
c
lu
d
e
d
a
ta
fr
o
m
K
a
n
s
a
s
.
d
C

222. a
n
c
e
rs
a
re
s
o
rt
e
d
in
d
e
s
c
e
n
d
in
g
o
rd
e
r

223. a
c
c
o
rd
in
g
to
s
e
x
-s
p
e
c
if
ic
ra
te
s
fo
r
a
ll
ra
c
e
s

224. /e
th
n
ic
it
ie
s
.
M
o
re
th
a
n
1
5
c
a
n
c
e
rs
m
a
y
a

225. p
p
e
a
r
u
n
d
e
r
m
a
le
s
a
n
d
fe
m
a
le
s
to
in
c
lu

226. d
e
th
e
to
p
1
5
c
a
n
c
e
rs
in
e
v
e
ry
ra
c
e
/e
th
n
ic
it
y

227. g
ro
u
p
.
e
R
a
te
s
a
re
p
e
r
1
0
0
,0
0
0
p
e
rs
o
n

228. s
a
n
d
w
e
re
a
g
e
s
ta
n
d
a
rd
iz
e
d
to
th
e
2
0
0
0

229. U
S
s
ta
n
d
a
rd
p
o
p
u
la
ti
o
n
(1
9
a
g
e
g
ro
u
p

230. s
;
U
S
B
u
re
a
u
o
f
th
e
C
e
n
s
u
s
,
C
u
rr
e
n
t
P

231. o
p
u
la
ti
o
n
R
e
p
o
rt
s
,
P
u
b
lic
a
ti
o
n
2
5
-1
1

232. 3
0
.
W
a
s
h
in
g
to
n
,
D
C
:
U
S
G
o
v
e
rn
m
e
n
t

233. P
ri
n
ti
n
g
O
ff
ic
e
;
2
0
0
0
[C
e
n
s
u
s
P
2
5
-1
1
3
0
])
.

234. f
T
h
e
A
A
P
C
is
th
e
a
v
e
ra
g
e
A
P
C
a
n
d
is
a

235. w
e
ig
h
te
d
a
v
e
ra
g
e
o
f
th
e
A
P
C
s
o
v
e
r
th
e

236. fi
x
e
d
in
te
rv
a
l
fr
o
m
2
0
1
0
to
2
0
1
4
u
s
in
g
th
e
u

237. n
d
e
rl
y
in
g
J
o
in
p
o
in
t
m
o
d
e
l
fo
r
th
e
p
e
ri

238. o
d
fr
o
m
1
9
9
9
to
2
0
1
4
.
J
o
in
p
o
in
t
m
o
d
e

239. ls
w
it
h
u
p
to
2
jo
in
p
o
in
ts
a
re
b
a
s
e
d
o
n
ra
te

240. s
p
e
r
1
0
0
,0
0
0
p
e
rs
o
n
s
a
n
d
a
g
e
s
ta
n
d

241. a
rd
iz
e
d
to
th
e
2
0
0
0
U
S
s
ta
n
d
a
rd
p
o
p
u
la
ti

242. o
n
(1
9
a
g
e
g
ro
u
p
s
;
C
e
n
s
u
s
P
2
5
-1
1
3
0
).

243. F
o
r
jo
in
p
o
in
t
a
n
a
ly
s
is
,
th
e
J
o
in
p
o
in
t
R

244. e
g
re
s
s
io
n
P
ro
g
ra
m
w
a
s
u
s
e
d
(v
e
rs
io
n
4
.5

245. .0
.1
;
B
e
th
e
s
d
a
,
M
D
:
S
ta
ti
s
ti
c
a
l
R
e
s
e
a

246. rc
h
a
n
d
A
p
p
lic
a
ti
o
n
s
B
ra
n
c
h
,
N
a
ti
o
n
a
l

247. C
a
n
c
e
r
In
s
ti
tu
te
;
J
u
n
e
2
0
1
7
).
g
F
o
r
a
ll

248. s
it
e
s
,
m
y
e
lo
d
y
s
p
la
s
ti
c
s
y
n
d
ro
m
e
s
a
re
in

249. c
lu
d
e
d
fo
r
th
e
ra
te
c
a
lc
u
la
ti
o
n
s
b
u
t
n
o

250. t
fo
r
th
e
A
P
C
c
a
lc
u
la
ti
o
n
s
;
th
e
y
a
re
e
x
c

251. lu
d
e
d
fr
o
m
c
a
n
c
e
r-
s
p
e
c
if
ic
a
n
a
ly
s
is
.
O

252. v
a
ry
e
x
c
lu
d
e
s
b
o
rd
e
rl
in
e
tu
m
o
rs
.
h
T
h
e

253. A
A
P
C
is
s
ta
ti
s
ti
c
a
lly
s
ig
n
if
ic
a
n
tl
y
d
if
fe
re
n
t

254. fr
o
m
z
e
ro
(t
w
o
-s
id
e
d
P
<
.0
5
).
Annual Report National Cancer Statistics/Cronin et al
Cancer July 1, 2018 2791
and larynx, except that rates were stable for bladder cancer
among AIs/ANs, were stable for stomach cancer among
whites and non-Hispanics, and increased for bladder

255. Figure 3. Age-standardized death rates and recent fixed-
interval trends (2011-2015) are illustrated for the 18 most
common cancers in men and the 20 most common cancers
in women, for all races/ethnicities combined, and by sex. The
5-year average annual percent change (AAPC) is based on
the joinpoint trend from 1999 to 2015. An asterisk indicates
that the AAPC is statistically significantly different from zero
(2-sided t test or Z test; P <.05). Rates were age-
standardized to the 2000 US standard population (19 age
groups; Bureau of the Census. Current Population Reports,
Publication 25-1130. Washington, DC: US Government Printing
Office; 2000 [Census P25-1130]). The AAPC is a weighted
average of the annual percent changes over the fixed interval
(2011-2015) using the underlying joinpoint model for the
period from 1999 to 2015. Joinpoint models with up to 3 join-
points are based on rates per 100,000 persons age standard-
ized to the 2000 US standard population (19 age groups;
Census P25-1130). For joinpoint analysis, the Joinpoint
Regression Program was used (version 4.5.0.1; Bethesda, MD:
Statistical Research and Applications Branch, National Cancer
Institute; June 2017).
T
A
B
L
E
2
.
U
S
C

256. a
n
c
e
r
D
e
a
th
R
a
te
s
a
n
d
F
ix
e
d
-I
n
te
rv
a
l

257. T
re
n
d
s
(2
0
11
-2
0
15
)
fo
r
th
e
M
o
s
t
C
o
m
m

258. o
n
C
a
n
c
e
rs
b
y
S
e
x
,
R
a
c
e
,
a
n
d
E
th
n
ic
it

259. y
a
A
ll
R
a
c
e
s
b
W
h
it
e
b
B
la
c
k
b
A
P
Ib
A
I/
A

260. N
(C
H
S
D
A
)b
H
is
p
a
n
ic
b
N
o
n
-H
is
p
a
n
ic
b
S

261. e
x
/C
a
n
c
e
r
S
it
e
o
r
T
y
p
e
c
R
a
n
k
R
a
te
d
2

262. 0
1
0
-2
0
1
5
A
A
P
C
e
P
R
a
n
k
R
a
te
d
2
0
1
1
-2
0

263. 1
5
A
A
P
C
e
P
R
a
n
k
R
a
te
d
2
0
1
1
-2
0
1
5
A
A

264. P
C
e
P
R
a
n
k
R
a
te
d
2
0
1
1
-2
0
1
5
A
A
P
C
e
P

265. R
a
n
k
R
a
te
d
2
0
1
1
-2
0
1
5
A
A
P
C
e
P
R
a
n
k
R

266. a
te
d
2
0
1
1
-2
0
1
5
A
A
P
C
e
P
R
a
n
k
R
a
te
d
2

267. 0
1
1
-2
0
1
5
A
A
P
C
e
P
A
ll
s
it
e
s
f
B
o
th
s
e
x
e

268. s
1
6
3
.5
2
1
.5
f
<
.0
0
1
1
6
3
.8
2
1
.4
f
<
.0
0
1
1
8

269. 9
.8
2
2
.1
f
<
.0
0
1
1
0
1
.3
2
1
.3
f
<
.0
0
1
1
5
0
.4
2

270. 0
.7
f
.0
0
1
1
1
4
.6
2
1
.3
f
<
.0
0
1
1
6
7
.7
2
1
.5
f
<

271. .0
0
1
M
a
le
s
1
9
6
.7
2
1
.8
f
<
.0
0
1
1
9
6
.4
2
1
.6
f

272. <
.0
0
1
2
3
9
.9
2
2
.7
f
<
.0
0
1
1
2
0
.4
2
1
.6
f
<
.0
0

273. 1
1
8
1
.4
2
0
.6
f
.0
0
9
1
4
0
.0
2
1
.6
f
<
.0
0
1
2
0
1

274. .4
2
1
.7
f
<
.0
0
1
F
e
m
a
le
s
1
3
9
.5
2
1
.4
f
<
.0
0
1

275. 1
4
0
.0
2
1
.3
f
<
.0
0
1
1
5
9
.0
2
1
.6
f
<
.0
0
1
8
7
.7

276. 2
1
.0
f
<
.0
0
1
1
2
7
.6
2
1
.4
f
<
.0
0
1
9
6
.7
2
1
.0

277. f
<
.0
0
1
1
4
3
.4
2
1
.4
f
<
.0
0
1
M
a
le
s
L
u
n
g
a
n

278. d
b
ro
n
c
h
u
s
1
5
3
.8
2
3
.8
f
<
.0
0
1
1
5
3
.9
2
3
.7

279. f
<
.0
0
1
1
6
5
.1
2
4
.4
f
<
.0
0
1
1
3
1
.0
2
2
.9
f
<
.0

280. 0
1
1
4
5
.0
2
1
.1
f
.0
0
9
1
2
6
.4
2
3
.0
f
<
.0
0
1
1
5

281. 6
.2
2
3
.7
f
<
.0
0
1
P
ro
s
ta
te
2
1
9
.5
2
2
.2
f
.0
1
2

282. 1
8
.2
2
1
.9
f
.0
2
2
3
9
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316. 0
3
Original Article
2792 Cancer July 1, 2018
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414. e
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454. it
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l.
Annual Report National Cancer Statistics/Cronin et al
Cancer July 1, 2018 2793
cancer among blacks. Incidence rates among men
increased in each racial and ethnic group for leukemia,
myeloma, and cancers of the kidney, thyroid, pancreas,
and liver, except that rates were stable for kidney and liver
cancers among Hispanics and for leukemia, myeloma,
and pancreas cancer among AIs/ANs.
Among women, overall cancer incidence rates inc-
reased during 2010 to 2014 among blacks, APIs, and AIs/
ANs but remained stable in whites, Hispanics, and non-
Hispanics. Incidence rates increased for female breast can-

455. cer in each racial and ethnic group (Table 1). Incidence
rates among women also increased for cancers of the thy-
roid, liver, and uterus in each racial and ethnic group,
except that rates remained stable for thyroid cancer and
liver cancer among APIs. Incidence rates among women
decreased for lung and bronchus cancer and colorectal
cancer in each racial and ethnic group, except that rates
were stable for lung and bronchus cancer among APIs and
for colorectal cancer among Hispanics. As with men, for
most cancer sites incidence trends for women in each
racial and ethnic group were similar in direction to those
for all women combined.
Current Cancer Death Rates and Trends by Sex,
Race, and Ethnicity
Average annual death rates and trends from 2011 to 2015
are presented by cancer site, sex, race, and ethnicity in
Table 2. For all cancer sites combined, similar to inci-
dence rates, death rates (per 100,000 persons) were higher
among men than among women overall (196.7 vs 139.5
for all races/ethnicities combined) and in every racial and
ethnic group. Black men and black women had the high-
est cancer death rates of any racial group for all cancer sites
combined, for 8 of the most common cancers in men, and
for 9 of the most common cancers in women. Non-
Hispanic men and women had higher overall cancer death
rates than those of Hispanic ethnicity. Among men, lung
and bronchus cancer was the leading cause of cancer death
in every racial and ethnic group, followed by prostate and
colorectal cancer in black, white, and Hispanic men; liver
and colorectal cancer in API men; and colorectal and
prostate cancer in AI/AN men. Among women, lung and
bronchus, breast, and colorectal cancers were the leading
causes of cancer death in every racial and ethnic group
except Hispanics, in whom breast cancer replaced lung

456. and bronchus cancer as the leading cause.
During 2011 to 2015, death rates declined overall
and for the most common cancers (lung and bronchus,
prostate, colorectal, breast) among men and women in all
racial and ethnic groups, except that breast cancer death
rates were stable among API and AI/AN women, colorec-
tal cancer death rates were stable among AI/AN men and
women, and prostate cancer death rates were stable among
AI/AN men (Table 2). Death rates for most of the other
cancer sites declined or were stable among men and
women in each racial and ethnic group. However, death
rates increased for some cancers in some racial and ethnic
groups: liver cancer in white men and women, black
women, AI/AN men, Hispanic women, and non-
Hispanic men and women; pancreas cancer in white men
and women and non-Hispanic men and women; uterus
cancer in white, black, API, Hispanic, and non-Hispanic
women; brain cancer in white men and women, non-
Hispanic men and women, and API women; oral cavity
and pharynx cancer in white men and non-Hispanic men;
nonmelanoma skin cancer in white men and non-
Hispanic men; and soft tissue (including heart) cancer in
white men and non-Hispanic men and women.
Incidence and Mortality Trends, Survival by
Stage, and Stage at Diagnosis for Female
Breast Cancer, Colorectal Cancer, Lung and
Bronchus Cancer, and Melanoma of the Skin
Figure 4 illustrates delay-adjusted incidence (1999-2014)
and mortality (1999-2015) trends, 5-year survival esti-
mates by stage (2007-2013), and the stage distribution at
diagnosis for female breast cancer, colorectal cancer, lung
and bronchus cancer, and melanoma of the skin. We focus

457. on these 4 cancer sites because they are among the 5 sites
that have the highest number of expected cases in 2017.41
In addition to these 4 cancer sites, prostate cancer is
among the top 5 sites based on the number of expected
cases, but we do not include prostate cancer here because
it is examined in detail in Part II of this report.
Female breast cancer incidence had been declining
before 2004 but has increased since then at an average rate
of 0.4% per year (Supporting Table 1). Female breast can-
cer mortality decreased during 1999 to 2015 (Supporting
Table 2). Seventy-eight percent of cases were diagnosed at
stage I or II, for which 5-year survival was high (100%
and 92%, respectively) (Fig. 4). Approximately 6% of
cases were diagnosed at stage IV, for which 5-year survival
was 26.5%.
Colorectal cancer incidence rates decreased during
1999 to 2012 among men and women, although rates
have been stable since 2012 (Supporting Table 1). Colo-
rectal cancer mortality decreased during 1999 to 2015
among men and women (Supporting Table 2). Five-year
survival for colorectal cancer (men and women combined)
varied from 88.1% for cases diagnosed at stage I (23% of
Original Article
2794 Cancer July 1, 2018
cases) to 12.6% for cases diagnosed at stage IV (20% of
cases) (Fig. 4).
Lung and bronchus cancer incidence and mortality

458. rates remain higher among men than among women, but
men have experienced a longer and more pronounced
decrease in both rates over time (Fig. 4, Supporting Tables
1 and 2). Among women, lung and bronchus cancer inci-
dence decreased during 2006 to 2014, and lung and bron-
chus cancer mortality decreased during 2002 to 2015
(Supporting Tables 1 and 2). Lung and bronchus cancer
survival (men and women combined) was low, ranging
from 55.1% for stage I (21% of cases) to 4.2% for cases
diagnosed at stage IV (44% of cases) (Fig. 4).
The incidence of melanoma of the skin increased
substantially since 1999 among men and among
women, although the rates of increase among women
began slowing in 2005 (Fig. 4 and Supporting Table
1). Melanoma mortality was stable during 1999 to
2015 in women; in men, it was stable during 2009 to
2013 and decreased during 2013 to 2015 (Supporting
Table 2). Sixty-two percent of cases were diagnosed
with stage I disease and 12% were diagnosed with stage
II disease, for which the 5-year survival rates were
99.5% and 75%, respectively. Four percent were diag-
nosed at stage IV, for which the 5-year survival rate was
16% (Fig. 4).
Figure 4. Delay-adjusted incidence (1999-2014) and mortality
(1999-2015) trends, 5-year survival estimates by stage (2007-
2013), and stage distribution at diagnosis are illustrated for (A)
female breast cancer, (B) colon and rectum cancer, (C) lung and
bronchus cancer, and (D) melanoma of the skin. Rates were age-
standardized to the 2000 US standard population (19 age
groups; Bureau of the Census. Current Population Reports,
Publication 25-1130. Washington, DC: US Government Printing
Office;
2000 [Census P25-1130]). Scattered points indicate observed
rates, and lines are fitted rates according to joinpoint

459. regression.
Incidence rates were delay-adjusted and covered 89% of the US
population, and mortality covered the entire United States. The
following registries were included for incidence: Alabama,
Alaska, Arizona, Arkansas, California, Colorado, Connecticut,
Delaware,
Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa,
Kentucky, Louisiana, Maine, Maryland, Massachusetts,
Michigan, Missouri,
Montana, Nebraska, New Hampshire, New Jersey, New York,
North Carolina, North Dakota, Ohio, Oklahoma, Oregon,
Pennsylva-
nia, Rhode Island, South Carolina, Texas, Utah, Vermont,
Washington, West Virginia, Wisconsin, and Wyoming.
Joinpoint models
with up to 2 joinpoints for incidence and up to 3 joinpoints for
mortality are based on rates per 100,000 persons age standard-
ized to the 2000 US standard population (19 age groups; Census
P25-1130). For joinpoint analysis, the Joinpoint Regression Pro-
gram was used (version 4.5.0.1; Bethesda, MD: Statistical
Research and Applications Branch, National Cancer Institute;
June
2017). Five-year relative survival rates covered 69.5% of the
US population. The following registries were included for
survival:
Alabama, Alaska, Arizona, California, Colorado, Connecticut,
Delaware, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana,
Iowa, Ken-
tucky, Louisiana, Maine, Maryland, Michigan, Montana,
Nebraska, New Hampshire, New Jersey, New York, North
Carolina, Pennsyl-
vania, Rhode Island, South Carolina, Utah, Vermont, Seattle,
West Virginia, Wisconsin, and Wyoming.
Annual Report National Cancer Statistics/Cronin et al

460. Cancer July 1, 2018 2795
Cancer Incidence and Mortality Among Children
The most common cancer sites for children vary by age.
Overall, the most common sites are leukemia, brain and
other nervous system, soft tissue, NHL, and kidney and
renal pelvis. Bone and joint cancer and Hodgkin lym-
phoma are more common in older children. Among chil-
dren ages birth to 14 years, the average annual, age-
standardized, delay-adjusted incidence rates (all cancer
types combined; per 100,000 persons) during 2010 to
2014 ranged from 12.6 among AIs/ANs to 17.3 among
whites (both sexes combined) (Table 3). The average,
annual age-standardized death rates during 2011 to 2015
ranged from 1.7 among APIs to 2.2 among whites. Inci-
dence rates increased during 2010 to 2014 for all racial/
ethnic groups combined (0.8% per year) and among chil-
dren in 4 racial/ethnic groups (APIs, 1.1% per year; non-
Hispanics, 1.0% per year; whites, 0.7% per year; and His-
panics, 0.4% per year). Among AI/AN and black chil-
dren, incidence rates were stable. In contrast, death rates
among children during 2011 to 2015 decreased overall
(21.5% per year; all races/ethnicities combined) and
among children in every racial and ethnic group, except
that the AAPC for AIs/ANs could not be calculated
because of sparse data (Table 3). The greatest decrease in
cancer mortality was observed among API children
(22.4%), and the smallest decreases were among white
children and non-Hispanic children (21.4% in each
group).
DISCUSSION

461. Cancer incidence rates for all races/ethnicities combined
continued to decline among men and were stable among
women. Incidence rates from 2010 to 2014 decreased for
7 of the 17 most common cancers among men and for 7
of the 18 most common cancers among women, and rates
increased for 8 cancer sites among men and 10 sites
among women.
The largest increases in incidence rates were ob-
served for liver cancer, myeloma, melanoma of the skin,
thyroid cancer, and leukemia. Additional cancers with ris-
ing incidence trends during the most recent years include
kidney and female breast. The increase in thyroid cancer
incidence rates is largely thought to be caused by increased
detection of small and indolent tumors through imag-
ing42,43; however, the rates increased for both small and
large tumors, suggesting a role for unidentified risk factors
TABLE 3. Delay-Adjusted Childhood Cancer Incidence Rates
for Areas With High-Quality Data and US
Childhood Cancer Death Rates by Race/Ethnicity, Both Sexes
Combined, and Their Fixed-Interval Trendsa,b
Children: Ages 0-14 Yearsc
Incidence (2010-2014) Mortality (2011-2015)
Race/Ethnicityd Ratee AAPCf 95% CI P Ratee AAPCf 95% CI P
All races 16.6 0.8g 0.6, 1.0 < .001 2.1 21.5g 21.8, 21.2 < .001
White 17.3 0.7g 0.5, 0.9 < .001 2.2 21.4g 21.7, 21.0 < .001
Black 12.9 21.1 23.7, 1.3 .30 2.0 21.6g 22.1, 21.0 < .001
API 13.7 1.1g 0.4, 1.7 .004 1.7 22.4g 23.9, 21.0 .003

462. AI/AN CHSDA 12.6 20.1 21.4, 1.2 .84 1.9 —h
Hispanic 16.1 0.4g 0.1, 0.6 .02 2.1 22.0g 22.5, 21.5 < .001
Non-Hispanic 16.8 1.0g 0.8, 1.1 < .001 2.1 21.4g 21.7, 21.0 <
.001
Abbreviations: AAPC, average annual percent change; AI/AN,
American Indian/Alaska Native; API, Asian/Pacific Islander;
CHSDA, Indian Health Service Con-
tract Health Services Delivery Area; CI, confidence interval.
a Source: National Program of Cancer Registries and
Surveillance, Epidemiology, and End Results areas reported by
the North American Association of Central
Cancer Registries as meeting high-quality incidence data
standards for the specified time periods.
b The following registries were included in the incidence rates
(2010-2014) and Joinpoint models (1999-2014) for all
race/ethnicities, white, black, AI/AN, API,
Hispanic, and non-Hispanic (42 states): Alabama, Alaska,
Arizona, Arkansas, California, Colorado, Connecticut,
Delaware, Florida, Georgia, Hawaii, Idaho, Illi-
nois, Indiana, Iowa, Kentucky, Louisiana, Maine, Maryland,
Massachusetts, Michigan, Missouri, Montana, Nebraska, New
Hampshire, New Jersey, New York,
North Carolina, North Dakota, Ohio, Oklahoma, Oregon,
Pennsylvania, Rhode Island, South Carolina, Texas, Utah,
Vermont, Washington, West Virginia, Wis-
consin, and Wyoming.

463. c For incidence, AI/AN (CHSDA 2012) statistics exclude data
from Kansas.
d White, black, API, and AI/AN (CHSDA 2012 counties)
include Hispanic and non-Hispanic; the race and ethnicity
categories are not mutually exclusive.
e Rates are per 100,000 persons and were age standardized to
the 2000 US standard population (19 age groups US Bureau of
the Census. Current Population
Reports, Publication 25-1130. Washington, DC: US Government
Printing Office; 2000 [Census P25-1130]).
f The AAPC is the average APC and is a weighted average of
the APCs over the fixed interval (2009-2013 for incidence;
2010-2014 for mortality) using the
underlying Joinpoint model for the period from 1999 to 2014 for
incidence and the period from 1999 to 2015 for mortality.
Joinpoint models with up to 2 join-
points for incidence and up to 3 joinpoints for mortality were
based on rates per 100,000 persons that were age standardized
to the 2000 US standard popula-
tion (19 age groups; Census P25-1130). For joinpoint analysis,
the Joinpoint Regression Program was used (version 4.5.0.1;
Bethesda, MD: Statistical
Research and Applications Branch, National Cancer Institute;
June 2017).
g The AAPC is statistically significantly different from zero (2-
sided P <.05).
h The statistic could not be calculated. The average APC is
based on <10 cases for at least 1 year within the time interval.
Original Article

464. 2796 Cancer July 1, 2018
in the rising trend.44,45 It is believed that the increase in
kidney cancer incidence rates in part reflects increased
detection resulting from wider application of imaging
techniques46 as well as the obesity epidemic.14 For all can-
cer sites combined, men had higher incidence rates than
women within every racial and ethnic group. Overall,
black men and white women had higher rates than other
racial groups, and non-Hispanic men and women had
higher rates than Hispanic individuals. These racial and
ethnic differences were driven largely by the incidence of
prostate cancer, female breast cancer, and lung cancer.
The increase in the breast cancer incidence rate con-
tinues the 0.4% increase observed in last year’s report.19
After decreasing in the early 2000s after cessation of
hormone-replacement therapy,47,48 the increase from
2004 to 2014 may in part reflect the obesity epidemic.17
Increased detection through mammography is unlikely to
have contributed to the recent trend, because mammogra-
phy rates remained unchanged during the corresponding
period.49 The continued increase in melanoma incidence
rates is thought to reflect increased harmful recreational
sun exposure and tanning bed use, as well as increased
detection.50 The survival rates for early stage breast cancer
and melanoma of the skin are extremely high (100% and
99.5% for stage I breast cancer and melanoma, respec-
tively), suggesting the influence of screening on survival.
These high survival rates may result from a combination
of better prognosis because of early detection, some level
of overdiagnosis associated with screening, and individu-

465. als with screen-detected disease being healthier than the
general population.51
Overall cancer death rates have continued to dec-
rease among both men and women for all major racial and
ethnic groups, with the greatest decrease among black
men and the smallest among AI/AN men. From 2011 to
2015, death rates for all races/ethnicities combined
decreased for 11 of the 18 most common cancers among
men and for 14 of the 20 most common cancers among
women, including lung and bronchus (men and women),
colorectal (men and women), female breast, and prostate.
In contrast, cancer death rates increased for liver, pan-
creas, and brain and other nervous system among men
and women; for oral cavity and pharynx, nonmelanoma
skin, and soft tissue (including heart) among men; and for
uterus among women. Black men and black women had
the highest cancer death rates of any racial group during
the most recent 5-year period. Except for female lung can-
cer, black men and black women had the highest death
rates for cancer sites with the highest mortality in the over-
all population: lung, prostate, female breast, colorectal,
and pancreas. Non-Hispanic men and women had higher
overall cancer death rates than men and women of His-
panic ethnicity.
Factors that have contributed to the continued
decreases in cancer death rates for the 4 most common
cancers have been discussed in previous reports.14-19
Briefly, the sustained decrease in lung and bronchus can-
cer death rates since the early 1990s among men and since
the early 2000s among women has been attributed to the
reduction in cigarette smoking over the past 5 decades.11