Understanding Scans 101

Melanoma Research Foundation
Melanoma Research FoundationAccount Director at Melanoma Research Foundation
Radiology Basics
David J. Eschelman, M.D., FSIR
Professor of Radiology,
Sidney Kimmel Medical College of Thomas Jefferson University
Co-Director of Interventional Radiology,
Thomas Jefferson University Hospital
So what is a radiologist?
So what is an
interventional radiologist?
Imaging Modalities
• CT (computed tomography)
• US (ultrasound)
• MRI
(magnetic resonance imaging)
• PET-CT
(positron emission tomography)
CT
• Pros:
– Available everywhere, consistent quality, best option
for whole-body evaluation
– Fast
• Cons:
– Less sensitive for small liver metastases than MRI
– Radiation (10-15 mSv)
Chest CT – Lung Metastases
Ultrasound
• Pros:
– Relatively inexpensive.
– No radiation.
– Can be very sensitive for small lesions
• Cons:
– Variable quality, depending on site and on patient.
– Not useful for whole-body surveillance.
Biopsy
MRI
• Pros:
– Most sensitive for liver mets.
– No radiation. No known harmful effects
• Cons:
– Does not cover entire body
– Can’t use in SOME people with pacers, anxiety, etc.
– Variability in how studies are done.
– Slow, noisy, easily affected by motion, etc.
Understanding Scans 101
Understanding Scans 101
8/11/2010
10/27/2010
12/23/2010
4/09/2010
MRI is better than CT (another example)
CT
MRI
MRI is better than CT (yet another example)
CT MRI
PET-CT
PET - CT
• Pros
– Unique: Images metabolic activity
– May give information about efficacy of treatment
• Cons
– Not universally available
– Expensive
– Not sensitive for small metastases
– Takes about 2 hours
– Radiation (30 mSv)
Understanding Scans 101
Surveillance Imaging
• Surveillance Scheduling
– No consensus: Varies from center to center
– Depends on tumor histology and genetics
• Jefferson protocol
– Low/intermediate risk: MRI q6-12 mo, CXR q12 mo
for 5 years
– High risk: MRI q3 mo + CT chest q 6 mo for 2 years,
then MRI q6 mo + CT q 12 mo for 3 years
NCCN Guidelines v1.2018
RISK OF DISTANT METASTASIS -
Low risk:
• Class 1A(x)
• Disomy 3
• Gain of chromosome 6p
• EIF1AX mutation
• T1 (AJCC) (See ST-1 and ST-2)
• Spindle cells
SYSTEMIC IMAGING BASED ON RISK STRATIFICATION
• Imaging to evaluate signs or symptoms as clinically indicated
• Consider surveillance imaging(y)
NCCN Guidelines v1.2018
RISK OF DISTANT METASTASIS -
Medium risk:
• Class 1B(x)
• SF3B1 mutation
• T2 and T3 (AJCC) (See ST-1 and ST-2)
• Mixed histology (spindle and epithelioid cells)
SYSTEMIC IMAGING BASED ON RISK STRATIFICATION
• Imaging to evaluate signs or symptoms as clinically indicated
• Consider surveillance imaging(y) every 6–12 months for
10 years, then as clinically indicated
NCCN Guidelines v1.2018
RISK OF DISTANT METASTASIS -
High risk:
• Class 2(x) • PRAME mutation
• Monosomy 3 • Epithelioid cells
• Gain of chromosome 8q • Extraocular extension
• BAP1 mutation • Ciliary body involvement
• T4 (AJCC) (See ST-1 and ST-2)
SYSTEMIC IMAGING BASED ON RISK STRATIFICATION
• Imaging to evaluate signs or symptoms as clinically indicated
• Consider surveillance imaging(y) every 3-6 months for 5 years,
then every 6-12 months for 10 years, then as clinically
indicated
NCCN Guidelines v1.2018
Surveillance:
The most frequent sites of metastasis are liver, lungs, skin/soft tissue,
and bones. At minimum, all patients should have contrast-enhanced MR
or ultrasound of the liver, with modality preference determined by
expertise at the treating institution. Additional imaging modalities may
include chest/abdominal/pelvic CT with contrast. However, screening
should limit radiation exposure whenever possible. Scans should be
performed with IV contrast unless contraindicated.
. . . . . but also add:
(y) Recognizing that there are limited options for systemic recurrence and
that regular imaging may cause patient anxiety, some patients may elect
to forgo surveillance imaging.
Background Radiation
Sources:
• Cosmic radiation
• Naturally occurring radioactive materials (radon, radium)
• Fallout
Exposure in US:
• Approximately 3 mSv/yr (low altitude)
• 30-50% higher in Denver
• Transatlantic flight – 0.08 mSv (2-3x higher over poles)
• 2x higher in US Capitol (8 hrs/day) – granite, marble
Radiation
Imaging Examples Effective Dose Range
(mSv)
Background Equivalent
Radiation Time
Radiation Risk Descriptora Probability of Cancer From
Imaging (%)
Probability of No Cancer
From Imaging (%)
CT scan or nuclear
medicine scan
1-10 Years Minor ∼0.05 ∼99.95
Abdominal radiograph 0.1-1 Months Minimal ∼0.005 ∼99.995
Chest radiograph or
mammogram
< 0.1-0.1 Days to weeks Negligible ∼0.0005 ∼99.9995
aDescriptors are from [78]
Dauer L et al. AJR 2011, 196
Brenner: DJ, Hall EJ: Computed Tomography — An Increasing Source of
Radiation Exposure. N Engl J Med 357:2277, November 29, 2007
Contrast Risks
• CT contrast and MR contrast are completely
unrelated materials
• Risk of reaction to CT contrast is very low
(0.15%)
• Risk of reaction to MR contrast is extremely low
(0.04%)
• Most reactions are minor
Contrast Reactions
Contrast and Renal Insufficiency
CT: “Contrast nephropathy”
MR: NSF
FDA Drug Safety Communication:
FDA warns that gadolinium-based
contrast agents (GBCAs) are
retained in the body; requires new
class warnings
May 22, 2017, updated December 19,2017
Gadolinium Contrast for MRI
• Per FDA:
Gadolinium retention has not been directly linked
to adverse health effects in patients with normal
kidney function, and we have concluded that the
benefit of all approved GBCAs continues to
outweigh any potential risks.
• Linear vs. macrocyclic
• Eovist is one of the lower linear “accumulators”
(lower dose administered, excreted by kidneys
and liver, more stable than other linear agents)
RECIST Criteria
Complete Response (CR)
Disappearance of liver lesions
Partial Response (PR)
> 30% decrease in the sum of the longest diameters
(“sum LD”) relative to baseline sum
Stable Disease (SD)
Absence of change which would qualify as
response or progression
Progression (PD)
> 20% increase in the sum LD in liver lesions OR
appearance of one or more new liver lesions
Initial Presentation
MRI was normal 6 months ago
Rapid Growth without Treatment
12/17/2013
4/30/2014 6/2/2014
Any Questions?
1 of 36

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Understanding Scans 101

  • 1. Radiology Basics David J. Eschelman, M.D., FSIR Professor of Radiology, Sidney Kimmel Medical College of Thomas Jefferson University Co-Director of Interventional Radiology, Thomas Jefferson University Hospital
  • 2. So what is a radiologist?
  • 3. So what is an interventional radiologist?
  • 4. Imaging Modalities • CT (computed tomography) • US (ultrasound) • MRI (magnetic resonance imaging) • PET-CT (positron emission tomography)
  • 5. CT • Pros: – Available everywhere, consistent quality, best option for whole-body evaluation – Fast • Cons: – Less sensitive for small liver metastases than MRI – Radiation (10-15 mSv)
  • 6. Chest CT – Lung Metastases
  • 7. Ultrasound • Pros: – Relatively inexpensive. – No radiation. – Can be very sensitive for small lesions • Cons: – Variable quality, depending on site and on patient. – Not useful for whole-body surveillance.
  • 9. MRI • Pros: – Most sensitive for liver mets. – No radiation. No known harmful effects • Cons: – Does not cover entire body – Can’t use in SOME people with pacers, anxiety, etc. – Variability in how studies are done. – Slow, noisy, easily affected by motion, etc.
  • 16. MRI is better than CT (another example) CT MRI
  • 17. MRI is better than CT (yet another example) CT MRI
  • 19. PET - CT • Pros – Unique: Images metabolic activity – May give information about efficacy of treatment • Cons – Not universally available – Expensive – Not sensitive for small metastases – Takes about 2 hours – Radiation (30 mSv)
  • 21. Surveillance Imaging • Surveillance Scheduling – No consensus: Varies from center to center – Depends on tumor histology and genetics • Jefferson protocol – Low/intermediate risk: MRI q6-12 mo, CXR q12 mo for 5 years – High risk: MRI q3 mo + CT chest q 6 mo for 2 years, then MRI q6 mo + CT q 12 mo for 3 years
  • 22. NCCN Guidelines v1.2018 RISK OF DISTANT METASTASIS - Low risk: • Class 1A(x) • Disomy 3 • Gain of chromosome 6p • EIF1AX mutation • T1 (AJCC) (See ST-1 and ST-2) • Spindle cells SYSTEMIC IMAGING BASED ON RISK STRATIFICATION • Imaging to evaluate signs or symptoms as clinically indicated • Consider surveillance imaging(y)
  • 23. NCCN Guidelines v1.2018 RISK OF DISTANT METASTASIS - Medium risk: • Class 1B(x) • SF3B1 mutation • T2 and T3 (AJCC) (See ST-1 and ST-2) • Mixed histology (spindle and epithelioid cells) SYSTEMIC IMAGING BASED ON RISK STRATIFICATION • Imaging to evaluate signs or symptoms as clinically indicated • Consider surveillance imaging(y) every 6–12 months for 10 years, then as clinically indicated
  • 24. NCCN Guidelines v1.2018 RISK OF DISTANT METASTASIS - High risk: • Class 2(x) • PRAME mutation • Monosomy 3 • Epithelioid cells • Gain of chromosome 8q • Extraocular extension • BAP1 mutation • Ciliary body involvement • T4 (AJCC) (See ST-1 and ST-2) SYSTEMIC IMAGING BASED ON RISK STRATIFICATION • Imaging to evaluate signs or symptoms as clinically indicated • Consider surveillance imaging(y) every 3-6 months for 5 years, then every 6-12 months for 10 years, then as clinically indicated
  • 25. NCCN Guidelines v1.2018 Surveillance: The most frequent sites of metastasis are liver, lungs, skin/soft tissue, and bones. At minimum, all patients should have contrast-enhanced MR or ultrasound of the liver, with modality preference determined by expertise at the treating institution. Additional imaging modalities may include chest/abdominal/pelvic CT with contrast. However, screening should limit radiation exposure whenever possible. Scans should be performed with IV contrast unless contraindicated. . . . . . but also add: (y) Recognizing that there are limited options for systemic recurrence and that regular imaging may cause patient anxiety, some patients may elect to forgo surveillance imaging.
  • 26. Background Radiation Sources: • Cosmic radiation • Naturally occurring radioactive materials (radon, radium) • Fallout Exposure in US: • Approximately 3 mSv/yr (low altitude) • 30-50% higher in Denver • Transatlantic flight – 0.08 mSv (2-3x higher over poles) • 2x higher in US Capitol (8 hrs/day) – granite, marble
  • 27. Radiation Imaging Examples Effective Dose Range (mSv) Background Equivalent Radiation Time Radiation Risk Descriptora Probability of Cancer From Imaging (%) Probability of No Cancer From Imaging (%) CT scan or nuclear medicine scan 1-10 Years Minor ∼0.05 ∼99.95 Abdominal radiograph 0.1-1 Months Minimal ∼0.005 ∼99.995 Chest radiograph or mammogram < 0.1-0.1 Days to weeks Negligible ∼0.0005 ∼99.9995 aDescriptors are from [78] Dauer L et al. AJR 2011, 196
  • 28. Brenner: DJ, Hall EJ: Computed Tomography — An Increasing Source of Radiation Exposure. N Engl J Med 357:2277, November 29, 2007
  • 29. Contrast Risks • CT contrast and MR contrast are completely unrelated materials • Risk of reaction to CT contrast is very low (0.15%) • Risk of reaction to MR contrast is extremely low (0.04%) • Most reactions are minor
  • 30. Contrast Reactions Contrast and Renal Insufficiency CT: “Contrast nephropathy” MR: NSF
  • 31. FDA Drug Safety Communication: FDA warns that gadolinium-based contrast agents (GBCAs) are retained in the body; requires new class warnings May 22, 2017, updated December 19,2017
  • 32. Gadolinium Contrast for MRI • Per FDA: Gadolinium retention has not been directly linked to adverse health effects in patients with normal kidney function, and we have concluded that the benefit of all approved GBCAs continues to outweigh any potential risks. • Linear vs. macrocyclic • Eovist is one of the lower linear “accumulators” (lower dose administered, excreted by kidneys and liver, more stable than other linear agents)
  • 33. RECIST Criteria Complete Response (CR) Disappearance of liver lesions Partial Response (PR) > 30% decrease in the sum of the longest diameters (“sum LD”) relative to baseline sum Stable Disease (SD) Absence of change which would qualify as response or progression Progression (PD) > 20% increase in the sum LD in liver lesions OR appearance of one or more new liver lesions
  • 34. Initial Presentation MRI was normal 6 months ago
  • 35. Rapid Growth without Treatment 12/17/2013 4/30/2014 6/2/2014