This document discusses the basics of radiotherapy treatment plan evaluation. It covers topics such as defining the gross tumor volume (GTV), clinical target volume (CTV), planning target volume (PTV) and organs at risk (OAR). It describes dose volume histograms (DVHs) and how to analyze metrics like the median dose, minimum and maximum doses received by the target and OARs. Other areas covered include isodose lines, equivalent radiation, conformity and homogeneity indices, and ensuring appropriate dose coverage of the target while sparing OARs. The document emphasizes balancing target coverage with OAR protection in treatment plan evaluation.
The vmat vs other recent radiotherapy techniquesM'dee Phechudi
VMAT is a new type of intensity-modulated radiation therapy (IMRT) treatment technique that uses the same hardware (i.e. a digital linear accelerator) as used for IMRT or conformal treatment, but delivers the radiotherapy treatment using a rotational or arc geometry rather than several static beams.
This technique uses continuous modulation (i.e. moving the collimator leaves) of the multileaf collimator (MLC) fields, continuous change of the fluence rate (the intensity of the X rays) and gantry rotation speed across a single or multiple 360 degree rotations
This seminar is presented as a part of weekly journal club and seminar presented in Apollo Hospital,Kolkata Department of Radiation Oncology.This seminar is moderated by Dr Tanweer Shahid.
The vmat vs other recent radiotherapy techniquesM'dee Phechudi
VMAT is a new type of intensity-modulated radiation therapy (IMRT) treatment technique that uses the same hardware (i.e. a digital linear accelerator) as used for IMRT or conformal treatment, but delivers the radiotherapy treatment using a rotational or arc geometry rather than several static beams.
This technique uses continuous modulation (i.e. moving the collimator leaves) of the multileaf collimator (MLC) fields, continuous change of the fluence rate (the intensity of the X rays) and gantry rotation speed across a single or multiple 360 degree rotations
This seminar is presented as a part of weekly journal club and seminar presented in Apollo Hospital,Kolkata Department of Radiation Oncology.This seminar is moderated by Dr Tanweer Shahid.
ICRU 83 report on dose prescription in IMRTAnagha pachat
this slide is about the report 83 which is published by international commission for units and measurements on the topic dose prescription reporting and recording in intensity modulated radiation therapy . it is useful for personals and students in the field of radiation oncology.
EBCTCG METAANALYSIS
INDICATION OF POST OP RADIOTHERAPY
Immobilization devices
Conventional planning
Alignment of the Tangential Beam with the Chest Wall Contour
Doses To Heart & Lung By Tangential Fields
ICRU 83 report on dose prescription in IMRTAnagha pachat
this slide is about the report 83 which is published by international commission for units and measurements on the topic dose prescription reporting and recording in intensity modulated radiation therapy . it is useful for personals and students in the field of radiation oncology.
EBCTCG METAANALYSIS
INDICATION OF POST OP RADIOTHERAPY
Immobilization devices
Conventional planning
Alignment of the Tangential Beam with the Chest Wall Contour
Doses To Heart & Lung By Tangential Fields
Assessing the Dosimetric Links between Organ-At-Risk Delineation Variability ...Wookjin Choi
Purpose: To determine the relative dosimetric impact of delineation variability (DV) when inter-observer and inter-technique planning variability (PV), and setup variability (SV) with are considered.
Methods: 409 plans for a single head-and-neck patient from the 2017 Radiation Knowledge plan competition were used. Plans were created with Eclipse (N=227), Pinnacle (N=49), RayStation (N=25), Monaco (N=75), and TomoTherapy (N=33) with delivery techniques conventional linac IMRT (N=142), volumetric modulated arc therapy (VMAT, N=234), and helical TomoTherapy (N=33). All plans were optimized using a consistent set of target volumes and a single OAR structure set. Four additional OAR structure sets were contoured by radiation oncologists (N=2) and medical physics residents (N=2) who had completed head-and-neck contouring training. Probabilistic DVHs, dose-volume coverage maps (DVCM), which shows the probability of achieving a dose metric, were computed for each OAR on the following scenarios: SV alone (N=1000), SV+PV (N=1000*409), SV+DV (N=1000*5), SV+PV+DV (total variability [TV], N=1000*409*5). Analysis focused on the probability of exceeding the maximum dose constraint exceeded 5% for each OAR.
Results: The primary source of variability was PV, which was expected due to inter-observer planning abilities and preferences during the optimization planning process, even when all participants utilized the same constraints. The parotid had the most significant interquartile range (IQR) on the PV scenario. Conversely, adding SV, DV, and TV each reduced the IQR, showing a washing out effect on the DVCM.
Conclusion: Assessment of OAR sensitivity to DV will be highly sensitive to the specific planning technique and planner, likely requiring plan-specific assessment of in-tolerance delineation variations. Incorporation SV and DV variabilities in plan assessments washes out their relative impacts on maximum dose.
These lecture slides, by Dr Sidra Arshad, offer a quick overview of physiological basis of a normal electrocardiogram.
Learning objectives:
1. Define an electrocardiogram (ECG) and electrocardiography
2. Describe how dipoles generated by the heart produce the waveforms of the ECG
3. Describe the components of a normal electrocardiogram of a typical bipolar leads (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
Study Resources:
1. Chapter 11, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 9, Human Physiology - From Cells to Systems, Lauralee Sherwood, 9th edition
3. Chapter 29, Ganong’s Review of Medical Physiology, 26th edition
4. Electrocardiogram, StatPearls - https://www.ncbi.nlm.nih.gov/books/NBK549803/
5. ECG in Medical Practice by ABM Abdullah, 4th edition
6. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
micro teaching on communication m.sc nursing.pdfAnurag Sharma
Microteaching is a unique model of practice teaching. It is a viable instrument for the. desired change in the teaching behavior or the behavior potential which, in specified types of real. classroom situations, tends to facilitate the achievement of specified types of objectives.
Lung Cancer: Artificial Intelligence, Synergetics, Complex System Analysis, S...Oleg Kshivets
RESULTS: Overall life span (LS) was 2252.1±1742.5 days and cumulative 5-year survival (5YS) reached 73.2%, 10 years – 64.8%, 20 years – 42.5%. 513 LCP lived more than 5 years (LS=3124.6±1525.6 days), 148 LCP – more than 10 years (LS=5054.4±1504.1 days).199 LCP died because of LC (LS=562.7±374.5 days). 5YS of LCP after bi/lobectomies was significantly superior in comparison with LCP after pneumonectomies (78.1% vs.63.7%, P=0.00001 by log-rank test). AT significantly improved 5YS (66.3% vs. 34.8%) (P=0.00000 by log-rank test) only for LCP with N1-2. Cox modeling displayed that 5YS of LCP significantly depended on: phase transition (PT) early-invasive LC in terms of synergetics, PT N0—N12, cell ratio factors (ratio between cancer cells- CC and blood cells subpopulations), G1-3, histology, glucose, AT, blood cell circuit, prothrombin index, heparin tolerance, recalcification time (P=0.000-0.038). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and PT early-invasive LC (rank=1), PT N0—N12 (rank=2), thrombocytes/CC (3), erythrocytes/CC (4), eosinophils/CC (5), healthy cells/CC (6), lymphocytes/CC (7), segmented neutrophils/CC (8), stick neutrophils/CC (9), monocytes/CC (10); leucocytes/CC (11). Correct prediction of 5YS was 100% by neural networks computing (area under ROC curve=1.0; error=0.0).
CONCLUSIONS: 5YS of LCP after radical procedures significantly depended on: 1) PT early-invasive cancer; 2) PT N0--N12; 3) cell ratio factors; 4) blood cell circuit; 5) biochemical factors; 6) hemostasis system; 7) AT; 8) LC characteristics; 9) LC cell dynamics; 10) surgery type: lobectomy/pneumonectomy; 11) anthropometric data. Optimal diagnosis and treatment strategies for LC are: 1) screening and early detection of LC; 2) availability of experienced thoracic surgeons because of complexity of radical procedures; 3) aggressive en block surgery and adequate lymph node dissection for completeness; 4) precise prediction; 5) adjuvant chemoimmunoradiotherapy for LCP with unfavorable prognosis.
Acute scrotum is a general term referring to an emergency condition affecting the contents or the wall of the scrotum.
There are a number of conditions that present acutely, predominantly with pain and/or swelling
A careful and detailed history and examination, and in some cases, investigations allow differentiation between these diagnoses. A prompt diagnosis is essential as the patient may require urgent surgical intervention
Testicular torsion refers to twisting of the spermatic cord, causing ischaemia of the testicle.
Testicular torsion results from inadequate fixation of the testis to the tunica vaginalis producing ischemia from reduced arterial inflow and venous outflow obstruction.
The prevalence of testicular torsion in adult patients hospitalized with acute scrotal pain is approximately 25 to 50 percent
Prix Galien International 2024 Forum ProgramLevi Shapiro
June 20, 2024, Prix Galien International and Jerusalem Ethics Forum in ROME. Detailed agenda including panels:
- ADVANCES IN CARDIOLOGY: A NEW PARADIGM IS COMING
- WOMEN’S HEALTH: FERTILITY PRESERVATION
- WHAT’S NEW IN THE TREATMENT OF INFECTIOUS,
ONCOLOGICAL AND INFLAMMATORY SKIN DISEASES?
- ARTIFICIAL INTELLIGENCE AND ETHICS
- GENE THERAPY
- BEYOND BORDERS: GLOBAL INITIATIVES FOR DEMOCRATIZING LIFE SCIENCE TECHNOLOGIES AND PROMOTING ACCESS TO HEALTHCARE
- ETHICAL CHALLENGES IN LIFE SCIENCES
- Prix Galien International Awards Ceremony
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Explore natural remedies for syphilis treatment in Singapore. Discover alternative therapies, herbal remedies, and lifestyle changes that may complement conventional treatments. Learn about holistic approaches to managing syphilis symptoms and supporting overall health.
Ozempic: Preoperative Management of Patients on GLP-1 Receptor Agonists Saeid Safari
Preoperative Management of Patients on GLP-1 Receptor Agonists like Ozempic and Semiglutide
ASA GUIDELINE
NYSORA Guideline
2 Case Reports of Gastric Ultrasound
Ethanol (CH3CH2OH), or beverage alcohol, is a two-carbon alcohol
that is rapidly distributed in the body and brain. Ethanol alters many
neurochemical systems and has rewarding and addictive properties. It
is the oldest recreational drug and likely contributes to more morbidity,
mortality, and public health costs than all illicit drugs combined. The
5th edition of the Diagnostic and Statistical Manual of Mental Disorders
(DSM-5) integrates alcohol abuse and alcohol dependence into a single
disorder called alcohol use disorder (AUD), with mild, moderate,
and severe subclassifications (American Psychiatric Association, 2013).
In the DSM-5, all types of substance abuse and dependence have been
combined into a single substance use disorder (SUD) on a continuum
from mild to severe. A diagnosis of AUD requires that at least two of
the 11 DSM-5 behaviors be present within a 12-month period (mild
AUD: 2–3 criteria; moderate AUD: 4–5 criteria; severe AUD: 6–11 criteria).
The four main behavioral effects of AUD are impaired control over
drinking, negative social consequences, risky use, and altered physiological
effects (tolerance, withdrawal). This chapter presents an overview
of the prevalence and harmful consequences of AUD in the U.S.,
the systemic nature of the disease, neurocircuitry and stages of AUD,
comorbidities, fetal alcohol spectrum disorders, genetic risk factors, and
pharmacotherapies for AUD.
New Drug Discovery and Development .....NEHA GUPTA
The "New Drug Discovery and Development" process involves the identification, design, testing, and manufacturing of novel pharmaceutical compounds with the aim of introducing new and improved treatments for various medical conditions. This comprehensive endeavor encompasses various stages, including target identification, preclinical studies, clinical trials, regulatory approval, and post-market surveillance. It involves multidisciplinary collaboration among scientists, researchers, clinicians, regulatory experts, and pharmaceutical companies to bring innovative therapies to market and address unmet medical needs.
1. MANAGEMENT OF DIFFUSE GLIOMAS
4/5/2022 1
DR KANHU CHARAN PATRO
MD,DNB(RADIATION ONCOLOGY),MBA,FAROI(USA),PDCR,CEPC
HOD,RADIATION ONCOLOGY
Mahatma Gandhi Cancer Hospital And Research Institute, Visakhapatnam
drkcpatro@gmail.com M-9160470564
Plan evaluation in high technique radiotherapy
19. MANAGEMENT OF DIFFUSE GLIOMAS
4/5/2022 19
Basics of plan evaluation – Michael Goitein
20. 4/5/2022 20
Basics of plan evaluation – PIXEL and VOXEL
In 3D computer graphics, a voxel represents a value on
a regular grid in three-dimensional space. As with pixel in a 2D
22. 4/5/2022 22
Basics of plan evaluation – Differential DVH
1. The generic form of any histogram, displaying the volume of the
organ that receives dose within each bin (1% or 0.5 to 1 Gy is a
typical dose bin width.
2. It is useful for display of the dose to target volumes, because one
can easily visualise the minimum dose, the maximum dose, and
the most representative of the dose to the entire target volume.
24. 0
5
10
15
20
25
30
35
40
0-1.5 1.8 2 2.1
Chart Title
4/5/2022 24
Basics of plan evaluation – differential histo
Dose bin Counts
0-1.5Gy 0
1.8Gy 36
2Gy 18
2.1Gy 26
Total 80
V
O
L
U
M
E
In
CC
Dose in Gy
25. 0
10
20
30
40
50
60
70
80
90
0-1.5 1.8 2 2.1
Chart Title
4/5/2022 25
Basics of plan evaluation – Cumulative Histo
Dose bin Counts Cum
0-1.5Gy 0 80
1.8Gy 36 80
2Gy 18 44
2.1Gy 26 26
Total 80 0
V
O
L
U
M
E
In
CC
Dose in Gy
26. 4/5/2022 26
Basics of plan evaluation – CUMULATIVE DVH
1. Volumes receiving at least a given dose value are ploted.
2. The cumulative DVH integrates the direct histogram, so it
always begins at 100% (100% of the organ receives at least 0
dose)
3. It ends at maximum dose
30. • D50% (Median Dose)
• Most representative of prescribed dose
• Dmean is nearly identical to D50%
• D98% (Near Minimum Dose)
• Dose received by 98% of PTV
• D2% (Near Maximum Dose)
• Dose received by 2% of PTV
4/5/2022 30
Basics of plan evaluation – Defining the dose
36. PUSHING BACKWARD AND FORWARD AT A TIME
DIFFICULT BUT NOT IMPOSSIBLE
OAR
TARGET
36
37. 4/5/2022 37
Basics of plan evaluation – DVH pitfalls
1. Insensitive to hot spot and cold spot
2. Shape of DVH alone can be misleading
3. DVH is the most direct and informative representation of a treatment
plan available
4. 3D dose distribution are large and cumbersome to analyse quantitatively
5. User interactivity is essential to extract the most information from dose
distribution.
6. Clinical studies have shown that DVH metrics correlate with patient
toxicity outcomes.
7. A drawback of the DVH methodology is that it offers no spatial
information; i.e., a DVH does not show where within a structure a
dose is received.
8. Also, DVHs from initial radiotherapy plans represent the doses to
structures at the start of radiation treatment.
9. As treatment progresses and time elapses, if there are changes
(i.e. if patients lose weight, if tumors shrink, if organs change
shape, etc.), the original DVH loses its accuracy
38. MANAGEMENT OF DIFFUSE GLIOMAS
4/5/2022 38
Basics of plan evaluation – plan evaluation
42. 4/5/2022 42
Basics of plan evaluation – dose displaying
1. Isodose Contours: Set of closed contours linking voxels of equal
dose
2. Color Wash: The coding of CT and Dose in the same voxel through
the modulation of both intensity (CT) and color (Dose)
3. Isodose Surfaces: The Shaded surface (pseudo 3D) representation
of the dose level and selected VOI
43. MANAGEMENT OF DIFFUSE GLIOMAS
4/5/2022 43
Basics of plan evaluation – CBCHOP
Mary Dean/Applied Radiation Oncology/2017
44. 4/5/2022 44
Basics of plan evaluation – COSID INDEX
Patro K C/Journal of Current Oncology/2022(UNDER REVIEW)
C
COVERAGE INDEX
O
OAR INDEX
S
SPILLAGE INDEX
I
IMAGING INDEX
D
DELIVERY INDEX
45. 4/5/2022 45
Basics of plan evaluation – Coverage Index
Patro K C/Journal of Current Oncology/2022(UNDER REVIEW)
PTV/CTV/GTV
D2/D98
95-107
46. 4/5/2022 46
Basics of plan evaluation – OAR INDEX
Patro K C/Journal of Current Oncology/2022(UNDER REVIEW)
Max dose in series organ
Mean dose in parallel organ
Volumetric analysis
47. 4/5/2022 47
Basics of plan evaluation – Spillage Index
Patro K C/Journal of Current Oncology/2022(UNDER REVIEW)
Conformity index
Homogeneity index
Gradient index
48. 4/5/2022 48
Basics of plan evaluation – Imaging Index
Patro K C/Journal of Current Oncology/2022(UNDER REVIEW)
Axial view
Coronal view
Sagittal View
49. 4/5/2022 49
Basics of plan evaluation – Delivery index
Patro K C/Journal of Current Oncology/2022(UNDER REVIEW)
Complexity of plan
MU
Complexity of Delivery
51. SL NO PARAMETER VALUE
1 D MAX 36.43Gy
2 D95% 31.01Gy
3 D100% 28.23Gy
4 V95% 99.99%
5 V30 Gy[V100%] 99.56%
6 V110% 44.45%
7 V120% 0.03%
8 V130% 0%
1. Prescription Isodose level is usually not 100% PD covering 100% PTV
2. Often 95% PD covering 95% PTV or higher
3. Or 100% PD covering 95% PTV or higher.
Michael Torrens,/J Neurosurg (Suppl 2)/2014
PTV coverage index
52. • Is your desired defined dose is confined to PTV ?
• FORMULA
• VOLUME OF PRESCRIPTION ISODOSE/PTV VOLUME
• 43.798/37.491=1.17
• DESIRABLE=1
[Sonja Petkovska
Proceedings of the Second
Conference on Medical Physics and
Biomedical Engineering]
RTOG conformity index
53. • FORMULA
(VOLUME OF PRESCRIPTION ISODOSE IN AREA OF INTEREST)2
PTV VOLUME X VOLUME OF PRESCRIPTION ISODOSE
• =39.764 x 39.764 /37.494 x43.798 =0.96
• IDEAL= > 0.85. AND <1
Michael Torrens,/J Neurosurg (Suppl 2)/2014
Paddick conformity index
54. • How homogeneous your dose inside the PTV?
• FORMULA
• MAXIMUM DOSE/PRESCRIPTION DOSE
• 36.43Gy/30Gy=1.21
• DESIRABLE = 1.1-1.3
HOMOGENITY index
55. • Dose fall off observation is very much needed in
this evaluation under headings
• Gradient index
• Difference between various isodose lines
• e.g between 80% and 60%- ideal- <2mm
• Between 80% and 40%- ideal- < 8mm
• For that reason, we must calculate equivalent
radius
Dose fall off
56. • To evaluate dose gradient, we must find out
difference between radius of various isodose
line
• But none is iso spherical
• We must find out equivalent radius from
formula
• First find out the specified isodose volume
• Then calculate the radius
• V=4/3 πr3
• r= (3V/4π)1/3
Equivalent radius
58. • FORMULA
• Difference of equivalent radius of prescription isodose
and equivalent radius of 50% isodose
• 2.19mm-3.15mm=0.96mm
• It should be between 0.3 to 0.9
Gradient index
59. • BETWEEN 80% AND 60%- IDEAL-<2mm
• HERE- 0. 4mm
• BETWEEN 80% AND 40%- IDEAL- <8mm
• HERE- 1mm
EORTC-22952-26001
Distance between various isodose lines
60. Isodose line
COLOUR ISODOSE LINE
Dark green 100%
Light green 80%
Sky green 60%
Pink 50%
Blue 40%
ISODOSE LINES
61. SL NO ORGAN DESIRABLE ACHIEVED
1 RT. EYE MAX <22.5Gy 1.97Gy
2 LT. EYE MAX <22.5Gy 4.4Gy
3 RT. OPTIC NERVE MAX <22.5Gy 2.3Gy
4 LT. OPTIC NERVE MAX <22.5Gy 5.5Gy
5 OPTIC CHIASM MAX <22.5Gy 7.5Gy
8 BRAIN STEM MAX 23-31Gy 10.01Gy
9 RT. COCHLEA MEAN <25Gy <1Gy
10 LT. COCHLEA MEAN <25Gy <1Gy
GG HANNA/CLINICAL ONCOLOGY/2016
OAR coverage
62. 4/5/2022 62
Basics of plan evaluation – junction volume
Accept under dosage in one of the Subvolumes