Conformal radiation therapy techniques like 3D CRT and IMRT aim to concentrate radiation dose in the tumor while sparing surrounding normal tissues. This is achieved through advances in imaging, treatment planning and delivery. 3D CRT uses geometric field shaping with multiple beams while IMRT further modulates beam intensity across each field. Both require contouring of target and organs at risk on imaging along with inverse or forward treatment planning to optimize dose distribution. Conformal techniques allow higher tumor doses with improved normal tissue sparing compared to conventional radiation therapy.
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
The vital importance of imaging techniques in radiation oncology now extends beyond diagnostic evaluation and treatment planning. Radiotherapy requires input from imaging for treatment planning and execution, when the treatment target is not located on the surface and, inspection and visual confirmation are not feasible. Traditional radiotherapy practices incorporate use of anatomic surface landmarks as well as radiologic correlation with 2D imaging in the form of port films or fluoroscopic imaging. Targets to be irradiated and normal tissues to be spared are delineated on CT scans in the planning process. Recent technical advances have enabled the integration of various imaging modalities into the everyday practice of radiotherapy directly at the linear accelerator. IGRT seeks to address geometric uncertainties in dose placement for target and normal tissues. It has become a routine part of current RT practice. Safe application of IGRT technology requires additional training and careful integration into the clinical process. IGRT reveals changes in anatomy during treatment which challenges conventional practices. IGRT facilitates the precise application of specialized irradiation techniques with narrow safety margins to radiosensitive organs.
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
The vital importance of imaging techniques in radiation oncology now extends beyond diagnostic evaluation and treatment planning. Radiotherapy requires input from imaging for treatment planning and execution, when the treatment target is not located on the surface and, inspection and visual confirmation are not feasible. Traditional radiotherapy practices incorporate use of anatomic surface landmarks as well as radiologic correlation with 2D imaging in the form of port films or fluoroscopic imaging. Targets to be irradiated and normal tissues to be spared are delineated on CT scans in the planning process. Recent technical advances have enabled the integration of various imaging modalities into the everyday practice of radiotherapy directly at the linear accelerator. IGRT seeks to address geometric uncertainties in dose placement for target and normal tissues. It has become a routine part of current RT practice. Safe application of IGRT technology requires additional training and careful integration into the clinical process. IGRT reveals changes in anatomy during treatment which challenges conventional practices. IGRT facilitates the precise application of specialized irradiation techniques with narrow safety margins to radiosensitive organs.
Conventional radiotherapy treatments are delivered with radiation beams that are of uniform intensity across the field (within the flatness specification limits). Wedges or compensators are used to modify the intensity profile to offset contour in irregularities and produce more uniform composite dose distributions such as in techniques using wedges. This process of changing beam intensity profile to meet the goals of a composite plan is called intensity modulation
IMRT refers to a radiation therapy technique in which nonuniform fluence is delivered to the patient from any given position of the treatment beam to optimize the composite dose distribution. The optimal fluence profiles for a given set of beam directions are determined through inverse planning. The fluence files thus generated are electronically transmitted to the linear accelerator, which is computer controlled, to deliver intensity modulated beams (IMBs) as calculated.
Intensity Modulated Radiation Therapy (IMRT) is an advanced mode of high-precision radiotherapy that uses computer-controlled linear accelerators to deliver precise radiation doses to a malignant tumor or specific areas within the tumor by reducing radiation dose to the nearby normal tissues.
A summary of recent innovations in radiation oncology focussing on the priniciples of different techniques and their application. An overview of clinical results has also been given
Similar to Three dimensional conformal radiotherapy - 3D-CRT and IMRT - Intensity modulated radiotherapy (20)
Management of acute lymphoblatic leukemia with light on etiology, clinical features, diagnosis and different aspects of management including chemotherapy and radiation therapy
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
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.
263778731218 Abortion Clinic /Pills In Harare ,sisternakatoto
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NVBDCP.pptx Nation vector borne disease control programSapna Thakur
NVBDCP was launched in 2003-2004 . Vector-Borne Disease: Disease that results from an infection transmitted to humans and other animals by blood-feeding arthropods, such as mosquitoes, ticks, and fleas. Examples of vector-borne diseases include Dengue fever, West Nile Virus, Lyme disease, and malaria.
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Ve...kevinkariuki227
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
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
The prostate is an exocrine gland of the male mammalian reproductive system
It is a walnut-sized gland that forms part of the male reproductive system and is located in front of the rectum and just below the urinary bladder
Function is to store and secrete a clear, slightly alkaline fluid that constitutes 10-30% of the volume of the seminal fluid that along with the spermatozoa, constitutes semen
A healthy human prostate measures (4cm-vertical, by 3cm-horizontal, 2cm ant-post ).
It surrounds the urethra just below the urinary bladder. It has anterior, median, posterior and two lateral lobes
It’s work is regulated by androgens which are responsible for male sex characteristics
Generalised disease of the prostate due to hormonal derangement which leads to non malignant enlargement of the gland (increase in the number of epithelial cells and stromal tissue)to cause compression of the urethra leading to symptoms (LUTS
Recomendações da OMS sobre cuidados maternos e neonatais para uma experiência pós-natal positiva.
Em consonância com os ODS – Objetivos do Desenvolvimento Sustentável e a Estratégia Global para a Saúde das Mulheres, Crianças e Adolescentes, e aplicando uma abordagem baseada nos direitos humanos, os esforços de cuidados pós-natais devem expandir-se para além da cobertura e da simples sobrevivência, de modo a incluir cuidados de qualidade.
Estas diretrizes visam melhorar a qualidade dos cuidados pós-natais essenciais e de rotina prestados às mulheres e aos recém-nascidos, com o objetivo final de melhorar a saúde e o bem-estar materno e neonatal.
Uma “experiência pós-natal positiva” é um resultado importante para todas as mulheres que dão à luz e para os seus recém-nascidos, estabelecendo as bases para a melhoria da saúde e do bem-estar a curto e longo prazo. Uma experiência pós-natal positiva é definida como aquela em que as mulheres, pessoas que gestam, os recém-nascidos, os casais, os pais, os cuidadores e as famílias recebem informação consistente, garantia e apoio de profissionais de saúde motivados; e onde um sistema de saúde flexível e com recursos reconheça as necessidades das mulheres e dos bebês e respeite o seu contexto cultural.
Estas diretrizes consolidadas apresentam algumas recomendações novas e já bem fundamentadas sobre cuidados pós-natais de rotina para mulheres e neonatos que recebem cuidados no pós-parto em unidades de saúde ou na comunidade, independentemente dos recursos disponíveis.
É fornecido um conjunto abrangente de recomendações para cuidados durante o período puerperal, com ênfase nos cuidados essenciais que todas as mulheres e recém-nascidos devem receber, e com a devida atenção à qualidade dos cuidados; isto é, a entrega e a experiência do cuidado recebido. Estas diretrizes atualizam e ampliam as recomendações da OMS de 2014 sobre cuidados pós-natais da mãe e do recém-nascido e complementam as atuais diretrizes da OMS sobre a gestão de complicações pós-natais.
O estabelecimento da amamentação e o manejo das principais intercorrências é contemplada.
Recomendamos muito.
Vamos discutir essas recomendações no nosso curso de pós-graduação em Aleitamento no Instituto Ciclos.
Esta publicação só está disponível em inglês até o momento.
Prof. Marcus Renato de Carvalho
www.agostodourado.com
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.
2. Radiation Therapy
Despite advancement from KV X-ray machines
to MV linear accelerators, basic approach to RT
planning & delivery has remained relatively
unchanged.
Radiotherapy is delivered conventionally using
limited set of beams.
3. LIMITATIONS OF CONVENTIONAL RT
1.Uncertainties in delineation of true spatial extent of
disease
2.Inadequate knowledge of exact shape & location of
normal structures.
3.Lack of tools for efficient planning & delivery
4.Limitations in producing optimal dose distributions.
These limitations results in
1.Incorporation of large safety margins
2.Tumor dose often has to be compromised to prevent normal
tissue complications leading to higher probability of local failures
4. CONFORMAL RADIOTHERAPY
To ‘‘concentrate’’ the radiation in the tumour while
sparing normal structures
Conformal RT became achievable because of
1. Introduction of Multileaf Collimator
2. Synergistic advances in mathematics & computers
3. 3D imaging modalities
4. Computerized therapy planning techniques & dose
delivery machines
7. Types of Conformal Radiation
Two broad subtypes :
Techniques aiming to
employ geometric field
shaping alone( 3D-CRT)
Techniques to modulate
the intensity of fluence
across the geometrically-
shaped field (IMRT)
Geometrical Field shaping
Geometrical Field shaping with
Intesity Modulation
8. WHAT IS 3-D CRT
To plan & deliver treatment based on 3D anatomic
information. such that resultant dose distribution
conforms to the target volume closely in terms of
Adequate dose to tumor &
Minimum dose to normal tissues.
The 3D CRT plans generally
use increased number of radiation beams
to improve dose conformation and conventional
beam modifiers (e.g., wedges and/or compensating
filters) are used.
9. IMRT
IMRT is an advanced form of 3D CRT
IMRT refers to a radiation therapy technique in
which
nonuniform fluence is delivered to the patient from any
given position of the treatment beam
using computer-aided optimization
to attain certain specified
dosimetric and clinical objectives.
10. ADVANTAGES OF IMRT
IMRT is used
To improve target dose uniformity
To selectively avoid critical structures & normal tissues.
To deliver higher than conventional doses.
To create concave isodose surfaces or low-dose areas surrounded
by high dose.
Focal dose escalation to specific sub volumes in the target vol.
i.e. SIB
Better sparing of critical structures specially during reirradiation.
11. Caveats: Conformal Therapy
Significantly increased expenditure:
Machine with conformal treatment capability
Advanced Imaging equipment: Planning and Verification
Software and Computer hardware
Extensive physics manpower and time is required.
Conformal nature – highly susceptible to motion and setup related errors – Achilles
heel of CFRT
Target delineation remains problematic.
Treatment and Planning time both significantly increased
Radiobiological disadvantage:
Decreased “dose-rate” to the tumor
Increased integral dose (Cyberknife > Tomotherapy > IMRT)
14. POSITIONING
• Important component of conformal RT
• Position
– Should be comfortable & Reproducible
– Should be suitable for beam entry, with minimum accessories in beam
path
• For this purpose positioning devices may be used
• Positioning devices are ancillary devices used to help maintain
the patient in a non-standard treatment position.
16. IMMOBILIZATION
• Patient is immobilized using individualized casts or moulds.
• An immobilization device is any device that helps to establish and
maintain the patient in a fixed, well-defined position from treatment to
treatment over a course of radiotherapy-reproduce the treatment
everyday
17. IMAGE ACQUISITION
• It provides foundation for treatment planning
• Usually more than one imaging modalities are required for better
delineation of target volume
• Images are acquired for :
– Treatment planning
– Image guidance and/or treatment verification
– Follow-up studies (during & after treatment)
18. IMAGING MODALITIES
• No single imaging modality produces all the
information, needed for the accurate
identification and delineation of the target
volume and critical organs.
• Various imaging modalities used are :
– CT
– MRI
– PET-CT
19. CT IMAGING
• Advantages of CT
– Gives quantitative data in
form of CT no. (electron
density) to account for
tissue heterogeneities while
computing dose distribution.
– Gives detailed information
of bony structures
– Potential for rapid scanning
– 4 -D imaging can be done.
– Widely available;
(relatively) inexpensive
20. MRI IMAGING
• Advantages of MRI
– No radiation dose to
patient
– Unparalleled soft tissue
delineation
– scans directly in axial,
sagittal, coronal or oblique
planes
– Vascular imaging with
contrast agents
21. PET/CT
• Recently introduced PET/CT
machines, integrating PET &
CT technologies , enables the
collection of both anatomical
& biological information
simultaneously
• ADV. of PET/CT
– Earlier diagnosis of tumor
– Precise localization
– Accurate staging
– Precise treatment
– Monitoring of response to
treatment
22. CT SIMULATOR
• Images are acquired on a
dedicated CT machine called
CT simulator with following
features
– A large bore (75-85cm) to
accommodate various treatment
positions along with treatment
accessories.
– A flat couch insert to simulate
treatment machine couch.
– A laser system consisting of
• Inner laser
• External moving laser
to position patients for
imaging & for marking
• A graphic work station
23. IMAGE ACQUISITION
• CT is done with pt in the treatment position with immobilization
device if used.
• Radio opaque fiducial are placed at the presumed isocentre.
• These fiducial assist in any coordinate transformation needed as
a result of 3D planning and eventual plan implementation.
• A topogram is generated to insure that patient alignment is
correct & then using localizer, area to be scanned is selected.
• The FOV is selected to permit visualization of the external
contour, which is required for accurate dose calculations.
• Using site dependent protocols, images are acquired.
• The planning CT data set is transferred to a 3D-TPS or
workstation via a computer network.
24. TREATMENT PLANNING SYSTEM
• TPS provides tools for
– Image registration
– Image segmentation or contouring
– Virtual Simulation
– Dose calculations
– Plan Evaluation
– Data Storage and transmission to console
– Treatment verification
25. IMAGE REGISTRATION
• Image registration allows use of complementary features of
different scan types.
• Employs a unique algorithm that allows full voxel to voxel
intensity match, Image Fusion automatically correlates thousands
of points from two image sets, providing true volumetric fusion
of anatomical data sets.
• This requires calculation of 3D transformation that relates
coordinates of a particular imaging study to planning CT
coordinates.
• Various registration techniques include
– Point-to-point fitting,
– Line or curve matching
– Surface or topography matching
– Volume matching
27. APPLICATIONS OF IMAGE
REGISTRATION
• Identifying the volume of a tumour on a preoperative scan and
transferring it to the postoperative treatment planning scan to
define the target volume.
• Visualizing CNS structures more clearly seen on MRI and
mapping them to CT image for planning-fusion
• Combining functional or biochemical signals from emission
tomography onto CT scans for planning purposes.
• For organ motion studies
• Image guidance
• For follow-up studies
• 4D CT
• Image registration allows computation of cumulative doses
from multiple plans done on different image sets for same
patient
28. IMAGE SEGMENTATION OR
CONTOURING
• Most labour-intensive component
of 3-D CRT
• Necessary for the qualitative and
quantitative evaluation of
treatment plan.
• Reconstructed sagittal & coronal
images provide additional
orientation cues & are useful in
defining spatially consistent
volumes of interest.
• Segmentation is done manually
or automatically delineating
anatomic regions of interest on a
slice-by-slice basis
29. IMAGE SEGMENTATION
• The segmented regions can be rendered
in different colors.
• High contrast structures e.g. lungs,
bones & air cavities can be contoured
with edge detection & edge tracking
techniques.
• The computer automatically tracks path
of a specified pixel value &connects
the pixels into a contour outline
• Basic features of contouring software
are manipulating image contrast and
brightness, zoom, pan, sampling pixel
values, distance measurement.
• Contours drawn on a limited number of
widely separated image sections can be
interpolated
30. VOLUME DEFINITION
• Volume definition is
prerequisite for 3-D
treatment planning.
• To aid in the treatment
planning process &
provide a basis for
comparison of treatment
outcomes.
• ICRU reports50 & 62
define & describe target
& critical structure
volumes.
31. VOLUME DEFINITION
• The Gross Tumor Volume (GTV) - is
gross palpable or
visible/demonstrable extent and
location of malignant growth
• defined with the help of
– Imaging modalities & clinical
examination
• The Clinical Target Volume (CTV) -
is tissue volume that contains GTV
and/or sub-clinical microscopic
malignant disease, which must be
eliminated.
• This volume thus has to be treated
adequately in order to achieve the aim
of therapy, cure or palliation.
32. VOLUME DEFINITION
• ITV-Internal target volume consists of
CTV plus internal margin.
• Internal margin accounts for variations
in the size & position of CTV relative
to the patient’s reference frame (usually
defined by the bony anatomy), i.e.,
variations due to organ motion, such as
breathing, bladder or rectal contents,
etc.
• PTV-Planning target voplume includes
the internal target margin & an
additional margin for:
– Set-up uncertainties
– Machine tolerances
– Intra-treatment variations
• The PTV does NOT include a margin
for dosimetric characteristics of the
radiation beam.
33. VOLUME DEFINITION
• Organ at Risk (OAR) - is an organ whose
sensitivity to radiation is such that the
dose received from a treatment plan may
be significant compared to its tolerance,
possibly requiring a change in beam
arrangement or a change in dose.
• PVR- planning organ at risk volume
margins need to be added to compensate
for its movements, internal as well as set-
up.
• The treated volume - volume enclosed by
an isodose surface that is selected and
specified by the Radiation Oncologist as
being appropriate to achieve the purpose
of treatment (e.g., 95% isodose surface)
• The irradiated volume - volume that
receives a dose considered significant in
relation to normal tissue tolerance.
34. Biological Target Volume
A target volume that
incorporated data from
molecular imaging techniques
Target volume drawn
incorporates information
regarding:
Cellular burden
Cellular metabolism
Tumor hypoxia
Tumor proliferation
Intrinsic Radioresistance or
sensitivity
35. Biological Target Volumes
Lung Cancer:
30 -60% of all GTVs and PTVs are changed with
PET.
Increase in the volume can be seen in 20 -40%.
Decrease in the volume in 20 – 30%.
Several studies show significant improvement in
nodal delineation.
Head and Neck Cancer:
PET fused images lead to a change in GTV volume
in 79%.
Can improve parotid sparing in 70% patients.
36. OAR TYPES
• Organs are made up of functional units.
• Radio sensitivity of an organ is determined by the arrangement
of these units.
• If functional units are arranged in series then inactivation of
one subunit causes loss of function of whole organ –spinal
cord
• In parallel organization of functional subunits, inactivation of a
large no. of subunits doesn’t affect overall organ function.
• Consequently,
– an organ with high tolerance may be lost by inactivation of a small part.
– While an organ with very low tolerance may sustain loss of even large
no. of subunits.
37. Digitally Reconstructed Radiograph-
DRR
• A synthetic radiographs produced
by tracing ray-lines from a virtual
source position through the CT
data to a virtual film plane .
• It is analogous to conventional
simulation radiographs.
• DRR is used
– for treatment portal design
– for verification of treatment portal by
comparison with port films or
electronic portal images
– provides planar reference image for
transferring 3D treatment plan to
clinical setting
38. Digitally Composite Radiograph -
DCR
• The digitally composite radiograph is a type of
DRR that allows different ranges of CT
numbers related to a certain tissue type to be
selectively suppressed or enhanced in the
image.
39. Beam Eye View-BEV
• In BEV observer’s viewing
point is at the source of
radiation looking out along axis
of radiation beam.
– Demonstrates geometric coverage
of target volume by the beam
– Shielding & MLCs are designed
on BEV
– Useful in identifying best gantry,
collimator, and couch angles to
irradiate target & avoid adjacent
normal structures by interactively
moving patient and treatment
beam.
40. Room Eye View-REV
• The REV display provides a
viewing point simulating any
arbitrary location within the
treatment room.
•
• The REV helps
– To better appreciate overall
treatment technique
geometry and placement of
the isocenter
41. PLANNING
• For planning, the 3D TPS must have the capability to simulate
each of the treatment machine motion functions, including
– Gantry angle,
– Collimator length, width & angle,
– MLC leaf settings,
– Couch latitude, longitude, height & angle.
42. FORWARD PLANNING
• For 3D CRT forward planning is used.
• Beam arrangement is selected based on clinical experience.
• Using BEV, beam aperture is designed
• Dose is prescribed.
• 3D dose distribution is calculated.
• Then plan is evaluated.
• Plan is modified based on dose distribution evaluation, using
various combinations of
– Beam , collimator & couch angle,
– Beam weights &
– Beam modifying devices (wedges, compensators) to get desired dose
distribution.
43. IMRT PLANNING
• IMRT planning is an inverse planning.
• It is so called because this approach starts with desired result (a
uniform target dose) & works backward toward incident beam
intensities.
• After contouring, treatment fields & their orientation ( beam
angle) around patient is selected.
• Next step is to select the parameters used to drive the
optimization algorithm to a particular solution.
• Optimization refers to mathematical technique of
– finding the best physical and technically possible treatment plan
– to fulfill specified physical and clinical criteria,
– under certain constraints
– using sophisticated computer algorithm
44. “Inverse” Planning
1. Dose distribution specified
Forward Planning
2. Intensity map created
3. Beam Fluence
modulated to recreate
intensity map
Inverse Planning
45. IMRT PLANNING
• Dose-volume constraints for the target and normal
tissues are entered into the optimization program of
TPS
– Maximum and minimum target doses
– Maximum normal tissues doses
– Priority scores for target and normal tissues
• The dose prescription for IMRT is more structured
and complex than single-valued prescription used
in 3-D CRT & conventional RT
• Ideally some dose value is prescribed to every
voxel.
46. Optimization
Refers to the technique of finding the best physical
and technically possible treatment plan to fulfill the
specified physical and clinical criteria.
A mathematical technique that aims to maximize (or
minimize) a score under certain constraints.
It is one of the most commonly used techniques for
inverse planning.
47. OPTIMIZATION
• During the optimization process, each beam is
divided into small “beamlets”
• Intensity of each is varied until the optimal
dose distribution is derived
• We can Optimize following parameters
– Intensity maps
– Number of intensity levels
– Beam angles
– Number of beams
– Beam Energy
Infections
48.
49.
50. Optimization Criteria
Refers to the constraints that need to be fulfilled during the planning
process
Types:
Physical Optimization Criteria: Based on physical
dose coverage
Biological Optimization Criteria: Based on TCP
and NTCP calculation
A total objective function (score) is then derived from these criteria.
Priorities are defined to tell the algorithm the relative importance of the
different planning objectives (penalties)
The algorithm attempts to maximize the score based on the criteria and
penalties.
51. PLAN EVALUATION
• The following tools are used in the evaluation
of the planned dose distribution:
– 2-D display
• Isodose lines
• Color wash
• DVHs (Dose volume histograms )
– Dose distribution statistics
52. 2D EVALUATION
• Isodose lines superimposed on
CT images
• Color wash - Spectrum of colors
superimposed on the anatomic
information represented by
modulation of intensity
– Gives quick over view of dose
distribution
– Easy to assess overdosage in
normal tissue that are not
contoured.
– To assess dose heterogeneity inside
PTV
• Slice by slice evaluation of dose
distribution can be done.
53. DOSE VOLUME HISTOGRAM - DVH
• DVHs summarize the information contained in
the 3-D dose distribution & quantitatively
evaluates treatment plans.
• DVHs are usually displayed in the form of ‘per
cent volume of total volume’ against dose.
• The DVH may be represented in two forms:
– Cumulative integral DVH
– Differential DVH.
54. CUMULATIVE DVH
• It is plot of volume of a given
structure receiving a certain
dose.
• Any point on the cumulative
DVH curve shows the volume
of a given structure that receives
the indicated dose or higher.
• It start at 100% of the volume
for zero dose, since all of the
volume receives at least more
than zero Gy.
55. DIFFERENTIAL DVH
• The direct or differential DVH is
a plot of volume receiving a dose
within a specified dose interval
(or dose bin) as a function of
dose.
• It shows extent of dose variation
within a given structure.
• The ideal DVH for a target
volume would be a single column
indicating that 100% of volume
receives prescribed dose.
• For a critical structure, the DVH
may contain several peaks
indicating that different parts of
the organ receive different doses.
DVH - target vol.
DVH - OAR
56. 3-D DOSE CLOUD
• Map isodoses in three
dimensions and
overlay the resulting
isosurface on a 3-D
display with surface
renderings of target
& other contoured
organs.
57. Dose statistics
• It provide quantitative information on the volume of the target or critical
structure and on the dose received by that volume.
• These include:
– The minimum dose to the volume
– The maximum dose to the volume
– The mean dose to the volume
– Modal dose
• Useful in dose reporting.
58. PLAN EVALUATION
• The planned dose distribution approved by the
radiation oncologist is one in which
– a uniform dose is delivered to the target volume
(e.g., +7% and –5% of prescribed dose)
– with doses to critical structures held below some
tolerance level specified by the radiation oncologist
• Acceptable dose distribution is one that differs
from desired dose distribution
– within preset limits of dose and
– only in regions where desired dose distribution can’t
be physically achieved.
59. PLAN IMPLEMENTATION
• Once the treatment plan has been evaluated &
approved, documentation for plan implementation
must be generated.
• It includes
– beam parameter settings transferred to the treatment
machine’s record and verify system,
– MLC parameters communicated to computer system
that controls MLC system of the treatment machine,
– DRR generation & printing or transfer to an image
database.
60. PLAN VERIFICATION FOR 3DCRT
• These include
– An independent check of the plan and monitor unit calculation by a
physicist,
– isocenter placement check on the treatment machine using orthogonal
radiographs,
– field-apertures check using portal films or electronic portal images, and
– to ensure that input data into the Record & Verification system are
correct
– to confirm the geometric validity and accuracy of the 3D treatment
plan.
– to confirm the correctness of the beam orientations in the physical
implementation by taking port film or image & comparing it with DRR.
61. IMRT PLAN VERIFICATION
• The goal is to verify that correct dose & dose distribution will
be delivered to the patient.
• One needs to check that
– the plan has been properly computed
– leaf sequence files & treatment parameters charted and/or stored in the
R/V server are correct &
– plan will be executable.
• Before first treatment, verification is done to check
– MU (or absolute dose to a point)
– MLC leaf sequences or fluence maps
– Dose distribution
62. PLAN VERIFICATION
• Specially designed IMRT
phantoms are used.
• These phantoms have various
inhomogeneity built in that
allow verification not only of
IMRT plans but also of the
algorithm used for tissue
inhomogeneity corrections.
• It is also possible, however, to
use simple phantoms made of
Lucite, polystyrene or other
water equivalent materials, in
which dosimeters can be
positioned.
IMRT PHANTOM
ionamatrixx
63. PLAN VERIFICATION
• Involves mapping the plan fields onto a
phantom, to create a verification plan &
comparing the results with measurements
made on that phantom.
• Assuming that validity of results for the
phantom can be extrapolated to the patient.
• CT images of the IMRT phantom with
ionization chamber in the slot, are taken with
2.5mm slice thickness.
• Phantom images are transferred to TPS & body
of phantom is contoured.
• A phantom plan is created by superimposing
the patient plan on to the IMRT phantom.
• All gantry angles are made to zero-degree
orientation for the measurement without
changing anything further so that isodose and
profile remained the same, & it is called
verification plan.
64.
65. IMRT DELIVERY
• Having calculated the fluence distributions or
fluence maps for each field angle, one now needs
to have a means of delivering those fluence maps.
• Methods to deliver an IMRT treatment are:
– Compensator based IMRT
– Multileaf collimator (MLC) based
• Static or step & shoot mode
• Dynamic mode
– Intensity modulated arc therapy (IMAT)
– Tomotherapy
66. COMPENSATOR BASED IMRT
• compensators are used to modulate intensity.
• compensators must be constructed for each gantry position
employed and then placed in the beam for each treatment.
• Adv. of physical attenuators are
– Highest MU efficiency
– Devoid of problems such as
• leaf positioning accuracy,
• interleaf leakage and
• intraleaf transmission,
• rounded leaf, and
• tongue-and-groove effect that are intrinsic to MLC systems.
• Disadv of physical attenuators
– issues related to material choice, machining accuracy, and placement
accuracy.
– Labour intensive as each field has unique intensity map & requires
separate compensator.
67. STEP & SHOOT IMRT
• In static or step & shoot mode the intensity modulated fields are delivered
with a sequence of small segments or subfields, each subfield with a uniform
intensity.
• The beam is only turned on when the MLC leaves are stationary in each of the
prescribed subfield positions.
• Adv. of SMLC
– Simple concept resembles conventional treatment
– Easy to plan, deliver & to verify
– an interrupted treatment is easy to resume
– fewer MUs in comparison to DMLC
– less demanding in terms of QA
• Disadv. of SMLC
– Slow dose delivery (5 min/field)
– Hard on MLC hardware
68. Step & Shoot IMRT
Intesntiy
Distance
Since beam is interrupted
between movements
leakage radiation is less.
Easier to deliver and plan.
More time consuming
69. DYNAMIC MODE
• In the DMLC or sliding window mode, the leaves of MLC are
moving during irradiation i.e. each pair of opposing leaf sweeps
across target volume under computer control.
• Adv. Of DMLC
– Better dose homogeneity for target volumes
– Shorter treatment time for complex IM beams
• Disadv of DMLC
– More demanding in terms of QA
• leaf position (gap), leaf speed need to be checked
– Beam remains on throughout – leakage radiation increased
– Total MU required is more than that for SMLC
• increased leakage dose
70. Dynamic IMRT
Faster than Static IMRT
Smooth intensity modulation
acheived
Beam remains on throughout
– leakage radiation increased
More susceptible to tumor
motion related errors.
Additional QA required for
MLC motion accuracy.
Intesntiy
Distance
71. IMAT
• Intensity-modulated arc therapy (IMAT)
technique uses MLC dynamically to shape
fields as gantry rotate in an arc.
• IMAT, which uses five to seven overlapping
concentric arcs to deliver a conformal dose
distribution
72. TOMOTHERAPY
• Historically, IMRT by tomotherapy preceded
IMRT by any MLC-based technique.
• Delivered by two methods:
– Slice based tomotherapy
– Helical tomotherapy
75. CONFORMAL RADIATION THERAPY
QUESTIONS
1. Do conformal techniques allow dose escalation ?
2. Have conformal techniques increased local control ?
3. Have conformal techniques increased survival rates ?
4. Have conformal techniques reduced late effects ?
76. CONFORMAL RADIATION THERAPY
1. Do conformal techniques allow dose escalation ?
Conformal techniques like 3-D CRT & IMRT has
definitely achieved escalation of radiation dose
compared to conventional radiotherapy at some
sites.
Dose has been increased from conventional 60-65
Gys. to 70-86 Gys., particularly in cancer of prostate
and head & neck cancers.
77. CONFORMAL RADIATION THERAPY
2. Have conformal techniques increased local control ?
Significant dose escalation has been possible so far in the
treatment of cancer of Prostate only.
Dose has been increased from 65 – 86 Gys.
Escalation of dose has increased both histological &
biochemical local control of prostate cancer.
The effect on survival is not very significant.
Conformal techniques have so far failed to achieve
significant dose escalation in other tumours with increase
in the local control.
78. CONFORMAL RADIATION THERAPY
3. Have conformal techniques increased survival rates ?
The 3-D CRT and IMRT has not led to desired &
expected increase in the survival rates for various
cancers treated by these techniques.
There is only 1-2%age increase in survival compared
to conventional radiation therapy.
Inspite of these techniques being introduced in 1980’s
& early 1990’s, clinical results reported are far from
few.
79. CONFORMAL RADIATION THERAPY
4. Have conformal techniques reduced late effects ?
The greatest impact of conformal techniques have
been seen in the reduction of late radiation morbidity,
which has been reduced by 1/3rd to2/3rd compared to
toxicity produced by conventional radiation therapy.
and
This is the only justification for use of these techniques.
80. Clinical applications- Prostate
Dosimetric data on Organs at risk
3DCRT can drastically reduce rectal and bladder dose (Perez et al)
Conv RT 3DCRT
Bladder > 65Gy~60% ~34%
Rectum > 65Gy ~50% ~22%
Clinical data on Toxicity
Rectal and bladder complication rates are reduced
Conv. RT 3DCRT IMRT
GrII ~50-60% 20-30% 5% (R) 15% (B)
GrIII ~3-4%
(20-30% with dose escalation)
Zelefsky et al 2000, 2003, 2005 . IMRT toxicity at 81Gy comparable with 3DCRT
to 65-75Gy.
81. CONFORMAL RADIATION THERAPY
Royal Marsden Hospital, London
Carcinoma Prostate – 3D CRT
_________________________________________________
Late Toxicity Conventional RT 3-D CRT
_________________________________________________
Proctitis
Grade – I 56 % 37 %
Grade – II 15 % 5 %
_________________________________________________
82. Clinical applications – Prostate
Clinical data on dose escalation
With 3DCRT – upto 81 Gy
With IMRT – upto 86 Gy
PSA failure free at 3 yrs
>77 Gy 95%
68-77 Gy 70%
<67 Gy 60%
(Pollack et.al, Kupelian et al, Fiveash et al)
MSKCC >81Gy IMRT 81-92%
83. IMRT in Carcinoma Prostate
Toxicity Profile
Toxicity Ghadjar P
2008
Coote, JH
2009
1. GIT toxicity
Grade-II
Acute
Late
Grade-III
3%
8%
None
--
4%
None
2. GU toxicity
Grade-II
Acute
Late
Grade-III
Acute
Late
56%
28%
8%
3%
--
4.25%
NIL
NIL
84. Clinical applications – Head & Neck
Oropharynx
Toxicity
Chao et al 2001 Conventional RT IMRT
Grade II xerostomia 78-84% 17-30%
Eisbruch et al 3DCRT
Severe xerostomia 33%
Results
Chao et al 2004
Stages I (2), II (3), III (14), IV (43)
Median FU 33 months – 10 locoregional
recurrences
85. Clinical applications – Head & Neck
Nasopharynx
Toxicity
Xia et al 2000
mean parotid dose 21Gy
significant dose reduction to brainstem,
optic chiasm, optic structures.
Results
LC OS
UCSF 94% 73%
HongKong 100%
86. Results of IMRT in Head & Neck Cancer
Survival Data
Study No.of pts. Residual
Disease
Local
Recurrenc
e
Nodal
Recurrenc
e
2 yrs.
Overall
survival
Studor G
2007
50% 16% 11% 82%
Studor G
2006
71
Post.Op.
-- 5% -- 71%
Studor G
2006
115
SIB-IMRT
-- -- -- 77%
Thorstad W
2005
356 -- 19% 14% 85%
Yao M
2005
Ghoshal,
2009
151
20
SIB-IMRT
--
--
8%
--
4%
--
85%
95%
87. Results of IMRT Vs. Conventional RT in
Head & Neck Cancer
Lee NY , 2006 Comparative Trial
Patients – 112
Disease Control 3 yrs. Survival
CVRT - 71 85%
IMRT - 41 95%
Toxicity
Died of toxicity CVRT - 3 , IMRT – None
Gastrostomy CVRT - 21%, IMRT – 4%
Survival
CVRT (3 yrs) 76%
IMRT (3 yrs) 82%
88. Clinical applications – Other Sites
Breast
improves dose coverage and reduced inhomogeneity
Lung
3DCRT improves dose distribution and reduces dose to
normal lung, heart, esophagus and spinal cord. IMRT improves the
conformity index compared with 3DCRT. IGRT is being used at
various institutions now.
Esophagus
reduces dose to lungs and heart.
Cervix
small bowel dose can be reduced by 50%, and rectal and
bladder doses by 23%.
89. CONFORMAL RADIATION THERAPY
CONCLUSIONS
Conventional treatment is still the best form of radiation
therapy for majority of our patients at most of the
treatment centers.
Conformal Radiation techniques are available for possible
better control and survival of cancer with reduced late
radiation morbidity.
However, the patient should be chosen properly who can
get required benefits.
Success of conformal techniques depends on meticulous
treatment planning.
90. CONFORMAL RADIATION THERAPY
CONCLUSIONS
These are time consuming and labor intense
techniques which may not be feasible for routine
practice of radiation therapy in our country for all
patients.
Finally the cost involved is prohibitive and
therefore, the facility should be established in
discrete manner.
91. CONFORMAL RADIATION THERAPY
“ We have never been near to the old dream of
the first Radiotherapist : Irradiating the entire
tumour and the only tumour”
“Mauric Tubiana, 2000”
Editor's Notes
Spatial dose distribution in the 3 dimensional volume is first defined.
Defination of dose coverage for the PTV(s)
Defination of sparing for the organ at risk
Establishment of a hierarchy of targets and organs at risk
Beam intensity distribution required to achieve this dose distribution goal would be calculated.
Photon Fluence required to deliver this intensity distribution is then generated.
Effecient delivery requires fast beam cycling – dark current in tube can cause unwanted radiation during movement.