IGBRT (Image Guided Brachytherapy)

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IGBRT (Image Guided Brachytherapy)

Fallacies of point A
 The location of the point A is at a point where significant cranio-caudal dose gradients exist, and
therefore use of this point for prescription and reporting of doses can lead to substantial inaccuracies.
 Dose point A does not correlate significantly with the complications or the control rates in various forms
of cervical brachytherapy.
 Prescription to this point, without regarding cervical anatomy can lead to substantial under dosing of a
large cervix.
 The location of the point A is determined based upon the applicator geometry instead of the anatomy of
the patient.
 ICRU bladder point is actually a point estimate of dose in the trigone. Doses may
vary in the bladder base, neck etc.
 ICRU bladder point dose not estimate the dose to hottest part of the bladder.
Which is usually 2cm superior. The dose in that area will be usually 2-4 times the
dose to ICRU bladder point.
 ICRU rectal point do not represent the maximum dose area which will be usually 2-4 cm cephalad.
Maximum dose is usually 3 time the ICRU rectal point.
 Dose to bowel is not checked in 2D
 Tandem insertion can be safe and easy if done under visualization, especially when large tumour
obscures the canal and also a retroverted uterus can be identified
 The original concept or the dose-limiting para-cervical triangle is now considered
invalid in light of recent clinical data, which show that the tolerance of this area
far exceeds that of the bladder or the rectum.
 Dose calculated to point A use in the Manchester system rules can be significantly
inaccurate with the use of modern-day radioisotopes and new applicator design,
where the arrangement of the applicator and the radioactive source do not follow
the recommendations of the Manchester system.

 The use of point A as a prescription point is not recommended in applicators where


the vaginal sources are parallel to the uterine sources.
Limitations of 2D planning
 Point A based dosimtery- Point A may over or under estimate the target dose
 Tumour dose escalation not feasible
 Optimization not feasible
IGBT

 Aim to
 1. localize the source positions.
 2. Localize the target.
 3. Localize the organs at risk.
 4. Determine the relationships between all the above
CT SCAN Plain CT scan is obtained after applicator insertion with 3-5mm
cuts Advantages:

 • verifies proper placement of applicator


 • reasonable estimate of the location of uterus
 • fairly good for visualizing bladder and rectum.
 • analyses 3D BT dose distribution
 • depicts changes in the OAR related to tumor shrinkage & filling status.
 • 3D dose calculations & optimization possible
 • long experience in treatment planning for EBRT
 • readily available in radiotherapy departments
Problems with CT treatment planning

 • produce artifact with metallic applicators • expensive • GTV not identified


 • overestimate tumor contours compared to MRI (although additional width
contoured on CT may not be detrimental)
 • fails to provide differentiation between the uterus, cervix, parauterine tissues so
CT-based contouring guidelines recommend delineating entire cervix and uterus.
 • contouring sigmoid difficult due to lack of contrast
 • contrast placed in OAR may cause artifact.in contouring wall of organ.
 • requiresmoving patient after application from CT to
treatment room: can produce motion artifact that nullifies the
increased accuracy of IGBT 
MRI Planning ADVANTAGES

 • multiplaner imaging
 • excellent soft tissue contrast
 • better visualization of tumor & parametrium. involvement
 • differentiate between uterus, cervix, tumor, other pelvic tissues & OAR
 • particularly useful in patients with advanced or deeply infiltrating tumors.
 • specific signal intensities allow for distinct separation on T1- and T2 WI cervix
(low T1, low T2), parametrium (high T1, high T2), tumor (low T1, high T2)
 • regression of cervical tumors can be documented so dose escalation possible
 • organ wall may be more clearly visualized for contouring OAR
DISADVANTAGES

 • requires special applicators. non-ferromagnetic metal or plastic/graphite


 • very expensive
 • can produce motion artifact
DELINEATION
  Advances in image guidance for applicator insertion and treatment planning have resulted
in 3D tissue contouring guidelines (GEC-ESTRO)
  After insertion of applicators, the target volumes and normal-tissue structures are
delineated on images in TPS.
  The delineation is to be performed at time of each BT application.
  The delineation process is based on clinical examination at diagnosis and at BT and on a
set of sectional images (preferably MRI T2 weighted) taken at diagnosis and at BT with
applicator in place
ICRU 38 to ICRU 89
Conceptual Changes

 Shift from an anatomical point based prescription to


“Residual high risk volume based” prescription.

 Unlike Point A, “HRCTV” Takes Disease Biology and Response into account

GTV D, GTV BT, HRCTV,IRCTV,LRCTV


Basic Concepts: GTV D and GTV BT

GTV D

GTV BT
HRCTV (Stage III B): Partial Responder

GTV Diagnosis

GTV BT

HRCTV (Including Gey Zones)

Zones that were signal intensive on the initial MRI depicting GTV-T but became gray indication
pathologic residual fibrotic tissue which might or might not contain macroscopic or microscopic
tumour

Grey Zones
Schmid, 2013 Strahlentherap Oncol
HRCTV (Stage II B) :Partial Responder

GTV baseline GTV baseline


GTV baseline

GTV BT
GTV BT
GTV BT HRCTV
HRCTV

HRCTV
Safety margins are more for a
complete responder to take
cognizance of initial disease

ICRU 89
Stage II B: IRCTV

GTV Diagnosis GTV Diagnosis


GTV Diagnosis

IRCTV
IRCTV IRCTV
HRCTV HRCTV HRCTV

GTV BT
GTV BT
GTV BT
CT Based Target Contouring
CT Based Contouring for IGBT

IB2/IIA IIB/IIIA IIIB

2cm

3 cm

IB2/IIA IIB/IIIA IIIB


HRCTV Cervix Cx+ 2 cm from lat edge of Cervix Cervix+Para Upto LPW
Inf Extent EUA
IRCTV 1 cm 1 cm 1 cm limited to LPW

IJROBP, Viswanathan,2007
NCCN 2018
 Intact Cervix 45(40-50) Gy EBRT followed by 30- 40 2cc Rectal dose 65-75 Gy
Gy LDR equivalent 2cc sigmoid dose 70 -75 Gy
2cc bladder dose 80-90 Gy
 80 gy for small volume d/s
 > 85-87 Gy for large volume d/s

 HDR
 6 Gy in 5 settings 30 Gy HDR = 48 LDR
 7 Gy in 4 settings 28 Gy HDR = 44.8 LDR
 7 Gy in 3 settings 21 HDR =33.6

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