IGBRT (Image Guided Brachytherapy)
IGBRT (Image Guided Brachytherapy)
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.
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:
• 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
Unlike Point A, “HRCTV” Takes Disease Biology and Response into account
GTV D
GTV BT
HRCTV (Stage III B): Partial Responder
GTV Diagnosis
GTV BT
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 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
IRCTV
IRCTV IRCTV
HRCTV HRCTV HRCTV
GTV BT
GTV BT
GTV BT
CT Based Target Contouring
CT Based Contouring for IGBT
2cm
3 cm
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