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CLINICAL APPLICATIONS
OF LDR-HDR
BRACHYTHERAPY

DR. SUGASHWARAN. J,
MODERATOR:PROF.DR.G. V. GIRI,
DEPT. OF RADIATION ONCOLOGY,
KMIO, BANGALORE.
BRACHYTHERAPY
ī‚§ Type of radiation treatment
ī‚§ Consists of placing sealed radioactive

sources very close to or in contact
with the target tissue.
CLINICAL ADVANTAGES
ī‚§ High biological efficacy
ī‚§ Rapid dose fall-off
ī‚§ High tolerance
ī‚§ Tolerable acute intense reaction
ī‚§ Decreased risk of tumor population
ī‚§ High control rate
ī‚§ Minimal radiation morbidity
ī‚§ Day care procedure
LIMITATIONS & DISADVANTAGES
Difficult for inaccessible regions
Limited for small tumors (T1_T2)
Invasive procedures, require GA
Higher dose inhomogeneity
Greater conformation –small errors in
placement of sources lead to extreme
changes from the intended dose distribution
ī‚§ Radioactive hazards (not now)
ī‚§ Costly
ī‚§
ī‚§
ī‚§
ī‚§
ī‚§
SELECTION CRITERIA
ī‚§ Easily accessible lesions
ī‚§ Early stage diseases (Ideal implant ≤ 5 cm)
ī‚§ Well localized tumor to organ of origin
ī‚§ No nodal or distant metastases (radical
ī‚§
ī‚§
ī‚§
ī‚§

intent)
No local infections or inflammation
Favorable histology- mod. diff. i.e. SCC
Well controlled DM / HTN
Proliferative/exophtic lesions preferred
(better outcome)
INDICATIONS
ī‚§ SOLE MODALITY
īƒē Skin malignanciesBCC, SCC
īƒē Head & neck cancers
īƒē Ca cx
īƒē Ca prostate

ī‚§ BOOST( AFTER

EXT.RTÂąCCT)

īƒē Head & neck cancers
īƒē Ca Breast
īƒē Esophagus
īƒē Anal canal
INDICATIONS...
ī‚§ PERIOPERTIVE
īƒē STS
īƒē Ca Breast
ī‚§ POSTOP
īƒē Ca Endometrium
īƒē Ca cx
īƒē Ca Breast

ī‚§ PALLIATIVE
īƒē Bronchogenic Ca
īƒē Biliary duct
malignancy
īƒē Ca Esophagus
īƒē Recurrent tumors
ī‚§ BENIGN
īƒē Keloids / Pterygium
ī‚§ OTHERS
īƒē Endovascular/Rad.
stent
CLASSIFICATION
ī‚§ SURGICAL APPROACH

/ POSITIONING

īƒē SOURCE IN TUMOR
ī‚ 
ī‚ 
ī‚ 
ī‚ 

INTERSTITIAL
INTRACAVITARY
INTRALUMINAL
ENDOVASCULAR

īƒē SOURCE IN CONTACT

BUT SUPERFICIAL
ī‚  SURFACE
BRACHYTHERAPY/
MOULD

ī‚§ DURATION OF

IRRADIATION

īƒē TEMPORARY-Cs137,Ir192
īƒē PERMANENT-I125,Au198

Pd 103 .Cs 131
DOSE RATE(ICRU 38)
ī‚§ LOW DOSE RATE (LDR)
īƒē 0.4-2 Gy/hr (clinical practice range 0.4 to 1 Gy per

hour)

ī‚§ MEDIUM DOSE RATE (MDR)
īƒē 2-12 Gy/hr

ī‚§ HIGH DOSE RATE (HDR)
īƒē > 12 Gy/hr

ī‚§ ULTRA LOW DOSE RATE
īƒē 0.01-0.3 Gy/hr
ADVANTAGES
LDR

HDR

ī‚§ Predictable clinical effects
ī‚§ Superior radiobiological

ī‚§ SHORT TREATMENT TIME

role
ī‚§ Less morbidity, control is
best
ī‚§ Well practised since long
ī‚§ Minimum intersession
variability in dose
distribution

īƒē Geometry well maintained
īƒē Better patient compliance /

comfort
īƒē Day care procedure

ī‚§ DOSE OPTIMIZATION
ī‚§ NO RADIATION HAZARDS
ī‚§ SMALL APPLICATOR
īƒē Less tissue trauma
īƒē Better packing
AFTER LOADING TECHNIQUE
ī‚§ MANUAL
īƒē Avoids radiation

īƒē
īƒē
īƒē
īƒē

protection issue of
preloading
Better applicator
placement
Verification prior to
source placement
More radiation hazard
Advantages of
preloading

ī‚§ REMOTE

CONTROLLED
īƒē
īƒē
īƒē
īƒē
īƒē
īƒē
īƒē
īƒē

No radiation hazard
Accurate placement
Geometry maintained
Better dose distribution
Highly precise
Short Treatment time
Day care procedure
Mainly used for HDR
RADIOBIOLOGY
ī‚§ Biological effects depend on
īƒē Prescribed dose
īƒē Treated volume
īƒē Dose rate
īƒē Fractionation
īƒē Treatment duration
RADIOBIOLOGY – 4 Rs
ī‚§
ī‚§
ī‚§
ī‚§

Repair
Reassortment / redistribution
Repopulation
Reoxygenation
INTERSTITIAL BRACHYTHERAPY
ī‚§ Sealed Radioactive sources directly

implanted into the tumor in a geometric
fashion
ī‚§ ADVANTAGES
īƒē
īƒē
īƒē
īƒē
īƒē
īƒē

Higher local dose in shorter time
Rapid dose fall
Better tumor control
Lesser radiation morbidities
Superior cosmetics
Functional preservation of organs
INTERSTITIAL BRACHYTHERAPYâ€Ļ
ī‚§ DISADVANTAGES
īƒē Invasive procedure
īƒē Costly

ī‚§ INTENTION OF TREATMENT
īƒē RADICAL INTENTION
ī‚  As radical brachytherapy alone (smaller lesions)
ī‚  Local boost in combination with EBRT (larger lesion)
SELECTION CRITERIA
ī‚§ Easily accessible lesions, at least from one

side
ī‚§ Early stage disease

īƒē T 1-T2 and sometimes early T3
īƒē Ideally total size of implant ≤ 5 cm

ī‚§ Well controlled DM /HTN
ī‚§ No local infection
CLINICAL APPLICATIONS
ī‚§ Head & neck tumors
īƒē Early stage oropharyngeal cancers

ī‚§ Ca breast- Boost /PBI
ī‚§ Ca prostate
ī‚§ Soft tissue sarcoma
ī‚§ Gynecologic malignancies
ī‚§ Ca anal canal and rectum
ī‚§ Ca lung and pancreas
TYPES OF INTERSTITIAL
IMPLANTS
ī‚§ TEMPORARY

ī‚§ PERMANENT

ACCORDING TO SIZE/LOCATION/PROXIMITY OF TUMOR TO NORMAL STRUCTURES

īƒē Radioactive sources

removed after desirable
dose has been delivered
īƒē Rigid stainless steel
needles/flexible Teflon /
nylon guides/plastic
tubes
īƒē Preloaded/After loaded

īƒē Preloaded – rigid needle

eg. Ra226 ,Cs137
īƒē After loaded – Manual/
Remote
īƒē Advantages

ī‚  Flexibility of implant
design
ī‚  Reduction of radiation
exposure levels resulting in
more accurate placement
of needles and guides
PERMANENT IMPLANTS
ADVANTAGES
īƒē Less accessible sites
īƒē ultra low dose rate/Max

biological effectiveness
īƒē Better tissue heal
īƒē Better effect in slow and
radio resistant tumors
īƒē Improved mobility

DISADVANTAGES
īƒē Environmental issue
īƒē Dosimetric uncertainties/

Later part of Treatment
becomes less effective
īƒē Source displacement
īƒē Large tumor /Difficult
procedure and geometry
īƒē Radio biologically less
effective for rapidly
proliferating tumors
CLINICAL APPLICATIONS

Oral Cavity:
ī‚§ LIP:

īƒē Indications: T1-2N0 Lesions (monotherapy- 0.5to5 cm or

boost therapy->5 cm)
T.V.: All visible & palpable tumour with 5-10 mm margin
īƒē Dose: 50-70Gy in 5-7 days LDR
īƒē Technique:
ī‚  Rigid after loading needles maintained in place by
Template
ī‚  Classical plastic tubes
īƒē Spacers to decrease dose to gingiva, teeth & other lip
CLINICAL APPLICATIONSâ€Ļ
Buccal Mucosa:
īƒē Indications:

īƒē
īƒē
īƒē
īƒē

ī‚  Brachytherapy alone indicated for small (<4cm), welldefined lesions in anterior 2/3rd
ī‚  As boost after EBRT for larger lesions
T.V.: GTV +0.5 to 1 cm margins
Dose: Alone 65-70 Gy
ī‚­ Boost 25-30 Gy
Technique: Guide Gutter Technique: Lesion < 2cm
Plastic tube technique: For other lesions
CLINICAL APPLICATIONSâ€Ļ
Oral Tongue:

ī‚§ Indications: T1 N0, T2 N0 < 3cm lesion
ī‚§ T.V.: GTV + 5 mm margin
ī‚§ Dose: Alone:60-65 Gy LDR
ī‚  Boost 20-25 Gy after EBRT dose of 45-50 Gy

ī‚§ Techniques: Guide-gutter technique

AP X-ray
CLINICAL APPLICATIONSâ€Ļ

Floor of Mouth:
īƒē Indications: T1-2N0 lesions, â‰Ĩ 5 mm away from

mandible
īƒē Dose: monotherapy-65Gy;boost-20 to 30 Gy
īƒē Complication: bone necrosis is most common, up
to 30%
Oropharynx:
īƒē Indications: Ca BOT, soft palate, tonsillar fossa &

vallecula usually as boost after EBRT
ī‚  Lesions < 5 cm (after EBRT)

īƒē T.V.: GTV + 10 mm margin
īƒē Dose: Tonsillar fossa-25-30 Gy; BOT 30-35 Gy
īƒē Technique: Classical Plastic Loop technique
CLINICAL APPLICATIONSâ€Ļ
ī‚§ Nasopharynx:
Ind- T1 AND T2 lesions
Dose: LDR -as a sole treatment 60Gy; as a boost 12 to 20 Gy.
HDR- 18 Gy in 6 fr

ī‚§ Opthalmic brachytherapy(I-125,Ru-106,Sr90)
Ind- malignant tumors of the conjuctiva, pterygium,wet macular
degeneration,neovascularization
Sr 90 dose rate-100Gy/hr,, I-125 dose rate 0.5 to 1 Gy/hr
Pterygium – Sr 90 dose varying from 20 to 60 Gy in 1 to 6 fr.
CLINICAL APPLICATIONSâ€Ļ
Breast

īƒēIndications: Boost after BCS & EBRT
ī‚­ Postoperative interstitial irradiation alone of

the primary tumor site after BCS in selected
low risk T1 and small T2N0 (PBI)
As sole modality

As Boost to EBRT

Patient choice: cannot come for
5-6 wks treatment :

Close, positive or unknown
margins

ī‚§ Distance
ī‚§ Lack of time

Elderly, frail, poor health patient EIC
Large breasts, unacceptable
toxicity with EBRT

Younger patients
Deep tumour in large breast
Irregularly thick target vol.

ī‚­ Chest wall recurrences
CLINICAL APPLICATIONSâ€Ļ
ī‚§ T.V.: Primary Tumor site + 2-3 cm margin
ī‚§ Dose: As Boost: 10-20 Gy LDR
ī‚  AS PBI: 45-50 Gy in 4-5 days LDR (30-70
cGy/hour)
ī‚­ 34 Gy/10fr, 2fr per day HDR

ī‚§ Technique:
īƒē Localization of PTV: Surgical clips (at least 6)
ī‚  USG, CT or MRI localization, Intra op USG
īƒē During primary surgery
īƒē Guide needle technique or
īƒē Plastic tube technique using Template
ī‚  Double plane implant
ī‚  Skin to source distance: Minimum 5 mm
MAMMOSITE
ī‚§ Used for Accelerated Partial Breast Irradiation(APBI)
ī‚§ Fluid filled balloon placed during surgery
Prescription
Reference Point at 1 cm
340cGy per fraction
2 fractions per day
6 hour separation
10 fractions total
Weekend break is allowed
Ideal patients for APBI(ASTRO)
ī‚§ Tumor Size < 2 cm
ī‚§ Absence of nodal involvement(N0)
ī‚§ Absence of Metastatic Status(M0)
ī‚§ Age > 60 yr
ī‚§ Negative margins
ī‚§ Invasive ductal histology in the absence of

DCIS
ī‚§ Estrogen receptor positive
HDR Brachytherapy with Savi
The Savi applicator is a new single insertion
multicatheter device used for partial breast
radiation.
It has a single central catheter and multiple
peripheral catheters.
This allows the radiation dose to be tailored to
the shape of the lumpectomy cavity.
Contura- multi lumen baloon
ī‚§ Consists of a central lumen and 4 outer lumen

offering a total of 40 dwell positions
ī‚§ Encased in a polyurethane balloon which
maintains symmetry and reduces potential
for balloon ruputre.
NEW ELLIPTICAL BALOON(2004)
ī‚§ Provides excellent conformance
ī‚§ Ellipsoidal implant parellel to the chest wall

provides appropriate symmentry
AXXENT:NEWER DEVICE
ī‚§ Uses a miniaturized x-ray source to deliver low energy x-rays within

a needle or catheter.

ī‚§ Use of this device for APBI
ī‚§ No need for heavy room shielding
ī‚§

Stay in room with patient during treatment

ī‚§

No radioactive materials license needed

ī‚§

No handling, storing, security concerns

ī‚§

One source per patient

ī‚§

Must calibrate source before each treatment
CLINICAL APPLICATIONSâ€Ļ
Prostate:

ī‚§ Indications

īƒē Brachytherapy as monotherapy:
ī‚  Stage T1-2a /Gleason score 2-6 / PSA ≤ 10 ng/ml
īƒē As boost after EBRT
ī‚  Stage T2b, T2c /Gleason score 7-10 /PSA > 10 ng/ml

ī‚§ Patient factors :
īƒē
īƒē
īƒē
īƒē
īƒē

Life expectancy > 5 yrs
IPSS<15
Prostate volume<60cm2
No defect if previous TURP
Minimal pubic arch interfence

ī‚§ T.V.: Whole prostate within capsule + 2-3 mm

margin
ī‚§ Methods: Permanent Implant (I125 or Pd103) or
Temporary Implant (Ir192)
CLINICAL APPLICATIONSâ€Ļ

Technique for Permanent implant

ī‚§ Retropubic approach with I125 seeds- Disappointing results
ī‚§ Modern technique: Transperineal Approach
īƒē TRUS guided
īƒē Two step approach

ī‚  Volume study of prostate
ī‚  pubic arch interfence assessment
īƒē Computer planning
ī‚§ Coverage check -USG & Flouroscopy
ī‚§ Bladder irrigation /Cystoscopy can be performed
ī‚§ Post-implant image based dosimetry
CLINICAL APPLICATIONS
ī‚§ Dose:
īƒē I125: 145 Gy as sole RT;100-110 Gy as boost to 40-50 Gy

EBRT
īƒē Pd103: 125 Gy as sole RT;90-100 Gy as boost to 40-50 Gy
EBRT
īƒē Cs 131 :115 GY as sole rt;85-95 Gy as boost to 40-50 Gy
EBRT

Temporary Implants with Ir192 (LDR or
HDR):
īƒē Procedure same as above; lesser no. of plastic

catheters required (8-15)
īƒē Dose:

ī‚  LDR 30-35 Gy seeds left for 3 days(Boost to 45 Gy
EBRT)
ī‚  HDR 20-25 Gy, 4-6 Gy/#(Boost to 45 Gy EBRT)
CLINICAL APPLICATIONS

Soft tissue Sarcomas (using Ir192 or I125)

ī‚§ Indications:

īƒē As sole postop RT:
ī‚  completely resected intermediate or high grade tumours
of extremity or superficial trunk with -ve margins
īƒē As boost to postop EBRT:
ī‚  Intermediate or high grade sarcoma with +/- margins
ī‚  Postop pts with small lesions & +ve/uncertain margins
ī‚  Deep lesions
ī‚  Low grade sarcomas

ī‚§ T.V.: GTV + 2-5 cm margin

ī‚  GTV based on preop MRI & clinical findings

ī‚§ Dose: LDR (Ir seeds or wires) as sole treatment

45-50 Gy in 4-6 days

ī‚  As boost to 45-50 Gy EBRT: 15-25 Gy in 2-3 days
HDR: as sole treatment 40 t0 50 Gy in 12 to 15 fr/ as boost
to 45-50 Gy EBRT:18-25 Gy in 4-8 fr
CLINICAL APPLICATIONSâ€Ļ
Technique:
īƒē Usually performed at time of surgery
īƒē Basic or sealed end temporary implant technique
īƒē To delay the start of brachytherapy for about 4 to 7

days after surgery
īƒē limit the allowable skin dose the 40 Gy isodoseline
to <25cm2 and the 25 Gy isodose line <100 cm2
CLINICAL APPLICATIONSâ€Ļ

Brain: Permanent or temporary (using I125 or Ir192

seeds/wires )
ī‚§ Indications:

īƒē As boost to EBRT or recurrence
īƒē Anaplastic astrocytoma or GBM, unifocal, well

cicumscribed, peripheral lesions & < 5 cm in diameter

ī‚§ T.V.: Contrast enhancing area on MRI +/- 5mm

margin
ī‚§ Dose: LDR 50-60 Gy, 0.4-0.5 Gy/hr
Gliasite
ī‚§ Used to treat brain tumors
ī‚§ Balloon filled with I-125

containing solution
ī‚§ Example: used to treat
glioblastoma multiformae to
50 Gy followed by EBRT
boost
CLINICAL APPLICATIONSâ€Ļ

Ca Anorectum

ī‚§ Indications: As boost to EBRT/ChemoRT
ī‚­ If T.V. does not exceeds 1/2 circumference, 5 mm thick, 5
cm long i.e. T1-2 & small T3 lesions
ī‚­ T1N0 adenocarcinoma of rectum 3-10 cm above anus

ī‚§ T.V.: Visible palpable tumor+5 mm
ī‚§ Dose: LDR 15-20 Gy at 0.3-0.6 Gy/hr
ī‚§ Technique: Guide needle technique with

plastic perineal template
CLINICAL APPLICATIONSâ€Ļ

Gynecological Tumors (Ir192 LDR or HDR)
ī‚§ Indications:

īƒē Ca Cervix
īƒē Ca Endometrium

ī‚  Postop local recurrence
īƒē Ca Vagina & Vulva
ī‚  Radical BT in early lesions (T1-2N0)
ī‚  Boost after EBRT in large lesions (T2-3N1)

ī‚§ Technique:

īƒē Guide-gutter technique
īƒē Blind plastic tube implant

(transperineal technique)
īƒē Plastic or guide needles
CLINICAL APPLICATION – CA
ABS Recommendations
CX

īƒē Bulky primary disease
īƒē Prior hysterectomy-inability to place tandem
īƒē Post hysterectomy
īƒē vault rec/cervical stump presentation

īƒē Extesive parametrial involvement
īƒē Distorted anatomy
īƒē Narrow vagina & fornices
īƒē Extensive / Distal vaginal wall involvement

īƒē Re-irradiation after recurrences
CLINICAL APPLICATIONSâ€Ļ
īƒē PERINEAL IMPLANTS

Martinez Universal Perineal
Interstitial Template
(MUPIT)

Syed-Neblett template
CLINICAL APPLICATIONSâ€Ļ
īƒē Ca Lung: Permanent perioperative BT, I125 seeds

ī‚­ Persistent or recurrent ds after EBRT or residual ds after
surgery
īƒē Ca Pancreas: Permanent perioperative BT, I125 seeds

ī‚­ Locally advanced unresectable ds
īƒē Ca Penis: scc predominant histology,
Indications – T1,T2 and T3(<4cm)that do not involve the
shaft of penis.
Based on paris system using templates(12 &18mm)
Dose ;60 Gy at a dose rate of 0.5 to0.65Gy/hr
īƒē Ca urethra: as sole treatment is 60 to 70 Gy in 3 to 5 days;
as a boost 20 to 25 Gy.
INTRACAVITARY APPLICATION
ī‚§ Radioactive sources are placed in a existing

cavity usually inside a predefined applicator
with special geometry
ī‚§ Uses:
īƒē Cervix
īƒē Endometrium
īƒē Vagina
īƒē Maxilla
īƒē Nasopharynx
DOSE SCHEDULE
ī‚§ LDR (<200cgy/hr)
īƒē 35-40 Gy at point A

ī‚§ MDR (200-1200cgy/hr)
īƒē 35 Gy LDR EQUIVALENT at point A

ī‚§ HDR(>1200cgy/hr)
īƒē 9 Gy in 2 fr
īƒē 6.8Gy in 3 fr at point A
EXTERNAL RT WITH
BRACHYTHERAPYfollow external irradiation
ī‚§ Brachytherapy can
īƒē SIMULTANEOUS
ī‚  Stage I - II with very minimal parametriun
involvement
ī‚  HDR -5 sessions (9gy /fr, 1week apart)
ī‚  40 Gy by EBRT simultaneously
īƒē SANDWICH
ī‚  Stage I-II
ī‚  40 Gy LDR eq.—â€ē EBRT 40 Gy

ī‚§ In both above cases a MIDLINE SHIELD is

used
POST OP/ VAULT
ī‚§ Vault RT
BRACHYTHERAPY
īƒē No residual disease

ī‚  8500 cGy at 5mm from the surface of the
vault
ī‚  2 sessions 1 week apart
īƒē Residual disease
ī‚  CTV of 2 cm given to gross tumor and the
prescription of 8500cgy encompassing the
whole CTV is made
ī‚  2 sessions 1 week apart

ī‚§ Mostly after EBRT
POST OP BRACHYTHERAPY
ī‚§ CONTRAINDICATIONS
īƒē Vaginal wall involvement ( middle- lower 13)
īƒē Heavy parametrium infiltration
īƒē VVF or VRF
īƒē Inadequate space
īƒē Medical contraindications
īƒē Metastatic disease

ī‚§ Supplementary radiation 2000 cGy 10fr
SURFACE MOULDS
Radiation is delivered by arranging RA
sources over the surface of tumor
ī‚§ Types
īƒē Planar
ī‚  Circular
ī‚  Square
ī‚  Rectangular
īƒē Line source
īƒē Cylinder
INDICATIONS

ī‚§ Superficial /Accessible tumors

keloid : Sr90 , 20 gy in 4 fr after surgery.
ī‚§ Skin ca – HAM applicator, Freiburg flab are
surface template applicators, dose – 35 to 50
Gy in 5 to 10 fr.
ī‚§ Post mastectomy recurrence – LDR- 65 Gy in
2 to 3 fr,monthly intervals.
ī‚§ Oral tumor
īƒē hard palate ,alveolus,oral cavity,lip
īƒē as a sole modality 60 GY,as boost to 45 to 50 GY-

15 TO 30 Gy.

ī‚§ Penile carcinoma
INTRALUMINAL BRACHYTHERAPY
ī‚§ Radioactive source is passed through a tube and

passed into a hollow lumen
ī‚§ Sites

īƒē Esophagus : TV-tumor+distal and proximal margin of

2 to 3 cm
Dose: palliative-16 GY IN 2 FR or 18 GY IN 3 FR.
as boost EBRT 50 Gy-HDR 10 Gy in 2 fr at 1 cm
from surface.
ILBT..
īƒē Bronchus : Bronchogenic carcinoma
ī‚  Definitive : T1-T2tumors

HDR- sole treatment-5Gy in 5 fr or 7.5 Gy in 2 fr
prescribed to 1cm.
as boost to EBRT treatment(45 TO 60 Gy)- three 5
Gy fr or two 7.5 GY fr
ī‚  Palliative :
ī‚­
ī‚­
ī‚­
ī‚­

Dyspnea,hemoptysis,post obstructive pneumonitis
Poor lung function
Previous EBRT
Dose : 7.5Gy/fr in3 weekly fr, 10Gy/fr in 2 fr, 6Gy/fr in 4
fr prescribed at 1 cm.
Boost treatment- 30 Gy in 10 to 12 fr
Biliary tract
ī‚§ Ind – unresectable tumors
ī‚§ Technique – endoscopic retrograde technique
ī‚§ BT delivered throug a transhepatic

cholangiogram
ī‚§ TV- tumor +1 to 2 cm proximal and distal
margin
ī‚§ Monotherapy- palliative dose 30 gy in 6 fr
ī‚§ As boost(45 Gy EBRT) – 15 TO 20 Gy in 3 to 4
fr.
Intra vascular
brachytherapy

Coronary artery disease caused
by occlusion of cardiac vessels
ī‚§ IVB used to prevent restenosis
after angioplasty
ī‚§ Radiation delivered either with
temporary implant or radioactive
stent
ī‚§
Intra operative Radiation
brachytherapy

ī‚§ Attractive for deep tumors

because the skin dose was
limiting prior to the invention
of megavoltage accelerators.
ī‚§ Applications include:
retroperitoneal
sarcoma, pancreatic cancer,
rectal cancer, pediatric
tumors,malignant thoracic
tumors.
ī‚§ dose of 10 to 20 Gy in single
fr over 10 to 30 minutes.
Image guided brachytherapy
ī‚§ Image-guided brachytherapy may provide

better dose distribution to the target tumor
and reduced dose volumes to surrounding
healthy tissues when compared with imageguided IMRT and IMPT.
ī‚§ The use of imaging techniques, such as
ultrasound,CT and MRI for treatment
planning, has led to improved visualization of
the tumor and surrounding organs.
IGBTâ€Ļ

ī‚§ Applicators used for IGBRT should be such

that the applicator does not produce an
artifact on the cross sectional imaging
technique being used. For this purpose
special CT/MRI Compatible applicators
should be used. The applicators are usually
made up of a titanium alloy Now a days
carbon fibre based brachytherapy
applicators are also available.
ī‚§ MR is an ideal image guidance modality
for image guided brachytherapy.
Outstanding visualization of pelvic
Adaptive Brachytherapy
ī‚§ Adaptive Brachytherapy can be defined as

temporally changing the treatment plan
delivered to a patient based on observed
anatomic changes caused by tumor shrinkage,
weight loss, or internal motion.
ī‚§ Plans are altered throughout the treatment
course for every course of treatment depending
on tumor volume.
ī‚§ Patient setup and organ motion obtained from
imaging during treatment to alter the treatment
plan.
ROBOTIC BRACHYTHERAPY
ī‚§ Improve accuracy of needle placement

and seed delivery
ī‚§ Improve consistency of seed implant
ī‚§ Improve avoidance of critical structures
ī‚§ Reduce radiation exposure
ī‚§ MAINLY USED FOR CA PROSTATE
ī‚§ Seed placement error is at sub millimeter

level.
Intensity modulated
brachytherapy
ī‚§ This modulation is specific for the patient and allows for high
intensity radiation treatment of tumor tissue with limited
destructive effects on surrounding normal tissue.
ī‚§ Intensity modulated sources based on Monte Carlo
simulations
ī‚§ a “modified TG43” (mTG43) dose calculation algorithm
developed specifically for IMBT dosimetry. the anisotropic
function of a IMBT source, is a function of both the position
of measurement and the intensity distribution of the source
ī‚§ an inverse IMBT treatment planning method based on Dose
Volume Histogram (DVH) or Dose Surface Histogram (DSH)
constraints and simulated annealing optimization algorithm.
clinical applications of ldr and hdr brachytherapy

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clinical applications of ldr and hdr brachytherapy

  • 1. CLINICAL APPLICATIONS OF LDR-HDR BRACHYTHERAPY DR. SUGASHWARAN. J, MODERATOR:PROF.DR.G. V. GIRI, DEPT. OF RADIATION ONCOLOGY, KMIO, BANGALORE.
  • 2. BRACHYTHERAPY ī‚§ Type of radiation treatment ī‚§ Consists of placing sealed radioactive sources very close to or in contact with the target tissue.
  • 3. CLINICAL ADVANTAGES ī‚§ High biological efficacy ī‚§ Rapid dose fall-off ī‚§ High tolerance ī‚§ Tolerable acute intense reaction ī‚§ Decreased risk of tumor population ī‚§ High control rate ī‚§ Minimal radiation morbidity ī‚§ Day care procedure
  • 4. LIMITATIONS & DISADVANTAGES Difficult for inaccessible regions Limited for small tumors (T1_T2) Invasive procedures, require GA Higher dose inhomogeneity Greater conformation –small errors in placement of sources lead to extreme changes from the intended dose distribution ī‚§ Radioactive hazards (not now) ī‚§ Costly ī‚§ ī‚§ ī‚§ ī‚§ ī‚§
  • 5. SELECTION CRITERIA ī‚§ Easily accessible lesions ī‚§ Early stage diseases (Ideal implant ≤ 5 cm) ī‚§ Well localized tumor to organ of origin ī‚§ No nodal or distant metastases (radical ī‚§ ī‚§ ī‚§ ī‚§ intent) No local infections or inflammation Favorable histology- mod. diff. i.e. SCC Well controlled DM / HTN Proliferative/exophtic lesions preferred (better outcome)
  • 6. INDICATIONS ī‚§ SOLE MODALITY īƒē Skin malignanciesBCC, SCC īƒē Head & neck cancers īƒē Ca cx īƒē Ca prostate ī‚§ BOOST( AFTER EXT.RTÂąCCT) īƒē Head & neck cancers īƒē Ca Breast īƒē Esophagus īƒē Anal canal
  • 7. INDICATIONS... ī‚§ PERIOPERTIVE īƒē STS īƒē Ca Breast ī‚§ POSTOP īƒē Ca Endometrium īƒē Ca cx īƒē Ca Breast ī‚§ PALLIATIVE īƒē Bronchogenic Ca īƒē Biliary duct malignancy īƒē Ca Esophagus īƒē Recurrent tumors ī‚§ BENIGN īƒē Keloids / Pterygium ī‚§ OTHERS īƒē Endovascular/Rad. stent
  • 8. CLASSIFICATION ī‚§ SURGICAL APPROACH / POSITIONING īƒē SOURCE IN TUMOR ī‚  ī‚  ī‚  ī‚  INTERSTITIAL INTRACAVITARY INTRALUMINAL ENDOVASCULAR īƒē SOURCE IN CONTACT BUT SUPERFICIAL ī‚  SURFACE BRACHYTHERAPY/ MOULD ī‚§ DURATION OF IRRADIATION īƒē TEMPORARY-Cs137,Ir192 īƒē PERMANENT-I125,Au198 Pd 103 .Cs 131
  • 9. DOSE RATE(ICRU 38) ī‚§ LOW DOSE RATE (LDR) īƒē 0.4-2 Gy/hr (clinical practice range 0.4 to 1 Gy per hour) ī‚§ MEDIUM DOSE RATE (MDR) īƒē 2-12 Gy/hr ī‚§ HIGH DOSE RATE (HDR) īƒē > 12 Gy/hr ī‚§ ULTRA LOW DOSE RATE īƒē 0.01-0.3 Gy/hr
  • 10. ADVANTAGES LDR HDR ī‚§ Predictable clinical effects ī‚§ Superior radiobiological ī‚§ SHORT TREATMENT TIME role ī‚§ Less morbidity, control is best ī‚§ Well practised since long ī‚§ Minimum intersession variability in dose distribution īƒē Geometry well maintained īƒē Better patient compliance / comfort īƒē Day care procedure ī‚§ DOSE OPTIMIZATION ī‚§ NO RADIATION HAZARDS ī‚§ SMALL APPLICATOR īƒē Less tissue trauma īƒē Better packing
  • 11. AFTER LOADING TECHNIQUE ī‚§ MANUAL īƒē Avoids radiation īƒē īƒē īƒē īƒē protection issue of preloading Better applicator placement Verification prior to source placement More radiation hazard Advantages of preloading ī‚§ REMOTE CONTROLLED īƒē īƒē īƒē īƒē īƒē īƒē īƒē īƒē No radiation hazard Accurate placement Geometry maintained Better dose distribution Highly precise Short Treatment time Day care procedure Mainly used for HDR
  • 12. RADIOBIOLOGY ī‚§ Biological effects depend on īƒē Prescribed dose īƒē Treated volume īƒē Dose rate īƒē Fractionation īƒē Treatment duration
  • 13. RADIOBIOLOGY – 4 Rs ī‚§ ī‚§ ī‚§ ī‚§ Repair Reassortment / redistribution Repopulation Reoxygenation
  • 14. INTERSTITIAL BRACHYTHERAPY ī‚§ Sealed Radioactive sources directly implanted into the tumor in a geometric fashion ī‚§ ADVANTAGES īƒē īƒē īƒē īƒē īƒē īƒē Higher local dose in shorter time Rapid dose fall Better tumor control Lesser radiation morbidities Superior cosmetics Functional preservation of organs
  • 15. INTERSTITIAL BRACHYTHERAPYâ€Ļ ī‚§ DISADVANTAGES īƒē Invasive procedure īƒē Costly ī‚§ INTENTION OF TREATMENT īƒē RADICAL INTENTION ī‚  As radical brachytherapy alone (smaller lesions) ī‚  Local boost in combination with EBRT (larger lesion)
  • 16. SELECTION CRITERIA ī‚§ Easily accessible lesions, at least from one side ī‚§ Early stage disease īƒē T 1-T2 and sometimes early T3 īƒē Ideally total size of implant ≤ 5 cm ī‚§ Well controlled DM /HTN ī‚§ No local infection
  • 17. CLINICAL APPLICATIONS ī‚§ Head & neck tumors īƒē Early stage oropharyngeal cancers ī‚§ Ca breast- Boost /PBI ī‚§ Ca prostate ī‚§ Soft tissue sarcoma ī‚§ Gynecologic malignancies ī‚§ Ca anal canal and rectum ī‚§ Ca lung and pancreas
  • 18. TYPES OF INTERSTITIAL IMPLANTS ī‚§ TEMPORARY ī‚§ PERMANENT ACCORDING TO SIZE/LOCATION/PROXIMITY OF TUMOR TO NORMAL STRUCTURES īƒē Radioactive sources removed after desirable dose has been delivered īƒē Rigid stainless steel needles/flexible Teflon / nylon guides/plastic tubes īƒē Preloaded/After loaded īƒē Preloaded – rigid needle eg. Ra226 ,Cs137 īƒē After loaded – Manual/ Remote īƒē Advantages ī‚  Flexibility of implant design ī‚  Reduction of radiation exposure levels resulting in more accurate placement of needles and guides
  • 19. PERMANENT IMPLANTS ADVANTAGES īƒē Less accessible sites īƒē ultra low dose rate/Max biological effectiveness īƒē Better tissue heal īƒē Better effect in slow and radio resistant tumors īƒē Improved mobility DISADVANTAGES īƒē Environmental issue īƒē Dosimetric uncertainties/ Later part of Treatment becomes less effective īƒē Source displacement īƒē Large tumor /Difficult procedure and geometry īƒē Radio biologically less effective for rapidly proliferating tumors
  • 20. CLINICAL APPLICATIONS Oral Cavity: ī‚§ LIP: īƒē Indications: T1-2N0 Lesions (monotherapy- 0.5to5 cm or boost therapy->5 cm) T.V.: All visible & palpable tumour with 5-10 mm margin īƒē Dose: 50-70Gy in 5-7 days LDR īƒē Technique: ī‚  Rigid after loading needles maintained in place by Template ī‚  Classical plastic tubes īƒē Spacers to decrease dose to gingiva, teeth & other lip
  • 21. CLINICAL APPLICATIONSâ€Ļ Buccal Mucosa: īƒē Indications: īƒē īƒē īƒē īƒē ī‚  Brachytherapy alone indicated for small (<4cm), welldefined lesions in anterior 2/3rd ī‚  As boost after EBRT for larger lesions T.V.: GTV +0.5 to 1 cm margins Dose: Alone 65-70 Gy ī‚­ Boost 25-30 Gy Technique: Guide Gutter Technique: Lesion < 2cm Plastic tube technique: For other lesions
  • 22. CLINICAL APPLICATIONSâ€Ļ Oral Tongue: ī‚§ Indications: T1 N0, T2 N0 < 3cm lesion ī‚§ T.V.: GTV + 5 mm margin ī‚§ Dose: Alone:60-65 Gy LDR ī‚  Boost 20-25 Gy after EBRT dose of 45-50 Gy ī‚§ Techniques: Guide-gutter technique AP X-ray
  • 23. CLINICAL APPLICATIONSâ€Ļ Floor of Mouth: īƒē Indications: T1-2N0 lesions, â‰Ĩ 5 mm away from mandible īƒē Dose: monotherapy-65Gy;boost-20 to 30 Gy īƒē Complication: bone necrosis is most common, up to 30% Oropharynx: īƒē Indications: Ca BOT, soft palate, tonsillar fossa & vallecula usually as boost after EBRT ī‚  Lesions < 5 cm (after EBRT) īƒē T.V.: GTV + 10 mm margin īƒē Dose: Tonsillar fossa-25-30 Gy; BOT 30-35 Gy īƒē Technique: Classical Plastic Loop technique
  • 24. CLINICAL APPLICATIONSâ€Ļ ī‚§ Nasopharynx: Ind- T1 AND T2 lesions Dose: LDR -as a sole treatment 60Gy; as a boost 12 to 20 Gy. HDR- 18 Gy in 6 fr ī‚§ Opthalmic brachytherapy(I-125,Ru-106,Sr90) Ind- malignant tumors of the conjuctiva, pterygium,wet macular degeneration,neovascularization Sr 90 dose rate-100Gy/hr,, I-125 dose rate 0.5 to 1 Gy/hr Pterygium – Sr 90 dose varying from 20 to 60 Gy in 1 to 6 fr.
  • 25. CLINICAL APPLICATIONSâ€Ļ Breast īƒēIndications: Boost after BCS & EBRT ī‚­ Postoperative interstitial irradiation alone of the primary tumor site after BCS in selected low risk T1 and small T2N0 (PBI) As sole modality As Boost to EBRT Patient choice: cannot come for 5-6 wks treatment : Close, positive or unknown margins ī‚§ Distance ī‚§ Lack of time Elderly, frail, poor health patient EIC Large breasts, unacceptable toxicity with EBRT Younger patients Deep tumour in large breast Irregularly thick target vol. ī‚­ Chest wall recurrences
  • 26. CLINICAL APPLICATIONSâ€Ļ ī‚§ T.V.: Primary Tumor site + 2-3 cm margin ī‚§ Dose: As Boost: 10-20 Gy LDR ī‚  AS PBI: 45-50 Gy in 4-5 days LDR (30-70 cGy/hour) ī‚­ 34 Gy/10fr, 2fr per day HDR ī‚§ Technique: īƒē Localization of PTV: Surgical clips (at least 6) ī‚  USG, CT or MRI localization, Intra op USG īƒē During primary surgery īƒē Guide needle technique or īƒē Plastic tube technique using Template ī‚  Double plane implant ī‚  Skin to source distance: Minimum 5 mm
  • 27. MAMMOSITE ī‚§ Used for Accelerated Partial Breast Irradiation(APBI) ī‚§ Fluid filled balloon placed during surgery Prescription Reference Point at 1 cm 340cGy per fraction 2 fractions per day 6 hour separation 10 fractions total Weekend break is allowed
  • 28. Ideal patients for APBI(ASTRO) ī‚§ Tumor Size < 2 cm ī‚§ Absence of nodal involvement(N0) ī‚§ Absence of Metastatic Status(M0) ī‚§ Age > 60 yr ī‚§ Negative margins ī‚§ Invasive ductal histology in the absence of DCIS ī‚§ Estrogen receptor positive
  • 29. HDR Brachytherapy with Savi The Savi applicator is a new single insertion multicatheter device used for partial breast radiation. It has a single central catheter and multiple peripheral catheters. This allows the radiation dose to be tailored to the shape of the lumpectomy cavity.
  • 30. Contura- multi lumen baloon ī‚§ Consists of a central lumen and 4 outer lumen offering a total of 40 dwell positions ī‚§ Encased in a polyurethane balloon which maintains symmetry and reduces potential for balloon ruputre.
  • 31. NEW ELLIPTICAL BALOON(2004) ī‚§ Provides excellent conformance ī‚§ Ellipsoidal implant parellel to the chest wall provides appropriate symmentry
  • 32. AXXENT:NEWER DEVICE ī‚§ Uses a miniaturized x-ray source to deliver low energy x-rays within a needle or catheter. ī‚§ Use of this device for APBI ī‚§ No need for heavy room shielding ī‚§ Stay in room with patient during treatment ī‚§ No radioactive materials license needed ī‚§ No handling, storing, security concerns ī‚§ One source per patient ī‚§ Must calibrate source before each treatment
  • 33. CLINICAL APPLICATIONSâ€Ļ Prostate: ī‚§ Indications īƒē Brachytherapy as monotherapy: ī‚  Stage T1-2a /Gleason score 2-6 / PSA ≤ 10 ng/ml īƒē As boost after EBRT ī‚  Stage T2b, T2c /Gleason score 7-10 /PSA > 10 ng/ml ī‚§ Patient factors : īƒē īƒē īƒē īƒē īƒē Life expectancy > 5 yrs IPSS<15 Prostate volume<60cm2 No defect if previous TURP Minimal pubic arch interfence ī‚§ T.V.: Whole prostate within capsule + 2-3 mm margin ī‚§ Methods: Permanent Implant (I125 or Pd103) or Temporary Implant (Ir192)
  • 34. CLINICAL APPLICATIONSâ€Ļ Technique for Permanent implant ī‚§ Retropubic approach with I125 seeds- Disappointing results ī‚§ Modern technique: Transperineal Approach īƒē TRUS guided īƒē Two step approach ī‚  Volume study of prostate ī‚  pubic arch interfence assessment īƒē Computer planning ī‚§ Coverage check -USG & Flouroscopy ī‚§ Bladder irrigation /Cystoscopy can be performed ī‚§ Post-implant image based dosimetry
  • 35. CLINICAL APPLICATIONS ī‚§ Dose: īƒē I125: 145 Gy as sole RT;100-110 Gy as boost to 40-50 Gy EBRT īƒē Pd103: 125 Gy as sole RT;90-100 Gy as boost to 40-50 Gy EBRT īƒē Cs 131 :115 GY as sole rt;85-95 Gy as boost to 40-50 Gy EBRT Temporary Implants with Ir192 (LDR or HDR): īƒē Procedure same as above; lesser no. of plastic catheters required (8-15) īƒē Dose: ī‚  LDR 30-35 Gy seeds left for 3 days(Boost to 45 Gy EBRT) ī‚  HDR 20-25 Gy, 4-6 Gy/#(Boost to 45 Gy EBRT)
  • 36. CLINICAL APPLICATIONS Soft tissue Sarcomas (using Ir192 or I125) ī‚§ Indications: īƒē As sole postop RT: ī‚  completely resected intermediate or high grade tumours of extremity or superficial trunk with -ve margins īƒē As boost to postop EBRT: ī‚  Intermediate or high grade sarcoma with +/- margins ī‚  Postop pts with small lesions & +ve/uncertain margins ī‚  Deep lesions ī‚  Low grade sarcomas ī‚§ T.V.: GTV + 2-5 cm margin ī‚  GTV based on preop MRI & clinical findings ī‚§ Dose: LDR (Ir seeds or wires) as sole treatment 45-50 Gy in 4-6 days ī‚  As boost to 45-50 Gy EBRT: 15-25 Gy in 2-3 days HDR: as sole treatment 40 t0 50 Gy in 12 to 15 fr/ as boost to 45-50 Gy EBRT:18-25 Gy in 4-8 fr
  • 37. CLINICAL APPLICATIONSâ€Ļ Technique: īƒē Usually performed at time of surgery īƒē Basic or sealed end temporary implant technique īƒē To delay the start of brachytherapy for about 4 to 7 days after surgery īƒē limit the allowable skin dose the 40 Gy isodoseline to <25cm2 and the 25 Gy isodose line <100 cm2
  • 38. CLINICAL APPLICATIONSâ€Ļ Brain: Permanent or temporary (using I125 or Ir192 seeds/wires ) ī‚§ Indications: īƒē As boost to EBRT or recurrence īƒē Anaplastic astrocytoma or GBM, unifocal, well cicumscribed, peripheral lesions & < 5 cm in diameter ī‚§ T.V.: Contrast enhancing area on MRI +/- 5mm margin ī‚§ Dose: LDR 50-60 Gy, 0.4-0.5 Gy/hr
  • 39. Gliasite ī‚§ Used to treat brain tumors ī‚§ Balloon filled with I-125 containing solution ī‚§ Example: used to treat glioblastoma multiformae to 50 Gy followed by EBRT boost
  • 40. CLINICAL APPLICATIONSâ€Ļ Ca Anorectum ī‚§ Indications: As boost to EBRT/ChemoRT ī‚­ If T.V. does not exceeds 1/2 circumference, 5 mm thick, 5 cm long i.e. T1-2 & small T3 lesions ī‚­ T1N0 adenocarcinoma of rectum 3-10 cm above anus ī‚§ T.V.: Visible palpable tumor+5 mm ī‚§ Dose: LDR 15-20 Gy at 0.3-0.6 Gy/hr ī‚§ Technique: Guide needle technique with plastic perineal template
  • 41. CLINICAL APPLICATIONSâ€Ļ Gynecological Tumors (Ir192 LDR or HDR) ī‚§ Indications: īƒē Ca Cervix īƒē Ca Endometrium ī‚  Postop local recurrence īƒē Ca Vagina & Vulva ī‚  Radical BT in early lesions (T1-2N0) ī‚  Boost after EBRT in large lesions (T2-3N1) ī‚§ Technique: īƒē Guide-gutter technique īƒē Blind plastic tube implant (transperineal technique) īƒē Plastic or guide needles
  • 42. CLINICAL APPLICATION – CA ABS Recommendations CX īƒē Bulky primary disease īƒē Prior hysterectomy-inability to place tandem īƒē Post hysterectomy īƒē vault rec/cervical stump presentation īƒē Extesive parametrial involvement īƒē Distorted anatomy īƒē Narrow vagina & fornices īƒē Extensive / Distal vaginal wall involvement īƒē Re-irradiation after recurrences
  • 43. CLINICAL APPLICATIONSâ€Ļ īƒē PERINEAL IMPLANTS Martinez Universal Perineal Interstitial Template (MUPIT) Syed-Neblett template
  • 44.
  • 45. CLINICAL APPLICATIONSâ€Ļ īƒē Ca Lung: Permanent perioperative BT, I125 seeds ī‚­ Persistent or recurrent ds after EBRT or residual ds after surgery īƒē Ca Pancreas: Permanent perioperative BT, I125 seeds ī‚­ Locally advanced unresectable ds īƒē Ca Penis: scc predominant histology, Indications – T1,T2 and T3(<4cm)that do not involve the shaft of penis. Based on paris system using templates(12 &18mm) Dose ;60 Gy at a dose rate of 0.5 to0.65Gy/hr īƒē Ca urethra: as sole treatment is 60 to 70 Gy in 3 to 5 days; as a boost 20 to 25 Gy.
  • 46. INTRACAVITARY APPLICATION ī‚§ Radioactive sources are placed in a existing cavity usually inside a predefined applicator with special geometry ī‚§ Uses: īƒē Cervix īƒē Endometrium īƒē Vagina īƒē Maxilla īƒē Nasopharynx
  • 47. DOSE SCHEDULE ī‚§ LDR (<200cgy/hr) īƒē 35-40 Gy at point A ī‚§ MDR (200-1200cgy/hr) īƒē 35 Gy LDR EQUIVALENT at point A ī‚§ HDR(>1200cgy/hr) īƒē 9 Gy in 2 fr īƒē 6.8Gy in 3 fr at point A
  • 48. EXTERNAL RT WITH BRACHYTHERAPYfollow external irradiation ī‚§ Brachytherapy can īƒē SIMULTANEOUS ī‚  Stage I - II with very minimal parametriun involvement ī‚  HDR -5 sessions (9gy /fr, 1week apart) ī‚  40 Gy by EBRT simultaneously īƒē SANDWICH ī‚  Stage I-II ī‚  40 Gy LDR eq.—â€ē EBRT 40 Gy ī‚§ In both above cases a MIDLINE SHIELD is used
  • 49. POST OP/ VAULT ī‚§ Vault RT BRACHYTHERAPY īƒē No residual disease ī‚  8500 cGy at 5mm from the surface of the vault ī‚  2 sessions 1 week apart īƒē Residual disease ī‚  CTV of 2 cm given to gross tumor and the prescription of 8500cgy encompassing the whole CTV is made ī‚  2 sessions 1 week apart ī‚§ Mostly after EBRT
  • 50. POST OP BRACHYTHERAPY ī‚§ CONTRAINDICATIONS īƒē Vaginal wall involvement ( middle- lower 13) īƒē Heavy parametrium infiltration īƒē VVF or VRF īƒē Inadequate space īƒē Medical contraindications īƒē Metastatic disease ī‚§ Supplementary radiation 2000 cGy 10fr
  • 51. SURFACE MOULDS Radiation is delivered by arranging RA sources over the surface of tumor ī‚§ Types īƒē Planar ī‚  Circular ī‚  Square ī‚  Rectangular īƒē Line source īƒē Cylinder
  • 52. INDICATIONS ī‚§ Superficial /Accessible tumors keloid : Sr90 , 20 gy in 4 fr after surgery. ī‚§ Skin ca – HAM applicator, Freiburg flab are surface template applicators, dose – 35 to 50 Gy in 5 to 10 fr. ī‚§ Post mastectomy recurrence – LDR- 65 Gy in 2 to 3 fr,monthly intervals. ī‚§ Oral tumor īƒē hard palate ,alveolus,oral cavity,lip īƒē as a sole modality 60 GY,as boost to 45 to 50 GY- 15 TO 30 Gy. ī‚§ Penile carcinoma
  • 53. INTRALUMINAL BRACHYTHERAPY ī‚§ Radioactive source is passed through a tube and passed into a hollow lumen ī‚§ Sites īƒē Esophagus : TV-tumor+distal and proximal margin of 2 to 3 cm Dose: palliative-16 GY IN 2 FR or 18 GY IN 3 FR. as boost EBRT 50 Gy-HDR 10 Gy in 2 fr at 1 cm from surface.
  • 54. ILBT.. īƒē Bronchus : Bronchogenic carcinoma ī‚  Definitive : T1-T2tumors HDR- sole treatment-5Gy in 5 fr or 7.5 Gy in 2 fr prescribed to 1cm. as boost to EBRT treatment(45 TO 60 Gy)- three 5 Gy fr or two 7.5 GY fr ī‚  Palliative : ī‚­ ī‚­ ī‚­ ī‚­ Dyspnea,hemoptysis,post obstructive pneumonitis Poor lung function Previous EBRT Dose : 7.5Gy/fr in3 weekly fr, 10Gy/fr in 2 fr, 6Gy/fr in 4 fr prescribed at 1 cm. Boost treatment- 30 Gy in 10 to 12 fr
  • 55. Biliary tract ī‚§ Ind – unresectable tumors ī‚§ Technique – endoscopic retrograde technique ī‚§ BT delivered throug a transhepatic cholangiogram ī‚§ TV- tumor +1 to 2 cm proximal and distal margin ī‚§ Monotherapy- palliative dose 30 gy in 6 fr ī‚§ As boost(45 Gy EBRT) – 15 TO 20 Gy in 3 to 4 fr.
  • 56. Intra vascular brachytherapy Coronary artery disease caused by occlusion of cardiac vessels ī‚§ IVB used to prevent restenosis after angioplasty ī‚§ Radiation delivered either with temporary implant or radioactive stent ī‚§
  • 57. Intra operative Radiation brachytherapy ī‚§ Attractive for deep tumors because the skin dose was limiting prior to the invention of megavoltage accelerators. ī‚§ Applications include: retroperitoneal sarcoma, pancreatic cancer, rectal cancer, pediatric tumors,malignant thoracic tumors. ī‚§ dose of 10 to 20 Gy in single fr over 10 to 30 minutes.
  • 58. Image guided brachytherapy ī‚§ Image-guided brachytherapy may provide better dose distribution to the target tumor and reduced dose volumes to surrounding healthy tissues when compared with imageguided IMRT and IMPT. ī‚§ The use of imaging techniques, such as ultrasound,CT and MRI for treatment planning, has led to improved visualization of the tumor and surrounding organs.
  • 59. IGBTâ€Ļ ī‚§ Applicators used for IGBRT should be such that the applicator does not produce an artifact on the cross sectional imaging technique being used. For this purpose special CT/MRI Compatible applicators should be used. The applicators are usually made up of a titanium alloy Now a days carbon fibre based brachytherapy applicators are also available. ī‚§ MR is an ideal image guidance modality for image guided brachytherapy. Outstanding visualization of pelvic
  • 60. Adaptive Brachytherapy ī‚§ Adaptive Brachytherapy can be defined as temporally changing the treatment plan delivered to a patient based on observed anatomic changes caused by tumor shrinkage, weight loss, or internal motion. ī‚§ Plans are altered throughout the treatment course for every course of treatment depending on tumor volume. ī‚§ Patient setup and organ motion obtained from imaging during treatment to alter the treatment plan.
  • 61. ROBOTIC BRACHYTHERAPY ī‚§ Improve accuracy of needle placement and seed delivery ī‚§ Improve consistency of seed implant ī‚§ Improve avoidance of critical structures ī‚§ Reduce radiation exposure ī‚§ MAINLY USED FOR CA PROSTATE ī‚§ Seed placement error is at sub millimeter level.
  • 62. Intensity modulated brachytherapy ī‚§ This modulation is specific for the patient and allows for high intensity radiation treatment of tumor tissue with limited destructive effects on surrounding normal tissue. ī‚§ Intensity modulated sources based on Monte Carlo simulations ī‚§ a “modified TG43” (mTG43) dose calculation algorithm developed specifically for IMBT dosimetry. the anisotropic function of a IMBT source, is a function of both the position of measurement and the intensity distribution of the source ī‚§ an inverse IMBT treatment planning method based on Dose Volume Histogram (DVH) or Dose Surface Histogram (DSH) constraints and simulated annealing optimization algorithm.