Clinical Trial Details
— Status: Completed
Administrative data
| NCT number |
NCT03511781 |
| Other study ID # |
EC/TMC/31/14 |
| Secondary ID |
|
| Status |
Completed |
| Phase |
N/A
|
| First received |
|
| Last updated |
|
| Start date |
September 2015 |
| Est. completion date |
March 2021 |
Study information
| Verified date |
December 2021 |
| Source |
Tata Medical Center |
| Contact |
n/a |
| Is FDA regulated |
No |
| Health authority |
|
| Study type |
Interventional
|
Clinical Trial Summary
This prospective phase I/II study to assess the clinical toxicity and investigate the
clinical response of breast cancers to a 10 fraction hypofractionated course of radiation
therapy in advanced incurable breast cancer patients. This study would also investigate the
feasibility of voluntary breath hold technique for heart sparing in left sided breast cancer
patients. An intervention radiation therapy dose of 35 Gray in 10 fractions over 2 weeks, 5
fractions per week, 1 fraction per day will be studied within this clinical trial. Primary
objective of the study is to assess the toxicity using CTCAE version 4 and LENTSOMA toxicity
criteria, in advanced incurable breast cancer patients treated with hypofractionated
radiotherapy schedule of 35 GY in 10 fractions . Secondary objectives are 1. response rate
after radiotherapy measured using the PERCIST criteria at 3 months. 2. Change in quality of
life measured using trial outcome index (TOI) at 2 weeks after radiotherapy. 3. Measure the
change in PHQ4 score at 2 weeks after radiotherapy.
Additionally to assess the feasibility of voluntary breath hold technique for heart sparing
in left sided breast cancer patients and to biobank tissue and blood for future radiobiology
tests. A total of 30 patients will be recruited in this study. Among these 30 patients at
least 10 patients will be recruited with left sided breast cancer on which feasibility of
voluntary breath hold technique for heart sparing will be tested. Patient will be followed up
weekly during radiotherapy, then monthly for 1st three months, then 3 monthly for two years,
then 6 monthly for next 3 years.
Description:
Study design: Prospective interventional phase I/II study Study area: Tata Medical Center,
Kolkata
Aims and objectives:
Primary objective To assess the toxicity using CTCAE version 4 and LENTSOMA toxicity
criteria, in advanced incurable breast cancer patients treated with hypofractionated
radiotherapy schedule of 35 GY in 10 fractions Secondary objectives
1. response rate after radiotherapy measured using the PERCIST criteria at 3 months. 2.
Change in quality of life measured using trial outcome index (TOI) at 2 weeks after
radiotherapy. 3. Measure the change in PHQ4 score at 2 weeks after radiotherapy.
To assess the impact of hypofractionated breast radiotherapy schedule of 35 GY in 10
fractions over 2 weeks on quality of life in advanced incurable breast cancer patients using
FACT B scores PHQ4 questionnaire
To assess the feasibility of voluntary breath hold technique for heart sparing in left sided
breast cancer patients.
To biobank tissue and blood for future radiobiology tests
Consent:
All patients will be recruited after obtaining informed consent.
Sample size:
A total of 30 patients will be recruited in this phase I/ II study. Among these 30 patients
at least 10 patients will be recruited with left sided breast cancer on which feasibility of
voluntary breath hold technique for heart sparing will be tested.
Statistical analysis:
Given that this is a phase I/II study a 30 patients sample is used as a feasibility study.
Primary end point of this study is acute toxicity and secondary endpoint is radiological
response, quality of life after radiotherapy ( from baseline) . Acute toxicities are defined
as toxicities happening during and at 3 months after radiotherapy. Medcalc version 12 will be
used for statistical analysis. Paired Student t test (2-tailed) was applied to compare the
results from the different time points. The level of significance will be taken as P < 0.05.
Stopping Rules:
6 patients will be recruited in the first phase of the study (20% of total number). If 1-2 of
the 6 patients have had more than grade 3 acute toxicity (radiation dermatitis) then the
study will recruit 4 further patients as phase 2. If more than 1 of these patients are found
to have more than Grade 3 dermatological toxicity then the study will be stopped. Similarly
after recruitment of 20 patients, another safety monitoring will be undertaken . At any
point, if more than 40% of the patients have more than grade 3 toxicity the study will be
closed.
Objective Imaging in the trial:
A regional positron emission computed -computed Tomography scan of breast done before
starting radiotherapy. The standardized uptake value by the tumour, size of the tumour along
with that of the regional lymph nodes will be recorded. 3 months post completion of
radiation, the PET-CT scan will be repeated and parameters re-recorded. PERCIST criteria will
be used to evaluate response to radiation therapy.
Radiation Therapy Technique:
Acquisition of planning CT scan-
The patient is positioned supine on all in one solution breast board with head rest, arms
above head as in treatment position such that the sternum is horizontal . The CT markers are
placed on the patient approximately at the lower end of sternum in free breathing.The
position of palpable breast tissue, drain sites and scars are marked with radio opaque wires
during the CT . Helical CT scan is obtained with 5 mm thickness. Couch height from the
lateral lasers are measured as reference height for reproducing in treatment table. CT marker
positions are tattooed.
Acquisition of Outlines- A full 3D set of outlines covering the whole breast and the organs
at risk must be collected with a slice separation of no more than 5 mm. The right breast
patients are scanned with standard institutional protocol and left breast will be scanned
with Voluntary breath Hold Technique . The position of palpable breast tissue, and scars are
marked with radio opaque wires during the CT scan. Bolus will be used as and when required
for dose build up to the surface during simulation and treatment.
Target Volume Definition-
Gross Tumour Volume (GTV)- GTV will be outlined as seen on the planning CT scan, with
information available from the PET-CT scan and clinical examination. This will include any
lymph nodes in the axilla or supraclavicular fossa.
Whole Breast Clinical Target Volume (WBCTV)- This is based on the recommendations in the
START trial protocol . The CTV includes the soft tissues of the whole breast from 5 mm below
the skin surface down to the deep fascia, excluding muscle and underlying rib cage. If the
tumor is seen to involve the muscle, skin or adjoining structures adequate margins must be
taken to include these in the target volume.
Planning Target Volumes (PTV)- A field-based whole breast PTV will be used and this method is
illustrated below.
Intended field limits:
Breast:
1. Lateral or central tumour - Superior edge - 1cm above the superior border of the
palpable breast tissue Inferior limit - 1cm below palpable breast tissue Lateral limit
-1cm lateral to palpable breast, at or anterior to mid axillary line.
Medial limit -1cm medial to palpable breast tissue at or ipsilateral to midline.
Anterior- Adequate margin on skin anteriorly to account for respiratory movements as
well as random and systematic errors
2. Medial tumour As above but medial edge may be beyond midline. The internal mammary nodes
are not routinely included in the treated volume.
Supraclavicular fossa Superior: At level of cricoid or 3 cm above medial end clavicle
(whichever is superior).
Inferior: Matchplane. In some patients with a lower match plane (for anatomy or mobility)
Lateral: Junction of medial 2/3rd and lateral 1/3rd of the clavicle, including coracoid
process
Medial: Medial margin of head of clavicle Axilla:Axilla will be included in tangential field
if there is involved node clinically or radiologically in axilla.
Organs at Risk (OAR):
It is mandatory to contour ipsilateral and contralateral lung and heart, brachial plexus for
dose volume histogram assessment. Left anterior descending coronary artery will be contoured
for left sided breast cancer patients.
Radiotherapy planning Prescribed Dose 35 Gy in 10 fraction; 5 fractions a week; 1 fraction a
day for 2 weeks. Ideally, prescribed to 100% (normalization point). Dose Planning two
standard isocentric tangential fields, one lateral tangential and another medial tangential
field (6 Mega Volt, 15 MV or both could be used depending on the site and geometry of the
breasts) will be used to treat the breast encompassing the axillary nodes in clinically or
radio-logically involved. Supraclavicular fossa will be treated with one direct anterior
field. Radiotherapy will be delivered to the whole breast using tangential photons . 3D dose
calculation will be done by Analytical Anisotropic Algorithm algorithm. Segmented fields with
multi leaf or wedges will be used to achieve dose homogeneity in accordance with the
guidelines of ICRU 50/62 i.e, within 95% to 107%. Dose reporting Tangential fields prescribed
at the normalization point (ICRU reference point). The Supraclavicular field is prescribed at
a depth of Dmax for 6MV beam.
Radiotherapy Treatment Setup:
Patient will be positioned in the treatment couch as in planning CT with the help of skin
reference markers. The patient is then moved to planned isocenter according to the plan.The
medial and lateral borders are marked and verified by light field and source-to-surface
distance. The superior border of tangential fields and inferior border of supraclavicular
field is matched on the skin with light field.
Radiotherapy Treatment Delivery:
After checking the alignment , the treatment commences. Every day the patient is moved from
reference CT-Isocenter to planned isocenter and field edge (as defined by light field) is
marked with marker at every fraction.
Planning Documentation:
Electronic Treatment prescription. Planning approval and treatment approval is given on
treatment planning system. A hard copy of the planning with electronic approvals is attached
with each patient file.
treatment planning system
Quality assurance and Treatment setup verification:
In-vivo dosimetry with thermoluminescence dosimeters (TLDs) and Gafchromic film will be
performed during patient treatment. TLDs will be used to verify the skin dose in the junction
of SCF and tangential fields and along the skin surface of intact breast for each patient for
first 3 days. Film dosimetry will be used in the junction of the of Supra clavicular fossa
and Tangential field. Online clinical breast coverage verification is carried out by Visually
checking the light field on the patient on the first day of treatment. Partial conebeam CT
scan will be taken to ascertain the treatment position verification for whole breast set-up
and 2D MV image for supraclavicular field setup, for all fractions. Treatment Review Patients
are reviewed weekly, unless specified otherwise by the clinician.
Dose Constraints for Organs at Risk (OAR):
The optimal dose constraints criterias are as follows-
- The volume of ipsilateral lung receiving 10.5 Gy should be less than 15%
- The volume of heart receiving 1.75 Gy and 8.75 Gy should be less than 30% and 5%
respectively.
- Brachial plexus: EQD2 = 60 Gy (conservative estimate based on α/β= 2 for brachial
plexus). Minimum , maximum and median dose to the left anterior descending artery will
be recorded for left sided breast cancer patients undergoing voluntary breadth hold
technique. In case where optimal dose constraints criteria for heart and lung could not
be met in order to cover the gross tumour volume in breast or axilla; essential criteria
should be met ( V10.5 Gy for lung <31%, V8.75 Gy for heart <11%).
Assessment of toxicity:
Acute toxicity will be assessed weekly during radiotherapy then monthy for 1st three month
after completion of radiotherapy. Acute toxicity will be graded according to CTCAE version 4
toxicity criteria. If CTCAE Gr 3 desquamation is seen the patient will be reviewed weekly
until the desquamation is resolved to CTCAE gr 1 or less. If the patient somehow fails to
attend for the toxicity assessment, a telephone questionnaire will be asked to assess grade
of skin toxicity. Modified LENT-SOMA scale will be used for scoring various grades of late
effects occurring in brachial plexus after radiation therapy at 3 months,6 months and 1year .
Assessment of response:
Clinical assessment:
Tumour size measurement will be done pretreatment and 3 months after completion of
radiotherapy. Patients will be assessed for symptoms like breast pain, ulcer, arm oedema ,
shoulder stiffness and others at baseline . If the patients have any of these symptoms then :
for Pain in breast visual analogue scale will be used to score the pain (score 0-10), ulcer
and arm oedema will be graded according to CTCAE version 4, shoulder stiffness will be
recored as yes/no response. Symptom assessment will be repeated at 2 wks, 1 month, 2 months,
3 months, 6 months, and 1 year.
Radiological assessment:
All patients will have a baseline regional PET-CT scan of breast (including axilla and
supraclavicular fossa) done before start of radiotherapy and three month after completion of
radiotherapy another regional PET-CT scan of breast will be done. Response will be assessed
using PERCIST 1.0 criteria .
Assessment of quality of life: Quality of life will be assessed by using FACT B scale and
anxiety/mood symptoms will be assessed by a 4 question screen (PHQ4) before start of
radiotherapy, after completion of radiotherapy and 3 month, 6 months and 1 year after
completion of radiotherapy. For patients who are unable to travel, the quality of life rating
will be done over telephone for the 3 months, 6 months and 1 year follow up.
Follow up:Weekly during radiotherapy, then monthly for 1st three months, then 3 monthly for
two years, then 6 monthly for next 3 years.
Data Safety Monitoring An independent data safety monitoring committee (IDMC) will be
instigated to monitor the progress of the trial. Two radiation oncologists, a surgeon and a
lay person will be in the committee to ensure safety of patients. The IDMC will meet in
confidence after a first phase of recruitment of 6 patients (20% of the sample size). The
second meeting will be done after 10 patients are recruited and the third meeting after 20
patients recruited. A report of the findings and recommendations will be produced following
each meeting and a summary of the minutes will be submitted to the PI, and if required, the
Institutional review board.
Liability/Indemnity/Insurance:
Indemnity arrangements will be made as required.
