| CTRI Number |
CTRI/2024/12/078804 [Registered on: 31/12/2024] Trial Registered Prospectively |
| Last Modified On: |
21/07/2025 |
| Post Graduate Thesis |
No |
| Type of Trial |
Interventional |
|
Type of Study
|
Other (Specify) [Interventional arm is No Radiation Therapy (observation)] |
| Study Design |
Randomized, Parallel Group Trial |
|
Public Title of Study
|
A study to check in DLBCL (a type of lymphoma) patients whose disease disappears with chemotherapy, if Radiation therapy is required for better disease control |
|
Scientific Title of Study
|
Role of COnsolidative RADiotherapy in bulky and/or extra-nodal DLBCL (CORAD-DLBCL) with complete metabolic response (CMR) after R-CHOP regimen: A Randomized Controlled Trial |
| Trial Acronym |
CORAD-DLBCL |
|
Secondary IDs if Any
|
| Secondary ID |
Identifier |
| CORAD DLBCL_Protocol V2.1_09.09.2024 |
Protocol Number |
|
|
Details of Principal Investigator or overall Trial Coordinator (multi-center study)
|
| Name |
Dr Sangeeta Kakoti |
| Designation |
Associate Professor |
| Affiliation |
Department of Radiation Oncology, ACTREC, Tata Memorial Centre Mumbai |
| Address |
Department of Radiation Oncology
ACTREC,
Tata Memorial Centre
Sector 22, Utsav Chowk - CISF Road, Owe Camp, Kharghar, Navi Mumbai,
Raigarh MAHARASHTRA 410210 India |
| Phone |
9769938230 |
| Fax |
|
| Email |
drsangeetakakoti@gmail.com |
|
Details of Contact Person Scientific Query
|
| Name |
Dr Sangeeta Kakoti |
| Designation |
Associate Professor |
| Affiliation |
Department of Radiation Oncology, ACTREC, Tata Memorial Centre Mumbai |
| Address |
Department of Radiation Oncology
ACTREC
Tata Memorial Centre, Sector 22, Utsav Chowk - CISF Road, Owe Camp, Kharghar, Navi Mumbai,
Raigarh MAHARASHTRA 410210 India |
| Phone |
9769938230 |
| Fax |
|
| Email |
drsangeetakakoti@gmail.com |
|
Details of Contact Person Public Query
|
| Name |
Dr Sangeeta Kakoti |
| Designation |
Associate Professor |
| Affiliation |
Department of Radiation Oncology, ACTREC, Tata Memorial Centre Mumbai |
| Address |
Department of Radiation Oncology
ACTREC
Tata Memorial Centre, Sector 22, Utsav Chowk - CISF Road, Owe Camp, Kharghar, Navi Mumbai,
Raigarh MAHARASHTRA 410210 India |
| Phone |
9769938230 |
| Fax |
|
| Email |
drsangeetakakoti@gmail.com |
|
|
Source of Monetary or Material Support
|
| TMC Research Administrative Council,
Tata Memorial Centre,
Advanced Centre for Treatment, Research & Education in Cancer
Institutional Ethics Committee
ACTREC, Sector 22, Utsav Chowk - CISF Road, Owe Camp, Kharghar, Navi Mumbai, 410210, Maharashtra, India |
|
|
Primary Sponsor
|
| Name |
Dr Sangeeta Kakoti |
| Address |
Department of Radiation Oncology
ACTREC
Tata Memorial Centre, Sector 22, Utsav Chowk - CISF Road, Owe Camp, Kharghar, Navi Mumbai, 410210
Maharashtra, India |
| Type of Sponsor |
Other [Principal investigator, investigator initiated study] |
|
|
Details of Secondary Sponsor
|
|
|
Countries of Recruitment
|
India |
|
Sites of Study
|
| No of Sites = 2 |
| Name of Principal
Investigator |
Name of Site |
Site Address |
Phone/Fax/Email |
| Dr Sangeeta Kakoti |
ACTREC, Tata Memorial Centre |
Room number 20, Proton therapy Centre, Radiation Oncology department, Adult Hematolymphoid disease management group division
Plot No. 1 and 2, Sector 22
Kharghar, Navi Mumbai 410210,
Maharashtra, India. Raigarh MAHARASHTRA |
9769938230
drsangeetakakoti@gmail.com |
| Dr Sangeeta Kakoti |
Tata Memorial Hospital, Tata Memorial Centre |
Room number 1123, Radiation Oncology department, Adult Hematolymphoid disease management group division, Dr. E Borges Road, Parel, Mumbai, 400012, Maharashtra, India Mumbai MAHARASHTRA |
9769938230
drsangeetakakoti@gmail.com |
|
Details of Ethics Committee
Modification(s)
|
| No of Ethics Committees= 1 |
| Name of Committee |
Approval Status |
| IEC III ACTREC |
Approved |
|
|
Regulatory Clearance Status from DCGI
|
|
|
Health Condition / Problems Studied
|
| Health Type |
Condition |
| Patients |
(1) ICD-10 Condition: C858||Other specified types of non-Hodgkin lymphoma, |
|
|
Intervention / Comparator Agent
|
| Type |
Name |
Details |
| Comparator Agent |
Consolidative Radiotherapy (RT) |
Consolidative Radiotherapy (RT) to a dose of 36 Gy in 20 fractions over the total duration of four weeks(one fraction daily, five fractions per week); to be started within 6 weeks from last chemotherapy |
| Intervention |
Observation |
Patients will not go for Radiotherapy. They will keep doing follow up as scheduled six monthly for total duration of five years and yearly after that. |
|
|
Inclusion Criteria
|
| Age From |
18.00 Year(s) |
| Age To |
90.00 Year(s) |
| Gender |
Both |
| Details |
1) Patients aged 18 years and above, with biopsy confirmed DLBCL (stage I-IV) and baseline bulky (more than 7 cm in maximum diameter) lymph node and/or extra-nodal sites of disease
2) Received 6 cycles of Immuno-chemotherapy (R-CHOP)
3) Complete metabolic response in interim or end-of-chemotherapy PET-CT scan
|
|
| ExclusionCriteria |
| Details |
1) Patients with relapsed/refractory DLBCL
2) Prior chemo/radiotherapy due to any other disease
3) Retro-positive patients
4) Patients with testicular/CNS lymphoma
5) Patients with background indolent NHL
6) Patients with disseminated extra-nodal sites, technically not feasible to be included in RT portal
|
|
|
Method of Generating Random Sequence
|
Computer generated randomization |
|
Method of Concealment
|
Not Applicable |
|
Blinding/Masking
|
Open Label |
|
Primary Outcome
|
| Outcome |
TimePoints |
| To compare 2-year Event Free Survival (EFS) |
2 years |
|
|
Secondary Outcome
|
| Outcome |
TimePoints |
1) To compare 2-year Local control (LC)
2) To compare 2-year Overall survival (OS)
3) To compare acute and late toxicities of patients with and without consolidative RT |
2 years |
|
|
Target Sample Size
|
Total Sample Size="934" Sample Size from India="934"
Final Enrollment numbers achieved (Total)= "Applicable only for Completed/Terminated trials"
Final Enrollment numbers achieved (India)="Applicable only for Completed/Terminated trials" |
|
Phase of Trial
|
Phase 3 |
|
Date of First Enrollment (India)
|
01/02/2025 |
| Date of Study Completion (India) |
Applicable only for Completed/Terminated trials |
| Date of First Enrollment (Global) |
Date Missing |
| Date of Study Completion (Global) |
Applicable only for Completed/Terminated trials |
|
Estimated Duration of Trial
|
Years="4" Months="0" Days="0" |
|
Recruitment Status of Trial (Global)
|
Not Applicable |
| Recruitment Status of Trial (India) |
Open to Recruitment |
|
Publication Details
|
N/A |
|
Individual Participant Data (IPD) Sharing Statement
|
Will individual participant data (IPD) be shared publicly (including data dictionaries)?
Response - YES
- What data in particular will be shared?
Response - All of the individual participant data collected during the trial, after de-identification.
- What additional supporting information will be shared?
Response - Study Protocol
- Who will be able to view these files?
Response - Researchers whose proposed use of the data has been approved by an independent review committee identified for this purpose.
- For what types of analyses will this data be available?
Response - To achieve aims in the approved proposal.
- By what mechanism will data be made available?
Response - Proposals should be directed to [drsangeetakakoti@gmail.com].
- For how long will this data be available start date provided 01-12-2030 and end date provided 31-12-2045?
Response - Immediately following publication. No end date.
- Any URL or additional information regarding plan/policy for sharing IPD?
Additional Information - Nil
|
|
Brief Summary
|
Diffuse large B cell lymphoma (DLBCL) consists of 60-70% of Non-Hodgkin’s Lymphoma (NHL)
patients in India (Nair R et al, Oncology 2016). Immuno-chemotherapy incorporating Rituximab,
Cyclophosphamide, Doxorubicin, vincristine and Prednisolone (R-CHOP) is the current standard
regimen for treatment of DLBCL. A proportion of DLBCL patients present with relapse after successful treatment, and a multitude of
factors have been associated with the same. PET CT-based response assessment using a 5-point
Deauville’s score is one predictive factor, with clinical implication.
Presence of bulky lymph nodes (defined as >5 cm to >10 cm in different studies) and extranodal disease at presentation is
another risk factor for relapse. Use of local radiotherapy (RT), to the site of bulky or extranodal disease, is practiced
by multiple groups across the world, to abrogate this risk. However, there is concern about potential
acute and especially long-term toxicities of RT, due to expected long-term survivorship of these
patients. Thus, a fine balance between the potential benefit and risk is crucial.
The evidence so far, to guide clinicians about the need of RT in DLBCL is very sparse. There were
randomized studies in the pre-Rituximab and/or pre-PET era comparing chemotherapy alone (CT)
versus combination of CT and RT; which showed superiority of combined regimen (namely the analysis
of National Cancer Database (NCDB), SWOG 8736, the ECOG 1484, the GELA LNH 93-1 and 93-4
study). In addition to the issues with design and patient characteristics, the applicability of those studies
in the present era is questionable.
Retrospective studies in the Rituximab and PET era showed benefit in PFS with consolidative RT.
Possibility of inherent bias, lack of details about the RT portals and toxicities limit adopting those results
in current clinical practice.
The prospective studies include the RCT by Aviles et al. (Precis. Radiat. Oncol. 2019) showing benefit
in OS in the RT arm (flaws being non-usage of PET CT for response assessment and use of 14-day
cycles of R-CHOP), the comparison of RICOVER and RICOVER NoRTh groups by Held et al (JCO
2013) showing benefit in EFS with consolidative RT (however was not used as a response assessment
tool and patients included partial responders also).
The UNFOLDER study (published in abstract form) had randomized patients after R-CHOP to RT
versus observation; and reported significant benefit in EFS with RT; leading to closure of the RT arm.
However, 11% of patients in this study had partial response to immuno-chemotherapy, which makes
applicability of the results to patients having CMR quite challenging. The OPTIMAL-60 study (Am.
Soc. Clin. Oncol. 2017) concluded no detriment in outcomes, if RT was omitted in elderly poor-risk
patients.
There are prospective single arm studies attempting a PET based omission of RT mainly from the
British Columbia group (Sehn et al, Blood 2019, Freeman et al, Blood 2021) where there were excellent
outcomes in patients observed after CMR. The FLYER trial (ref) also showed non-inferiority of lesser
cycles of R-CHOP in favorable risk patients and none of the patients received consolidative RT.
Gaps in the evidence:
1) When a patient with bulky or extranodal disease at presentation obtains CMR after 6 cycles of R-CHOP, does
consolidative RT to the bulky site improve outcomes?
2) Sites of RT used differ across studies; some using IFRT to only the bulky site while others irradiated
all sites irrespective of baseline extent of disease. The latter is often technically and practically (higher
anticipated toxicities) challenging. Whether benefits of consolidative RT only to the baseline bulky
disease adds benefit, is yet to be defined. To address the above lacunae in scientific evidence, in the specified patient population, we are planning
this RCT.
|