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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  
Name  Address 
NIL  NIL 
 
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  
Status 
Not Applicable 
 
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
  1. What data in particular will be shared?
    Response - All of the individual participant data collected during the trial, after de-identification.

  2. What additional supporting information will be shared?
    Response -  Study Protocol

  3. 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.

  4. For what types of analyses will this data be available?
    Response - To achieve aims in the approved proposal.

  5. By what mechanism will data be made available?
    Response - Proposals should be directed to [drsangeetakakoti@gmail.com].

  6. 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.

  7. 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.

 
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