A Prospective Phase III Study Comparing Standard Radiotherapy (24 Gy) With a PET REsponse-guided Very Low Dose (4 Gy) Staged Radiotherapy Strategy for Potentially Curable, Indolent B-cell Lymphomas

Status: Recruiting
Location: See all (7) locations...
Intervention Type: Radiation
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

The researchers are doing this study to find out whether a very low dose of radiation therapy (VLDRT) is an effective treatment for people with follicular lymphoma (FL) or marginal zone lymphoma (MZL) and works as well as the standard dose of radiation therapy. The researchers will see if VLDRT works against cancer in the area that is currently affected by cancer and if the therapy prevents new spots of lymphoma from developing. The researchers will also compare VLDRT with the standard dose of radiation therapy to see if VLDRT causes fewer side effects. Radiation therapy uses beams of intense energy to kill cancer cells. Standard doses of radiation therapy can cause short- and long-term side effects. Researchers think VLDRT may be as effective as standard doses, and, because VLDRT uses less radiation, researchers think VLDRT may cause fewer side effects than standard doses.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Patients must be diagnosed with a follicular lymphoma or marginal zone lymphoma. Of note, there are now two widely-utilized pathology classification criteria used for mature B-cell lymphomas, the World Health Organization (WHO) 5th Edition Classification of Lymphoid Neoplasms and the International Consensus Classification (ICC) of Mature Lymphoid Neoplasms. Either criteria is acceptable and for the purposes of this protocol, the following diagnoses are included:

‣ Follicular lymphoma

• WHO 5th Edition

‣ Classic follicular lymphoma (cFL)

⁃ Follicular lymphoma with uncommon features (uFL)

⁃ Pediatric type follicular lymphoma

⁃ Duodenal type follicular lymphoma

∙ ICC

‣ Follicular lymphoma, grades 1-2 or 3A

⁃ BCL2 rearrangement negative, CD23 positive follicle center lymphoma

⁃ Pediatric type follicular lymphoma

⁃ Duodenal type follicular lymphoma

⁃ Marginal zone lymphoma

• WHO 5th Edition and ICC

‣ Nodal marginal zone lymphoma

⁃ Pediatric nodal marginal zone lymphoma

⁃ Extranodal marginal zone lymphoma of mucosa associated lymphoid tissue (MALT)

• Patients must have stage I or II disease (with stage I defined as involvement of one nodal region and stage II as two or more nodal regions involved on the same side of the diaphragm)

• Patients should be newly diagnosed or previously observed with no prior lymphoma-directed therapy

• If the patient is referred for localized gastric MALT lymphoma, there should be documented negative H. Pylori testing within 6 months prior to proposed radiotherapy

• Age at the time of enrollment of ≥18 years

• Patients must be able to start radiation within 2 months from time of randomization

Locations
United States
New Jersey
Memorial Sloan Kettering Basking Ridge (All Protocol Activities)
RECRUITING
Basking Ridge
Memorial Sloan Kettering Monmouth (All Protocol Activities)
RECRUITING
Middletown
Memorial Sloan Kettering Bergen (All Protocol Activities)
RECRUITING
Montvale
New York
Memorial Sloan Kettering Suffolk - Commack (All Protocol Activities)
RECRUITING
Commack
Memorial Sloan Kettering Westchester (All Protocol Activities)
RECRUITING
Harrison
Memorial Sloan Kettering Cancer Center (All Protocol Activities)
RECRUITING
New York
Memorial Sloan Kettering Nassau (All Protocol Activities)
RECRUITING
Uniondale
Contact Information
Primary
Brandon Imber, MD
imberb@mskcc.org
631-212-6346
Backup
Joachim Yahalom, MD
646-608-2639
Time Frame
Start Date: 2025-06-09
Estimated Completion Date: 2028-06
Participants
Target number of participants: 375
Treatments
Active_comparator: Very low dose of Radiation
Patients will receive a total of 4 Gy in 1-2 consecutive daily fractions comprehensively to all initially involved sites of disease. At 12 weeks (+/- 4 weeks) post VLDRT, the patient will undergo repeat imaging and clinical evaluation.
Experimental: Standard dose of Radiation
Patients will receive a total of 24 Gy in 12 fractions comprehensively to all initially involved sites of disease over 12 consecutive business days. At 12 weeks (+/- 4 weeks) post VLDRT, the patient will undergo repeat imaging and clinical evaluation.
Sponsors
Leads: Memorial Sloan Kettering Cancer Center
Collaborators: The Leukemia and Lymphoma Society

This content was sourced from clinicaltrials.gov