RecruitingPhase 3NCT05045664

Early Stage Follicular LymphOma and RadioTherapy PLUS Anti-CD20 Antibody


Sponsor

Heidelberg University

Enrollment

100 participants

Start Date

Jul 6, 2022

Study Type

INTERVENTIONAL

Conditions

Summary

The MIR study proved the effect of Rituximab in combination with a localized irradiation given in a standard dose. Together with the TROG 99.03 trial, this led to the recommendation of using this combined approach in early stage nodal follicular lymphoma. The GAZAI study is currently looking for the effect of a low dose radiotherapy of 2x2 Gy in combination with Obinutuzumab. The combination seems to show a high CR rate based on the 50% of the patients. This is in contrast to the FORT trial, which showed an inferiority of the 4 Gy dose compared to the standard dose (24 Gy) in terms of response and progression free survival. The goal of the FORTplus trial is to prove (1) the non-inferiority of LDRT (4Gy) in a combined approach with an anti-CD20-antibody. In case of non-inferiority, a possible (2) superiority of the Obinutuzumab + LDRT should be tested against Rituximab + standard dose using the same test set. The radiation dose can significantly be reduced to 16% of the standard dose if (1) is confirmed. Knowing the data of the FORT trial, this would have a significant influence on the treatment of the disease worldwide even if the difference in the CR rate at week 18 is not as high as currently in the historical comparison expected.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This trial is testing whether adding an anti-CD20 antibody (a drug that targets a protein on lymphoma cells) to radiation therapy improves outcomes for patients with early-stage follicular lymphoma — a slow-growing type of blood cancer. **You may be eligible if...** - You are 18 or older with confirmed stage I or II follicular lymphoma (grade 1, 2, or 3a) - Your lymphoma has not been treated before (no radiation, chemotherapy, or immunotherapy) - Your largest lymphoma site is 7 cm or smaller - Your blood counts are adequate (normal hemoglobin, white cells, platelets) - You are in good health (ECOG 0–2) **You may NOT be eligible if...** - Your lymphoma is more advanced (stage III or IV) - You have a different lymphoma subtype (e.g., grade 3b or transformed) - You have had prior treatment for lymphoma - You have significant heart disease or active autoimmune conditions requiring immune-suppressing drugs - You are pregnant or breastfeeding Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

RADIATIONStandard

12 x 2 Gy involved site radiotherapy plus Rituximab

RADIATIONExperimental

2 x2 Gy involved site radiotherapy plus Obinutuzumab

DRUGStandard

Rituximab with 12 x 2 Gy involved site radiotherapy

DRUGExperimental

Obinutuzumab with 2 x2 Gy involved site radiotherapy


Locations(12)

Vivantes Klinikum Berlin

Berlin, Germany

University of Essen

Essen, Germany

University of Göttingen

Göttingen, Germany

University Hospital Heidelberg

Heidelberg, Germany

Strahlentherapie KH Maria Hilf

Mönchengladbach, Germany

LMU München

Munich, Germany

Technische Universität München

Munich, Germany

Krankenhaus Barmherzige Brüder

Regensburg, Germany

University of Rostock

Rostock, Germany

Katharinen Hospital Stuttgart

Stuttgart, Germany

University of Tübingen

Tübingen, Germany

University of Ulm

Ulm, Germany

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NCT05045664