Phase 1/Dose Expansion Trial of Brentuximab Vedotin and Lenalidomide in Relapsed or Refractory Diffuse Large B-Cell Lymphoma
A Phase 1 study evaluated the combination of brentuximab vedotin and lenalidomide in 37 patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL) ineligible for autologous transplant. The therapy was well-tolerated, showing an overall response rate of 57% and a complete response rate of 35%. The study suggests this combination as a promising treatment option, currently under further investigation in a Phase 3 trial.
Diffuse large B-cell lymphoma (DLBCL) is a prevalent form of non-Hodgkin lymphoma, with a significant portion of patients relapsing or becoming refractory to initial treatments. The study explores the efficacy of combining brentuximab vedotin (BV), a CD30-targeted antibody-drug conjugate, with lenalidomide (Len), an immunomodulator, in treating relapsed or refractory DLBCL.
Thirty-seven patients with relapsed or refractory DLBCL, ineligible for autologous stem cell transplant, were treated with BV every 21 days and continuous Len for up to 16 cycles. The study aimed to determine the safety, maximum tolerated dose, and efficacy of this combination.
The combination therapy was well-tolerated, with the most common adverse events being neutropenia and thrombocytopenia. The overall response rate was 57%, with a complete response rate of 35%. The median progression-free survival was 10.2 months, and the median overall survival was 14.3 months. Notably, patients with CD30+ DLBCL showed a higher response rate of 73%.
The combination of brentuximab vedotin and lenalidomide presents a promising treatment option for patients with relapsed or refractory DLBCL, especially those ineligible for autologous transplant. The favorable safety profile and efficacy outcomes support further investigation in a Phase 3 trial to confirm these findings and potentially establish a new standard of care for this challenging patient population.

Stay Updated with Our Daily Newsletter
Get the latest pharmaceutical insights, research highlights, and industry updates delivered to your inbox every day.
Related Clinical Trials
Seagen, a wholly owned subsidiary of Pfizer
Posted 8/20/2020
Washington University School of Medicine
Posted 9/18/2014
Related Topics
Reference News
[1]
Phase 1/dose expansion trial of brentuximab vedotin and ...
pmc.ncbi.nlm.nih.gov · Mar 31, 2022
A Phase 1 study evaluated brentuximab vedotin and lenalidomide in 37 relapsed/refractory DLBCL patients, showing a 57% o...