by Dr. C.H. Weaver M.D. 11/2019
Topline results from Re-MIND, an observational retrospective study, demonstrated that the combination of MOR208 with Revlimid (lenalidomide) appears promising for the treatment of patients with relapsed/refractory diffuse large B-cell lymphoma (DLBCL) who were not eligible for high-dose chemotherapy and stem cell transplant.1
MOR208 is a humanized monoclonal antibody precision medicine directed against the CD19 antigen which is expressed on early B lymphocytes and B cell lymphomas which makes it a potential target for the treatment of non-Hodgkin’s lymphoma (NHL), including diffuse large B cell lymphoma (DLBCL), as well as chronic lymphocytic leukemia (CLL).
In the L-MIND clinical trial, 81 patients who had failed 1 to 3 prior lines of systemic treatment were treated with a combination of MOR208 combined with Revlimid.(2) The treatment results of the 81 patients were then compared to matched patients selected from 490 transplant-ineligible patients with relapsed/refractory DLBCL who had been previously treated with single-agent Revlimid in the Re-MIND clinical study. (1)
Preliminary findings from the L-MIND trial, presented at the 2018 ASH Annual Meeting demonstrated that MOR208 + Revlimid combination therapy was fairly well tolerated however 42% of patients did require a Revlimid dose reduction. An overall response rate of 58% and 33% complete remissions were reported following treatment with the MOR208 + Revlimid combination. Patients survived and average of 16.2 without lymphoma progression and the one year survival rate was 73%. (1)
When the study authors compared the MOR208 + Revlimid treated patients to those treated with Revlimid alone 67% of patients treated with the combination regimen responded to treatment compared to 34% of matched patients treated with Revlimid. The complete remission rate was 40% for MOR208+Revlimid compared to only 12% for treatment with Revlimid alone.
MOR208 appears to represent a new precision medicine with promise for the treatment of B cell NHL and will undergo continued evaluation and ultimately submission to the United States Food and Drug Administration for approval.
- MorphoSys AG: Primary Endpoint met in Real-World Data Study Demonstrating Clinical Superiority of the Combination of Tafasitamab and Lenalidomide compared to Lenalidomide alone [press release]. Planegg/Munich: MorphoSys AG; October 29, 2019. <a href="https://www.morphosys.com/media-investors/media-center/morphosys-ag-primary-endpoint-met-in-real-world-data-study.">https://www.morphosys.com/media-investors/media-center/morphosys-ag-primary-endpoint-met-in-real-world-data-study.</a> Accessed October 30, 2019.
- MorphoSys Provides Updates on L-MIND and B-MIND Clinical Trials of MOR208 in Relapsed/Refractory DLBCL [press release]. Planegg/Munich: MorphoSys AG; March 7, 2019. <a href="https://bit.ly/2IYLR5T.">https://bit.ly/2IYLR5T.</a> Accessed October 30, 2019.
- Salles GA, Guell J, González-Barca E, et al. Single-arm phase II study of MOR208 combined with lenalidomide in patients with relapsed or refractory diffuse large B-cell lymphoma: L-mind. Blood.2018;132(suppl 1; abstr 227). doi: 10.1182/blood-2018-99-113399.