Dr Grajales-Cruz on Real-World Responses With Teclistamab in Pretreated R/R Multiple Myeloma

Commentary
Video

In Partnership With:

Ariel Grajales-Cruz, MD, discusses real-world safety and efficacy outcomes with teclistamab in select patients with relapsed/refractory multiple myeloma.

Ariel Grajales-Cruz, MD, assistant Member, Department of Malignant Hematology, Multiple Myeloma Section, Moffitt Cancer Center, discusses real-world safety and efficacy outcomes from treatment with the bispecific antibody teclistamab (Tecvayli) in heavily pretreated patients with relapsed/refractory multiple myeloma who progressed on aprior BCMA-directed therapy.

A retrospective, single-center study assessed the real-world efficacy of this standard-of-care therapy relative to results from the phase 1/2 MajesTEC-1 trial (NCT03145181; NCT04557098), Ariel Grajales-Cruz, MD begins. In this trial, teclistamab produced an objective response rate of 63%, he reports, and a median progression-free survival (PFS) of 11.3 months. Such findings supported the FDA approval of teclistamab in October 2022 in the treatment of patients with relapsed/refractory multiple myeloma who had received at least 4 previous lines of therapy, including a proteasome inhibitor, an immunomodulatory agent, and an anti-CD38 monoclonal antibody.

Results presented at the 2023 ASH Annual Meetingdemonstrated a favorable overall response rate of 63% with teclistamab in heavily pretreated patients in clinic, with a complete response rate of 36%, Grajales-Cruz states. These response rates were comparable to that of patients in the MajesTEC-1 trial, who were not previously exposed to prior BCMA therapy, he emphasizes. No new safety signals were identified.

Unlike the MajesTEC-1 trial, this real-world cohort comprised of more heavily pretreated patients, Grajales-Cruz reports, adding that 36 individuals had been treated with BCMA-directed therapies, including CAR T-cell therapy, antibody-drug conjugates, or other bispecific antibodies. The study also enrolled approximately 45% of patients with high-risk features as well as frailer patients with an ECOG performance status of 2 or greater, Grajales-Cruz states. Despite including a more difficult-to-treat patient population, the study demonstrated results with teclistamab that align closely with outcomes observed in the original MajesTEC-1 trial, Grajales-Cruz says. This underscores the robustness and effectiveness of teclistamab across diverse patient profiles, he concludes.

Related Videos
Krina K. Patel, MD, MSc
Erin Crane, MD, MPH
Ibrahim Aldoss, MD
Minoo Battiwalla, MD
Arlene O. Siefker-Radtke, MD
Heinz-Josef Lenz, MD, FACP
Roger Li, MD, of Moffitt Cancer Center
Rohan Garje, MD, chief, Genitourinary Medical Oncology, Baptist Health Miami Cancer Institute
Changchun Deng, MD, PhD, associate professor, hematology/oncology, University Hospitals Seidman Cancer Center; member, Immune Oncology Program, Case Comprehensive Cancer Center
Jaime R. Merchán, MD