
Dr Grajales-Cruz on Real-World Responses With Teclistamab in Pretreated R/R Multiple Myeloma
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
Results presented at the
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.



































