Abdulraheem Yacoub, MD, on Advancing Outcomes for Patients With Myelofibrosis and Myeloproliferative Neoplasms

Video

CancerNetwork® spoke with Abdulraheem Yacoub, MD, during the American Association for Cancer Research Annual Meeting 2021 to discuss how predictors of response to therapy may be just as important as the development of new therapies for advancing outcomes in myelofibrosis and myeloproliferative neoplasms.

CancerNetwork® sat down with Abdulraheem Yacoub, MD, to discuss some of the data to come out of the American Association for Cancer Research (AACR) Annual Meeting 2021. He explained that predictors of response to therapy and the incorporation of early transplantation in these patients had the potential to significantly influence the field.

Transcript:

The next step in the advancements of myelofibrosis and myeloproliferative neoplasms is to be able to predict responses in patients. There are many agents in development. There are many novel drugs with very unique and different mechanisms of actions. Although completing all these clinical trials is necessary to try to define the data and find if this drug will help patients, it’s very challenging to complete all those trials simultaneously. The next wave of improvement in patient outcomes is to try to be able to identify early predictors of response. And in this way, hopefully, the treatment for myelofibrosis will be more individualized and will be more personalized. [Clinicians] will be, based on the baseline biomarkers, more likely to predict [response to] different therapies and hopefully, that will improve outcomes substantially.

Also, trying to incorporate more transplantation early on in myelofibrosis, we try also to identify which therapies can improve patient outcomes through the transplant or against transplant or maybe make patients more likely to have a successful transplant. So that’s also an area for improvement that we’re hopefully going to hear more about in the future.

Recent Videos
Findings from David Rimm, MD, PhD, suggest that there may be an inverse relationship between HER2 and TROP2 expression among patients with breast cancer.
Tissue samples collected from patients with breast cancer during treatment may help explore therapy selection and predict toxicities.
The mechanism of CTO1681 may allow it to reduce the production of a broad range of proinflammatory cytokines in DLBCL.
Younger and fitter patients with relapsed/refractory multiple myeloma were more likely to receive bispecific antibodies in community oncology settings.
Mechanistic treatment benefits were observed in the phase 2 STEM trial for patients with multiple myeloma.
Data from a retrospective cohort study showed that one-fifth of patients with multiple myeloma received bispecific antibodies in rural community settings.
Being able to treat patients with cevostamab who have multiple myeloma after 1 to 3 prior lines of therapy vs 4 lines may allow for better outcomes.
Using the monitoring of symptoms and quality of life platform may provide a quick and efficient system for patients to submit outcome data.
Although a greater risk of CNS relapse may emerge with immunotherapy-based backbones, toxicities associated with chemotherapy are avoided.
Related Content