Reid Merryman, MD, on Potential Clinical Designs with MRD-Guidance for Patients with DLBCL

News
Video

Expert details the potential for a clinical trial using minimal residual disease to guide therapy for patients with DLBCL.

Reid Merryman, MD, of the Dana-Farber Cancer Institute, spoke with CancerNetwork® about the detailed the future potential research building off an oral presentation investigating the prognostic value of circulating tumor DNA among patients with diffuse large B-cell lymphoma (DLBCL) from the 2020 American Society of Hematology (ASH) Annual Meeting & Exposition.

Transcription:

Yeah, I think you can think of different potential clinical trial designs. So, I think, The data that I presented at ASH suggests that there’s this high-risk patient population, but I don’t think we’re quite ready yet to use this in the clinical setting. I think the next step would be a clinical trial that would use MRD [minimal residual disease] to guide therapy for patients with relapsed or refractory DLBCL. So, You can imagine collecting samples for patients after salvage chemotherapy and directing MRD-negative patients to transplant and MRD-positive patients to an alternative treatment, for example CAR [chimeric antigen receptor] T-cell therapy, as part of a clinical trial.

Recent Videos
Co-hosts Kristie L. Kahl and Andrew Svonavec highlight what to look forward to at the 67th Annual ASH Meeting in Orlando.
Patients with mediastinal lymph node involved-lung cancer may benefit from chemoimmunotherapy in the neoadjuvant setting.
Stressing the importance of prompt AE disclosure before they become severe can ensure that a patient can still undergo resection with curative intent.
Thomas Marron, MD, PhD, presented a session on clinical data that established standards of care for stage II and III lung cancer treatment at CFS 2025.
Sonia Jain, PhD, stated that depatuxizumab mafodotin, ABBV-221, and ABBV-321 were 3 of the most prominent ADCs in EGFR-amplified glioblastoma.
Skin toxicities are common with targeted therapies for GI malignancies but can be remedied by preventative measures and a collaboration with dermatology.
Computational models help researchers anticipate how ADCs may behave in later lines of development, while they are still in the early stages.
ADC payloads with high levels of potency can sometimes lead to higher levels of toxicity, which can eliminate the therapeutic window for patients with cancer.
According to Greg Thurber, PhD, target-mediated uptake is the biggest driver of efficacy for antibody-drug conjugates as a cancer treatment.
Related Content