Bispecific Antibodies are Helping to Advance the Field of Lymphoma

News
Video

Julie M. Vose, MD, MBA, and Avyakta Kallam, MD, highlighted research advances in the lymphoma field they’ve witnessed throughout their careers.

A recent Breaking Barriers: Women in Oncology episode focused on key research advances each clinician has been a part of during their careers. Julie M. Vose, MD, MBA, and Avyakta Kallam, MD, spoke with CancerNetwork® about their research focusing on the use of bispecific antibodies and how these efforts have helped to advance the field of lymphoma.

Vose, is division chief, Neumann M. and Mildred E. Harris Professor at the University of Nebraska Medical Center, and co-editor-in-chief of ONCOLOGY®. Kallam is an assistant professor in the Division of Lymphoma and Department of Hematology & Hematopoietic Cell Transplantation from City of Hope in Duarte, California. Vose began her career working with autologous stem cell transplantation before researching CAR T-cell therapy and bispecific antibodies as the field evolved.

Kallam alluded to learning from her various mentors at the University of Nebraska, where she formerly worked as an assistant professor of hematology/oncology. During the early stages of her career, she witnessed various breakthroughs in the development of CAR T-cell therapy. She also highlighted her ongoing work with bispecific antibodies in central nervous system (CNS) lymphomas.

Transcript:

Vose:

I was involved early with autologous stem cell transplantation and trying new therapeutic regimens for that as well as new cancer therapies against lymphoma. [Work involved] a lot of monoclonal antibodies, radiolabelled antibodies, and, more recently, CAR T cells and bispecific antibodies. [There are] lots of different therapies and opportunities for our patients. There has been tremendous improvement over the years and a lot of research that’s been exciting to be involved in.

Kallam:

During training, I had the opportunity to work with Vose, James O. Armitage, MD, and Matthew Lunning, DO, FACP, when CAR T-cell therapy was just starting out. I had the privilege to witness the clinical trials and then eventually see CAR T cells being approved and becoming standard of care at this point. Right now, some of the research studies that I’m involved in involve bispecific antibodies, particularly in the field of CNS lymphomas. Bispecific antibodies are approved for systemic lymphomas, and they’re very effective. What we’re doing here is trying to see if they would be equally efficacious in the central nervous system.

Recent Videos
Preliminary phase 2 trial data show durvalumab plus lenalidomide was superior to durvalumab alone in refractory/advanced cutaneous T-cell lymphoma.
Developing odronextamab combinations following CAR T-cell therapy failure may help elicit responses in patients with diffuse large B-cell lymphoma.
Cytokine release syndrome was primarily low or intermediate in severity, with no grade 5 instances reported among those with diffuse large B-cell lymphoma.
Safety results from a phase 2 trial show that most toxicities with durvalumab treatment were manageable and low or intermediate in severity.
Investigators are currently evaluating mosunetuzumab in relapsed disease or comparing it with rituximab in treatment-naïve follicular lymphoma.
Harmonizing protocols across the health care system may bolster the feasibility of giving bispecifics to those with lymphoma in a community setting.
Establishment of an AYA Lymphoma Consortium has facilitated a process to better understand and address gaps in knowledge for this patient group.
Adult and pediatric oncology collaboration in assessing nivolumab in advanced Hodgkin lymphoma facilitated the phase 3 SWOG S1826 findings.
Treatment paradigms differ between adult and pediatric oncologists when treating young adults with lymphoma.
No evidence indicates synergistic toxicity when combining radiation with CAR T-cell therapy in this population, according to Timothy Robinson, MD, PhD.
Related Content