Creating a “Watershed Moment” for Novel Therapeutic Access in Lymphoma

Commentary
Video

A new clinical trial aims to offer a novel allogenic CAR T-cell product for patients with lymphoma closer to home.

An ongoing phase 1 trial could create a “watershed moment” for providing safe CAR T-cell therapy in a setting closer to home among patients with lymphoma, according to Suman Kambhampati, MD.

In a discussion ahead of the 2025 ICE-T (Immune Cell Effector Therapy) Congress, Kambhampati spoke with CancerNetwork® about ongoing research that aims to mitigate barriers to treatment access among patients with lymphoma and other hematologic cancers, especially those who reside in rural communities. He highlighted this initiative in the context of a panel discussion he would attend at the meeting titled “Access with CAR-T and Bispecifics.”

The phase 1 trial, Kambhampati described, is designed to offer a novel allogenic CAR T-cell product to patients with relapsed/refractory lymphoma without requiring them to travel all the way to a tertiary care center. If the trial yields success, he stated that the study’s principles may also be applicable to the use of bispecific antibodies. Overall, Kambhampati explained that this collaboration with different community and rural practices may be “terrific” for expanding access to treatment for patients.

Kambhampati is an associate professor of Medicine and director of KU-VA Integration and Infrastructure Development in the Division of Hematologic Malignancies and Cellular Therapeutics of the Department of Internal Medicine at The University of Kansas Cancer Center.

Transcript:

As a tertiary care facility and an NCI-funded comprehensive cancer center, one of the big asks for us is to decrease the disparity between rural and urban patients. We take that seriously, and the Department of Hematology and Cell Therapy is now leading a national trial offering allogeneic CAR T cells for [patients with] relapsed and refractory lymphoma. This study is being led by Joseph P. McGuirk, DO, the chair of our program. We are collaborating with many community and rural practices to offer a novel allogeneic CAR T-cell product for [patients with] relapsed/refractory lymphoma close to home. They do not need to come all the way to Kansas City; these patients will be treated and managed close to home.

That could be the watershed moment, about designing these types of safe treatments that could be done or delivered close to home. If successful, I would argue the same principles could apply to bispecific drugs wherein these patients could be [treated] in a hybrid fashion. For the early phase of treatment, [they] come to a tertiary care facility and then immediately [get] sent back to community practices once they are on a safe and maintenance phase of their treatment. These new treatments are changing rapidly, and I would bet that in the next 3 to 5 years, the adoption rates for these new treatments would increase significantly. We would then be tasked to make sure that these patients have recurring access to these new drugs. This collaboration would be terrific in expanding these sorts of drugs to other tertiary care [facilities] and rural collaborations.

Reference

Birch K. “Triple Threat” CAR T-cell therapy clinical trial debuts at KU Cancer Center. News release. KU Medical Center. August 5, 2025. Accessed October 1, 2025. https://tinyurl.com/2eb2r2xp

Recent Videos
According to Greg Thurber, PhD, target-mediated uptake is the biggest driver of efficacy for antibody-drug conjugates as a cancer treatment.
Combining daratumumab with other agents is one strategy that investigators are exploring in the smoldering multiple myeloma field.
Antibody-drug conjugates are effective, but strategies such as better understanding the mechanisms of action may lead to enhanced care for patients with cancer. Antibody-drug conjugates are effective, but strategies such as better understanding the mechanisms of action may lead to enhanced care for patients with cancer.
Co-hosts Kristie L. Kahl and Andrew Svonavec highlight what to expect at the 43rd Annual Chemotherapy Foundation Symposium, such as new chemotherapeutics and targeted therapies.
A substantial portion of patients who received daratumumab in the AQUILA study were able to delay disease progression to active multiple myeloma.
Results showed no “deleterious reactions” with chlorotoxin-directed cellular therapy in a small cohort of patients with recurrent glioblastoma.
Although 1 of 21 patients with liver-dominant NETs died due to RILD in the phase 1 study, no RILD-induced deaths were observed in the phase 2 trial.
A novel CAR T-cell therapy may bind with more avidity, rather than affinity, to glioblastoma cells, said Michael Barish, PhD.
Using chlorotoxin as a targeting element may bind to more glioblastoma cells than other targeting entities, according to Michael Barish, PhD.
ADCs demonstrate superior efficacy vs chemotherapy but maintain a similar efficacy profile that requires multidisciplinary collaboration to optimally treat.
Related Content