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ASH 2024 | Key predictors of success when administering CAR-T for DLBCL

Frederick Locke, MD, Moffitt Cancer Center, Tampa, FL, comments on the key predictors of success when administering CAR T-cell therapy for diffuse large B-cell lymphoma (DLBCL), highlighting the importance of disease burden and markers of inflammation, such as CRP and ferritin, in predicting patient outcomes. Dr Locke notes that patients with large tumors and a greater number of prior lines of therapy are less likely to respond to CAR T-cell therapy and that early referral for treatment is crucial in this setting. This interview took place at the 66th ASH Annual Meeting and Exposition, held in San Diego, CA.

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Transcript (AI-generated)

So when we think about the patients who are getting CAR T-cell therapy for treatment of diffuse large B-cell lymphoma, there are some things we can use to predict the likelihood that they have toxicity or the opportunity for a durable response. One of the predictors that I use in my clinic is just the disease burden. How much disease does that patient have on imaging, particularly on PET scan? In our research endeavors, we look at metabolic tumor volume, but it’s often not measured in our patients...

So when we think about the patients who are getting CAR T-cell therapy for treatment of diffuse large B-cell lymphoma, there are some things we can use to predict the likelihood that they have toxicity or the opportunity for a durable response. One of the predictors that I use in my clinic is just the disease burden. How much disease does that patient have on imaging, particularly on PET scan? In our research endeavors, we look at metabolic tumor volume, but it’s often not measured in our patients. So I just kind of have an idea, and patients who have large tumors with lymphoma that’s over five centimeters, I often send them for radiation bridging after we’ve collected. Other factors that I use in my practice include measurements of inflammation. We recently published a paper in Blood Cancer Discovery where we created a scoring system for these markers of inflammation. IL-6 is the cytokine that we often look at and think about, but it’s not clinically available. So we look at CRP and ferritin, and by measuring these values prior to CAR-T treatment, we can actually predict the patients who are most likely to progress quickly after CAR T-cell therapy and similarly, most likely to have toxicities. And so again, CRP, ferritin, if those are elevated, that’s a poor prognostic factor. And then of course, the more prior lines of therapy patients have, the less likely they are to respond to CAR-T. And so the sooner they’re referred to get treatment, the better.

 

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Disclosures

Aptitude Health: Honoraria; American Society of Hematology: Honoraria, Other: travel, accomodation, expenses; BioPharma Communications CARE Education: Honoraria; A2: Consultancy; Allogene: Consultancy, Research Funding; Amgen: Consultancy; Bluebird Bio: Consultancy; Bristol-Myers Squibb: Consultancy, Research Funding; Calibr: Consultancy; Caribou: Consultancy; Kite, a Gilead Company: Consultancy, Other: institutional, travel, accomodation, expenses, Research Funding; Allogene: Other: Institutional, Research Funding; CERo Therapeutics: Research Funding; Moffitt Cancer Center: Patents & Royalties; Communications CARE Education: Honoraria; Clinical Care Options Oncology: Honoraria; Imedex: Honoraria; Society for Immunotherapy of Cancer: Honoraria; Cowen: Consultancy; EcoR1: Consultancy; Gerson Lehrman Group (GLG): Consultancy; Iovance: Consultancy; Janssen: Consultancy; Legend Biotech: Consultancy; Novartis: Consultancy, Research Funding; Sana: Consultancy; Umoja: Consultancy; Pfizer: Consultancy; 2SeventyBio: Other: Institutional, Research Funding; National Cancer Institute: Other: Institutional, Research Funding; Leukemia and Lymphoma Society Scholar in Clinical Research: Other: Institutional, Research Funding.