Expert Interview
Discussing Iovance's TIL therapy AMTAGVI (lifileucel) recently FDA approved for unresectable or metastatic melanoma previously treated with a PD-1 blocking antibody.
Ticker(s): IOVAInstitution: University of Washington
- Director of the Melanoma and Renal Cancer Team at Fred Hutchinson Cancer Center and Professor of Medical Oncology at the University of Washington School of Medicine
- Treats ~ 100 patients per year with melanoma, ~50 of which are Stage IV
- Clinical interest in advanced skin cancers, including melanoma, ocular melanoma, Merkel cell carcinoma and other non-melanoma skin cancers; Research interest in novel immunotherapies, targeted therapies, and intra-tumoral immunotherapy.
The phase 2 C-144-01 trial showed early and durable responses in advanced melanoma patients treated with Lifileucel. Can you elaborate on the significance of these findings, especially considering the challenges faced in treating patients who have progressed on checkpoint inhibitors?
Added By: catalin_adminWith an objective response rate of 31.4% and a substantial reduction in tumor burden observed, how does Lifileucel's performance compare to existing treatments for advanced melanoma?
Added By: catalin_adminThe trial revealed different patterns of response and their impact on long-term survival. Could you discuss how these patterns might influence treatment decisions and patient outcomes?
Added By: catalin_adminSeveral patients converted to a complete response more than a year after treatment. What does this indicate about the long-term efficacy and potential of Lifileucel in melanoma therapy?
Added By: catalin_adminHow do factors like lactate dehydrogenase (LDH) levels and the number of lesions influence the efficacy of Lifileucel, and what does this mean for patient selection?
Added By: catalin_adminConsidering the safety profile of Lifileucel, particularly in relation to lymphodepletion and IL-2, how should clinicians approach the management of treatment-emergent adverse effects?
Added By: catalin_adminWhere do you see AMTAGVI fitting into the current treatment paradigm for advanced melanoma, especially for patients with resistance to checkpoint inhibitors?
Added By: catalin_adminNow that AMTAGVI is FDA approved, what future directions might research and clinical application take?
Added By: catalin_adminAre You Interested In These Questions?
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