Amod Sarnaik, MD, on Lifileucel’s Place in the Treatment Lanscape for Advanced Melanoma

Video

Sarnaik discussed the investigational TIL therapy’s potential as an additional option for patients.

“There are definitely challenges associated with implementation of a product as complex as lifileucel. This requires mobilization of resources that as a medical field we're not quite used to. The treatment does involve extensive patient and caregiver education, as well as mobilization of resources associated with practitioners of surgical oncology, medical oncology, as well as cellular therapy. Of note, cellular therapy is still a relatively emerging field, and therefore represents a relatively scarce resource.”

While there are various treatments available for patients with advanced melanoma, many of these treatments have substantial limitations or drawbacks, leaving some patients with few viable options. In this situation, some patients will turn to investigational therapies being evaluated in clinical trials.

Amod A. Sarnaik, MD, FACS, Moffitt Cancer Center and University of South Florida, recently presented data from the phase 2 C-144-01 (NCT02360579) clinical trial evaluating lifileucel (LN-144), an investigational autologous tumor infiltrating lymphocyte (TIL) therapy, at the Society for Immunotherapy of Cancer’s (SITC) 37th Annual Meeting, November 8-12, 2022, in Boston, Massachusetts.

In an interview with CGTLive, Sarnaik discussed the current treatment landscape for advanced melanoma, going over the various options available and their respective limitations, and then gave his view on where lifileucel could fit into this landscape if it becomes an approved therapy. He also discussed some of the challenges of implementing lifileucel in the clinic, going over the infrastructural limitations that currently make cell therapy options less accessible for patients than more conventional treatments.

Recent Videos
Nirav Shah, MD, MSHP, associate professor of medicine, at the Medical College of Wisconsin
Bhagirathbhai R. Dholaria, MD, an associate professor of medicine in malignant hematology & stem cell transplantation at Vanderbilt University Medical Center
Reena Sharma, MD, an adult metabolic consultant at Salford Royal Hospital
Mark Hamilton, MD, PhD, a hematology-oncology and bone marrow transplant (BMT) cell therapy fellow at Stanford University
Barry J Byrne, MD, PhD, the chief medical advisor of MDA and a physician-scientist at the University of Florida
Barry J Byrne, MD, PhD, the chief medical advisor of MDA and a physician-scientist at the University of Florida
Sarah Larson, MD, the medical director of the Immune Effector Cell Therapy Program in the Division of Hematology/Oncology at David Geffen School of Medicine at University of California, Los Angeles (UCLA)
David Porter, MD, the director of cell therapy and transplant at Penn Medicine
David Porter, MD, the director of cell therapy and transplant at Penn Medicine
Georg Schett, MD, vice president research and chair of internal medicine at the University of Erlangen – Nuremberg
Related Content
© 2025 MJH Life Sciences

All rights reserved.