Adoptive Cell Transfer of Tumor-Infiltrating Lymphocytes for Metastatic Acral Lentiginous Melanoma
Abstract
PURPOSE Acral lentiginous melanoma is a subtype of cutaneous melanoma arising from palmar, plantar, or subungual skin. These tumors are characterized by aggressive biology, a low tumor mutational burden (TMB), and diminished sensitivity to immune checkpoint blockade. It is unknown whether adoptive cell transfer of tumor-infiltrating lymphocytes (ACT-TIL) has efficacy in patients with acral melanoma. METHODS We analyzed prospectively collected data from 442 patients with metastatic cutaneous melanoma who were treated on clinical trials of ACT-TIL at a single institution between 1999 and 2018. Although blinded to treatment outcome and genomic data, we retrospectively identified patients who had acral subtype on the basis of clinicopathologic data available at the time of diagnosis. We then evaluated the ACT-TIL treatment outcomes of patients with acral melanoma and compared them with contemporaneously treated patients with nonacral melanoma. RESULTS Out of 442 included patients, 30 (7%) had acral melanoma while 412 (93%) had nonacral melanoma. Cohorts had similar clinical characteristics, protocol enrollment, and treatment-related factors. The objective response rate to ACT-TIL in patients with acral and nonacral melanomas was 43% and 40%, respectively ( P = .87), with 3% and 16% having complete responses (CRs; P = .07). Median progression-free survival was 3.5 and 4.1 months ( P = .40) and median overall survival was 13 and 17 months ( P = .79), respectively. Acral melanomas had lower TMB and ultraviolet mutational signature scores than nonacral melanomas. CONCLUSION ACT-TIL can mediate objective responses in patients with metastatic acral melanoma, and outcomes in patients with acral disease were unexpectedly comparable with those of contemporaneously treated patients with nonacral cutaneous melanoma. Further research is necessary to understand the immunologic basis of responses to ACT-TIL in acral melanoma and to increase the frequency of CRs.
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (18)
Paul H. McClelland
Surgery Branch, National Cancer Institute, Bethesda, MD
Shirley K. Nah
Surgery Branch, National Cancer Institute, Bethesda, MD
Alexandra M. Gustafson
Surgery Branch, National Cancer Institute, Bethesda, MD
Aaron J. Dinerman
Surgery Branch, National Cancer Institute, Bethesda, MD
Bradley S. White
Surgery Branch, National Cancer Institute, Bethesda, MD
Billel Gasmi
Surgery Branch, National Cancer Institute, Bethesda, MD
Donald E. White
Surgery Branch, National Cancer Institute, Bethesda, MD
Sivasish Sindiri
Surgery Branch, National Cancer Institute, Bethesda, MD
Jared J. Gartner
Surgery Branch, National Cancer Institute, Bethesda, MD
Todd D. Prickett
Surgery Branch, National Cancer Institute, Bethesda, MD
Paul F. Robbins
Surgery Branch, National Cancer Institute, Bethesda, MD
Maria R. Parkhurst
Surgery Branch, National Cancer Institute, Bethesda, MD
Hyunmi Halas
Surgery Branch, National Cancer Institute, Bethesda, MD
Mei Li M. Kwong
Surgery Branch, National Cancer Institute, Bethesda, MD
Stephanie L. Goff
Surgery Branch, National Cancer Institute, Bethesda, MD
James C. Yang
Surgery Branch, National Cancer Institute, Bethesda, MD
Steven A. Rosenberg
Surgery Branch, National Cancer Institute, Bethesda, MD
Nicholas D. Klemen
Surgery Branch, National Cancer Institute, Bethesda, MD