Durable Complete Responses in Heavily Pretreated Patients with Metastatic Melanoma Using T-Cell Transfer Immunotherapy

医学 黑色素瘤 过继性细胞移植 养生 免疫疗法 醛类白血病 内科学 转移性黑色素瘤 肿瘤科 CD8型 进行性疾病 实体瘤疗效评价标准 临床试验 外科 化疗 白细胞介素2 胃肠病学 T细胞 免疫学 癌症 免疫系统 癌症研究 细胞因子
作者
Steven A. Rosenberg,James Chih‐Hsin Yang,Richard Mark Sherry,Udai S. Kammula,Marybeth S. Hughes,Giao Q. Phan,Deborah E. Citrin,Nicholas P. Restifo,Paul F. Robbins,John R. Wunderlich,Kathleen E. Morton,Carolyn M. Laurençot,Seth M. Steinberg,Donald Edward White,Mark E. Dudley
出处
期刊:Clinical Cancer Research [American Association for Cancer Research]
卷期号:17 (13): 4550-4557 被引量:2145
标识
DOI:10.1158/1078-0432.ccr-11-0116
摘要

PURPOSE: Most treatments for patients with metastatic melanoma have a low rate of complete regression and thus overall survival in these patients is poor. We investigated the ability of adoptive cell transfer utilizing autologous tumor-infiltrating lymphocytes (TIL) to mediate durable complete regressions in heavily pretreated patients with metastatic melanoma. EXPERIMENTAL DESIGN: Ninety-three patients with measurable metastatic melanoma were treated with the adoptive transfer of autologous TILs administered in conjunction with interleukin-2 following a lymphodepleting preparative regimen on three sequential clinical trials. Ninety-five percent of these patients had progressive disease following a prior systemic treatment. Median potential follow-up was 62 months. RESULTS: Objective response rates by Response Evaluation Criteria in Solid Tumors (RECIST) in the 3 trials using lymphodepleting preparative regimens (chemotherapy alone or with 2 or 12 Gy irradiation) were 49%, 52%, and 72%, respectively. Twenty of the 93 patients (22%) achieved a complete tumor regression, and 19 have ongoing complete regressions beyond 3 years. The actuarial 3- and 5-year survival rates for the entire group were 36% and 29%, respectively, but for the 20 complete responders were 100% and 93%. The likelihood of achieving a complete response was similar regardless of prior therapy. Factors associated with objective response included longer telomeres of the infused cells, the number of CD8(+)CD27(+) cells infused, and the persistence of the infused cells in the circulation at 1 month (all P(2) < 0.001). CONCLUSIONS: Cell transfer therapy with autologous TILs can mediate durable complete responses in patients with metastatic melanoma and has similar efficacy irrespective of prior treatment. Clin Cancer Res; 17(13); 4550-7. ©2011 AACR.
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