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PMID: 21498393 Published · ppublish English Clinical Trial Journal Article

Durable complete responses in heavily pretreated patients with metastatic melanoma using T-cell transfer immunotherapy.

Rosenberg SA, Yang JC, Sherry RM, Kammula US, Hughes MS, Phan GQ, Citrin DE, Restifo NP, Robbins PF, Wunderlich JR, Morton KE, Laurencot CM, Steinberg SM, White DE, Dudley ME

Abstract

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. 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. 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). 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.

MeSH Terms
Adolescent Adult Aged Combined Modality Therapy Female Humans Immunotherapy, Adoptive Lymphocyte Count Lymphocytes, Tumor-Infiltrating/immunology Male Melanoma/mortality,pathology,therapy Middle Aged Survival Analysis Telomere/genetics Treatment Outcome Young Adult
Authors & Affiliations
15 authors, click to expand affiliations / ORCID
Rosenberg Steven A
Surgery Branch, National Cancer Institute, NIH, Bethesda, Maryland, USA. sar@nih.gov
Yang James C
Sherry Richard M
Kammula Udai S
Hughes Marybeth S
Phan Giao Q
Citrin Deborah E
Restifo Nicholas P
Robbins Paul F
Wunderlich John R
Morton Kathleen E
Laurencot Carolyn M
Steinberg Seth M
White Donald E
Dudley Mark E
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Article Info
Journal
Clinical cancer research : an official journal of the American Association for Cancer Research
Abbr.
Clin Cancer Res
ISSN
1557-3265
Published
2011-07-01
Epub
2011-00-15
Pages
4550-7
Language
English
Region
United States
NLM ID
9502500
PMCID
PMC3131487
Subset
IM
Grants
Intramural NIH HHS · Z01 SC003811-33 · United States
Corrections
CommentIn
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