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Lifileucel, a Tumor-Infiltrating Lymphocyte Therapy, in Metastatic Melanoma
Effective treatment options are limited for patients with advanced (metastatic or unresectable) melanoma who progress after immune checkpoint inhibitors and targeted therapies. Adoptive cell therapy using tumor-infiltrating lymphocytes has demonstrated efficacy in advanced melanoma. Lifileucel is an...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8376325/ https://www.ncbi.nlm.nih.gov/pubmed/33979178 http://dx.doi.org/10.1200/JCO.21.00612 |
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author | Sarnaik, Amod A. Hamid, Omid Khushalani, Nikhil I. Lewis, Karl D. Medina, Theresa Kluger, Harriet M. Thomas, Sajeve S. Domingo-Musibay, Evidio Pavlick, Anna C. Whitman, Eric D. Martin-Algarra, Salvador Corrie, Pippa Curti, Brendan D. Oláh, Judit Lutzky, Jose Weber, Jeffrey S. Larkin, James M. G. Shi, Wen Takamura, Toshimi Jagasia, Madan Qin, Harry Wu, Xiao Chartier, Cecile Graf Finckenstein, Friedrich Fardis, Maria Kirkwood, John M. Chesney, Jason A. |
author_facet | Sarnaik, Amod A. Hamid, Omid Khushalani, Nikhil I. Lewis, Karl D. Medina, Theresa Kluger, Harriet M. Thomas, Sajeve S. Domingo-Musibay, Evidio Pavlick, Anna C. Whitman, Eric D. Martin-Algarra, Salvador Corrie, Pippa Curti, Brendan D. Oláh, Judit Lutzky, Jose Weber, Jeffrey S. Larkin, James M. G. Shi, Wen Takamura, Toshimi Jagasia, Madan Qin, Harry Wu, Xiao Chartier, Cecile Graf Finckenstein, Friedrich Fardis, Maria Kirkwood, John M. Chesney, Jason A. |
author_sort | Sarnaik, Amod A. |
collection | PubMed |
description | Effective treatment options are limited for patients with advanced (metastatic or unresectable) melanoma who progress after immune checkpoint inhibitors and targeted therapies. Adoptive cell therapy using tumor-infiltrating lymphocytes has demonstrated efficacy in advanced melanoma. Lifileucel is an autologous, centrally manufactured tumor-infiltrating lymphocyte product. METHODS: We conducted a phase II open-label, single-arm, multicenter study in patients with advanced melanoma who had been previously treated with checkpoint inhibitor(s) and BRAF ± MEK targeted agents. Lifileucel was produced from harvested tumor specimens in central Good Manufacturing Practice facilities using a streamlined 22-day process. Patients received a nonmyeloablative lymphodepletion regimen, a single infusion of lifileucel, and up to six doses of high-dose interleukin-2. The primary end point was investigator-assessed objective response rate (ORR) per RECIST, version 1.1. RESULTS: Sixty-six patients received a mean of 3.3 prior therapies (anti–programmed death 1 [PD-1] or programmed death ligand 1 [PD-L1]: 100%; anticytotoxic T-lymphocyte-associated protein-4: 80%; BRAF ± MEK inhibitor: 23%). The ORR was 36% (95% CI, 25 to 49), with two complete responses and 22 partial responses. Disease control rate was 80% (95% CI, 69 to 89). Median duration of response was not reached after 18.7-month median study follow-up (range, 0.2-34.1 months). In the primary refractory to anti–PD-1 or PD-L1 therapy subset, the ORR and disease control rate were 41% (95% CI, 26 to 57) and 81% (95% CI, 66 to 91), respectively. Safety profile was consistent with known adverse events associated with nonmyeloablative lymphodepletion and interleukin-2. CONCLUSION: Lifileucel demonstrated durable responses and addresses a major unmet need in patients with metastatic melanoma with limited treatment options after approved therapy, including the primary refractory to anti–PD-1 or PD-L1 therapy subset. |
format | Online Article Text |
id | pubmed-8376325 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-83763252022-08-20 Lifileucel, a Tumor-Infiltrating Lymphocyte Therapy, in Metastatic Melanoma Sarnaik, Amod A. Hamid, Omid Khushalani, Nikhil I. Lewis, Karl D. Medina, Theresa Kluger, Harriet M. Thomas, Sajeve S. Domingo-Musibay, Evidio Pavlick, Anna C. Whitman, Eric D. Martin-Algarra, Salvador Corrie, Pippa Curti, Brendan D. Oláh, Judit Lutzky, Jose Weber, Jeffrey S. Larkin, James M. G. Shi, Wen Takamura, Toshimi Jagasia, Madan Qin, Harry Wu, Xiao Chartier, Cecile Graf Finckenstein, Friedrich Fardis, Maria Kirkwood, John M. Chesney, Jason A. J Clin Oncol RAPID COMMUNICATIONS Effective treatment options are limited for patients with advanced (metastatic or unresectable) melanoma who progress after immune checkpoint inhibitors and targeted therapies. Adoptive cell therapy using tumor-infiltrating lymphocytes has demonstrated efficacy in advanced melanoma. Lifileucel is an autologous, centrally manufactured tumor-infiltrating lymphocyte product. METHODS: We conducted a phase II open-label, single-arm, multicenter study in patients with advanced melanoma who had been previously treated with checkpoint inhibitor(s) and BRAF ± MEK targeted agents. Lifileucel was produced from harvested tumor specimens in central Good Manufacturing Practice facilities using a streamlined 22-day process. Patients received a nonmyeloablative lymphodepletion regimen, a single infusion of lifileucel, and up to six doses of high-dose interleukin-2. The primary end point was investigator-assessed objective response rate (ORR) per RECIST, version 1.1. RESULTS: Sixty-six patients received a mean of 3.3 prior therapies (anti–programmed death 1 [PD-1] or programmed death ligand 1 [PD-L1]: 100%; anticytotoxic T-lymphocyte-associated protein-4: 80%; BRAF ± MEK inhibitor: 23%). The ORR was 36% (95% CI, 25 to 49), with two complete responses and 22 partial responses. Disease control rate was 80% (95% CI, 69 to 89). Median duration of response was not reached after 18.7-month median study follow-up (range, 0.2-34.1 months). In the primary refractory to anti–PD-1 or PD-L1 therapy subset, the ORR and disease control rate were 41% (95% CI, 26 to 57) and 81% (95% CI, 66 to 91), respectively. Safety profile was consistent with known adverse events associated with nonmyeloablative lymphodepletion and interleukin-2. CONCLUSION: Lifileucel demonstrated durable responses and addresses a major unmet need in patients with metastatic melanoma with limited treatment options after approved therapy, including the primary refractory to anti–PD-1 or PD-L1 therapy subset. Wolters Kluwer Health 2021-08-20 2021-05-12 /pmc/articles/PMC8376325/ /pubmed/33979178 http://dx.doi.org/10.1200/JCO.21.00612 Text en © 2021 by American Society of Clinical Oncology https://creativecommons.org/licenses/by-nc-nd/4.0/Creative Commons Attribution Non-Commercial No Derivatives 4.0 License: https://creativecommons.org/licenses/by-nc-nd/4.0/ |
spellingShingle | RAPID COMMUNICATIONS Sarnaik, Amod A. Hamid, Omid Khushalani, Nikhil I. Lewis, Karl D. Medina, Theresa Kluger, Harriet M. Thomas, Sajeve S. Domingo-Musibay, Evidio Pavlick, Anna C. Whitman, Eric D. Martin-Algarra, Salvador Corrie, Pippa Curti, Brendan D. Oláh, Judit Lutzky, Jose Weber, Jeffrey S. Larkin, James M. G. Shi, Wen Takamura, Toshimi Jagasia, Madan Qin, Harry Wu, Xiao Chartier, Cecile Graf Finckenstein, Friedrich Fardis, Maria Kirkwood, John M. Chesney, Jason A. Lifileucel, a Tumor-Infiltrating Lymphocyte Therapy, in Metastatic Melanoma |
title | Lifileucel, a Tumor-Infiltrating Lymphocyte Therapy, in Metastatic Melanoma |
title_full | Lifileucel, a Tumor-Infiltrating Lymphocyte Therapy, in Metastatic Melanoma |
title_fullStr | Lifileucel, a Tumor-Infiltrating Lymphocyte Therapy, in Metastatic Melanoma |
title_full_unstemmed | Lifileucel, a Tumor-Infiltrating Lymphocyte Therapy, in Metastatic Melanoma |
title_short | Lifileucel, a Tumor-Infiltrating Lymphocyte Therapy, in Metastatic Melanoma |
title_sort | lifileucel, a tumor-infiltrating lymphocyte therapy, in metastatic melanoma |
topic | RAPID COMMUNICATIONS |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8376325/ https://www.ncbi.nlm.nih.gov/pubmed/33979178 http://dx.doi.org/10.1200/JCO.21.00612 |
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