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Phase I study of adjuvant immunotherapy with autologous tumor-infiltrating lymphocytes in locally advanced cervical cancer
BACKGROUND: Adoptive cell therapy (ACT) with tumor-infiltrating lymphocytes (TILs) has achieved remarkable clinical efficacy in metastatic cancers such as melanoma and cervical cancer (CC). Here, we explored the safety, feasibility, and preliminary tumor response and performed translational investig...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Clinical Investigation
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9337833/ https://www.ncbi.nlm.nih.gov/pubmed/35727633 http://dx.doi.org/10.1172/JCI157726 |
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author | Huang, He Nie, Cai-ping Liu, Xiu-feng Song, Bin Yue, Jian-hui Xu, Jing-xiao He, Jia Li, Kui Feng, Yan-ling Wan, Ting Zheng, Min Zhang, Yan-Na Ye, Wei-Jun Li, Jun-Dong Li, Yan-Fang Li, Jun-yun Cao, Xin-Ping Liu, Zhi-min Zhang, Xiao-shi Liu, Qing Zhang, Xi Liu, Ji-Hong Li, Jiang |
author_facet | Huang, He Nie, Cai-ping Liu, Xiu-feng Song, Bin Yue, Jian-hui Xu, Jing-xiao He, Jia Li, Kui Feng, Yan-ling Wan, Ting Zheng, Min Zhang, Yan-Na Ye, Wei-Jun Li, Jun-Dong Li, Yan-Fang Li, Jun-yun Cao, Xin-Ping Liu, Zhi-min Zhang, Xiao-shi Liu, Qing Zhang, Xi Liu, Ji-Hong Li, Jiang |
author_sort | Huang, He |
collection | PubMed |
description | BACKGROUND: Adoptive cell therapy (ACT) with tumor-infiltrating lymphocytes (TILs) has achieved remarkable clinical efficacy in metastatic cancers such as melanoma and cervical cancer (CC). Here, we explored the safety, feasibility, and preliminary tumor response and performed translational investigations of adjuvant immunotherapy using infusion of autogenous TILs (auto-TILs) following concurrent chemoradiotherapy (CCRT) in patients with CC who had locally advanced disease. METHODS: Twenty-seven patients with CC with stage III–IV disease were recruited in this single-center, phase I study. TILs were isolated from lesions in the uterine cervix and generated under good manufacturing practice (GMP) conditions and then infused after CCRT plus i.m. IL-2 injections. RESULTS: TILs from 20 of the 27 patients were successfully expanded, with a feasibility of 74.1%. Twelve patients received TILs following CCRT. Adverse events (AEs) were primarily attributable to CCRT. Only 1 (8.3%) patient experienced severe toxicity with a grade 3 hypersensitivity reaction after TIL infusion. No autoimmune AEs, such as pneumonitis, hepatitis, or myocarditis, occurred, and there were no treatment-related mortalities. Nine of 12 patients (75.0%) attained a complete response, with a disease control duration of 9–22 months. Translational investigation showed that the transcriptomic characteristics of the infused TIL products and some immune biomarkers in the tumor microenvironment and serum of patients with CC at baseline were correlated with the clinical response. CONCLUSION: TIL-based ACT following CCRT was safe in an academic center setting, with potentially effective responses in patients with locally advanced CC. “Hot” inflammatory immune environments were beneficial to the clinical efficacy of TIL-based ACT as adjuvant therapy. TRIAL REGISTRATION: ClinicalTrials.gov NCT04443296. FUNDING: National Key R&D Program; Sci-Tech Key Program of the Guangzhou City Science Foundation; the Guangdong Province Sci-Tech International Key Program; the National Natural Science Foundation of China. |
format | Online Article Text |
id | pubmed-9337833 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Society for Clinical Investigation |
record_format | MEDLINE/PubMed |
spelling | pubmed-93378332022-08-03 Phase I study of adjuvant immunotherapy with autologous tumor-infiltrating lymphocytes in locally advanced cervical cancer Huang, He Nie, Cai-ping Liu, Xiu-feng Song, Bin Yue, Jian-hui Xu, Jing-xiao He, Jia Li, Kui Feng, Yan-ling Wan, Ting Zheng, Min Zhang, Yan-Na Ye, Wei-Jun Li, Jun-Dong Li, Yan-Fang Li, Jun-yun Cao, Xin-Ping Liu, Zhi-min Zhang, Xiao-shi Liu, Qing Zhang, Xi Liu, Ji-Hong Li, Jiang J Clin Invest Clinical Medicine BACKGROUND: Adoptive cell therapy (ACT) with tumor-infiltrating lymphocytes (TILs) has achieved remarkable clinical efficacy in metastatic cancers such as melanoma and cervical cancer (CC). Here, we explored the safety, feasibility, and preliminary tumor response and performed translational investigations of adjuvant immunotherapy using infusion of autogenous TILs (auto-TILs) following concurrent chemoradiotherapy (CCRT) in patients with CC who had locally advanced disease. METHODS: Twenty-seven patients with CC with stage III–IV disease were recruited in this single-center, phase I study. TILs were isolated from lesions in the uterine cervix and generated under good manufacturing practice (GMP) conditions and then infused after CCRT plus i.m. IL-2 injections. RESULTS: TILs from 20 of the 27 patients were successfully expanded, with a feasibility of 74.1%. Twelve patients received TILs following CCRT. Adverse events (AEs) were primarily attributable to CCRT. Only 1 (8.3%) patient experienced severe toxicity with a grade 3 hypersensitivity reaction after TIL infusion. No autoimmune AEs, such as pneumonitis, hepatitis, or myocarditis, occurred, and there were no treatment-related mortalities. Nine of 12 patients (75.0%) attained a complete response, with a disease control duration of 9–22 months. Translational investigation showed that the transcriptomic characteristics of the infused TIL products and some immune biomarkers in the tumor microenvironment and serum of patients with CC at baseline were correlated with the clinical response. CONCLUSION: TIL-based ACT following CCRT was safe in an academic center setting, with potentially effective responses in patients with locally advanced CC. “Hot” inflammatory immune environments were beneficial to the clinical efficacy of TIL-based ACT as adjuvant therapy. TRIAL REGISTRATION: ClinicalTrials.gov NCT04443296. FUNDING: National Key R&D Program; Sci-Tech Key Program of the Guangzhou City Science Foundation; the Guangdong Province Sci-Tech International Key Program; the National Natural Science Foundation of China. American Society for Clinical Investigation 2022-08-01 2022-08-01 /pmc/articles/PMC9337833/ /pubmed/35727633 http://dx.doi.org/10.1172/JCI157726 Text en © 2022 Huang et al. https://creativecommons.org/licenses/by/4.0/This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Clinical Medicine Huang, He Nie, Cai-ping Liu, Xiu-feng Song, Bin Yue, Jian-hui Xu, Jing-xiao He, Jia Li, Kui Feng, Yan-ling Wan, Ting Zheng, Min Zhang, Yan-Na Ye, Wei-Jun Li, Jun-Dong Li, Yan-Fang Li, Jun-yun Cao, Xin-Ping Liu, Zhi-min Zhang, Xiao-shi Liu, Qing Zhang, Xi Liu, Ji-Hong Li, Jiang Phase I study of adjuvant immunotherapy with autologous tumor-infiltrating lymphocytes in locally advanced cervical cancer |
title | Phase I study of adjuvant immunotherapy with autologous tumor-infiltrating lymphocytes in locally advanced cervical cancer |
title_full | Phase I study of adjuvant immunotherapy with autologous tumor-infiltrating lymphocytes in locally advanced cervical cancer |
title_fullStr | Phase I study of adjuvant immunotherapy with autologous tumor-infiltrating lymphocytes in locally advanced cervical cancer |
title_full_unstemmed | Phase I study of adjuvant immunotherapy with autologous tumor-infiltrating lymphocytes in locally advanced cervical cancer |
title_short | Phase I study of adjuvant immunotherapy with autologous tumor-infiltrating lymphocytes in locally advanced cervical cancer |
title_sort | phase i study of adjuvant immunotherapy with autologous tumor-infiltrating lymphocytes in locally advanced cervical cancer |
topic | Clinical Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9337833/ https://www.ncbi.nlm.nih.gov/pubmed/35727633 http://dx.doi.org/10.1172/JCI157726 |
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