Phase I study of adjuvant immunotherapy with autologous tumor-infiltrating lymphocytes in locally advanced cervical cancer

He Huang(Sun Yat-sen University), Caiping Nie(Sun Yat-sen University), Xiufeng Liu(Sun Yat-sen University), Bin Song(BGI Group (China)), Jianhui Yue(BGI Group (China)), Jing-xiao Xu(Sun Yat-sen University), Jia He(Sun Yat-sen University), Kui Li(Sun Yat-sen University), Yanling Feng(Sun Yat-sen University), Ting Wan(Sun Yat-sen University), Min Zheng(Sun Yat-sen University), Yanna Zhang(Sun Yat-sen University), Weijun Ye(Sun Yat-sen University), Jun‐Dong Li(Sun Yat-sen University), Yanfang Li(Sun Yat-sen University), Junyun Li(Sun Yat-sen University), Xinping Cao(Sun Yat-sen University), Zhimin Liu(Sun Yat-sen University), Xiaoshi Zhang(BGI Group (China)), Qing Liu(Sun Yat-sen University), Xi Zhang(BGI Group (China)), Jihong Liu(Sun Yat-sen University), Li Jiang(Sun Yat-sen University)
Journal of Clinical Investigation
June 23, 2022
Cited by 54Open Access
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Abstract

BACKGROUNDAdoptive 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.METHODSTwenty-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.RESULTSTILs 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.CONCLUSIONTIL-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 REGISTRATIONClinicalTrials.gov NCT04443296.FUNDINGNational 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.


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