Tumor-infiltrating lymphocyte treatment for anti-PD-1-resistant metastatic lung cancer: a phase 1 trial

医学 无容量 肺癌 肿瘤浸润淋巴细胞 肿瘤科 内科学 环磷酰胺 癌症 免疫疗法 临床终点 氟达拉滨 免疫学
作者
BC Creelan,C Wang,JK Teer,EM Toloza,J Yao,S Kim,AM Landin,JE Mullinax,JJ Saller,AN Saltos,DR Noyes,LB Montoya,W Curry,SA Pilon-Thomas,AA Chiappori,T Tanvetyanon,FJ Kaye,ZJ Thompson,SJ Yoder,B Fang,JM Koomen,AA Sarnaik,DT Chen,JR Conejo-Garcia,EB Haura,SJ Antonia
标识
DOI:10.21417/bcc2021nm
摘要

Adoptive cell therapy using tumor-infiltrating lymphocytes (TILs) has shown activity in melanoma, but has not been previously evaluated in metastatic non-small cell lung cancer. We conducted a single-arm open-label phase 1 trial ( NCT03215810 ) of TILs administered with nivolumab in 20 patients with advanced non-small cell lung cancer following initial progression on nivolumab monotherapy. The primary end point was safety and secondary end points included objective response rate, duration of response and T cell persistence. Autologous TILs were expanded ex vivo from minced tumors cultured with interleukin-2. Patients received cyclophosphamide and fludarabine lymphodepletion, TIL infusion and interleukin-2, followed by maintenance nivolumab. The end point of safety was met according to the prespecified criteria of ≤17% rate of severe toxicity (95% confidence interval, 3-29%). Of 13 evaluable patients, 3 had confirmed responses and 11 had reduction in tumor burden, with a median best change of 35%. Two patients achieved complete responses that were ongoing 1.5 years later. In exploratory analyses, we found T cells recognizing multiple types of cancer mutations were detected after TIL treatment and were enriched in responding patients. Neoantigen-reactive T cell clonotypes increased and persisted in peripheral blood after treatment. Cell therapy with autologous TILs is generally safe and clinically active and may constitute a new treatment strategy in metastatic lung cancer.
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