作者
Benjamin C. Creelan,Chao Wang,Jamie K. Teer,Eric M. Toloza,Jiqiang Yao,Sungjune Kim,Ana Marie Landin,John E. Mullinax,James J. Saller,Andreas Saltos,David Noyes,Leighann B. Montoya,Wesley Curry,Shari Pilon‐Thomas,Alberto Chiappori,Tawee Tanvetyanon,Frederic J. Kaye,Zachary Thompson,Sean Yoder,Bin Fang,John M. Koomen,Amod A. Sarnaik,Dung‐Tsa Chen,José R. Conejo-Garcia,Eric B. Haura,Scott Antonia
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.