SAKK 16/14: Durvalumab in Addition to Neoadjuvant Chemotherapy in Patients With Stage IIIA(N2) Non–Small-Cell Lung Cancer—A Multicenter Single-Arm Phase II Trial

医学 杜瓦卢马布 多西紫杉醇 化疗 临床终点 顺铂 围手术期 内科学 肺癌 外科 肿瘤科 癌症 阶段(地层学) 泌尿科 新辅助治疗 临床试验 免疫疗法 乳腺癌 无容量 古生物学 生物
作者
Sacha I. Rothschild,Alfred Zippelius,Eric Innocents Eboulet,Spasenija Savic Prince,Daniel Betticher,Adrienne Bettini,Martin Früh,Markus Joerger,Didier Lardinois,Hans Gelpke,Laetitia Mauti,Christian Britschgi,Walter Weder,Solange Peters,Michael Mark,Richard Cathomas,Adrian F. Ochsenbein,Wolf-Dieter Janthur,Christine Waibel,Nicolas Mach,Patrizia Froesch,Martin Buess,Pierre Bohanes,Gilles Godar,Corinne Rusterholz,Michel Gonzalez,Miklos Pless
出处
期刊:Journal of Clinical Oncology [American Society of Clinical Oncology]
卷期号:39 (26): 2872-2880 被引量:169
标识
DOI:10.1200/jco.21.00276
摘要

PURPOSE For patients with resectable stage IIIA(N2) non–small-cell lung cancer, neoadjuvant chemotherapy with cisplatin and docetaxel followed by surgery resulted in a 1-year event-free survival (EFS) rate of 48% in the SAKK 16/00 trial and is an accepted standard of care. We investigated the additional benefit of perioperative treatment with durvalumab. METHODS Neoadjuvant treatment consisted of three cycles of cisplatin 100 mg/m 2 and docetaxel 85 mg/m 2 once every 3 weeks followed by two doses of durvalumab 750 mg once every 2 weeks. Durvalumab was continued for 1 year after surgery. The primary end point was 1-year EFS. The hypothesis for statistical considerations was an improvement of 1-year EFS from 48% to 65%. RESULTS Sixty-eight patients were enrolled, 67 were included in the full analysis set. Radiographic response rate was 43% (95% CI, 31 to 56) after neoadjuvant chemotherapy and 58% (95% CI, 45 to 71) after sequential neoadjuvant immunotherapy. Fifty-five patients were resected, of which 34 (62%) achieved a major pathologic response (MPR; ≤ 10% viable tumor cells) and 10 (18%) among them a complete pathologic response. Postoperative nodal downstaging (ypN0-1) was observed in 37 patients (67%). Fifty-one (93%) resected patients had an R0 resection. There was no significant effect of pretreatment PD-L1 expression on MPR or nodal downstaging. The 1-year EFS rate was 73% (two-sided 90% CI, 63 to 82). Median EFS and overall survival were not reached after 28.6 months of median follow-up. Fifty-nine (88%) patients had an adverse event grade ≥ 3 including two fatal adverse events that were judged not to be treatment-related. CONCLUSION The addition of perioperative durvalumab to neoadjuvant chemotherapy in patients with stage IIIA(N2) non–small-cell lung cancer is safe and exceeds historical data of chemotherapy alone with a high MPR and an encouraging 1-year EFS rate of 73%.
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