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855MO Adjuvant immunotherapy after salvage surgery in head and neck cancer squamous cell carcinoma (HNSCC): Phase II trial evaluating the efficacy and the toxicity of Nivolumab (ADJORL1)

医学 无容量 佐剂 毒性 内科学 头颈部鳞状细胞癌 临床终点 人口 外科 癌症 临床研究阶段 肿瘤科 头颈部癌 放射治疗 免疫疗法 随机对照试验 环境卫生
作者
Joanne Guerlain,Nathalie Cozic,Amaury Daste,O. Malard,Jérôme Fayette,Frédéric Rolland,Olivier Mauvais,Alison Johnson,Sébastien Salas,Marie Vinches,Alexandre Bozec,S. Vergèz,Erwan de Monès,Ingrid Breuskin,Mariana Iacob,Baptiste Archambaud,François Janot,Caroline Even
出处
期刊:Annals of Oncology [Elsevier BV]
卷期号:34: S557-S557 被引量:3
标识
DOI:10.1016/j.annonc.2023.09.2001
摘要

Treatment of locoregional failures or second primary in HNSCC in previously irradiated areas is a challenge. Reirradiation is currently the only treatment which can improve disease-free survival (DFS) after salvage surgery (SS) even if it has no impact on the overall survival (OS) because of high toxicity, showing the need to investigate other adjuvant therapies (AT) such as immunotherapy. The objectives of this study were to evaluate the 2-year DFS and OS of patients (pts) treated with nivolumab (N) after SS, the toxicity of N in this population and to determine biomarkers of response. This multicentric non-randomized phase II add trial pts with recurrence or second primary of HNSCC in previously irradiated area, operated by SS with curative intent, more than 6 months after initial radiotherapy and of bad prognosis justifying an AT. Within 8 weeks of SS, 240 mg of adjuvant N was administrated every 2 weeks during the first 3 months, and then N 480 mg every 4 weeks was administrated for the next 3 months. The design was performed using a binomial test with a 2-year DFS < 40% as ineffective (α=10%, power=80%). Between February 2018 and March 2021, 57 patients were included and treated. Median age was 61 years, 80% male. Median number of cycles of N was 9 (from 3 to 10). The reasons for off treatment were: 60% treatment completion, 21% tumor progression, 12% toxicity, 7% Others. 2-year DFS was 46.6%, 90%CI[36.1-57.5%] for the main endpoint and 2-year OS was 67.3%, 95%CI[54.2-78.2%]. Median follow-up was 48.2 months (from 5.3 to 59.6). 17 adverse events (AEs) grade ≥3 were related to N (mainly pancreatic hepatobiliary disorders, colitis, myositis andmyocarditis) and occurred in 11 pts (19%). No drug-related death occurred. Biomarkers data (CPS, Immunoscore) will be presented. N as AT after SS is well tolerated. The 2-year DFS and OS compared favorably with those from historical data of reirradiation trials. In JANORL2 trial (Radiother Oncol 2018), 2-year DFS and OS were respectively 33.4%, 95%CI [22.1-47.0%] and 54.0%, 95%CI [40.6-66.8%]. These encouraging results warrant further investigations.

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