Intensity-Modulated Reirradiation Therapy With Nivolumab in Recurrent or Second Primary Head and Neck Squamous Cell Carcinoma

医学 耐受性 无容量 头颈部癌 临床终点 头颈部鳞状细胞癌 内科学 放射治疗 颈淋巴结清扫术 肿瘤科 外科 粘膜炎 临床试验 癌症 不利影响 免疫疗法
作者
Nabil F. Saba,Stuart J. Wong,Tahseen H. Nasti,Ashley A. McCook‐Veal,Mark W. McDonald,William Stokes,Allyson M. Anderson,Asari Ekpenyong,Manali Rupji,Marin Abousaud,Soumon Rudra,James E. Bates,Jill Remick,Nikhil Joshi,N.M. Woody,Musaddiq Awan,J.L. Geiger,Aditya Shreenivas,Julia Samsa,Matthew C. Ward,Nicole C. Schmitt,Mihir R. Patel,Kristin Higgins,Yong Teng,Conor Steuer,Dong M. Shin,Yong‐Yu Liu,Rafi Ahmed,Shlomo A. Koyfman
出处
期刊:JAMA Oncology [American Medical Association]
卷期号:10 (7): 896-896
标识
DOI:10.1001/jamaoncol.2024.1143
摘要

Importance Intensity-modulated radiation therapy (IMRT) reirradiation of nonmetastatic recurrent or second primary head and neck squamous cell carcinoma (HNSCC) results in poor progression-free survival (PFS) and overall survival (OS). Objective To investigate the tolerability, PFS, OS, and patient-reported outcomes with nivolumab (approved standard of care for patients with HNSCC) during and after IMRT reirradiation. Design, Setting, and Participants In this multicenter nonrandomized phase 2 single-arm trial, the treatment outcomes of patients with recurrent or second primary HNSCC who satisfied recursive partitioning analysis class 1 and 2 definitions were evaluated. Between July 11, 2018, and August 12, 2021, 62 patients were consented and screened. Data were evaluated between June and December 2023. Intervention Sixty- to 66-Gy IMRT in 30 to 33 daily fractions over 6 to 6.5 weeks with nivolumab, 240 mg, intravenously 2 weeks prior and every 2 weeks for 5 cycles during IMRT, then nivolumab, 480 mg, intravenously every 4 weeks for a total nivolumab duration of 52 weeks. Main Outcomes and Measures The primary end point was PFS. Secondary end points included OS, incidence, and types of toxic effects, including long-term treatment-related toxic effects, patient-reported outcomes, and correlatives of tissue and blood biomarkers. Results A total of 62 patients were screened, and 51 were evaluable (median [range] age was 62 [56-67] years; 42 [82%] were male; 6 [12%] had p16+ disease; 38 [75%] had salvage surgery; and 36 [71%.] had neck dissection). With a median follow-up of 24.5 months (95% CI, 19.0-25.0), the estimated 1-year PFS was 61.7% (95% CI, 49.2%-77.4%), rejecting the null hypothesis of 1-year PFS rate of less than 43.8% with 1-arm log-rank test P = .002 within a 1-year timeframe. The most common treatment-related grade 3 or higher adverse event (6 [12%]) was lymphopenia with 2 patients (4%) and 1 patient each (2%) exhibiting colitis, diarrhea, myositis, nausea, mucositis, and myasthenia gravis. Functional Assessment of Cancer Therapy–General and Functional Assessment of Cancer Therapy–Head and Neck Questionnaire quality of life scores remained stable and consistent across all time points. A hypothesis-generating trend favoring worsening PFS and OS in patients with an increase in blood PD1+, KI67+, and CD4+ T cells was observed. Conclusions and Relevance This multicenter nonrandomized phase 2 trial of IMRT reirradiation therapy and nivolumab suggested a promising improvement in PFS over historical controls. The treatment was well tolerated and deserves further evaluation. Trial Registration ClinicalTrials.gov Identifier: NCT03521570
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