Atezolizumab With or Without Radiotherapy for Advanced Squamous Cell Carcinoma of the Penis (The PERICLES Study): A Phase II Trial

医学 阿替唑单抗 阴茎 基底细胞 内科学 放射治疗 癌症 肿瘤科 外科 泌尿科 免疫疗法 彭布罗利珠单抗
作者
Hielke M. de Vries,Tynisha S. Rafael,Alberto Gil-Jimenez,Jeantine M. de Feijter,Elise M. Bekers,Elsbeth van der Laan,Marta López‐Yurda,Erik Hooijberg,Annegien Broeks,Dennis Peters,Iris M. Seignette,Floris J. Pos,Simon Horenblas,Bas W.G. van Rhijn,Ekaterina S. Jordanova,Oscar R. Brouwer,Eva Schaake,Michiel S. van der Heijden
出处
期刊:Journal of Clinical Oncology [American Society of Clinical Oncology]
卷期号:41 (31): 4872-4880 被引量:29
标识
DOI:10.1200/jco.22.02894
摘要

Patients with advanced penile squamous cell carcinoma have a poor prognosis (21% 2-year overall survival [OS] from diagnosis). We assessed the activity of atezolizumab (anti-PD-L1) in patients with advanced penile cancer, with or without radiotherapy (RT).A single-center, nonrandomized phase II study with two treatment arms was conducted in 32 patients with histologically confirmed advanced penile cancer. All patients received atezolizumab (1,200 mg) once every 3 weeks. Twenty patients, who were expected to benefit from RT for locoregional disease control, received additional irradiation. The primary end point was 1-year progression-free survival (PFS) for the complete cohort and was reached if the actual 1-year PFS was at least 35%. Secondary end points included OS, objective response rate (ORR), and tolerability. Exploratory biomarker analyses were conducted in pretreatment specimens.Median follow-up was 29.1 months (IQR, 18.1-33.5). Grade 3-4 adverse events related to atezolizumab or RT were observed in 3/32 (9.4%) and 13/20 (65%) patients, respectively. One-year PFS was 12.5% (95% CI, 5.0 to 31.3), which did not meet the study's primary end point. Median OS was 11.3 months (95% CI, 5.5 to 18.7). In the objective response-evaluable population (n = 30; 93.8%), the ORR was 16.7% (95% CI, 6 to 35), including 2 (6.7%) complete responders and 3 (10%) partial responders. Improved PFS was observed in patients with high-risk human papillomavirus (hrHPV)-positive tumors (P = .003) and those with high infiltration of intratumoral CD3+CD8+ T cells (P = .037).Although the primary end point of 1-year PFS was not met, durable antitumor activity to atezolizumab was observed in a subset of patients. Biomarkers, such as hrHPV and intratumoral CD3+CD8+ T-cell infiltration, may help to better select responders.
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