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一项 I 期/ Ib 期临床试验及生物相关性分析:HPV 无关局部晚期头颈部鳞癌新辅助 SBRT 单次剂量 durvalumab 的疗效。

A phase I/Ib trial and biological correlate analysis of neoadjuvant SBRT with single-dose durvalumab in HPV-unrelated locally advanced HNSCC.

机构信息

Radiation Oncology, University of Colorado Denver at Anschutz Medical Campus, Aurora, CO, USA.

Department of Immunology, University of Colorado Denver at Anschutz Medical Campus, Aurora, CO, USA.

出版信息

Nat Cancer. 2022 Nov;3(11):1300-1317. doi: 10.1038/s43018-022-00450-6. Epub 2022 Nov 25.

Abstract

Five-year survival for human papilloma virus-unrelated head and neck squamous cell carcinomas remain below 50%. We assessed the safety of administering combination hypofractionated stereotactic body radiation therapy with single-dose durvalumab (anti-PD-L1) neoadjuvantly (n = 21) ( NCT03635164 ). The primary endpoint of the study was safety, which was met. Secondary endpoints included radiographic, pathologic and objective response; locoregional control; progression-free survival; and overall survival. Among evaluable patients at an early median follow-up of 16 months (448 d or 64 weeks), overall survival was 80.1% with 95% confidence interval (95% CI) (62.0%, 100.0%), locoregional control and progression-free survival were 75.8% with 95% CI (57.5%, 99.8%), and major pathological response or complete response was 75% with 95% exact CI (51.6%, 100.0%). For patients treated with 24 Gy, 89% with 95% CI (57.1%, 100.0%) had MPR or CR. Using high-dimensional multi-omics and spatial data as well as biological correlatives, we show that responders had: (1) an increase in effector T cells; (2) a decrease in immunosuppressive cells; and (3) an increase in antigen presentation post-treatment.

摘要

人乳头瘤病毒相关性头颈部鳞状细胞癌的 5 年生存率仍低于 50%。我们评估了联合低分割立体定向体放射治疗与单次剂量度伐利尤单抗(抗 PD-L1)新辅助治疗(n=21)(NCT03635164)的安全性。该研究的主要终点是安全性,安全性得到了满足。次要终点包括影像学、病理学和客观缓解率;局部区域控制;无进展生存期;总生存期。在中位随访时间为 16 个月(448 天或 64 周)的可评估患者中,总生存期为 80.1%,95%置信区间(95%CI)为(62.0%,100.0%),局部区域控制和无进展生存期分别为 75.8%和 95%CI(57.5%,99.8%),主要病理学缓解或完全缓解率为 75%,95%精确 CI(51.6%,100.0%)。对于接受 24Gy 治疗的患者,89%,95%CI(57.1%,100.0%)有 MPR 或 CR。通过高维多组学和空间数据以及生物学相关性,我们发现应答者具有:(1)效应 T 细胞增加;(2)抑制性细胞减少;(3)治疗后抗原呈递增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cdac/9701140/8fb733d2a857/43018_2022_450_Fig1_HTML.jpg

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