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Ann Oncol. 2022 Apr;33(4):406-415. doi: 10.1016/j.annonc.2021.12.014. Epub 2022 Jan 10.
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Avelumab plus standard-of-care chemoradiotherapy versus chemoradiotherapy alone in patients with locally advanced squamous cell carcinoma of the head and neck: a randomised, double-blind, placebo-controlled, multicentre, phase 3 trial.avelumab 联合标准治疗放化疗对比单纯放化疗用于局部晚期头颈部鳞状细胞癌患者:一项随机、双盲、安慰剂对照、多中心、III 期临床试验。
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2021 American Thyroid Association Guidelines for Management of Patients with Anaplastic Thyroid Cancer.2021 年美国甲状腺协会甲状腺间变性癌患者管理指南。
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Association of tumour mutational burden with outcomes in patients with advanced solid tumours treated with pembrolizumab: prospective biomarker analysis of the multicohort, open-label, phase 2 KEYNOTE-158 study.帕博利珠单抗治疗的晚期实体瘤患者肿瘤突变负荷与结局的相关性:多队列、开放标签、Ⅱ期 KEYNOTE-158 研究的前瞻性生物标志物分析。
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durvalumab(MEDI4736)联合 tremelimumab 与图像引导立体定向放射治疗治疗转移性间变性甲状腺癌的初步研究。

A Pilot Study of Durvalumab (MEDI4736) with Tremelimumab in Combination with Image-Guided Stereotactic Body Radiotherapy in the Treatment of Metastatic Anaplastic Thyroid Cancer.

机构信息

Department of Radiation Oncology, MSKCC, New York, New York, USA.

Division of Head and Neck Medical Oncology, Department of Medicine, MSKCC, New York, New York, USA.

出版信息

Thyroid. 2022 Jul;32(7):799-806. doi: 10.1089/thy.2022.0050. Epub 2022 Jun 21.

DOI:10.1089/thy.2022.0050
PMID:35521657
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9293682/
Abstract

Metastatic anaplastic thyroid cancer (ATC) has a poor prognosis. This pilot study aims to evaluate tremelimumab plus durvalumab with stereotactic body radiotherapy (SBRT) to improve overall survival (OS). Eligible patients received up to 4 doses tremelimumab (75 mg) given q4 weeks and up to 1 year of durvalumab (1500 mg) given q4 weeks. SBRT at 9 Gy × 3 fractions was given within the first 2 weeks of the start of treatment. Paired biopsies (pretreatment and between 3 and 10 weeks after the first dose of the drug treatment) were done in the medically qualified patients. Major inclusion criteria are metastatic ATC, Eastern Cooperative Oncology Group (ECOG) performance status 0-2, no prior immunotherapy, and last anticancer treatment >7 days before starting the study. The primary endpoint was 1 year OS with the combination of durvalumab, tremelimumab, and SBRT in metastatic ATC patients with a target of 1 year OS in ≥2 out of 12 patients. A total of 13 patients signed consent but only 12 patients ultimately participated in this trial. One patient who consented to the protocol became ineligible for this study due to continued decline in performance status. Patient characteristics were as follows: male ( = 6) with a median age of 71 years (range: 49-82), and ECOG = 1. Nine patients had prior neck radiation and nine patients had prior chemotherapy. Next-generation sequencing and PD-L1 staining were done in the nine patients where tissue was available. High microsatellite instability (MSI) corresponding to mismatch repair defect was noted in two patients. There were zero confirmed responses and only one patient had stable disease and was treated with ≥4 cycles of study drugs. The median time that the patients were under treatment was 11 weeks (1-28 weeks). MSI status did not affect treatment response. High MSI patients were on treatment for 8-14 weeks before disease progression. The median OS was 14.5 weeks with only 1 patient alive beyond 1 year. The presence of a BRAF or p53 mutation did not appear to affect treatment outcome. Tremelimumab and durvalumab with SBRT did not improve OS for ATC. Future research is needed to examine other novel immunotherapy combinations with or without radiotherapy in the treatment of ATC. Clinical Trial Registration: NCT03122496.

摘要

转移性间变性甲状腺癌 (ATC) 预后不良。本研究旨在评估替西木单抗联合度伐利尤单抗联合立体定向体部放疗 (SBRT) 是否能提高总生存率 (OS)。符合条件的患者接受多达 4 剂替西木单抗(75mg),每 4 周 1 次,1 年内接受多达 1 剂度伐利尤单抗(1500mg),每 4 周 1 次。SBRT 在治疗开始后的前 2 周内给予 9 Gy × 3 次分割。对符合条件的患者进行了配对活检(治疗前和首次药物治疗后 3 至 10 周)。主要纳入标准为转移性 ATC、东部合作肿瘤学组(ECOG)体能状态 0-2 分、无既往免疫治疗史、最后一次抗癌治疗在开始研究前 >7 天。主要终点是替西木单抗、度伐利尤单抗联合 SBRT 治疗转移性 ATC 患者的 1 年 OS,目标是 12 例患者中有 2 例以上达到 1 年 OS。共有 13 名患者签署了知情同意书,但最终只有 12 名患者参与了这项试验。由于体能状态持续下降,一名同意方案的患者被认为不符合本研究标准。患者特征如下:男性( = 6),中位年龄 71 岁(范围:49-82 岁),ECOG = 1。9 名患者曾接受过颈部放疗,9 名患者曾接受过化疗。对 9 名有组织标本的患者进行了下一代测序和 PD-L1 染色。两名患者存在高度微卫星不稳定 (MSI),对应错配修复缺陷。没有确认的应答,只有 1 名患者疾病稳定,并接受了≥4 个周期的研究药物治疗。患者接受治疗的中位时间为 11 周(1-28 周)。MSI 状态并不影响治疗反应。高 MSI 患者在疾病进展前接受治疗 8-14 周。中位 OS 为 14.5 周,只有 1 名患者在 1 年后仍存活。BRAF 或 p53 突变的存在似乎不影响治疗结果。替西木单抗联合度伐利尤单抗联合 SBRT 并不能提高 ATC 的 OS。需要进一步研究其他新型免疫疗法联合或不联合放疗治疗 ATC。临床试验注册:NCT03122496。