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Nivolumab 联合姑息性放疗治疗 HER2 阴性转移性乳腺癌骨转移患者的 Ib/II 期研究。

Phase Ib/II study of nivolumab combined with palliative radiation therapy for bone metastasis in patients with HER2-negative metastatic breast cancer.

机构信息

Department of Breast Surgery, Kyoto University Graduate School of Medicine, 54 Kawaharacho, Shogoin, Sakyo-Ku, Kyoto, 606-8507, Japan.

Department of Radiation Oncology and Image-Applied Therapy, Kyoto University Graduate School of Medicine, Kyoto, Japan.

出版信息

Sci Rep. 2022 Dec 27;12(1):22397. doi: 10.1038/s41598-022-27048-3.

Abstract

Radiation therapy (RT) can enhance the abscopal effect of immune checkpoint blockade. This phase I/II study investigated the efficacy and safety of nivolumab plus RT in HER2-negative metastatic breast cancer requiring palliative RT for bone metastases. Cohort A included luminal-like disease, and cohort B included both luminal-like and triple-negative disease refractory to standard systemic therapy. Patients received 8 Gy single fraction RT for bone metastasis on day 0. Nivolumab was administered on day 1 for each 14-day cycle. In cohort A, endocrine therapy was administered. The primary endpoint was the objective response rate (ORR) of the unirradiated lesions. Cohorts A and B consisted of 18 and 10 patients, respectively. The ORR was 11% (90% CI 4-29%) in cohort A and 0% in cohort B. Disease control rates were 39% (90% CI 23-58%) and 0%. Median progression-free survival was 4.1 months (95% CI 2.1-6.1 months) and 2.0 months (95% CI 1.2-3.7 months). One patient in cohort B experienced a grade 3 adverse event. Palliative RT combined with nivolumab was safe and showed modest anti-tumor activity in cohort A. Further investigations to enhance the anti-tumor effect of endocrine therapy combined with RT plus immune checkpoint blockade are warranted.Trial registration number and date of registration UMIN: UMIN000026046, February 8, 2017; ClinicalTrials.gov: NCT03430479, February 13, 2018; Date of the first registration: June 22, 2017.

摘要

放射治疗(RT)可增强免疫检查点阻断的远隔效应。这项 I/II 期研究调查了尼伏单抗联合 RT 在需要姑息性 RT 治疗骨转移的 HER2 阴性转移性乳腺癌中的疗效和安全性。队列 A 包括 luminal 样疾病,队列 B 包括 luminal 样和对标准系统治疗耐药的三阴性疾病。患者在第 0 天接受 8Gy 单次分割 RT 治疗骨转移。尼伏单抗在每个 14 天周期的第 1 天给药。在队列 A 中,给予内分泌治疗。主要终点是未照射病变的客观缓解率(ORR)。队列 A 和 B 分别包括 18 例和 10 例患者。队列 A 的 ORR 为 11%(90%CI 4-29%),队列 B 为 0%。疾病控制率分别为 39%(90%CI 23-58%)和 0%。中位无进展生存期为 4.1 个月(95%CI 2.1-6.1 个月)和 2.0 个月(95%CI 1.2-3.7 个月)。队列 B 中有 1 例患者发生 3 级不良事件。姑息性 RT 联合尼伏单抗是安全的,在队列 A 中显示出适度的抗肿瘤活性。进一步的研究需要增强内分泌治疗联合 RT 加免疫检查点阻断的抗肿瘤作用。

试验注册号和注册日期 UMIN:UMIN000026046,2017 年 2 月 8 日;ClinicalTrials.gov:NCT03430479,2018 年 2 月 13 日;首次注册日期:2017 年 6 月 22 日。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e690/9794767/c9449591819d/41598_2022_27048_Fig1_HTML.jpg

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