Abstract OT1-12-02: Biomarker study of patients with HER2-negative metastatic breast cancer receiving combination therapy with nivolumab, bevacizumab and paclitaxel as first-line treatment (WJOG9917BTR)

Y. Ozaki, S. Kitano, Koji Matsumoto, Maiko Takahashi, T. Mukohara, M. Futamura, N. Masuda, J. Tsurutani, K. Yoshimura, H. Minami, T. Takano
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引用次数: 2

Abstract

Background : In recent years, anti-PD-1 antibody, an immune checkpoint inhibitor, has been developed for the treatment of various types of cancer, including breast cancer. Synergistic effects of nivolumab, paclitaxel and bevacizumab are expected, based on various preclinical data, when these drugs are administered in combination. A biomarker study is ongoing to evaluate the immune status of patients participating in the NEWBEAT trial, which is a phase II trial of nivolumab + paclitaxel + bevacizumab therapy as first-line treatment for patients with metastatic or recurrent HER2-negative breast cancer. Methods : HER2-negative breast cancer patients from the WJOG9917B (NEWBEAT) trial are enrolled in this biomarker study. To explore new biomarkers for combined treatment of breast cancer with immune-checkpoint inhibitors and anti-vascular endothelial growth factor antibodies, we propose to conduct multicolor immunohistochemistry (IHC) assays for immunomonitoring of the intra-tumor environment, such as the expressions of PD-L1, CD4 and CD8. Blood samples are collected before the start of treatment and at four time-points during the treatment, to determine, using a multicolor flow cytometry panel, the numbers of circulating immunosuppressive cells, such as regulatory T cells, myeloid-derived suppressor cells and tumor-associated macrophages (M2). In the NEWBEAT trial, patients receive nivolumab 240 mg/body on days 1 and 15, paclitaxel 90 mg/m2 on days 1, 8 and 15, and bevacizumab 10 mg/kg on days 1 and 15 every 4 weeks until disease progression. The primary endpoint is the objective response rate, and the key secondary endpoints include progression-free survival, overall survival, and toxicity of the protocol treatment. A total of 51 patients will be enrolled and the enrollment period will be one year. This trial opened to accrual in February 2018. Clinical trial registry number: UMIN000029590 Citation Format: Ozaki Y, Kitano S, Matsumoto K, Takahashi M, Mukohara T, Futamura M, Masuda N, Tsurutani J, Yoshimura K, Minami H, Takano T. Biomarker study of patients with HER2-negative metastatic breast cancer receiving combination therapy with nivolumab, bevacizumab and paclitaxel as first-line treatment (WJOG9917BTR) [abstract]. In: Proceedings of the 2018 San Antonio Breast Cancer Symposium; 2018 Dec 4-8; San Antonio, TX. Philadelphia (PA): AACR; Cancer Res 2019;79(4 Suppl):Abstract nr OT1-12-02.
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OT1-12-02: her2阴性转移性乳腺癌患者接受纳武单抗、贝伐单抗和紫杉醇联合一线治疗的生物标志物研究(WJOG9917BTR)
背景:近年来,抗pd -1抗体(一种免疫检查点抑制剂)已被开发用于治疗包括乳腺癌在内的各种类型的癌症。根据各种临床前数据,当这些药物联合使用时,预计纳武单抗、紫杉醇和贝伐单抗会产生协同效应。一项生物标志物研究正在进行中,以评估参加NEWBEAT试验的患者的免疫状态,该试验是一项将纳武单抗+紫杉醇+贝伐单抗治疗作为转移性或复发性her2阴性乳腺癌患者一线治疗的II期试验。方法:将WJOG9917B (NEWBEAT)试验中her2阴性的乳腺癌患者纳入这项生物标志物研究。为了探索新的生物标志物,联合免疫检查点抑制剂和抗血管内皮生长因子抗体治疗乳腺癌,我们建议进行多色免疫组织化学(IHC)检测肿瘤内环境的免疫监测,如PD-L1, CD4和CD8的表达。在治疗开始前和治疗期间的四个时间点采集血液样本,使用多色流式细胞仪检测循环免疫抑制细胞的数量,如调节性T细胞、髓源性抑制细胞和肿瘤相关巨噬细胞(M2)。在NEWBEAT试验中,患者在第1天和第15天接受纳武单抗240 mg/体,在第1、8和15天接受紫杉醇90 mg/m2,在第1天和第15天每4周接受贝伐单抗10 mg/kg,直到疾病进展。主要终点是客观缓解率,关键的次要终点包括无进展生存期、总生存期和方案治疗的毒性。共纳入51例患者,入组期为1年。该试验于2018年2月开始。临床试验注册号:UMIN000029590引用格式:Ozaki Y, Kitano S, Matsumoto K, Takahashi M, Mukohara T, Futamura M, Masuda N, Tsurutani J, Yoshimura K, Minami H, Takano T. her2阴性转移性乳腺癌患者纳武单抗、贝伐单抗和紫杉醇联合治疗的生物标志物研究(WJOG9917BTR)[摘要]。2018年圣安东尼奥乳腺癌研讨会论文集;2018年12月4-8日;费城(PA): AACR;中国癌症杂志,2019;79(4增刊):1-12-02。
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