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紫杉醇联合每两周 cetuximab 治疗复发或转移性头颈部癌患者的 II 期试验,这些患者之前接受过铂类化疗和抗 PD-1 抗体治疗。

A phase II trial of paclitaxel plus biweekly cetuximab for patients with recurrent or metastatic head and neck cancer previously treated with both platinum-based chemotherapy and anti-PD-1 antibody.

机构信息

Department of Medical Oncology and Hematology, Kobe University Hospital, Kobe. Electronic address: https://twitter.com/hnoncoid.

Department of Medical Oncology and Hematology, Kobe University Hospital, Kobe; Cancer Center, Kobe University Hospital, Kobe.

出版信息

ESMO Open. 2024 Jun;9(6):103476. doi: 10.1016/j.esmoop.2024.103476. Epub 2024 Jun 3.

Abstract

BACKGROUND

An important unmet need for new treatment options remains for patients with recurrent or metastatic head and neck squamous cell carcinoma (R/M-HNSCC) previously treated with both platinum-based chemotherapy and anti-programmed cell death protein 1 (PD-1) antibody. Retrospective studies suggest that previous treatment with immune checkpoint inhibitor might augment the efficacy of subsequent chemotherapy. Here, we conducted a phase II trial aimed to evaluate the efficacy and safety of paclitaxel plus biweekly cetuximab for patients in this setting.

PATIENTS AND METHODS

This was a single-arm, multicenter, phase II trial. Key eligibility criteria were R/M-HNSCC, and previous treatment with both platinum-based chemotherapy and PD-1 antibody. Paclitaxel plus biweekly cetuximab consisted of weekly paclitaxel 100 mg/m (days 1, 8, 15) and biweekly cetuximab 500 mg/m (days 1, 15) with a cycle of 28 days until progression or unacceptable toxicity. Primary endpoint was objective response rate (ORR). Secondary endpoints included progression-free survival (PFS), overall survival (OS), disease control rate (DCR), and adverse events (AEs) (Common Terminology Criteria for Adverse Events version 5.0).

RESULTS

Between August 2020 and August 2022, 35 patients were enrolled, of whom 33 were assessable for response. ORR was 69.6% (95% confidence interval 51.2% to 84.4%). With a median follow-up period for survivors of 16.6 months, median PFS and OS were 5.5 and 13.3 months, respectively. DCR was 93.7%. Twenty-three patients (65%) experienced grade 3 or 4 AEs, including neutropenia (34%), infection (14%), leukopenia (11%), mucositis (8%), and pneumonitis (8%). Eight patients discontinued study treatment due to treatment-related AEs, and no treatment-related death was observed.

CONCLUSIONS

Paclitaxel plus biweekly cetuximab showed highly encouraging efficacy and manageable toxicities in R/M-HNSCC patients previously treated with both platinum-based chemotherapy and PD-1 antibody. This combination therapy warrants further investigation in this setting.

摘要

背景

对于先前接受过铂类化疗和抗程序性死亡蛋白 1(PD-1)抗体治疗的复发性或转移性头颈部鳞状细胞癌(R/M-HNSCC)患者,仍存在对新治疗选择的重要未满足需求。回顾性研究表明,先前接受免疫检查点抑制剂治疗可能会增强后续化疗的疗效。在这里,我们进行了一项 II 期临床试验,旨在评估紫杉醇联合每周两次西妥昔单抗在这种情况下患者的疗效和安全性。

患者和方法

这是一项单臂、多中心、II 期临床试验。主要入选标准为 R/M-HNSCC,先前接受过铂类化疗和 PD-1 抗体治疗。紫杉醇联合每周两次西妥昔单抗方案包括每周紫杉醇 100mg/m²(第 1、8、15 天)和每周两次西妥昔单抗 500mg/m²(第 1、15 天),每 28 天为一个周期,直至疾病进展或不可接受的毒性。主要终点为客观缓解率(ORR)。次要终点包括无进展生存期(PFS)、总生存期(OS)、疾病控制率(DCR)和不良事件(AE)(不良事件通用术语标准 5.0 版)。

结果

2020 年 8 月至 2022 年 8 月期间,共纳入 35 例患者,其中 33 例可评估疗效。ORR 为 69.6%(95%置信区间 51.2%至 84.4%)。在幸存者的中位随访期为 16.6 个月时,中位 PFS 和 OS 分别为 5.5 个月和 13.3 个月,DCR 为 93.7%。23 例患者(65%)发生 3 级或 4 级 AE,包括中性粒细胞减少症(34%)、感染(14%)、白细胞减少症(11%)、黏膜炎(8%)和肺炎(8%)。8 例患者因治疗相关 AE 停止研究治疗,无治疗相关死亡。

结论

紫杉醇联合每周两次西妥昔单抗在先前接受过铂类化疗和 PD-1 抗体治疗的 R/M-HNSCC 患者中显示出高度令人鼓舞的疗效和可管理的毒性。这种联合治疗方案在这种情况下值得进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9564/11179070/cfc85cb27df1/gr1.jpg

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