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在化疗联合西妥昔单抗治疗复发性或转移性头颈部鳞状细胞癌的日本患者中的真实世界临床结局和预后因素:一项前瞻性观察研究(JROSG12-2)。

Real-world clinical outcomes and prognostic factors in Japanese patients with recurrent or metastatic squamous cell carcinoma of head and neck treated with chemotherapy plus cetuximab: a prospective observation study (JROSG12-2).

机构信息

Division of Gastrointestinal Oncology, Shizuoka Cancer Center, 1007 Shimonagakubo, Nagaizumi, Sunto-gun, Shizuoka, 411-8777, Japan.

Department of Radiation Oncology, Hyogo Cancer Center Hospital, Akashi, Hyogo, Japan.

出版信息

Int J Clin Oncol. 2021 Feb;26(2):316-325. doi: 10.1007/s10147-020-01817-4. Epub 2020 Oct 30.

Abstract

BACKGROUND

The aims of this study are to evaluate the efficacy and safety of first-line treatment with chemotherapy plus cetuximab in real-world patients with recurrent or metastatic squamous cell carcinoma of the head and neck (RM-SCCHN) and to identify prognostic factors for overall survival (OS).

METHODS

This is a prospective observation study involving 20 oncology institutions in Japan. Patients with RM-SCCHN treated with a first-line therapy consisting of cetuximab plus any chemotherapy regimen between December 2013 and February 2017 were enrolled. The primary objective of the study was 1-year OS. Secondary objectives included response rate and adverse events.

RESULTS

Of 120 patients recruited, 114 patients were analyzed. Median age was 64 years. Cetuximab in combination with platinum plus 5-FU (EXTREME regimen) was chosen in 86 patients (75.4%). The median OS was 12.4 months. A point estimate of the 1-year survival rate was 51.1%. Overall response rate was 26.3%. Grade 3 or worse adverse events included neutropenia (22.8%), hypokalemia (9.6%), acneiform rash (7.0%), pneumonitis (1.8%), and infusion-related reaction (0.9%). On multivariate analysis, regional lymph node metastasis, absence of intervention by dermatologists, lack of response to therapy, skin metastasis, and non-EXTREME regimen were identified as independent unfavorable prognostic factors for OS.

CONCLUSION

The combination of cetuximab plus chemotherapy was tolerable and efficacious in patients with RM-SCCHN in a real-world setting. Clinical outcomes and prognostic factors extracted from this study provide a reference of the current clinical practice as well as for the future development of novel therapy in RM-SCCHN.

摘要

背景

本研究旨在评估在真实世界中接受含西妥昔单抗的一线化疗治疗的复发性或转移性头颈部鳞状细胞癌(RM-SCCHN)患者的疗效和安全性,并确定总生存(OS)的预后因素。

方法

这是一项涉及日本 20 家肿瘤学机构的前瞻性观察研究。2013 年 12 月至 2017 年 2 月期间,接受西妥昔单抗联合任何化疗方案一线治疗的 RM-SCCHN 患者被纳入研究。研究的主要目的是评估 1 年 OS。次要终点包括缓解率和不良事件。

结果

在招募的 120 例患者中,114 例患者被纳入分析。中位年龄为 64 岁。86 例患者(75.4%)选择西妥昔单抗联合铂类加 5-FU(EXTREME 方案)。中位 OS 为 12.4 个月。1 年生存率的点估计值为 51.1%。总缓解率为 26.3%。3 级或更高级别的不良事件包括中性粒细胞减少症(22.8%)、低钾血症(9.6%)、痤疮样皮疹(7.0%)、肺炎(1.8%)和输注相关反应(0.9%)。多变量分析显示,区域淋巴结转移、皮肤科医生未干预、治疗无反应、皮肤转移和非 EXTREME 方案是 OS 的独立不良预后因素。

结论

在真实环境中,西妥昔单抗联合化疗治疗 RM-SCCHN 患者是耐受且有效的。本研究中提取的临床结果和预后因素为当前临床实践以及 RM-SCCHN 新型治疗方法的未来发展提供了参考。

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