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一项比较尼妥珠单抗联合顺铂放化疗与单纯顺铂放化疗治疗局部晚期头颈部癌的随机 3 期临床试验。

A randomized phase 3 trial comparing nimotuzumab plus cisplatin chemoradiotherapy versus cisplatin chemoradiotherapy alone in locally advanced head and neck cancer.

机构信息

Department of Medical Oncology, Tata Memorial Hospital, Homi Bhabha National Institute (HBNI), Mumbai, India.

Department of Radiation Oncology, Tata Memorial Hospital, HBNI, Mumbai, India.

出版信息

Cancer. 2019 Sep 15;125(18):3184-3197. doi: 10.1002/cncr.32179. Epub 2019 May 31.

Abstract

BACKGROUND

Because the addition of nimotuzumab to chemoradiation in patients with locally advanced head and neck cancer improved outcomes in a phase 2 study, the authors conducted a phase 3 study to confirm these findings.

METHODS

This open-label, investigator-initiated, phase 3, randomized trial was conducted from 2012 to 2018. Adult patients with locally advanced head and neck cancer who were fit for radical chemoradiation were randomized 1:1 to receive either radical radiotherapy (66-70 grays) with concurrent weekly cisplatin (30 mg/m ) (CRT) or the same schedule of CRT with weekly nimotuzumab (200 mg) (NCRT).The primary endpoint was progression-free survival (PFS); key secondary endpoints were disease-free survival (DFS), duration of locoregional control (LRC), and overall survival (OS). An intent-to-treat analysis also was performed.

RESULTS

In total, 536 patients were allocated equally to both treatment arms. The median follow-up was 39.13 months. The addition of nimotuzumab improved PFS (hazard ratio [HR], 0.69; 95% CI, 0.53-0.89; P = .004), LRC (HR, 0.67; 95% CI, 0.50-0.89; P = .006), and DFS (HR, 0.71; 95% CI, 0.55-0.92; P = .008) and had a trend toward improved OS (HR, 0.84; 95% CI, 0.65-1.08; P = .163). Grade 3 through 5 adverse events were similar between the 2 arms, except for a higher incidence of mucositis in the NCRT arm (66.7% vs 55.8%; P = .01).

CONCLUSIONS

The addition of nimotuzumab to concurrent weekly CRT improves PFS, LRC, and DFS. This combination provides a novel alternative therapeutic option to a 3-weekly schedule of 100 mg/m cisplatin in patients with locally advanced head and neck cancer who are treated with radical-intent CRT.

摘要

背景

由于尼妥珠单抗联合放化疗可改善局部晚期头颈部癌患者的预后,因此研究者开展了一项 3 期临床试验以确认这一发现。

方法

这是一项由研究者发起的、开放标签的 3 期随机临床试验,于 2012 年至 2018 年开展。符合根治性放化疗条件的局部晚期头颈部癌成年患者按 1:1 随机分配至接受根治性放疗(66-70 戈瑞)联合同期每周顺铂(30mg/m2)(CRT)或相同方案 CRT 联合每周尼妥珠单抗(200mg)(NCRT)。主要终点为无进展生存期(PFS);关键次要终点为无病生存期(DFS)、局部区域控制持续时间(LRC)和总生存期(OS)。还进行了意向治疗分析。

结果

共有 536 例患者按比例随机分配至两组。中位随访时间为 39.13 个月。尼妥珠单抗的添加改善了 PFS(风险比[HR],0.69;95%CI,0.53-0.89;P=0.004)、LRC(HR,0.67;95%CI,0.50-0.89;P=0.006)和 DFS(HR,0.71;95%CI,0.55-0.92;P=0.008),OS 有改善趋势(HR,0.84;95%CI,0.65-1.08;P=0.163)。两组间 3-5 级不良事件相似,仅 NCRT 组的黏膜炎发生率较高(66.7%比 55.8%;P=0.01)。

结论

尼妥珠单抗联合每周 CRT 可改善 PFS、LRC 和 DFS。对于接受根治性 CRT 的局部晚期头颈部癌患者,与每周 100mg/m2顺铂的 3 周方案相比,该联合方案为患者提供了一种新的治疗选择。

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