Department of Medical Oncology, Tata Memorial Hospital, Homi Bhabha National Institute (HBNI), Mumbai, India.
Department of Radiation Oncology, Tata Memorial Hospital, HBNI, Mumbai, India.
Cancer. 2019 Sep 15;125(18):3184-3197. doi: 10.1002/cncr.32179. Epub 2019 May 31.
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.
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.
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).
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.
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。
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。
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)。
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。