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首页> 外文期刊>British Journal of Cancer >Efficacy and safety of pembrolizumab in recurrent/metastatic head and neck squamous cell carcinoma: pooled analyses after long-term follow-up in KEYNOTE-012
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Efficacy and safety of pembrolizumab in recurrent/metastatic head and neck squamous cell carcinoma: pooled analyses after long-term follow-up in KEYNOTE-012

机译:派姆单抗在复发/转移性头颈部鳞状细胞癌中的疗效和安全性:KEYNOTE-012长期随访后的汇总分析

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摘要

Background Second-line treatment options for advanced head and neck squamous cell carcinoma (HNSCC) are limited. The phase Ib KEYNOTE-012 study evaluated the safety and the efficacy of pembrolizumab for the treatment of HNSCC after long-term follow-up. Methods Multi-centre, non-randomised trial included two HNSCC cohorts (initial and expansion) in which 192 patients were eligible. Patients received pembrolizumab 10?mg/kg every 2 weeks (initial cohort; N ?=?60) or 200?mg every 3 weeks (expansion cohort; N ?=?132). Co-primary endpoints were safety and overall response rate (ORR; RECIST v1.1; central imaging vendor review). Results Median follow-up was 9 months (range, 0.2–32). Treatment-related adverse events (AEs) of any grade and grade 3/4 occurred in 123 (64%) and 24 (13%) patients, respectively. No deaths were attributed to treatment-related AEs. ORR was 18% (34/192; 95% CI, 13–24%). Median response duration was not reached (range, 2+ to 30+ months); 85% of responses lasted ≥6 months. Overall survival at 12 months was 38%. Conclusions Some patients received 2 years of treatment and the responses were ongoing for more than 30 months; the durable anti-tumour activity and tolerable safety profile, observed with long-term follow-up, support the use of pembrolizumab as a treatment for recurrent/metastatic HNSCC.
机译:背景技术晚期头颈部鳞状细胞癌(HNSCC)的二线治疗选择有限。 Ib KEYNOTE-012期研究评估了长期随访后派姆单抗治疗HNSCC的安全性和有效性。方法多中心,非随机试验包括两个HNSCC队列(初始和扩展),其中192例患者合格。患者每2周接受pembrolizumab 10?mg / kg(初始队列;N≥60)或每3周200?mg(扩展队列;N≥132)。共同的主要终点是安全性和总体响应率(ORR; RECIST v1.1;中央成像供应商审查)。结果中位随访时间为9个月(范围0.2–32)。任何级别和3/4级的治疗相关不良事件(AE)分别发生在123(64%)和24(13%)位患者中。没有死亡归因于治疗相关的不良事件。 ORR为18%(34/192; 95%CI,13-24%)。未达到中位反应持续时间(范围2+到30+个月); 85%的反应持续≥6个月。 12个月的总生存率为38%。结论一些患者接受了2年的治疗,并且反应持续了30个月以上。长期随访观察到的持久抗肿瘤活性和可耐受的安全性,支持使用派姆单抗作为复发/转移性HNSCC的治疗方法。

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