Department of Otolaryngology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Department of Medical Oncology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
Int J Clin Oncol. 2022 Jan;27(1):95-104. doi: 10.1007/s10147-021-02047-y. Epub 2021 Nov 13.
We have previously reported the effectiveness and safety of nivolumab in patients with head and neck cancer (HNC) in real-world clinical practice in Japan. Here, we report long-term outcomes from this study in the overall population and subgroups stratified by subsequent chemotherapy.
In this multicenter, retrospective observational study, Japanese patients with recurrent or metastatic (R/M) HNC receiving nivolumab were followed up for 2 years. Effectiveness endpoints included overall survival (OS), OS rate, progression-free survival (PFS), and PFS rate. Safety endpoints included the incidence of immune-related adverse events (irAEs).
Overall, 256 patients received a median of 6.0 doses (range: 1-52) of nivolumab over a median duration of 72.5 days (range: 1-736). Median OS was 9.5 months [95% confidence interval (CI) 8.2-12.0] and median PFS was 2.1 months (95% CI 1.8-2.7). A significant difference between 2-year survivors (n = 62) and non-2-year survivors was observed by median age (P = 0.0227) and ECOG PS (P = 0.0001). Of 95 patients who received subsequent chemotherapy, 54.7% received paclitaxel ± cetuximab. The median OS and PFS from the start of paclitaxel ± cetuximab were 6.9 months (95% CI 5.9-11.9) and 3.5 months (95% CI 2.3-5.5), respectively. IrAEs were reported in 17.2% of patients. Endocrine (7.0%) and lung (4.3%) disorders were the most common irAEs; kidney disorder (n = 1) was newly identified in this follow-up analysis.
Results demonstrated the long-term effectiveness of nivolumab and potential effectiveness of subsequent chemotherapy in patients with R/M HNC in the real-world setting. Safety was consistent with that over the 1-year follow-up.
我们之前报道了纳武利尤单抗在日本真实世界临床实践中对头颈癌(HNC)患者的有效性和安全性。在此,我们报告了这项研究在总人群中的长期结果,并按后续化疗进行了亚组分层。
在这项多中心、回顾性观察性研究中,接受纳武利尤单抗治疗的复发性或转移性(R/M)HNC 日本患者接受了为期 2 年的随访。有效性终点包括总生存期(OS)、OS 率、无进展生存期(PFS)和 PFS 率。安全性终点包括免疫相关不良事件(irAEs)的发生率。
总体而言,256 名患者接受了中位数为 6.0 剂(范围:1-52)纳武利尤单抗治疗,中位治疗时间为 72.5 天(范围:1-736)。中位 OS 为 9.5 个月[95%置信区间(CI)8.2-12.0],中位 PFS 为 2.1 个月(95%CI 1.8-2.7)。通过中位年龄(P=0.0227)和 ECOG PS(P=0.0001)观察到 2 年幸存者(n=62)和非 2 年幸存者之间存在显著差异。在接受后续化疗的 95 名患者中,54.7%接受了紫杉醇±西妥昔单抗。紫杉醇±西妥昔单抗起始后的中位 OS 和 PFS 分别为 6.9 个月(95%CI 5.9-11.9)和 3.5 个月(95%CI 2.3-5.5)。17.2%的患者报告了 irAEs。内分泌(7.0%)和肺部(4.3%)疾病是最常见的 irAEs;在本次随访分析中,新发现了肾脏疾病(n=1)。
结果表明,在真实环境中,纳武利尤单抗对 R/M HNC 患者具有长期疗效,且后续化疗具有潜在疗效。安全性与 1 年随访时一致。