Princess Margaret Cancer Centre, Toronto, ON.
Tom Baker Cancer Centre, Calgary, AB.
Curr Oncol. 2020 Aug;27(4):204-214. doi: 10.3747/co.27.5985. Epub 2020 Aug 1.
The combination of nivolumab and ipilimumab is approved in several jurisdictions (United States, European Union, Canada) for the first-line treatment of patients with advanced melanoma. CheckMate 218 is a North American expanded-access program (eap) of nivolumab plus ipilimumab in patients with advanced melanoma. Here, we report safety and survival outcomes for the Canadian cohort in the eap.
Eligible patients were those 18 years of age or older with unresectable stage iii or iv melanoma, an Eastern Cooperative Oncology Group performance status of 0 or 1, and no prior anti-PD-1 or anti-ctla-4 therapy. Patients were treated with nivolumab 1 mg/kg and ipilimumab 3 mg/kg every 3 weeks for 4 cycles (induction phase); they then continued with nivolumab 3 mg/kg every 2 weeks (maintenance phase) until progression, unacceptable toxicity, or a maximum of 48 weeks, whichever occurred first. Safety and overall survival (os) data were collected.
Of 194 patients enrolled, 174 were treated, and 51% continued on nivolumab maintenance. Median follow-up was 12.9 months. All-grade and grades 3-4 treatment-related adverse events were reported in 98% and 60% of patients respectively and led to treatment discontinuation in 40% and 28% of patients. Two treatment-related deaths were reported. The 12- and 18-month os rates were 80% [95% confidence interval (ci): 73% to 86%] and 76% (95% ci: 67% to 82%) respectively.
In this Canadian population, nivolumab plus ipilimumab demonstrated a safety profile and survival outcomes consistent with phase ii and iii clinical trial data.
纳武单抗和伊匹单抗联合治疗已在多个司法管辖区(美国、欧盟、加拿大)获得批准,用于治疗晚期黑色素瘤患者的一线治疗。CheckMate 218 是一项纳武单抗联合伊匹单抗在晚期黑色素瘤患者中的北美扩大准入计划(eap)。在这里,我们报告 eap 中加拿大队列的安全性和生存结果。
符合条件的患者为年龄 18 岁或以上、不可切除的 iii 期或 iv 期黑色素瘤、东部合作肿瘤学组表现状态 0 或 1 且无既往抗 pd-1 或抗 ctla-4 治疗的患者。患者接受纳武单抗 1 mg/kg 和伊匹单抗 3 mg/kg,每 3 周 1 次,共 4 个周期(诱导期);然后继续纳武单抗 3 mg/kg,每 2 周 1 次(维持期),直至疾病进展、不可接受的毒性或最长 48 周,以先发生者为准。收集安全性和总生存(os)数据。
在 194 名入组患者中,174 名患者接受了治疗,51%的患者继续接受纳武单抗维持治疗。中位随访时间为 12.9 个月。分别有 98%和 60%的患者报告了所有级别和 3-4 级治疗相关不良事件,分别有 40%和 28%的患者因治疗中断。报告了 2 例治疗相关死亡。12 个月和 18 个月的 os 率分别为 80%(95%ci:73%至 86%)和 76%(95%ci:67%至 82%)。
在加拿大人群中,纳武单抗联合伊匹单抗的安全性和生存结果与 ii 期和 iii 期临床试验数据一致。