Horisaki Ken, Yoshikawa Shusuke, Omata Wataru, Tsutsumida Arata, Kiyohara Yoshio
Department of Dermatology, Shizuoka Cancer Center, Shizuoka, Japan.
Department of Dermatology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
J Dermatol. 2025 Apr;52(4):651-662. doi: 10.1111/1346-8138.17672. Epub 2025 Mar 5.
Combination therapy with nivolumab and ipilimumab (NIVO+IPI) is highly effective in treating advanced malignant melanoma (MM) but it is associated with a high incidence of treatment-related adverse events (TRAEs). This retrospective, cohort study evaluated the efficacy and TRAEs of NIVO+IPI in Japanese patients with unresectable stage III and IV MM, comparing outcomes based on the number of treatment cycles and the IPI dose. We reviewed data from 57 patients with advanced or recurrent MM who received NIVO+IPI at the Shizuoka Cancer Center between August 2015 and July 2024. Patients who received two or fewer NIVO + IPI cycles (NIVO+IPI ≤2 cycles) generally had worse Eastern Cooperative Oncology Group performance status and more advanced stages compared to those who received three or more cycles (NIVO+IPI ≥3 cycles). The analysis revealed that the NIVO+IPI ≥3 cycles group had significantly better overall survival compared to the NIVO+IPI ≤2 cycles group, although receiving three or more cycles was not an independent prognostic factor in multivariate analysis. There was no significant difference in the frequency or severity of TRAEs between the two groups, but the incidence of grade ≥3 TRAEs increased significantly between the first and second cycles of NIVO+IPI. Additionally, reducing the IPI dose from 3 mg/kg to 2 mg/kg appeared to lower the risk of grade ≥3 TRAEs. In conclusion, further research is needed to determine the optimal number of NIVO+IPI cycles for Japanese patients with advanced MM. However, assessing efficacy after the second cycle may help avoid unnecessary NIVO+IPI administration. Reducing the IPI dose to 2 mg/kg may also offer a safer treatment approach for these patients.
纳武利尤单抗和伊匹木单抗联合治疗(NIVO+IPI)在治疗晚期恶性黑色素瘤(MM)方面非常有效,但它与治疗相关不良事件(TRAEs)的高发生率相关。这项回顾性队列研究评估了NIVO+IPI在日本不可切除的III期和IV期MM患者中的疗效和TRAEs,比较了基于治疗周期数和伊匹木单抗剂量的结果。我们回顾了2015年8月至2024年7月期间在静冈癌症中心接受NIVO+IPI治疗的57例晚期或复发性MM患者的数据。与接受三个或更多周期(NIVO+IPI≥3周期)的患者相比,接受两个或更少NIVO + IPI周期(NIVO+IPI≤2周期)的患者一般东部肿瘤协作组体能状态更差,分期更晚。分析显示,NIVO+IPI≥3周期组的总生存期明显优于NIVO+IPI≤2周期组,尽管在多变量分析中接受三个或更多周期并不是一个独立的预后因素。两组之间TRAEs的频率或严重程度没有显著差异,但NIVO+IPI的第一周期和第二周期之间≥3级TRAEs的发生率显著增加。此外,将伊匹木单抗剂量从3mg/kg降至2mg/kg似乎降低了≥3级TRAEs的风险。总之,需要进一步研究以确定日本晚期MM患者NIVO+IPI的最佳周期数。然而,在第二个周期后评估疗效可能有助于避免不必要的NIVO+IPI给药。将伊匹木单抗剂量降至2mg/kg也可能为这些患者提供更安全的治疗方法。