Cancer Institute Hospital, Japanese Foundation for Cancer Research, 3-8-31, Ariake, Koto, Tokyo, 135-8550, Japan.
National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo, 104-0045, Japan.
Int J Clin Oncol. 2023 Oct;28(10):1354-1368. doi: 10.1007/s10147-023-02390-2. Epub 2023 Aug 7.
In CheckMate 227 Part 1 (NCT02477826), first-line nivolumab plus ipilimumab demonstrated long-term durable overall survival (OS) benefit versus chemotherapy in patients with metastatic non-small cell lung cancer (NSCLC), regardless of tumor programmed death ligand 1 (PD-L1) expression. We report results in Japanese patients with ≥ 5-year follow-up.
Adults with stage IV/recurrent NSCLC without EGFR/ALK aberrations were randomized 1:1:1 to nivolumab plus ipilimumab, nivolumab alone, or chemotherapy (patients with tumor PD-L1 ≥ 1%), or nivolumab plus ipilimumab, nivolumab plus chemotherapy, or chemotherapy (patients with tumor PD-L1 < 1%). Five-year efficacy and safety were assessed in Japanese patients.
At 62.1 months' minimum follow-up, 143 Japanese patients with PD-L1 ≥ 1% or < 1% were randomized to nivolumab plus ipilimumab (n = 66) or chemotherapy (n = 77). Five-year OS rates were 46% with nivolumab plus ipilimumab versus 34% with chemotherapy (PD-L1 ≥ 1%) and 36% versus 19% (PD-L1 < 1%). Median duration of response was 59.1 versus 7.1 months (PD-L1 ≥ 1%) and 17.3 versus 3.0 months (PD-L1 < 1%). Among 5-year survivors treated with nivolumab plus ipilimumab (PD-L1 ≥ 1% and < 1%; n = 27), 59% (95% CI, 39%-75%) were off treatment for ≥ 3 years without receiving subsequent therapy. No new safety signals were observed.
At 5-year follow-up, nivolumab plus ipilimumab continued to show long-term durable clinical benefit versus chemotherapy, regardless of tumor PD-L1 expression. Consistent with findings for the global population, these data support the use of nivolumab plus ipilimumab as first-line treatment in Japanese patients with metastatic NSCLC.
在 CheckMate 227 第 1 部分(NCT02477826)中,一线纳武利尤单抗联合伊匹单抗与化疗相比,为转移性非小细胞肺癌(NSCLC)患者带来了长期持久的总生存(OS)获益,无论肿瘤程序性死亡配体 1(PD-L1)表达情况如何。我们报告了在日本患者中随访时间超过 5 年的结果。
成人 IV 期/复发性无 EGFR/ALK 异常的 NSCLC 患者按 1:1:1 的比例随机分配至纳武利尤单抗联合伊匹单抗、纳武利尤单抗单药或化疗(肿瘤 PD-L1≥1%),或纳武利尤单抗联合伊匹单抗、纳武利尤单抗联合化疗或化疗(肿瘤 PD-L1<1%)。在日本患者中评估了 5 年的疗效和安全性。
在 62.1 个月的最小随访时间内,有 143 名 PD-L1≥1%或<1%的日本患者被随机分配至纳武利尤单抗联合伊匹单抗(n=66)或化疗(n=77)。纳武利尤单抗联合伊匹单抗的 5 年 OS 率为 46%,化疗为 34%(PD-L1≥1%),36%和 19%(PD-L1<1%)。中位缓解持续时间为 59.1 个月与 7.1 个月(PD-L1≥1%)和 17.3 个月与 3.0 个月(PD-L1<1%)。纳武利尤单抗联合伊匹单抗(PD-L1≥1%和<1%;n=27)治疗的 5 年幸存者中,59%(95%CI,39%-75%)在未接受后续治疗的情况下停药≥3 年。未观察到新的安全性信号。
在 5 年随访时,纳武利尤单抗联合伊匹单抗与化疗相比继续显示出长期持久的临床获益,无论肿瘤 PD-L1 表达情况如何。与全球人群的研究结果一致,这些数据支持在日本转移性 NSCLC 患者中使用纳武利尤单抗联合伊匹单抗作为一线治疗。