Center for Clinical Oncology, Okayama University Hospital, Okayama, Japan.
Allergy and Respiratory Medicine, Okayama University Hospital, Okayama.
Jpn J Clin Oncol. 2020 Dec 16;50(12):1447-1453. doi: 10.1093/jjco/hyaa152.
Immune checkpoint inhibitors offer longer survival than chemotherapy in several clinical trials for advanced non-small cell lung cancer. In subset analyses of clinical trials, immune checkpoint inhibitors extended survival in patients aged ≥65 years, but the effects in patients aged ≥75 years are controversial. We performed multicenter, collaborative and retrospective analyses of immune checkpoint inhibitor efficacy and safety in non-small cell lung cancer patients aged ≥75 years.
We retrospectively studied 434 advanced non-small cell lung cancer patients who received immune checkpoint inhibitors from December 2015 to December 2017, and retrospectively applied the Geriatric (G) 8 screening tool with medical records.
Of the 434 patients who received immune checkpoint inhibitors, 100 were aged ≥75 years. Five patients with performance status 3 were omitted from the final analysis. Immune checkpoint inhibitors were given as a first-line treatment to 20 patients. The objective response rates, median progression-free survival rates and median survival times were 35.0%, 6.1 months and 10.7 months for first-line treatment, and 20.0%, 2.9 months and 14.7 months for second- or later-line treatments, respectively. The median modified G8 score was 11.0. The median survival time was longer in the high modified G8 (≥12.0) group than in the low modified G8 (≤11.0) group (18.7 vs. 8.7 months; P = 0.02). Likewise, the median survival time was 15.5 months (performance status 0-1) vs. 3.2 months (performance status 2) (P < 0.01). The grade ≥ 2 immune-related adverse events incidence was 36.8%.
In this study, immune checkpoint inhibitors were effective and tolerable for patients aged ≥75 years. The modified G8 screening tool and performance status were associated with the outcome of older non-small cell lung cancer patients treated with immune checkpoint inhibitors.
免疫检查点抑制剂在几项晚期非小细胞肺癌的临床试验中提供的生存时间长于化疗。在临床试验的亚组分析中,免疫检查点抑制剂延长了≥65 岁患者的生存时间,但≥75 岁患者的效果存在争议。我们对≥75 岁的非小细胞肺癌患者进行了免疫检查点抑制剂疗效和安全性的多中心、协作和回顾性分析。
我们回顾性研究了 2015 年 12 月至 2017 年 12 月期间接受免疫检查点抑制剂治疗的 434 例晚期非小细胞肺癌患者,并通过病历回顾性应用老年(G)8 筛选工具。
在接受免疫检查点抑制剂治疗的 434 例患者中,有 100 例年龄≥75 岁。有 5 例体能状态 3 的患者被排除在最终分析之外。免疫检查点抑制剂被用作一线治疗的患者有 20 例。一线治疗的客观缓解率、中位无进展生存期和中位总生存期分别为 35.0%、6.1 个月和 10.7 个月,二线或以上治疗的分别为 20.0%、2.9 个月和 14.7 个月。中位改良 G8 评分为 11.0。中位总生存期在改良 G8 评分较高(≥12.0)组比改良 G8 评分较低(≤11.0)组更长(18.7 个月比 8.7 个月;P=0.02)。同样,中位总生存期为 15.5 个月(体能状态 0-1)比 3.2 个月(体能状态 2)更长(P<0.01)。≥2 级免疫相关不良事件发生率为 36.8%。
在这项研究中,免疫检查点抑制剂对≥75 岁患者有效且耐受良好。改良 G8 筛选工具和体能状态与接受免疫检查点抑制剂治疗的老年非小细胞肺癌患者的结局相关。