Toyoda Shingo, Fukuokaya Wataru, Mori Keiichiro, Kawada Tatsushi, Katayama Satoshi, Nishimura Shingo, Maenosono Ryoichi, Tsujino Takuya, Adachi Takahiro, Hirasawa Yosuke, Saruta Masanobu, Komura Kazumasa, Nukaya Takuhisa, Yanagisawa Takafumi, Takahara Kiyoshi, Hashimoto Takeshi, Azuma Haruhito, Ohno Yoshio, Shiroki Ryoichi, Araki Motoo, Kimura Takahiro, Fujita Kazutoshi
Department of Urology, Kindai University Faculty of Medicine, 377-2, Ohnohigashi, Osaka-Sayama City, Osaka Prefecture, Japan.
Department of Urology, The Jikei University School of Medicine, 3-19-18 Nishi-Shinbashi, Minato-ku, Tokyo, Japan.
Jpn J Clin Oncol. 2024 Dec 7;54(12):1336-1342. doi: 10.1093/jjco/hyae108.
Metastatic nonclear cell renal cell carcinoma (nccRCC) is a heterogeneous disease with poor prognosis. The clinical characteristics and prognostic factors of immuno-oncology (IO) combination therapy for nccRCC are not well known. This study analyzed patients with metastatic nccRCC treated with IO combination therapy.
We retrospectively collected data from 447 patients with metastatic RCC treated with IO-based combination therapy as first-line treatment between September 2018 and July 2023 in a Japanese multicenter study. The primary endpoints were objective response rate, progression-free survival (PFS), and overall survival (OS), comparing groups treated with IO-IO and IO-tyrosine kinase inhibitor (TKI) therapies.
Seventy-five patients with metastatic nccRCC were eligible for analysis: 39 were classified into the IO-IO group and 36 into the IO-TKI group. Median PFS was 5.4 months (95% CI: 1.6-9.1) for the IO-IO group and 5.6 (95% CI: 3.4-12.0) for the IO + TKI group. Median OS was 24.2 months (95% CI: 7.5-NA) for the IO-IO group and 23.4 (95% CI: 18.8-NA) for the IO + TKI group, with no significant difference. In univariate analysis, International Metastatic Renal Cell Carcinoma Database Consortium scores, Karnofsky performance status, neutrophil-to-lymphocyte ratio, and the presence of liver metastases were significantly associated with OS, whereas in multivariate analysis, only the presence of liver metastases was significantly associated with OS (P = .035).
There was no significant difference in OS or PFS between IO-IO and IO-TKI combination therapy as first-line treatment for patients with nccRCC. Liver metastasis is a poor prognostic factor for such patients.
转移性非透明细胞肾细胞癌(nccRCC)是一种预后较差的异质性疾病。免疫肿瘤学(IO)联合治疗nccRCC的临床特征和预后因素尚不清楚。本研究分析了接受IO联合治疗的转移性nccRCC患者。
我们回顾性收集了2018年9月至2023年7月在一项日本多中心研究中接受以IO为基础的联合治疗作为一线治疗的447例转移性肾细胞癌患者的数据。主要终点是客观缓解率、无进展生存期(PFS)和总生存期(OS),比较接受IO-IO和IO-酪氨酸激酶抑制剂(TKI)治疗的组。
75例转移性nccRCC患者符合分析条件:39例分为IO-IO组,36例分为IO-TKI组。IO-IO组的中位PFS为5.4个月(95%CI:1.6-9.1),IO+TKI组为5.6个月(95%CI:3.4-12.0)。IO-IO组的中位OS为24.2个月(95%CI:7.5-无可用数据),IO+TKI组为23.4个月(95%CI:18.8-无可用数据),无显著差异。单因素分析中,国际转移性肾细胞癌数据库联盟评分、卡诺夫斯基体能状态、中性粒细胞与淋巴细胞比值和肝转移的存在与OS显著相关,而多因素分析中,只有肝转移的存在与OS显著相关(P= .035)。
对于nccRCC患者,IO-IO和IO-TKI联合治疗作为一线治疗的OS或PFS无显著差异。肝转移是此类患者的不良预后因素。