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帕博利珠单抗和阿昔替尼作为晚期肾细胞癌一线治疗的疗效和安全性:日本的真实世界经验。

Efficacy and safety of pembrolizumab and axitinib as first-line treatment for patients with advanced renal cell carcinoma: Real-world experience in Japan.

机构信息

Department of Urology, University of Occupational and Environmental Health, Kitakyushu, Japan.

Department of Urology, Hamamatsu University School of Medicine, Hamamatsu, Japan.

出版信息

Int J Urol. 2023 Sep;30(9):772-777. doi: 10.1111/iju.15230. Epub 2023 Jun 22.

Abstract

OBJECTIVES

The objective of this study was to assess the clinical outcomes following combined treatment with pembrolizumab and axitinib as first-line therapy for patients with advanced RCC.

METHODS

This study retrospectively included 47 consecutive Japanese patients who were diagnosed with advanced RCC and subsequently received pembrolizumab and axitinib between February 2020 and January 2022. Efficacy and safety of this combined therapy in these patients were comprehensively investigated.

RESULTS

The 47 included patients were classified into the following 3 groups by the IMDC system: favorable, 7 (14.9%); intermediate, 24 (51.1%) and poor, 16 (34.0%). Responses to this combined therapy in the 47 patients were as follows: CR, 8 (17.0%); PR, 20 (42.6%); SD, 16 (34.0%) and PD, 3 (6.4%); thus, the ORR was 59.6%. During the observation period, disease progression and death occurred in 19 (40.4%) and 9 (19.1%) patients, respectively, and the median PFS and OS were 18 months and not reached, respectively. Univariate analyses identified the following significant predictors for poor prognostic outcomes: lack of nephrectomy, liver metastasis, bone metastasis, elevated CRP and IMDC poor risk for PFS; and lack of nephrectomy, non-CCC and elevated CRP for OS. AEs and those corresponding to grade ≥ 3 occurred in all (100%) and 30 (63.8%) patients, respectively.

CONCLUSIONS

To our knowledge, this is the first study focusing on real-world outcomes following pembrolizumab and axitinib for treatment-naïve advanced Japanese RCC patients, which showed the efficacy and safety of this combined therapy being similar or even superior to those in clinical trial.

摘要

目的

本研究旨在评估帕博利珠单抗联合阿昔替尼作为晚期肾细胞癌(RCC)一线治疗的临床疗效。

方法

本研究回顾性纳入 2020 年 2 月至 2022 年 1 月期间接受帕博利珠单抗联合阿昔替尼治疗的 47 例日本晚期 RCC 患者。综合评估该联合治疗方案在这些患者中的疗效和安全性。

结果

根据 IMDC 系统,47 例患者分为以下 3 组:有利组 7 例(14.9%),中等组 24 例(51.1%)和不良组 16 例(34.0%)。47 例患者对联合治疗的反应如下:完全缓解(CR)8 例(17.0%),部分缓解(PR)20 例(42.6%),疾病稳定(SD)16 例(34.0%)和疾病进展(PD)3 例(6.4%),因此,总缓解率(ORR)为 59.6%。在观察期间,19 例(40.4%)患者发生疾病进展,9 例(19.1%)患者死亡,中位无进展生存期(PFS)和总生存期(OS)分别为 18 个月和未达到。单因素分析发现,以下因素与预后不良显著相关:未行肾切除术、肝转移、骨转移、C 反应蛋白(CRP)升高和 IMDC 预后不良与 PFS;未行肾切除术、非透明细胞癌(CCC)和 CRP 升高与 OS。所有患者(100%)和 30 例(63.8%)患者均出现治疗相关不良事件(AE)和≥3 级 AE。

结论

据我们所知,这是第一项关于帕博利珠单抗联合阿昔替尼治疗未经治疗的日本晚期 RCC 患者的真实世界研究,该研究显示该联合治疗方案的疗效和安全性与临床试验相似,甚至更优。

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