Real-world outcomes with avelumab + axitinib in patients with advanced renal cell carcinoma in Japan: subgroup analyses from the J-DART2 study by International Metastatic Renal Cell Carcinoma Database Consortium risk classification.

IF 2.8 3区 医学 Q3 ONCOLOGY International Journal of Clinical Oncology Pub Date : 2025-04-01 Epub Date: 2025-02-11 DOI:10.1007/s10147-024-02655-4
Junya Furukawa, Taigo Kato, Toshinari Yamasaki, Keisuke Monji, Toshiaki Tanaka, Norihiko Tsuchiya, Tomoaki Miyagawa, Hiroshi Yaegashi, Tomoyasu Sano, Takashi Karashima, Kazutoshi Fujita, Jun-Ichi Hori, Takayuki Ito, Masahiro Kajita, Yoshihiko Tomita, Nobuo Shinohara, Masatoshi Eto, Mototsugu Oya, Hirotsugu Uemura
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Abstract

Background: Avelumab + axitinib was approved for the treatment of advanced renal cell carcinoma (aRCC) in Japan in December 2019. We report long-term real-world subgroup analyses with first-line avelumab + axitinib in patients with aRCC by International Metastatic RCC Database Consortium (IMDC) risk classification from the J-DART2 study in Japan.

Methods: J-DART2 was a multicenter, noninterventional, retrospective study examining characteristics, treatment patterns, and outcomes in patients with aRCC who started first-line avelumab + axitinib in Japan between December 2019 and October 2022.

Results: Data from 150 patients across 19 sites were analyzed. IMDC risk was favorable in 39 patients (26.0%), intermediate (1 risk factor) in 46 (30.7%), intermediate (2 risk factors) in 36 (24.0%), and poor in 29 (19.3%). Baseline characteristics were generally consistent across IMDC risk subgroups. In subgroups with favorable, intermediate (1 risk factor), intermediate (2 risk factors), and poor risk, median progression-free survival was 31.0, 15.3, 16.4, and 8.1 months; median overall survival (OS) was not reached, but 24-month OS rates were 95.2%, 91.3%, 85.3%, and 57.6%, respectively. Objective response rates were 54.5%, 56.8%, 47.1%, and 54.2%, respectively. High-dose corticosteroid treatment for immune-related adverse events was administered in 5.1%, 8.7%, 8.3%, and 6.9% of patients, respectively.

Conclusion: Subgroup analyses from J-DART2 confirm the long-term real-world effectiveness of first-line avelumab + axitinib across IMDC risk groups in patients with aRCC in Japan. Our findings were consistent with previous analyses by IMDC risk and support the favorable benefit-risk profile of avelumab + axitinib in clinical practice in Japan.

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日本晚期肾癌患者使用avelumab + axitinib的真实结果:来自国际转移性肾癌数据库联盟风险分类J-DART2研究的亚组分析。
背景:Avelumab + axitinib于2019年12月在日本被批准用于治疗晚期肾细胞癌(aRCC)。根据日本J-DART2研究的国际转移性RCC数据库联盟(IMDC)风险分类,我们报告了一线阿维单抗+阿西替尼在aRCC患者中的长期现实亚组分析。方法:J-DART2是一项多中心、非介入性、回顾性研究,研究了2019年12月至2022年10月期间在日本开始一线阿维单抗+阿西替尼治疗的aRCC患者的特征、治疗模式和结局。结果:分析了来自19个部位的150例患者的数据。IMDC高危39例(26.0%),中度(1个危险因素)46例(30.7%),中度(2个危险因素)36例(24.0%),不良29例(19.3%)。IMDC风险亚组的基线特征基本一致。在有利、中等(1个危险因素)、中等(2个危险因素)和不良风险亚组中,中位无进展生存期分别为31.0个月、15.3个月、16.4个月和8.1个月;中位总生存期(OS)未达到,但24个月的OS率分别为95.2%、91.3%、85.3%和57.6%。客观有效率分别为54.5%、56.8%、47.1%和54.2%。高剂量皮质类固醇治疗免疫相关不良事件的患者比例分别为5.1%、8.7%、8.3%和6.9%。结论:J-DART2的亚组分析证实了一线avelumab + axitinib在日本aRCC患者IMDC风险组中的长期实际有效性。我们的研究结果与之前的IMDC风险分析一致,并支持日本临床实践中avelumab + axitinib有利的获益-风险概况。
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来源期刊
CiteScore
6.80
自引率
3.00%
发文量
175
审稿时长
2 months
期刊介绍: The International Journal of Clinical Oncology (IJCO) welcomes original research papers on all aspects of clinical oncology that report the results of novel and timely investigations. Reports on clinical trials are encouraged. Experimental studies will also be accepted if they have obvious relevance to clinical oncology. Membership in the Japan Society of Clinical Oncology is not a prerequisite for submission to the journal. Papers are received on the understanding that: their contents have not been published in whole or in part elsewhere; that they are subject to peer review by at least two referees and the Editors, and to editorial revision of the language and contents; and that the Editors are responsible for their acceptance, rejection, and order of publication.
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