Real-world outcomes of avelumab plus axitinib in patients with advanced renal cell carcinoma in Japan: long-term follow-up from the J-DART2 retrospective study.

IF 2.4 3区 医学 Q3 ONCOLOGY International Journal of Clinical Oncology Pub Date : 2024-11-16 DOI:10.1007/s10147-024-02618-9
Taigo Kato, Junya Furukawa, Nobuyuki Hinata, Kosuke Ueda, Isao Hara, Fumiya Hongo, Ryuichi Mizuno, Teppei Okamoto, Hiroshi Okuno, Takayuki Ito, Masahiro Kajita, Mototsugu Oya, Yoshihiko Tomita, Nobuo Shinohara, Masatoshi Eto, Hirotsugu Uemura
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Abstract

Background: Avelumab + axitinib was approved for advanced renal cell carcinoma (aRCC) in Japan in December 2019. We report long-term real-world outcomes with first-line avelumab + axitinib from the J-DART2 study in Japan.

Methods: J-DART2 was a multicenter, noninterventional, retrospective study examining clinical data from patients with curatively unresectable locally advanced or metastatic RCC who started treatment with first-line avelumab + axitinib in Japan between December 2019 and October 2022. Endpoints included patient characteristics, treatment patterns, and outcomes.

Results: Data from 150 patients across 19 sites were analyzed; median follow-up was 18.7 months (95% CI, 16.3-20.6 months). Median age was 70.5 years; 26.0% of patients were aged ≤64 years, 42.7% were aged 65-74 years, and 31.3% were aged ≥75 years. International Metastatic RCC Database Consortium risk was favorable in 26.0%, intermediate in 54.7% (1 risk factor in 30.7%; 2 risk factors in 24.0%), and poor in 19.3% of patients. Median progression-free survival (PFS) was 17.1 months, with 1- and 2-year PFS rates of 57.7% and 37.5%, respectively. Median overall survival (OS) was not reached, with 1- and 2-year OS rates of 90.6% and 84.7%, respectively. Objective response rate was 53.3%; disease control rate was 88.9%. Outcomes were similar across age groups, including patients aged ≥75 years.

Conclusions: J-DART2 is the largest retrospective study to report long-term real-world outcomes in patients with aRCC treated with avelumab + axitinib in Japan. Findings were similar to those observed in previous studies and support the benefit of avelumab + axitinib in clinical practice in Japan.

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日本晚期肾细胞癌患者使用阿维列单抗联合阿西替尼的实际疗效:J-DART2回顾性研究的长期随访。
背景:2019年12月,日本批准阿维列单抗+阿西替尼治疗晚期肾细胞癌(aRCC)。我们报告了日本J-DART2研究中使用阿维单抗+阿西替尼一线治疗的长期真实结果: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月期间在日本开始接受一线阿维列单抗+阿西替尼治疗的治愈性不可切除的局部晚期或转移性RCC患者的临床数据。终点包括患者特征、治疗模式和结果:分析了来自19个地区150名患者的数据;中位随访时间为18.7个月(95% CI,16.3-20.6个月)。中位年龄为70.5岁;26.0%的患者年龄≤64岁,42.7%的患者年龄为65-74岁,31.3%的患者年龄≥75岁。国际转移性 RCC 数据库联盟风险为良好的患者占 26.0%,中等风险的患者占 54.7%(30.7% 的患者存在 1 个风险因素;24.0% 的患者存在 2 个风险因素),不良风险的患者占 19.3%。中位无进展生存期(PFS)为17.1个月,1年和2年PFS率分别为57.7%和37.5%。中位总生存期(OS)未达标,1年和2年OS率分别为90.6%和84.7%。客观反应率为53.3%;疾病控制率为88.9%。各年龄组的结果相似,包括年龄≥75岁的患者:J-DART2是报告日本接受阿维列单抗+阿西替尼治疗的aRCC患者长期实际疗效的最大规模回顾性研究。研究结果与之前的研究结果相似,支持阿维列单抗+阿西替尼在日本临床实践中的益处。
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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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