Characteristics of patients with metastatic renal cell carcinoma who do not respond to axitinib treatment.

IF 2.8 3区 医学 Q3 ONCOLOGY International Journal of Clinical Oncology Pub Date : 2025-04-01 Epub Date: 2025-02-14 DOI:10.1007/s10147-025-02715-3
Kojiro Ohba, Takahiro Osawa, Takahiro Kojima, Tomohiko Hara, Mikio Sugimoto, Masatoshi Eto, Keita Minami, Yasutomo Nakai, Kosuke Ueda, Sei Naito, Norio Nonomura, Sachiyo Murai, Hiroyuki Nishiyama, Hiromi Nakanishi, Yuta Mukae, Kensuke Mitsunari, Tomohiro Matsuo, Ryoichi Imamura, Nobuo Shinohara
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Abstract

Background: Axitinib is a widely used tyrosine kinase inhibitor (TKI) in metastatic renal cell carcinoma (mRCC) treatment. Here, we analyzed the characteristics of patients who did not respond to axitinib and evaluated alternative options for their treatment.

Methods: We retrospectively analyzed data for 449 patients with mRCC who were administered axitinib following another TKI as initial therapy. Patients with progressive disease (PD) at their first assessment were defined as showing early-PD. We analyzed the characteristics of patients at risk of early-PD and evaluated the relationship between the treatment following axitinib and their prognosis.

Results: Early-PD was diagnosed in 102 patients, and was more common in those who had not undergone nephrectomy (p < 0.001), those treated with a TKI for a short period (p < 0.001), and those in the International Metastatic Renal Cell Carcinoma Database Consortium (IMDC) poor risk category for mRCC (p < 0.001). Multivariate analysis showed that these were independent risk factors for early-PD (all p < 0.001). Of those with early-PD, 52 changed to next-line treatment. The progression-free survival periods were 5.5 (95% confidence interval (CI) 2.4-8.6) months for patients administered TKIs, 4.2 (95% CI 0.3-8.1) months for those on nivolumab, and 2.2 (1.8-2.6) months for those on mammalian target of rapamycin inhibitors (p = 0.030).

Conclusion: Patients who have not undergone nephrectomy, those previously treated with another TKI for a short period, and those in the IMDC poor risk category are more likely to experience early-PD when taking axitinib. Furthermore, TKIs are the best treatment for patients with early-PD who have previously been administered axitinib.

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对阿西替尼治疗无效的转移性肾细胞癌患者的特征。
背景:阿西替尼是一种广泛应用于转移性肾细胞癌(mRCC)治疗的酪氨酸激酶抑制剂(TKI)。在这里,我们分析了对阿西替尼没有反应的患者的特征,并评估了他们的治疗方案。方法:我们回顾性分析了449例mRCC患者的数据,这些患者在另一次TKI作为初始治疗后给予阿西替尼。首次评估进行性疾病(PD)的患者被定义为早期PD。我们分析了早期pd风险患者的特征,并评估了阿西替尼治疗与预后的关系。结果:102例患者被诊断为早期pd,在未行肾切除术的患者中更常见(p结论:未行肾切除术的患者、曾短期接受另一种TKI治疗的患者以及IMDC低风险类别的患者在服用阿西替尼时更容易发生早期pd。此外,tki是早期pd患者的最佳治疗方法,这些患者之前曾接受过阿西替尼的治疗。
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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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