晚期肾细胞癌患者一线免疫检查点抑制剂联合疗法后卡博替尼的实际治疗顺序和疗效:CARINA 研究结果

IF 2.3 3区 医学 Q3 ONCOLOGY
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引用次数: 0

摘要

关于晚期肾细胞癌(aRCC)一线(1L)免疫检查点抑制剂(CPI)联合治疗后的治疗顺序和疗效,真实世界的数据非常有限。在这项基于英国真实世界的回顾性研究(CARINA;NCT04957160)中,数据来自医院和电子处方记录。患者在确诊 aRCC 时年龄≥ 18 岁,在接受包括卡博替尼在内的二线(2L)治疗前接受过 1L CPI-CPI 或酪氨酸激酶抑制剂 (TKI)-CPI 联合治疗。我们描述了治疗结果,包括1L和2L治疗持续时间(DoT)和总生存期(OS)。我们收集了2015年4月至2022年6月期间英国9个中心281名患者的数据。CPI-CPI 疗法的中位 1L DoT 为 2.3 个月(n = 171),TKI-CPI 疗法的中位 1L DoT 为 5.0 个月(n = 58)。在 CPI-CPI 或 TKI-CPI 治疗 1L 后,卡博替尼(n = 163)的中位 2L DoT 分别为 5.8 个月和 4.2 个月,其他疗法(n = 118)的中位 2L DoT 分别为 3.8 个月和 2.4 个月;卡博替尼的中位 2L OS 分别为 15.2 个月和 15.3 个月,其他疗法的中位 2L OS 分别为 14.6 个月和 24.2 个月。卡博替尼2L治疗的DoT在数字上优于其他疗法,1L CPI-CPI治疗后的DoT优于1L TKI-CPI治疗后的DoT。卡博替尼2L疗法和其他2L疗法的中位OS相似,卡博替尼2L疗法和1L疗法的中位OS相似。这些结果表明,无论采用1L CPI-CPI还是TKI-CPI疗法,在基于1L CPI的联合治疗后,包括卡博替尼在内的2L疗法都具有抗肿瘤作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Real-world Treatment Sequencing and Outcomes With Cabozantinib After First-line Immune Checkpoint Inhibitor-based Combination Therapy For Patients With Advanced Renal Cell Carcinoma: CARINA Study Results

Introduction

Real-world data are limited on treatment sequencing and outcomes after first-line (1L) immune checkpoint inhibitor (CPI)-based combination treatment of advanced renal cell carcinoma (aRCC).

Patients and Methods

In this real-world, UK-based, retrospective study (CARINA; NCT04957160), data were obtained from hospital and electronic prescribing records. Patients were aged ≥ 18 years at aRCC diagnosis and had received 1L CPI–CPI or tyrosine kinase inhibitor (TKI)–CPI combination therapy before second-line (2L) therapy including cabozantinib. We describe treatment outcomes including 1L and 2L durations of treatment (DoT) and overall survival (OS).

Results

Data from April 2015 to June 2022 were collected on 281 patients from nine UK centres. Median 1L DoT was 2.3 months for CPI–CPI therapy (n = 171) and 5.0 months for TKI–CPI therapy (n = 58). After 1L CPI–CPI or TKI–CPI therapy, median 2L DoT was 5.8 versus 4.2 months, respectively, for cabozantinib (n = 163), and 3.8 versus 2.4 months for other therapies (n = 118); median 2L OS was 15.2 and 15.3 months, respectively, for cabozantinib, and 14.6 and 24.2 months for other therapies.

Conclusion

DoT for 2L treatment was numerically better for cabozantinib than for other therapies, and after 1L CPI–CPI therapy than after 1L TKI–CPI therapy. Median OS was similar for 2L cabozantinib and other 2L therapies, and median OS for 2L cabozantinib was similar after both 1L therapy types. These results demonstrate the antitumour effect of 2L therapies, including cabozantinib, after 1L CPI-based combination treatment, regardless of whether 1L CPI–CPI or TKI–CPI therapy is used.

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来源期刊
Clinical genitourinary cancer
Clinical genitourinary cancer 医学-泌尿学与肾脏学
CiteScore
5.20
自引率
6.20%
发文量
201
审稿时长
54 days
期刊介绍: Clinical Genitourinary Cancer is a peer-reviewed journal that publishes original articles describing various aspects of clinical and translational research in genitourinary cancers. Clinical Genitourinary Cancer is devoted to articles on detection, diagnosis, prevention, and treatment of genitourinary cancers. The main emphasis is on recent scientific developments in all areas related to genitourinary malignancies. Specific areas of interest include clinical research and mechanistic approaches; drug sensitivity and resistance; gene and antisense therapy; pathology, markers, and prognostic indicators; chemoprevention strategies; multimodality therapy; and integration of various approaches.
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