Cabazitaxel versus abiraterone or enzalutamide for metastatic castration-resistant prostate cancer following docetaxel failure: a systematic review and meta-analysis.

IF 2.8 3区 医学 Q2 ONCOLOGY
Izael Pereira da Silva, Lucas Guimarães Campos Roriz de Amorim, Gabriel Vieira Piredda, Marcelo Mass-Lindenbaum, Francisco Cezar Aquino de Moraes, Pedro F S Freitas, Bárbara Vieira Lima Aguiar Melão, Helisandro Montenegro Brandão, Karine Martins da Trindade
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引用次数: 0

Abstract

Purpose: Treatment for metastatic castration-resistant prostate cancer (mCRPC) includes chemotherapy and inhibition of the androgen receptor pathway. However, the optimal treatment sequence in this scenario is not yet fully understood. Therefore, we conducted a systematic review and meta-analysis comparing cabazitaxel versus abiraterone or enzalutamide for efficacy and safety outcomes as second-line therapy in mCRPC patients after docetaxel failure.

Methods: We searched PubMed, Embase, and Cochrane databases for interventional studies comparing cabazitaxel versus abiraterone or enzalutamide for patients with mCRPC who have experienced treatment failure with docetaxel as their first-line therapy. We computed hazard ratios (HRs) or odds ratios (ORs) with 95% confidence intervals (CIs).

Results: Eight studies, comprising 1,897 patients were included, of whom 548 (28.8%) received cabazitaxel. Mean follow-up time ranged from 3 to 16.4 months. Median age ranged from 68.1 to 73.9 years in the cabazitaxel group, and 68.0 to 73.1 years in the abiraterone or enzalutamide group. In our meta-analysis, cabazitaxel significantly improved progression-free survival (PFS) rates (HR 0.60; 95% CI 0.47-0.78; p < 0.001) compared to abiraterone or enzalutamide. There were no differences between groups in overall survival (HR 0.76; 95% CI 0.46-1.24; p = 0.27), therapy-related grade ≥ 3 adverse events (AEs) (OR 3.00; 95% CI 0.72-12.40; p = 0.12), and PSA decline ≥ 50% (OR 1.20; 95% CI 0.51-2.80; p = 0.67).

Conclusions: In this systematic review and meta-analysis of men with mCRPC after docetaxel failure, second-line therapy with cabazitaxel was associated with a longer PFS compared with abiraterone or enzalutamide, though without a significant difference in OS.

卡巴他赛与阿比特龙或恩杂鲁胺治疗多西他赛失败后转移性去势抵抗性前列腺癌:一项系统回顾和荟萃分析
目的:转移性去势抵抗性前列腺癌(mCRPC)的治疗包括化疗和雄激素受体途径的抑制。然而,在这种情况下的最佳处理顺序尚未完全了解。因此,我们进行了一项系统回顾和荟萃分析,比较卡巴他赛与阿比特龙或恩杂鲁胺作为多西他赛失败后mCRPC患者二线治疗的有效性和安全性。方法:我们检索PubMed、Embase和Cochrane数据库,比较卡巴他赛与阿比特龙或恩杂鲁胺对多西他赛作为一线治疗失败的mCRPC患者的介入性研究。我们计算了95%置信区间(ci)的风险比(hr)或优势比(ORs)。结果:纳入8项研究,1897例患者,其中548例(28.8%)接受卡巴他赛治疗。平均随访时间3 ~ 16.4个月。卡巴他赛组的中位年龄为68.1 ~ 73.9岁,阿比特龙或恩杂鲁胺组的中位年龄为68.0 ~ 73.1岁。在我们的荟萃分析中,卡巴他赛显著提高了无进展生存(PFS)率(HR 0.60;95% ci 0.47-0.78;结论:在这项对多西他赛失败后mCRPC患者的系统回顾和荟萃分析中,与阿比特龙或恩杂鲁胺相比,二线治疗卡巴他赛与更长的PFS相关,尽管OS没有显着差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.20
自引率
2.90%
发文量
240
审稿时长
1 months
期刊介绍: Clinical and Translational Oncology is an international journal devoted to fostering interaction between experimental and clinical oncology. It covers all aspects of research on cancer, from the more basic discoveries dealing with both cell and molecular biology of tumour cells, to the most advanced clinical assays of conventional and new drugs. In addition, the journal has a strong commitment to facilitating the transfer of knowledge from the basic laboratory to the clinical practice, with the publication of educational series devoted to closing the gap between molecular and clinical oncologists. Molecular biology of tumours, identification of new targets for cancer therapy, and new technologies for research and treatment of cancer are the major themes covered by the educational series. Full research articles on a broad spectrum of subjects, including the molecular and cellular bases of disease, aetiology, pathophysiology, pathology, epidemiology, clinical features, and the diagnosis, prognosis and treatment of cancer, will be considered for publication.
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