卡博替尼对转移性或晚期肾细胞癌患者的疗效和安全性:系统综述和荟萃分析。

Q3 Medicine Baylor University Medical Center Proceedings Pub Date : 2024-06-17 eCollection Date: 2024-01-01 DOI:10.1080/08998280.2024.2363616
Majd M AlBarakat, Yaman B Ahmed, Sakhr Alshwayyat, Asmaa Ellaithy, Yaqoub Y Al-Shammari, Youssef Soliman, Hazem Rezq, Basel Abdelazeem, Arvind Kunadi
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引用次数: 0

摘要

背景:卡博替尼是治疗晚期肾细胞癌(aRCC)的一种新的一线疗法,它以重要的酪氨酸激酶为靶点,在各种疗效结果方面优于既有的比较药(舒尼替尼)。本系统综述和荟萃分析旨在评估卡博替尼与其他aRCC治疗方法相比的疗效和安全性:按照 PRISMA 和 Cochrane 指南,我们的研究方案在 PROSPERO 上进行了注册。截至 2023 年 10 月 8 日,我们在 PubMed、Cochrane、Web of Science 和 EMBASE 上进行了无日期限制的系统性检索。数据提取包括研究细节、基线信息和结果。每种结果都采用了带有95%置信区间的危险比(HR)和风险比(RR),并采用随机效应模型来考虑预期的异质性:我们的分析包括三项研究,共涉及 967 名患者。在疗效方面,卡博替尼的总生存率明显优于其他药物。然而,在亚组分析中,卡博替尼仅在统计学上优于依维莫司。在无进展生存期和肿瘤客观反应率方面,卡博替尼优于依维莫司和舒尼替尼。在不良反应方面,与舒尼替尼相比,卡博替尼除恶心和口腔炎在两组间无差异外,几乎在所有评估方面都表现出劣势。相反,在各种副作用方面,卡博替尼与依维莫司的风险状况相当:卡博替尼在延长总生存期、无进展生存期和肿瘤客观反应率方面疗效显著,尽管与舒尼替尼相比,卡博替尼发生不良反应的风险可能更高。这些研究结果支持将卡博替尼作为aRCC的一线疗法,无论是作为初始疗法还是在既往接受过VEGFR靶向疗法之后。
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The efficacy and safety of cabozantinib in patients with metastatic or advanced renal cell carcinoma: a systematic review and meta-analysis.

Background: Cabozantinib, a new first-line treatment for advanced renal cell carcinoma (aRCC), targets essential tyrosine kinases and outperforms the established comparator (sunitinib) in various efficacy outcomes. This systematic review and meta-analysis aimed to assess the efficacy and safety of cabozantinib compared to other aRCC treatments.

Methods: Following PRISMA and Cochrane guidelines, our protocol was registered in PROSPERO. A systematic search, without date limits, was conducted on PubMed, Cochrane, Web of Science, and EMBASE until October 8, 2023. Data extraction encompassed study details, baseline information, and outcomes. Hazard ratios (HR) and risk ratios (RR) with 95% confidence intervals were employed for each outcome, and a random-effects model was applied to account for expected heterogeneity.

Results: Three studies, encompassing 967 patients, were included in our analysis. In terms of efficacy, the pooled rate for overall survival significantly favored cabozantinib. However, in subgroup analyses, cabozantinib was only statistically superior to everolimus. For progression-free survival and tumor objective response rate, cabozantinib outperformed both everolimus and sunitinib. In adverse events, compared to sunitinib, cabozantinib exhibited inferiority in nearly all evaluated aspects, except for nausea and stomatitis, which showed no difference between the two groups. Conversely, it demonstrated a comparable risk profile with everolimus across various side effects.

Conclusion: Cabozantinib shows significant efficacy in extending overall survival, progression-free survival, and tumor objective response rate despite a potentially higher risk of adverse events compared to sunitinib. These findings support cabozantinib as a first-line therapy for aRCC, either as an initial treatment or after prior VEGFR-targeted therapies.

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