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Lancet. 2023 Jul 15;402(10397):185-195. doi: 10.1016/S0140-6736(23)00922-4. Epub 2023 Jun 5.
2
Cabozantinib plus Nivolumab and Ipilimumab in Renal-Cell Carcinoma.卡博替尼联合纳武利尤单抗和伊匹单抗治疗肾细胞癌。
N Engl J Med. 2023 May 11;388(19):1767-1778. doi: 10.1056/NEJMoa2212851.
3
Outcomes based on plasma biomarkers in METEOR, a randomized phase 3 trial of cabozantinib vs everolimus in advanced renal cell carcinoma.基于 METEOR 研究中血浆生物标志物的结果,该研究为卡博替尼对比依维莫司治疗晚期肾细胞癌的随机 3 期临床试验。
BMC Cancer. 2021 Aug 7;21(1):904. doi: 10.1186/s12885-021-08630-w.
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The PRISMA 2020 statement: an updated guideline for reporting systematic reviews.PRISMA 2020 声明:系统评价报告的更新指南。
BMJ. 2021 Mar 29;372:n71. doi: 10.1136/bmj.n71.
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Nivolumab plus Cabozantinib versus Sunitinib for Advanced Renal-Cell Carcinoma.纳武利尤单抗联合卡博替尼对比舒尼替尼用于晚期肾细胞癌。
N Engl J Med. 2021 Mar 4;384(9):829-841. doi: 10.1056/NEJMoa2026982.
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A comparison of sunitinib with cabozantinib, crizotinib, and savolitinib for treatment of advanced papillary renal cell carcinoma: a randomised, open-label, phase 2 trial.舒尼替尼与卡博替尼、克唑替尼和索凡替尼治疗晚期乳头状肾细胞癌的比较:一项随机、开放标签、二期临床试验。
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卡博替尼治疗转移性或晚期肾细胞癌患者的疗效和安全性:一项系统评价和荟萃分析。

The efficacy and safety of cabozantinib in patients with metastatic or advanced renal cell carcinoma: a systematic review and meta-analysis.

作者信息

AlBarakat Majd M, Ahmed Yaman B, Alshwayyat Sakhr, Ellaithy Asmaa, Y Al-Shammari Yaqoub, Soliman Youssef, Rezq Hazem, Abdelazeem Basel, Kunadi Arvind

机构信息

Faculty of Medicine, Jordan University of Science and Technology, Irbid, Jordan.

Faculty of Medicine, Suez Canal University, Ismailia, Egypt.

出版信息

Proc (Bayl Univ Med Cent). 2024 Jun 17;37(5):822-830. doi: 10.1080/08998280.2024.2363616. eCollection 2024.

DOI:10.1080/08998280.2024.2363616
PMID:39165809
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11332639/
Abstract

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.

摘要

背景

卡博替尼是晚期肾细胞癌(aRCC)的一种新型一线治疗药物,可作用于关键酪氨酸激酶,在多种疗效指标上优于已有的对照药物(舒尼替尼)。本系统评价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。

方法

按照PRISMA和Cochrane指南,我们的方案在PROSPERO中进行了注册。在PubMed、Cochrane、科学网和EMBASE上进行了无日期限制的系统检索,直至2023年10月8日。数据提取包括研究细节、基线信息和结果。每个结果采用95%置信区间的风险比(HR)和风险率(RR),并应用随机效应模型来考虑预期的异质性。

结果

我们的分析纳入了3项研究,共967例患者。在疗效方面,总生存的合并率显著有利于卡博替尼。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缓解率方面,卡博替尼优于依维莫司和舒尼替尼。在不良事件方面,与舒尼替尼相比,卡博替尼在几乎所有评估方面均表现较差,除恶心和口腔炎外,两组之间无差异。相反,在各种副作用方面,它与依维莫司的风险特征相当。

结论

尽管与舒尼替尼相比,卡博替尼发生不良事件的风险可能更高,但在延长总生存期、无进展生存期和肿瘤客观缓解率方面显示出显著疗效。这些发现支持卡博替尼作为aRCC的一线治疗药物,无论是作为初始治疗还是在先前接受过VEGFR靶向治疗之后。