舒尼替尼替代方案(AS)在亚洲和非亚洲患者群体中治疗转移性肾细胞癌(mRCC)的安全性和有效性的比较评价:一项荟萃分析

IF 1.1 Q4 ONCOLOGY
Kidney Cancer Pub Date : 2022-01-20 DOI:10.3233/kca-210122
A. Joshi, Ishan J. Patel, Pratiksha Kapse, Manmohan Singh
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引用次数: 0

摘要

背景:使用舒尼替尼的传统方案(TS, 4/2)治疗转移性肾细胞癌(mRCC)与替代方案(AS, 2/1前期或从TS切换时)相比,不良反应更高。目的:本荟萃分析旨在比较亚洲(AP)和非亚洲(NAP)人群接受舒尼替尼AS治疗的安全性、有效性和需要减量或中断剂量的患者百分比。方法:检索电子数据库(PubMed, EMBASE, Cochrane Library),以确定2009年5月至2019年5月期间以英语发表的研究,其中包括接受舒尼替尼治疗的mRCC患者(bb0 - 18岁)。数据分析采用随机效应模型和t检验。P < 0.05为差异有统计学意义。结果:1922年共纳入16项研究(8项AP, 8项NAP)。在所有ae中,粘膜炎(RR:0.22;95% CI: 0.12-0.40),心脏毒性(RR: 0.52;95% CI: 0.31-0.88),恶心(RR:0.21;95% CI: 0.10-0.44),手足综合征(RR:0.33;95% CI: 0.13-0.83),皮疹(RR: 0.52;95% CI: 0.34-0.79)和天冬氨酸转氨酶(RR:0.57;95% CI: 0.33-0.98)在AP中更为常见。白细胞减少(RR:2.57;95% CI: 1.47-4.49),蛋白血症(RR:4.45;95% CI: 2.12-9.33)和口炎(RR:4.33;95% CI: 2.6-7.23)更常见于NAP。此外,NAP患者的PFS明显更长,AP患者的OS更长(p < 0.001)。AP组的剂量减少率明显高于NAP组(52.08%比40.6%,p = 0.0088)。结论:舒尼替尼的AS安全性相似,但AP与NAP在疗效、剂量减少方面存在差异。调整舒尼替尼的剂量或方案可以通过延长治疗时间来减轻mRCC的不良反应并提高疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative Evaluation of Safety and Efficacy of Alternate Schedule (AS) of Sunitinib in Asian and Non-Asian Patient Population for the Treatment of Metastatic Renal Cell Cancer (mRCC): A Meta-Analysis
Background: Treatment of metastatic renal cell carcinoma (mRCC) using traditional schedule (TS, 4/2) of Sunitinib is associated with higher adverse effects compared to the alternate schedule (AS, 2/1 upfront or when switched from TS). Objective: This meta-analysis aims to compare the safety, efficacy, and percentage of patients requiring dose reduction or dose interruption between Asian (AP) and non-Asian population (NAP) receiving AS of sunitinib. Methods: Electronic databases (PubMed, EMBASE, Cochrane Library) were searched to identify studies published in the English language between May 2009- May 2019, which included patients (>18 years) with mRCC receiving AS of sunitinib. Data were analyzed using the random effect model and t-test. P <  0.05 was considered statistically significant. Results: Of 1922, 16 studies were included (eight AP, eight NAP). Among all grade AEs, mucositis (RR:0.22; 95% CI:0.12–0.40), cardiotoxicity (RR: 0.52; 95% CI: 0.31–0.88), nausea (RR:0.21; 95% CI: 0.10–0.44), hand-foot syndrome (RR:0.33; 95% CI:0.13–0.83), rash (RR: 0.52; 95% CI: 0.34–0.79), and aspartate transaminase (RR:0.57; 95% CI:0.33–0.98) were more common in AP. Leukopenia (RR:2.57; 95% CI:1.47–4.49), proteinemia (RR:4.45; 95% CI:2.12–9.33), and stomatitis (RR:4.33; 95% CI:2.6–7.23) occurred more commonly in NAP. Further, PFS was significantly longer in NAP, while longer OS was observed in AP (p <  0.001). Dose reduction was significantly higher in AP than NAP (52.08% vs. 40.6%, p = 0.0088). Conclusion: Safety profile of AS of sunitinib was similar with variations in the efficacy, dose reduction between AP and NAP. Sunitinib dose or schedule modification may mitigate AEs and enhance efficacy outcomes in mRCC by extending the treatment duration.
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来源期刊
Kidney Cancer
Kidney Cancer Multiple-
CiteScore
0.90
自引率
8.30%
发文量
23
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