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新型 TKI(安罗替尼)治疗晚期消化系统肿瘤的疗效和安全性:系统评价和荟萃分析。

Efficacy and safety of a novel TKI (anlotinib) for the treatment of advanced digestive system neoplasms: a systematic review and meta-analysis.

机构信息

Department of Central Laboratory, Liaocheng People's Hospital, Liaocheng, Shandong, China.

Department of Gastroenterology, Liaocheng People's Hospital, Liaocheng, Shandong, China.

出版信息

Front Immunol. 2024 Aug 14;15:1393404. doi: 10.3389/fimmu.2024.1393404. eCollection 2024.

DOI:10.3389/fimmu.2024.1393404
PMID:39206183
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11349560/
Abstract

OBJECTIVE

To systematically evaluate the efficacy and safety of anlotinib targeted therapy for the treatment of patients with advanced digestive system neoplasms (DSNs).

METHODS

Clinical trials were extracted from PubMed, the Cochrane Library, Web of Science, Embase, China National Knowledge Infrastructure (CNKI) and the Wanfang database up to October 2023. Outcome measures, including therapeutic efficacy, quality of life (QOL) and adverse events, were extracted and evaluated.

RESULTS

Twenty trials, including 1,613 advanced DSNs patients, were included. The results indicated that, compared with conventional treatment alone, the combination of anlotinib targeted therapy with conventional treatment significantly improved the patients' 6-months overall survival (OS, OR=1.76, CI=1.53 to 2.02, <0.00001), overall response (ORR, OR=1.76, CI=1.53 to 2.02, <0.00001) and disease control rate (DCR, OR=1.51, 95% CI=1.25 to 1.84, <0.0001). Moreover, the group that received the combined therapy had higher rates of hypertension (<0.00001), proteinuria (<0.00001), fatigue (<0.00001), diarrhea (<0.00001), hypertriglyceridemia (=0.02), alanine aminotransfease (ALT)increased (=0.004), aspartate transaminase (AST) increased (=0.006), anorexia (<0.00001), weight loss (=0.002), abdominal pain (=0.0006), hypothyroidism (=0.02), prolonged QT interval (=0.04). Analyses of other adverse events, such as gastrointestinal reaction, leukopenia, and neutropenia, did not reveal significant differences (>0.05).

CONCLUSION

The combination of anlotinib targeted therapy and conventional treatment is more effective for DSNs treatment than conventional treatment alone. However, this combined treatment could lead to greater rates of hypertension, albuminuria and hand-foot syndrome. Therefore, the benefits and risks should be considered before treatment.

摘要

目的

系统评价安罗替尼靶向治疗晚期消化系统肿瘤(DSN)的疗效和安全性。

方法

检索 PubMed、Cochrane 图书馆、Web of Science、Embase、中国知网(CNKI)和万方数据库建库至 2023 年 10 月的临床试验,提取治疗效果、生活质量(QOL)和不良反应等结局指标并进行评价。

结果

共纳入 20 项试验,包括 1613 例晚期 DSN 患者。结果显示,与单纯常规治疗相比,安罗替尼靶向治疗联合常规治疗可显著提高患者 6 个月总生存(OS,OR=1.76,95%CI=1.53 至 2.02,<0.00001)、总缓解率(ORR,OR=1.76,95%CI=1.53 至 2.02,<0.00001)和疾病控制率(DCR,OR=1.51,95%CI=1.25 至 1.84,<0.0001)。且联合治疗组高血压(<0.00001)、蛋白尿(<0.00001)、乏力(<0.00001)、腹泻(<0.00001)、高甘油三酯血症(=0.02)、丙氨酸氨基转移酶(ALT)升高(=0.004)、天门冬氨酸氨基转移酶(AST)升高(=0.006)、食欲减退(<0.00001)、体重下降(=0.002)、腹痛(=0.0006)、甲状腺功能减退(=0.02)、QT 间期延长(=0.04)发生率更高。而胃肠道反应、白细胞减少、中性粒细胞减少等其他不良反应发生率的差异均无统计学意义(>0.05)。

结论

安罗替尼靶向治疗联合常规治疗较单纯常规治疗更能有效治疗 DSN,但会增加高血压、蛋白尿和手足综合征的发生率。因此,治疗前应权衡利弊。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/398b/11349560/959ded0287d8/fimmu-15-1393404-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/398b/11349560/b15cdaf65795/fimmu-15-1393404-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/398b/11349560/411e8aebfa38/fimmu-15-1393404-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/398b/11349560/eaffcf825b9d/fimmu-15-1393404-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/398b/11349560/37e7b6fe618f/fimmu-15-1393404-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/398b/11349560/8ac7e069179e/fimmu-15-1393404-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/398b/11349560/cb49f765a4ec/fimmu-15-1393404-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/398b/11349560/959ded0287d8/fimmu-15-1393404-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/398b/11349560/b15cdaf65795/fimmu-15-1393404-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/398b/11349560/411e8aebfa38/fimmu-15-1393404-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/398b/11349560/eaffcf825b9d/fimmu-15-1393404-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/398b/11349560/37e7b6fe618f/fimmu-15-1393404-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/398b/11349560/8ac7e069179e/fimmu-15-1393404-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/398b/11349560/cb49f765a4ec/fimmu-15-1393404-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/398b/11349560/959ded0287d8/fimmu-15-1393404-g007.jpg

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