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在局部晚期直肠癌患者新辅助治疗中添加贝伐单抗的疗效和安全性:一项系统评价和荟萃分析。

The efficacy and safety of adding bevacizumab in neoadjuvant therapy for locally advanced rectal cancer patients: A systematic review and meta-analysis.

作者信息

Zhou Yue, Guo Zhexu, Wu Zhonghua, Shi Jinxin, Zhou Cen, Sun Jie, Hidasa Iko, Lu Xuefei, Lu Chong

机构信息

Department of Medical Oncology, The First Affiliated Hospital of China Medical University, 155 North Nanjing Street, Heping District, Shenyang 110001, China.

Department of Surgical Oncology and General Surgery, The First Affiliated Hospital of China Medical University, 155 North Nanjing Street, Heping District, Shenyang City, 110001, China.

出版信息

Transl Oncol. 2021 Jan;14(1):100964. doi: 10.1016/j.tranon.2020.100964. Epub 2020 Nov 25.

Abstract

BACKGROUND

Patients with locally advanced rectal cancer (LARC) are more likely to suffer local recurrence and distant metastases, contributing to worse prognoses. Considering the provided dramatic reduction of local recurrences, neoadjuvant CRT (nCRT) followed by curative resection with total mesorectal excision (TME) and adjuvant chemotherapy has been established as standard therapy for LARC patients. However, the efficacy of adding bevacizumab in neoadjuvant therapy, especially in induction therapy-containing nCRT for LARC patients remains uncertain.

MATERIALS

PubMed, Embase, and Web of Science were searched to retrieve records on the application of bevacizumab in a neoadjuvant setting for LARC patients. The endpoints of interest were pCR and the rates of patients suffering Grade 3/4 bevacizumab-specific adverse events, namely bleeding, wound healing complications, and gastrointestinal perforation.

RESULTS

29 cohorts covering 1134 subjects were included in this systematic review. The pooled pCR rate for bevacizumab-relevant cohorts was 21% (95% confidence interval (95% CI), 17-25%; I = 61.8%), the pooled estimates of Grade 3/4 bleeding, Grade 3/4 wound healing complication, Grade 3/4 gastrointestinal perforation were 1% (95% CI, 0-3%; I = 0%), 2% (95% CI, 1-5%; I = 4.7%), and 2% (95% CI, 0-5%; I = 0%), respectively.

CONCLUSION

The addition of bevacizumab in the nCRT, especially in the TNT, for LARC patients provides promising efficacy and acceptable safety. However, the results should be interpreted cautiously due to the small amount of relevant data and need further confirmation by future studies.

摘要

背景

局部晚期直肠癌(LARC)患者更易发生局部复发和远处转移,导致预后较差。鉴于局部复发率显著降低,新辅助放化疗(nCRT)后行根治性全直肠系膜切除术(TME)及辅助化疗已成为LARC患者的标准治疗方案。然而,在新辅助治疗中添加贝伐单抗的疗效,尤其是在含诱导治疗的LARC患者nCRT中的疗效仍不确定。

材料

检索了PubMed、Embase和Web of Science,以获取有关贝伐单抗在LARC患者新辅助治疗中应用的记录。感兴趣的终点是病理完全缓解(pCR)以及发生3/4级贝伐单抗特异性不良事件(即出血、伤口愈合并发症和胃肠道穿孔)的患者比例。

结果

本系统评价纳入了29个队列,共1134名受试者。与贝伐单抗相关队列的汇总pCR率为21%(95%置信区间(95%CI),17 - 25%;I² = 61.8%),3/4级出血、3/4级伤口愈合并发症、3/4级胃肠道穿孔的汇总估计值分别为1%(95%CI,0 - 3%;I² = 0%)、2%(95%CI,1 - 5%;I² = 4.7%)和2%(95%CI,0 - 5%;I² = 0%)。

结论

在LARC患者的nCRT中,尤其是在TNT方案中添加贝伐单抗具有良好的疗效和可接受的安全性。然而,由于相关数据量较少,结果应谨慎解读,需要未来研究进一步证实。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2417/7704460/66625c55fcd5/fx1.jpg

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