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局部晚期直肠癌患者新辅助治疗中添加靶向药物的疗效:一项荟萃分析。

The efficacy of adding targeted agents to neoadjuvant therapy for locally advanced rectal cancer patients: a meta-analysis.

机构信息

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

出版信息

Cancer Med. 2018 Mar;7(3):565-582. doi: 10.1002/cam4.1298. Epub 2018 Feb 21.

Abstract

Patients with locally advanced rectal cancer (LARC) are at tremendous risk of metastatic diseases. To improve the prognoses of LARC patients, the efficacy of adding targeted agents to neoadjuvant therapy has been investigated by many researchers but remains controversial. A literature search of relevant databases was conducted through December 2016, 804 studies were identified and 32 investigations were ultimately included. A total of 1196 patients from 31 cohorts of 29 studies were eligible for quantitative synthesis in this single-arm setting meta-analysis. As pathologic complete response (pCR) shows promise as a prognosis indicator, we focused on pCR rates to evaluate whether adding targeted agents to neoadjuvant therapies improves the outcome of LARC patients. In our study, we revealed pooled estimates of pCR of 27% (95%CI, 21-34%) and 14% (95%CI, 9-21%) for bevacizumab-relevant cohorts and cetuximab-relevant cohorts, respectively. The safety of adding targeted agents to neoadjuvant therapy was also evaluated by pooling the data of Grade 3/4 toxicity. In conclusion, our study revealed that adding bevacizumab to the neoadjuvant therapy regimens provides appreciable pCR for LARC patients. Meanwhile, the efficacy of cetuximab remains inconclusive, RCTs with larger scale and better study design that stress more on mutational status are needed.

摘要

局部晚期直肠癌(LARC)患者存在发生转移性疾病的巨大风险。为改善 LARC 患者的预后,许多研究人员研究了在新辅助治疗中添加靶向药物的疗效,但结果仍存在争议。通过对相关数据库进行文献检索,截至 2016 年 12 月共识别出 804 项研究,最终纳入 32 项研究。在这一单项研究的荟萃分析中,来自 29 项研究的 31 个队列的 1196 例患者符合定量综合的条件。由于病理完全缓解(pCR)作为预后指标显示出一定的前景,因此我们重点关注 pCR 率,以评估将靶向药物添加到新辅助治疗中是否能改善 LARC 患者的结局。在我们的研究中,我们发现贝伐珠单抗相关队列和西妥昔单抗相关队列的 pCR 率分别为 27%(95%CI,21-34%)和 14%(95%CI,9-21%)。我们还通过汇总 3/4 级毒性数据来评估添加靶向药物到新辅助治疗中的安全性。总之,我们的研究表明,将贝伐珠单抗添加到新辅助治疗方案中可为 LARC 患者带来可观的 pCR。同时,西妥昔单抗的疗效仍不确定,需要开展规模更大、设计更好的 RCT,并且需要更加注重突变状态。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25da/5852374/b19c4d82378c/CAM4-7-565-g001.jpg

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