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

机译:在局部晚期直肠癌患者的新辅助治疗中添加靶向药物的疗效:一项荟萃分析

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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.
机译:局部晚期直肠癌(LARC)患者处于转移性疾病的巨大风险中。为了改善LARC患者的预后,许多研究人员已经研究了将靶向药物添加到新辅助治疗中的功效,但仍存在争议。截至2016年12月,对相关数据库进行了文献检索,确定了804项研究,最终纳入了32项调查。在该单臂荟萃分析中,来自29个研究的31个队列的1196名患者符合定量综合要求。由于病理完全缓解(pCR)显示出有希望作为预后指标,因此我们将重点放在pCR率上,以评估在新辅助治疗中添加靶向药物是否可以改善LARC患者的预后。在我们的研究中,我们揭示了贝伐单抗相关人群和西妥昔单抗相关人群的pCR合并估计分别为27%(95%CI,21–34%)和14%(95%CI,9–21%)。还通过汇总3/4级毒性数据评估了在新辅助治疗中添加靶向药物的安全性。总之,我们的研究表明,在新辅助治疗方案中加入贝伐单抗可为LARC患者提供明显的pCR。同时,西妥昔单抗的疗效尚无定论,需要更大规模的RCT和更好的研究设计以强调突变状态。

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