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Neoadjuvant chemotherapy regimens in treatment of breast cancer: a systematic review and network meta-analysis protocol

机译:Neoadjuvant化疗治疗乳腺癌的治疗方案:系统审查与网络元分析方案

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摘要

Abstract Background Neoadjuvant chemotherapy (NACT), a standard of care for locally advanced breast cancer patients, is widely used for early breast cancer patients also. The varying role of regimens used as NACT needs to be investigated. Despite availability of some randomized controlled trials (RCTs), it is unclear which treatment regimen suits best. Further, there is no study comparing all the three regimens. Accordingly, present study will compare the efficacy of anthracyclines, taxanes, and targeted therapy administered in neoadjuvant setting on the basis of oncological outcomes and functional outcomes. Method/design Online databases PubMed and Cochrane Register of Controlled Trials will be searched to acquire eligible studies. Further, content of relevant journals, references of relevant articles, and proceedings of major related conference will also be searched. The RCTs comparing any of abovementioned regimen as NACT on breast cancer patients will be eligible. Two reviewers independently and in duplicate will screen the records on the basis of title and abstract and complete full-text review to determine eligibility. Similarly, data extraction and risk of bias assessment will be done by two independent reviewers. The pair-wise meta-analysis as well as network meta-analysis will be conducted to assess the relative efficacy of anthracyclines, taxanes, and targeted therapy regimens. Discussion The present systematic review will improve the understanding of the relative efficacies of the three treatment regimens and possibly guide the clinical practices by providing the current best evidence on the efficacy of various regimens of NACT in the management of breast cancer patients. Systematic review registration PROSPERO (CRD42016027236).
机译:摘要背景Neoadjuvant化疗(结构),局部晚期乳腺癌患者的护理标准,广泛用于早期乳腺癌患者。需要调查用作结构的方案的不同作用。尽管有一些随机对照试验(RCT),但目前还不清楚哪种治疗方案最佳。此外,没有研究所有三个方案的研究。因此,目前的研究将基于肿瘤的肿瘤结果和功能结果对新辅助设定中施用蒽环素,紫杉烷和靶向治疗的疗效。方法/设计在线数据库对受控试验的PubMed和Cochrane注册将被搜查以获取合格的研究。此外,还将搜索相关期刊的内容,相关文章的参考文章和主要相关会议的程序。将任何上述方案与乳腺癌患者的NACT进行比较的RCT将有资格。两个审阅者独立和重复将根据标题和抽象的基础筛选记录,并完成全文审查以确定资格。同样,数据提取和偏见评估的风险将由两个独立审稿人完成。将进行一对明智的元分析以及网络元分析,以评估蒽环类,紫杉烷和有针对性治疗方案的相对疗效。讨论本系统评价将提高三个治疗方案的相对功效的认识,并可能通过提供对乳腺癌患者的管理新辅助化疗的各种治疗方案的疗效目前的最佳证据指导临床实践。系统审查登记Prospero(CRD42016027236)。

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