Lyman Gary H, Allcott Kim, Garcia Jacob, Stryker Scott, Li Yanli, Reiner Maureen T, Weycker Derek
Fred Hutchinson Cancer Research Center and University of Washington, 1100 Fairview Avenue North, Seattle, WA, 98109, USA.
Oxford PharmaGenesis Ltd., Oxford, UK.
Support Care Cancer. 2017 Aug;25(8):2619-2629. doi: 10.1007/s00520-017-3703-y. Epub 2017 May 8.
Granulocyte colony-stimulating factors (G-CSF) are commonly used in clinical practice to prevent febrile neutropenia (FN). US and EU prescribing information and treatment guidelines from the NCCN, ASCO, and EORTC specify that pegfilgrastim, a long-acting (LA) G-CSF, should be administered at least 24 h after myelosuppressive chemotherapy. Nevertheless, many patients receive LA G-CSFs on the same day as chemotherapy. This systematic literature review evaluated the relative merits of same-day versus next-day dosing of LA G-CSFs.
A broad Ovid MEDLINE® and Embase® literature search was conducted that examined all publications indexed before May 9, 2016 that compared same-day versus next-day LA G-CSF administration. A congress abstract literature search included congresses from January 1, 2011 to April 6, 2016. The parameters for this review were prospectively delineated in a research protocol and adhered to the PRISMA Guidelines.
The first part of the systematic literature search identified 1736 publications. After elimination of duplicates, title/abstract screening was conducted on 1440 records, and full text review was conducted on 449 publications. Eleven publications met all criteria and are included in this systematic review; of these, four included data from randomized or single arm prospective studies, and seven were retrospective studies. In most studies included in this review and across a variety of tumor types, administration of pegfilgrastim at least 24 h after myelosuppressive chemotherapy resulted in improved patient outcomes.
Data from multiple publications support administration of pegfilgrastim at least 1 day after chemotherapy.
粒细胞集落刺激因子(G-CSF)在临床实践中常用于预防发热性中性粒细胞减少症(FN)。美国和欧盟的处方信息以及美国国立综合癌症网络(NCCN)、美国临床肿瘤学会(ASCO)和欧洲肿瘤内科学会(EORTC)的治疗指南规定,长效(LA)G-CSF培非格司亭应在骨髓抑制性化疗后至少24小时给药。然而,许多患者在化疗当天接受LA G-CSF治疗。本系统文献综述评估了LA G-CSF当日给药与次日给药的相对优缺点。
在Ovid MEDLINE®和Embase®数据库中进行广泛的文献检索,检索2016年5月9日前收录的所有比较LA G-CSF当日给药与次日给药的出版物。会议摘要文献检索涵盖2011年1月1日至2016年4月6日的会议。本综述的参数在研究方案中预先划定,并遵循PRISMA指南。
系统文献检索的第一部分共识别出1736篇出版物。剔除重复项后,对1440条记录进行了标题/摘要筛选,并对449篇出版物进行了全文审查。11篇出版物符合所有标准,纳入本系统综述;其中4篇包含随机或单臂前瞻性研究的数据,7篇为回顾性研究。在本综述纳入的大多数研究以及各种肿瘤类型中,骨髓抑制性化疗后至少24小时给予培非格司亭可改善患者预后。
多篇出版物的数据支持化疗后至少1天给予培非格司亭。