Thomas J. Smith, Johns Hopkins Sidney Kimmel Comprehensive Cancer Center, Baltimore, MD; Kari Bohlke, American Society of Clinical Oncology, Alexandria; Scott J. Cross, Virginia Oncology Associates, Norfolk; James L. Khatcheressian, Virginia Cancer Institute, Richmond, VA; Gary H. Lyman, Fred Hutchinson Cancer Research Center and University of Washington, Seattle, WA; Kenneth R. Carson, Washington University, St Louis, MO; Jeffrey Crawford, Duke Medicine, Durham, NC; John M. Goldberg, University of Miami Miller School of Medicine, Miami, FL; Natasha B. Leighl, Princess Margaret Cancer Centre, Toronto, Ontario, Canada; Cheryl L. Perkins, patient representative, Dallas, TX; George Somlo, City of Hope National Medical Center, Duarte, CA; James L. Wade, Cancer Care Specialists of Central Illinois, Decatur, IL; Antoinette J. Wozniak, Karmanos Cancer Institute, Detroit, MI; and James O. Armitage, University of Nebraska Medical Center, Omaha, NE.
J Clin Oncol. 2015 Oct 1;33(28):3199-212. doi: 10.1200/JCO.2015.62.3488. Epub 2015 Jul 13.
PURPOSE: To update the 2006 American Society of Clinical Oncology guideline on the use of hematopoietic colony-stimulating factors (CSFs). METHODS: The American Society of Clinical Oncology convened an Update Committee and conducted a systematic review of randomized clinical trials, meta-analyses, and systematic reviews from October 2005 through September 2014. Guideline recommendations were based on the review of the evidence by the Update Committee. RESULTS: Changes to previous recommendations include the addition of tbo-filgrastim and filgrastim-sndz, moderation of the recommendation regarding routine use of CSFs in older patients with diffuse aggressive lymphoma, and addition of recommendations against routine dose-dense chemotherapy in lymphoma and in favor of high-dose-intensity chemotherapy in urothelial cancer. The Update Committee did not address recommendations regarding use of CSFs in acute myeloid leukemia or myelodysplastic syndromes in adults. RECOMMENDATIONS: Prophylactic use of CSFs to reduce the risk of febrile neutropenia is warranted when the risk of febrile neutropenia is approximately 20% or higher and no other equally effective and safe regimen that does not require CSFs is available. Primary prophylaxis is recommended for the prevention of febrile neutropenia in patients who are at high risk on the basis of age, medical history, disease characteristics, and myelotoxicity of the chemotherapy regimen. Dose-dense regimens that require CSFs should only be used within an appropriately designed clinical trial or if supported by convincing efficacy data. Current recommendations for the management of patients exposed to lethal doses of total-body radiotherapy, but not doses high enough to lead to certain death as a result of injury to other organs, include the prompt administration of CSFs.
目的:更新 2006 年美国临床肿瘤学会关于使用造血细胞集落刺激因子(CSFs)的指南。
方法:美国临床肿瘤学会召集了一个更新委员会,并对 2005 年 10 月至 2014 年 9 月期间的随机临床试验、荟萃分析和系统评价进行了系统回顾。指南建议是基于更新委员会对证据的审查。
结果:与以前的建议相比,此次更新增加了 tbo-filgrastim 和 filgrastim-sndz,缓和了关于在弥漫性侵袭性淋巴瘤老年患者中常规使用 CSFs 的建议,并增加了反对常规剂量密集化疗在淋巴瘤和支持高强度化疗在膀胱癌中的建议。更新委员会没有涉及在成人急性髓细胞白血病或骨髓增生异常综合征中使用 CSFs 的建议。
建议:当发热性中性粒细胞减少症的风险约为 20%或更高,并且没有其他同样有效和安全且不需要 CSFs 的方案时,使用 CSFs 预防发热性中性粒细胞减少症是合理的。对于基于年龄、病史、疾病特征和化疗方案的骨髓毒性等高危因素的患者,建议进行一级预防以预防发热性中性粒细胞减少症。需要 CSFs 的密集剂量方案仅应在适当设计的临床试验中使用,或在有令人信服的疗效数据支持的情况下使用。对于暴露于全身放射治疗致死剂量但未因其他器官损伤而导致确定性死亡的患者,目前的管理建议包括立即使用 CSFs。
Cochrane Database Syst Rev. 2012-10-17
Cochrane Database Syst Rev. 2016-4-24
Cochrane Database Syst Rev. 2020-10-19
Cochrane Database Syst Rev. 2015-10-5
Cochrane Database Syst Rev. 2013-8-22
J Clin Oncol. 2025-7-10