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MONITOR-GCSF 的背景和方法学:生物类似物粒细胞集落刺激因子非格司亭预防发热性中性粒细胞减少症的多层次决定因素、预测因素和临床结局的药物流行病学研究。

Background and methodology of MONITOR-GCSF, a pharmaco-epidemiological study of the multi-level determinants, predictors, and clinical outcomes of febrile neutropenia prophylaxis with biosimilar granulocyte-colony stimulating factor filgrastim.

机构信息

Division of Medical Oncology, Department of Hematology-Oncology, Hospital Clínic de Barcelona, University of Barcelona, Spain.

出版信息

Crit Rev Oncol Hematol. 2011 Mar;77(3):184-97. doi: 10.1016/j.critrevonc.2010.01.014. Epub 2010 Mar 1.

DOI:10.1016/j.critrevonc.2010.01.014
PMID:20189821
Abstract

The MONITOR-GCSF study is an international, prospective, observational, pharmaco-epidemiological study to evaluate the multi-level factors and outcomes associated with the use of Zarzio(®) in the prophylaxis of febrile neutropenia in chemotherapy-treated cancer patients. Driven by a novel, integrated, multi-focal framework for post-approval observational studies, it examines determinants of response at both the patient and the physician level; integrates statistical methodologies from the social and behavioral sciences; assesses factors predictive of poor treatment response; and evaluates the congruence of treatment with EORTC guidelines and the approved label. This pan-European study will recruit at least 1000 patients from a minimum of 75 centers and follow them for maximum 6 cycles of chemotherapy. Apart from descriptive and associative procedures, statistical analysis will include variance attribution methods; hierarchical linear, logistic, and Poisson modeling; Kaplan-Meier time-to-event analysis, Mantel-Cox log-rank or generalized Wilcoxon-Breslow tests, and Cox proportional hazards modeling; and clustering and related data mining techniques.

摘要

MONITOR-GCSF 研究是一项国际性、前瞻性、观察性、药物流行病学研究,旨在评估 Zarzio(®) 在化疗治疗癌症患者中预防发热性中性粒细胞减少症的使用相关的多层次因素和结果。该研究采用了一种新颖的、综合的、多焦点的批准后观察研究框架,检查了患者和医生层面的反应决定因素;整合了来自社会和行为科学的统计方法;评估了不良治疗反应的预测因素;并评估了治疗与 EORTC 指南和批准标签的一致性。这项泛欧洲研究将从至少 75 个中心招募至少 1000 名患者,并对他们进行最多 6 个化疗周期的随访。除了描述性和关联性程序外,统计分析还将包括方差归因方法;分层线性、逻辑和泊松建模;卡普兰-迈耶生存时间分析、曼特尔-考克斯对数秩或广义威尔科克森-布雷斯洛检验和 Cox 比例风险模型;以及聚类和相关的数据挖掘技术。

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1
Background and methodology of MONITOR-GCSF, a pharmaco-epidemiological study of the multi-level determinants, predictors, and clinical outcomes of febrile neutropenia prophylaxis with biosimilar granulocyte-colony stimulating factor filgrastim.MONITOR-GCSF 的背景和方法学:生物类似物粒细胞集落刺激因子非格司亭预防发热性中性粒细胞减少症的多层次决定因素、预测因素和临床结局的药物流行病学研究。
Crit Rev Oncol Hematol. 2011 Mar;77(3):184-97. doi: 10.1016/j.critrevonc.2010.01.014. Epub 2010 Mar 1.
2
Update on the MONITOR-GCSF study of biosimilar filgrastim to reduce the incidence of chemotherapy-induced febrile neutropenia in cancer patients: Protocol amendments.监测-GCSF 研究中生物类似物非格司亭降低癌症患者化疗引起的发热性中性粒细胞减少症发生率的更新:方案修正案。
Crit Rev Oncol Hematol. 2011 Mar;77(3):198-200. doi: 10.1016/j.critrevonc.2011.01.006.
3
Treatment patterns and outcomes in the prophylaxis of chemotherapy-induced (febrile) neutropenia with biosimilar filgrastim (the MONITOR-GCSF study).使用生物类似药非格司亭预防化疗引起的(发热性)中性粒细胞减少症的治疗模式及结果(MONITOR-GCSF研究)
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4
Biosimilar filgrastim treatment patterns and prevention of febrile neutropenia: a prospective multicentre study in France in patients with solid tumours (the ZOHé study).生物类似物非格司亭治疗模式与发热性中性粒细胞减少症预防:法国一项针对实体瘤患者的前瞻性多中心研究(ZOHé 研究)。
BMC Cancer. 2018 Nov 16;18(1):1127. doi: 10.1186/s12885-018-4986-1.
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Chemotherapy-induced (febrile) neutropenia prophylaxis with biosimilar filgrastim in elderly versus non-elderly cancer patients: Patterns, outcomes, and determinants (MONITOR-GCSF study).生物类似物非格司亭在老年与非老年癌症患者中预防化疗引起的(发热性)中性粒细胞减少症:模式、结局和决定因素(MONITOR-GCSF 研究)。
J Geriatr Oncol. 2017 Mar;8(2):86-95. doi: 10.1016/j.jgo.2016.09.006. Epub 2016 Nov 6.
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Pegfilgrastim: a recent advance in the prophylaxis of chemotherapy-induced neutropenia.聚乙二醇化重组人粒细胞刺激因子:化疗引起的中性粒细胞减少症预防方面的一项最新进展。
Eur J Cancer Care (Engl). 2004 Sep;13(4):371-9. doi: 10.1111/j.1365-2354.2004.00503.x.
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Granulocytic growth factors and cancer-related neutropenia: limited effects.粒细胞生长因子与癌症相关中性粒细胞减少症:效果有限。
Prescrire Int. 2006 Oct;15(85):189-91.
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Risk of hospitalization for neutropenic complications of chemotherapy in patients with primary solid tumors receiving pegfilgrastim or filgrastim prophylaxis: a retrospective cohort study.接受培非格司亭或非格司亭预防性治疗的原发性实体瘤患者化疗中性粒细胞减少并发症的住院风险:一项回顾性队列研究。
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Efficacy of granulocyte colony stimulating factor as a secondary prophylaxis along with full-dose chemotherapy following a prior cycle of febrile neutropenia.粒细胞集落刺激因子作为发热性中性粒细胞减少症前一周期全剂量化疗后的二级预防的疗效。
Biosci Trends. 2010 Oct;4(5):273-8.

引用本文的文献

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Meta-Analysis of Same-Day Pegfilgrastim Administration Stratified by Myelotoxic Febrile Neutropenia Risk and Tumor Type.根据骨髓毒性发热性中性粒细胞减少风险和肿瘤类型分层的当日给予培非格司亭的荟萃分析。
J Adv Pract Oncol. 2022 Nov;13(8):796-811. doi: 10.6004/jadpro.2022.13.8.6. Epub 2022 Nov 1.
2
Treatment patterns and outcomes in patients with non-small cell lung cancer receiving biosimilar filgrastim for prophylaxis of chemotherapy-induced/febrile neutropaenia: Results from the MONITOR-GCSF study.接受生物类似物非格司亭预防化疗引起的/发热性中性粒细胞减少症的非小细胞肺癌患者的治疗模式和结局:MONITOR-GCSF 研究结果。
Eur J Cancer Care (Engl). 2019 Jul;28(4):e13034. doi: 10.1111/ecc.13034. Epub 2019 Apr 10.
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Outcomes of chemotherapy-induced (febrile) neutropenia prophylaxis with biosimilar filgrastim (Zarzio®) initiated "same-day" (< 24 h), "per-guidelines" (24-72 h), and "late" (> 72 h): findings from the MONITOR-GCSF study.
生物类似物非格司亭(Zarzio®)预防化疗引起的(发热性)中性粒细胞减少症的起始时间为“同日”(<24 小时)、“按指南”(24-72 小时)和“延迟”(>72 小时):来自 MONITOR-GCSF 研究的结果。
Support Care Cancer. 2019 Jun;27(6):2301-2312. doi: 10.1007/s00520-018-4513-6. Epub 2018 Oct 20.
4
Over- and under-prophylaxis for chemotherapy-induced (febrile) neutropenia relative to evidence-based guidelines is associated with differences in outcomes: findings from the MONITOR-GCSF study.相对于基于证据的指南,化疗诱导的(发热性)中性粒细胞减少症预防过度和不足与结局差异相关:MONITOR-GCSF研究的结果
Support Care Cancer. 2017 Jun;25(6):1819-1828. doi: 10.1007/s00520-017-3572-4. Epub 2017 Jan 22.
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