Ray-Coquard Isabelle, Borg Christophe, Bachelot Thomas, Fayette Jérome, Zufferey Laura, Guastalla Jean-Paul, Ghesquière Hervé, Blay Jean-Yves, Sebban Catherine, Marec-Bérard Perrine, Biron Pierre
Centre Léon-Bérard, 28, rue Laennec, 69008 Lyon, France.
Bull Cancer. 2006 May;93(5):501-6.
Cytotoxic chemotherapy suppresses the haematopoietic system, impairing host protective mechanisms and limiting the doses of chemotherapy that can be tolerated. Febrile neutropenia, the most serious haematological toxicity, is associated with the risk of life-threatening infections as well as chemotherapy dose reductions and delays that may compromise treatment outcomes. The recent literature in chemotherapy-induced neutropenia and its complications and impact was provided an update on research, and the implications for improving the management of patients with cancer who are treated with myelosuppressive chemotherapy was discussed. Despite its importance as the primary dose-limiting toxicity of chemotherapy, much concerning neutropenia and its consequences and impact remains unknown. Recent surveys indicate that neutropenia remains a prevalent problem associated with substantial morbidity, mortality, and costs. The colony-stimulating factors (CSFs) have been used effectively in a variety of clinical settings to prevent or treat febrile neutropenia and to assist patients receiving dose-intensive chemotherapy. A meta-analysis of the available randomized controlled trials (RCTs) has confirmed the efficacy of prophylactic CSFs. Much research has sought to identify risk factors that may predispose patients to neutropenic complications, including febrile neutropenia, in an effort to predict better which patients are at risk and to use preventive strategies, such as prophylactic colony-stimulating factors, more cost-effectively. Research in quantifying the risk of neutropenic complications may make it possible in the near future to target patients at greater risk with appropriate preventive strategies, thereby maximizing the benefits and minimizing the costs.
细胞毒性化疗会抑制造血系统,损害宿主保护机制,并限制可耐受的化疗剂量。发热性中性粒细胞减少是最严重的血液学毒性反应,与危及生命的感染风险以及可能影响治疗效果的化疗剂量减少和延迟有关。近期有关化疗引起的中性粒细胞减少及其并发症和影响的文献对研究进展进行了更新,并讨论了对改善接受骨髓抑制性化疗的癌症患者管理的意义。尽管中性粒细胞减少作为化疗的主要剂量限制性毒性反应很重要,但其许多方面以及后果和影响仍不清楚。近期调查表明,中性粒细胞减少仍然是一个普遍存在的问题,与严重的发病率、死亡率和成本相关。集落刺激因子(CSF)已在多种临床环境中有效用于预防或治疗发热性中性粒细胞减少,并帮助接受剂量密集型化疗的患者。对现有随机对照试验(RCT)的荟萃分析证实了预防性使用CSF的疗效。许多研究试图确定可能使患者易发生中性粒细胞减少并发症(包括发热性中性粒细胞减少)的危险因素,以便更好地预测哪些患者有风险,并更经济有效地使用预防性策略,如预防性集落刺激因子。量化中性粒细胞减少并发症风险的研究可能在不久的将来使针对高风险患者采取适当的预防策略成为可能,从而使益处最大化并使成本最小化。