促红细胞生成素在非血液学肿瘤化疗患者中的应用。系统治疗计划委员会。

I Quirt, S Micucci, L A Moran, J Pater, G Browman
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引用次数: 0

摘要

指南问题:1)促红细胞生成素(EPO)是否能减少接受非血液学癌症化疗的患者输血红细胞的需要?2)给药EPO是否能改善这些癌症患者的生活质量?目的:提出关于使用促红细胞生成素(EPO)以减少非血液学癌症化疗患者输血需要的建议。结果:从化疗开始的第一次输血需求是主要的结果。生活质量和成本也被考虑在内。观点(价值观):证据由安大略省癌症治疗实践指南倡议(OCTPGI)和系统治疗计划委员会(STPC)的5名成员选择和审查。本文件的草稿已分发给STPC成员并由其审查。STPC由肿瘤学家、药剂师、支持性护理人员和行政人员组成。没有社区代表参与该实践指南的制定。证据质量:11个随机对照试验(rct),大多数为安慰剂对照,可用于回顾。我们对8项具有临床相关结局指标的试验进行了荟萃分析。只有1项试验评估了生活质量。益处:荟萃分析显示EPO患者输血的相对风险为0.64(95%置信区间0.53-0.78),这意味着需要输血的患者比例相对降低36% (p = 0.00001)。输血需求的减少在不同的层次是相似的,由方法学质量、EPO剂量、血液学状况、试验开始时的肿瘤类型和化疗方案来定义。在评估生活质量的1项试验中,EPO与生活质量的改善有关。危害:epo治疗的癌症患者很少出现高血压。在随访期间,随机对照试验未报告epo治疗患者与对照组患者的不良反应。长期副作用尚不清楚。EPO比输血更昂贵,但没有正式的成本效益研究。实践指南:对于接受非血液学癌症化疗且预期会出现贫血症状且红细胞输注不被认为是可接受的治疗选择的患者,可推荐促生成素作为一种安全、有效的治疗选择。与接受非铂类化疗方案的患者相比,接受铂类化疗方案的患者使用EPO的支持证据更强。临床实践指南日期:1997年4月4日。
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Erythropoietin in the management of patients with nonhematologic cancer receiving chemotherapy. Systemic Treatment Program Committee.

Guideline questions: 1) Does erythropoietin (EPO) reduce the need for transfusion of red blood cells in patients receiving chemotherapy for a nonhematologic cancer? 2) Does the administration of EPO improve the quality of life of these cancer patients?

Objective: To make recommendations regarding the use of EPO to reduce the need for transfusion of red blood cells in patients receiving chemotherapy for a nonhematologic cancer.

Outcomes: First transfusion requirement from the start of chemotherapy is the main outcome of interest. Quality of life and costs are also considered.

Perspective (values): Evidence was selected and reviewed by 5 members of the Ontario Cancer Treatment Practice Guidelines Initiative (OCTPGI) and the Systemic Treatment Program Committee (STPC). Drafts of this document have been circulated to and reviewed by members of the STPC. The STPC comprises medical oncologists, pharmacists, supportive care personnel and administrators. No community representative participated in the development of this practice guideline.

Quality of evidence: Eleven randomized controlled trials (RCTs), most placebo-controlled, were available for review. A meta-analysis was performed with 8 trials that shared a clinically relevant outcome measure. Only 1 trial assessed quality of life.

Benefits: The meta-analysis showed a relative risk for transfusion among EPO patients of 0.64 (95% confidence interval 0.53-0.78), which translates into a 36% relative reduction in the proportion of patients requiring transfusion (p = 0.00001). Reduction in transfusion requirements was similar across strata defined by methodological quality, EPO dose, hematologic status, tumour type at trial entry and chemotherapy regimen. In the 1 trial that assessed quality of life, EPO was associated with improved quality of life.

Harms: Hypertension has been noted rarely in EPO-treated cancer patients. The RCTs did not report adverse effects in EPO-treated patients compared with control patients during the follow-up period. Long-term adverse effects are unknown. EPO is more costly than transfusion, but formal cost-effectiveness studies are unavailable.

Practice guideline: For patients receiving chemotherapy for nonhematologic cancer in whom symptoms of anemia are expected and in whom transfusion of red blood cells is not considered an acceptable treatment option, EPO can be recommended as a safe, effective treatment alternative. The evidence in support of using EPO is stronger for patients receiving platinum-based chemotherapy regimens that for those receiving non-platinum-based regimens. CLINICAL PRACTICE GUIDELINE DATE: Apr. 4, 1997.

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