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实体瘤化疗所致血小板减少症患者出血、化疗剂量调整的发生率、成本及结局

Incidence, cost, and outcomes of bleeding and chemotherapy dose modification among solid tumor patients with chemotherapy-induced thrombocytopenia.

作者信息

Elting L S, Rubenstein E B, Martin C G, Kurtin D, Rodriguez S, Laiho E, Kanesan K, Cantor S B, Benjamin R S

机构信息

Department of Health Services Research, The University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA.

出版信息

J Clin Oncol. 2001 Feb 15;19(4):1137-46. doi: 10.1200/JCO.2001.19.4.1137.

Abstract

PURPOSE

To describe the incidence and outcomes of bleeding and chemotherapy dose modifications associated with chemotherapy-induced thrombocytopenia (platelets < 50,000/microL).

PATIENTS AND METHODS

Six hundred nine patients with solid tumors or lymphoma were followed-up during 1,262 chemotherapy cycles complicated by thrombocytopenia for development of bleeding, delay or dose reduction of the subsequent cycle, survival, and resource utilization. The association between survival and bleeding or dose modification was examined using the Cox proportional hazards model. Predisposing factors were identified by logistic regression.

RESULTS

Bleeding occurred during 9% of cycles among patients with previous bleeding episodes (P <.0001), baseline platelets less than 75,000/microL (P <.0001), bone marrow metastases (P =.001), poor performance status (P =.03), and cisplatin, carboplatin, carmustine or lomustine administration (P =.0002). Major bleeding episodes resulted in shorter survival and higher resource utilization (P <.0001). Chemotherapy delays occurred during 6% of cycles among patients with more than five previous cycles (P =.003), radiotherapy (P =.03), and disseminated disease (P =.04). They experienced similar clinical outcomes but used significantly more resources. Dose reductions occurred during 15% of cycles but were not associated with poor clinical outcomes or excess resource utilization. Significantly shorter survival and higher resource utilization were observed among the 20% of patients who failed to achieve an adequate response to platelet transfusion.

CONCLUSION

The incidence of bleeding is low among solid tumor patients overall but exceeds 20% in some subgroups. These subgroups are easily identifiable using routinely available clinical information. A clinical prediction rule is being developed. Poor response to platelet transfusion is a clinically and financially significant downstream effect of thrombocytopenia and warrants further investigation.

摘要

目的

描述与化疗诱导的血小板减少症(血小板计数<50,000/微升)相关的出血发生率及化疗剂量调整情况和预后。

患者与方法

609例实体瘤或淋巴瘤患者在1262个伴有血小板减少症的化疗周期中接受随访,观察出血情况、后续周期化疗的延迟或剂量减少情况、生存情况及资源利用情况。使用Cox比例风险模型检验生存与出血或剂量调整之间的关联。通过逻辑回归确定易感因素。

结果

既往有出血史的患者中,9%的周期发生出血(P<.0001);基线血小板计数低于75,000/微升的患者中,9%的周期发生出血(P<.0001);有骨髓转移的患者中,9%的周期发生出血(P =.001);体能状态差的患者中,9%的周期发生出血(P =.03);接受顺铂、卡铂、卡莫司汀或洛莫司汀治疗的患者中,9%的周期发生出血(P =.0002)。严重出血事件导致生存期缩短和资源利用增加(P<.0001)。在既往化疗周期超过5个的患者中,6%的周期出现化疗延迟(P =.003);接受放疗的患者中,6%的周期出现化疗延迟(P =.03);有播散性疾病的患者中,6%的周期出现化疗延迟(P =.04)。这些患者的临床结局相似,但资源利用显著增加。15%的周期出现剂量减少,但与不良临床结局或资源利用过度无关。在对血小板输注反应不佳的2�%的患者中,观察到生存期显著缩短和资源利用增加。

结论

实体瘤患者总体出血发生率较低,但某些亚组超过20%。使用常规可得的临床信息可轻松识别这些亚组。正在制定临床预测规则。对血小板输注反应不佳是血小板减少症在临床和经济方面的显著下游效应,值得进一步研究。

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