首页> 外文期刊>Journal of Clinical Oncology >Incidence, cost, and outcomes of bleeding and chemotherapy dose modification among solid tumor patients with chemotherapy-induced thrombocytopenia.
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Incidence, cost, and outcomes of bleeding and chemotherapy dose modification among solid tumor patients with chemotherapy-induced thrombocytopenia.

机译:实体瘤患者化疗诱发的血小板减少症的发生率,费用以及出血和化疗剂量调整的结果。

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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.
机译:目的:描述与化疗引起的血小板减少症(血小板<50,000 / microL)相关的出血和化疗剂量调整的发生率和结果。患者和方法:在1,262例化疗并发血小板减少的化疗周期中对699例实体瘤或淋巴瘤患者进行了随访,以了解出血的发生,后续周期的延迟或剂量减少,生存率和资源利用率。使用Cox比例风险模型检查了生存与出血或剂量调整之间的关联。通过逻辑回归确定诱发因素。结果:既往有出血事件(P <.0001),基线血小板低于75,000 / microL(P <.0001),骨髓转移(P = .001),表现差的患者(9%的周期内发生出血) P = .03),以及顺铂,卡铂,卡莫司汀或洛莫司汀的给药(P = .0002)。严重的出血事件导致生存期缩短和资源利用率更高(P <.0001)。在先前五个周期以上(P = .003),放疗(P = .03)和播散性疾病(P = .04)的患者中,化学治疗延迟发生在周期的6%内。他们经历了相似的临床结果,但使用了更多的资源。剂量减少发生在15%的周期内,但与不良的临床结果或过多的资源利用无关。在未能对血小板输注产生足够反应的20%的患者中,观察到生存期明显缩短,资源利用率更高。结论:整体实体瘤患者的出血发生率总体较低,但在某些亚组中超过20%。使用常规可获得的临床信息可轻松识别这些亚组。临床预测规则正在制定中。对血小板输注的不良反应是血小板减少症的临床和财务意义重大的下游效应,值得进一步研究。

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