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晚期非霍奇金淋巴瘤中的中性粒细胞减少并发症:对预防性使用重组人粒细胞集落刺激因子(G-CSF)的影响。

Neutropenic complications in advanced-stage non-Hodgkin's lymphoma: implications for the use of prophylactic recombinant human granulocyte-colony stimulating factor (G-CSF).

作者信息

Bobey N, Woodman R C

机构信息

Department of Medicine, University of Calgary, Alta.

出版信息

Clin Invest Med. 1998 Apr;21(2):63-70.

PMID:9562926
Abstract

OBJECTIVES

To determine the incidence of neutropenic complications in patients receiving chemotherapy for advanced-stage non-Hodgkin's lymphoma (NHL), to predict which patients are at high risk for neutropenic complications and to develop an economic model for subsequent testing to assess the potential cost-effectiveness of prophylactic treatment with recombinant human granulocyte-colony stimulating factor (G-CSF).

DESIGN

Retrospective chart review.

PATIENTS

Forty-two patients with advanced-stage NHL treated at the Tom Baker Cancer Centre, Calgary, between Jan. 1, 1992, and Dec. 31, 1993.

OUTCOME MEASURES

Neutropenic complications including incidence of febrile neutropenic events, documented infections, and chemotherapy dose delays or dose reductions.

RESULTS

Of the 42 patients, 8 (19%) experienced febrile neutropenic events and 18 (43%) required chemotherapy dose modifications (delays or reductions or both) because of neutropenia. Fifteen patients (36%) were identified as being at high risk for neutropenic complications and may have benefited from the administration of prophylactic G-CSF. An economic model developed to assess the potential cost-effectiveness of prophylactic G-CSF therapy estimated that, for high-risk patients, the theoretical incremental cost per life year saved was $3300.

CONCLUSIONS

Febrile neutropenia and infection cause significant morbidity and mortality in patients receiving combination chemotherapy for the treatment of advanced-stage NHL. Secondary prophylactic G-CSF therapy has been proven to decrease the incidence of febrile neutropenia and infection in these patients. Considering the reduction in neutropenic complications and resulting increase in chemotherapy dose intensity received by patients on G-CSF, the theoretical incremental cost per life year saved of $3300 with G-CSF therapy is relatively low compared with other medical interventions.

摘要

目的

确定晚期非霍奇金淋巴瘤(NHL)患者接受化疗时中性粒细胞减少并发症的发生率,预测哪些患者发生中性粒细胞减少并发症的风险较高,并建立一个经济模型用于后续检测,以评估重组人粒细胞集落刺激因子(G-CSF)预防性治疗的潜在成本效益。

设计

回顾性病历审查。

患者

1992年1月1日至1993年12月31日期间在卡尔加里汤姆·贝克癌症中心接受治疗的42例晚期NHL患者。

观察指标

中性粒细胞减少并发症,包括发热性中性粒细胞减少事件的发生率、有记录的感染以及化疗剂量延迟或减少。

结果

42例患者中,8例(19%)发生发热性中性粒细胞减少事件,18例(43%)因中性粒细胞减少需要调整化疗剂量(延迟或减少或两者兼有)。15例患者(36%)被确定为发生中性粒细胞减少并发症的高风险患者,可能从预防性使用G-CSF中获益。为评估预防性G-CSF治疗的潜在成本效益而建立的经济模型估计,对于高风险患者,每挽救1年生命的理论增量成本为3300美元。

结论

发热性中性粒细胞减少和感染在接受联合化疗治疗晚期NHL的患者中导致显著的发病率和死亡率。二级预防性G-CSF治疗已被证明可降低这些患者发热性中性粒细胞减少和感染的发生率。考虑到中性粒细胞减少并发症的减少以及接受G-CSF治疗的患者化疗剂量强度的增加,与其他医疗干预措施相比,G-CSF治疗每挽救1年生命的理论增量成本3300美元相对较低。

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