Risk of Mortality in Patients With Cancer Who Experience Febrile Neutropenia

被引:182
|
作者
Lyman, Gary H. [1 ,2 ]
Michels, Shannon L. [3 ]
Reynolds, Matthew W. [3 ]
Barron, Rich [4 ]
Tomic, Karen Smoyer [5 ]
Yu, Jingbo [5 ]
机构
[1] Duke Univ, Sch Med, Durham, NC 27705 USA
[2] Duke Comprehens Canc Ctr, Durham, NC 27705 USA
[3] United BioSource Corp, Lexington, MA USA
[4] Amgen Corp, Thousand Oaks, CA 91320 USA
[5] HealthCore, Wilmington, DE USA
关键词
neutropenia; infection; mortality; chemotherapy; propensity score; NON-HODGKINS-LYMPHOMA; CHEMOTHERAPY-INDUCED NEUTROPENIA; PATIENTS RECEIVING CHEMOTHERAPY; COLONY-STIMULATING FACTOR; BREAST-CANCER; ADJUVANT CHEMOTHERAPY; FOLLOW-UP; DOSE INTENSITY; MANAGEMENT; MORBIDITY;
D O I
10.1002/cncr.25332
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: Febrile neutropenia (FN) is a serious and potentially life-threatening condition that may develop in patients with cancer who receive myelosuppressive chemotherapy. The risk of mortality from FN is not well characterized in current clinical practice. METHODS: Patients with cancer who were receiving chemotherapy in clinical practice were identified from a large US healthcare claims database, and mortality was confirmed using the National Death Index. Patients with FN had their propensity scores matched within tumor types of interest (non-Hodgkin lymphoma and breast, lung, colorectal, and ovarian cancers) to patients who did not experience FN. Study endpoints of overall mortality (anytime during follow-up), early mortality (during the first 12 months of the first chemotherapy course), and hospitalization were examined using univariate and multivariate techniques, RESULTS: Matched FN and control groups each included 5990 patients, and the average follow-up for both groups was 17.6 months. Crude incidence rates of early mortality were significantly higher for patients with FN compared with controls for all tumor types. Proportional hazards regression demonstrated a significant increase in the risk of overall and early mortality in patients with FN compared with controls (hazard ratio [HR], 1.15 [95% confidence interval, 1.02-1.29] and HR, 1.35 [95% confidence interval, 1.09-1.67], respectively). CONCLUSIONS: The adjusted risk of mortality in patients who experienced FN was at least 15% higher than in comparably matched patients without FN, supporting the inference that infectious complications because of neutropenia resulting from myelosuppressive chemotherapy are clinically important. Cancer 2010;116:5555-63. (C) 2070 American Cancer Society.
引用
收藏
页码:5555 / 5563
页数:9
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