Reduced Mortality of Cytomegalovirus Pneumonia After Hematopoietic Cell Transplantation Due to Antiviral Therapy and Changes in Transplantation Practices

被引:93
作者
Erard, Veronique [1 ,4 ]
Guthrie, Katherine A. [2 ,3 ]
Seo, Sachiko [1 ]
Smith, Jeremy [1 ]
Huang, MeeiLi
Chien, Jason [2 ]
Flowers, Mary E. D. [2 ]
Corey, Lawrence [1 ,5 ,6 ]
Boeckh, Michael [1 ,2 ,6 ]
机构
[1] Fred Hutchinson Canc Res Ctr, Vaccine & Infect Dis Div, Seattle, WA 98109 USA
[2] Fred Hutchinson Canc Res Ctr, Div Clin Res, Seattle, WA 98109 USA
[3] Fred Hutchinson Canc Res Ctr, Div Publ Hlth Sci, Seattle, WA 98109 USA
[4] Hop Fribourgeois Fribourg, Clin Med, Fribourg, Switzerland
[5] Univ Washington, Dept Lab Med, Seattle, WA 98195 USA
[6] Univ Washington, Dept Med, Seattle, WA 98195 USA
基金
美国国家卫生研究院;
关键词
hematopoeitic cell transplantation; cytomegalovirus; pneumonia; immunoglobulin; antiviral treatment; T-cell therapy; BONE-MARROW-TRANSPLANTATION; INTRAVENOUS IMMUNE GLOBULIN; VIRUS PNEUMONIA; CMV DISEASE; INVASIVE ASPERGILLOSIS; TREATMENT STRATEGY; VIRAL-INFECTIONS; RECIPIENTS; GANCICLOVIR; PREVENTION;
D O I
10.1093/cid/civ215
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Despite major advances in the prevention of cytomegalovirus (CMV) disease, the treatment of CMV pneumonia in recipients of hematopoietic cell transplant remains a significant challenge. Methods. We examined recipient, donor, transplant, viral, and treatment factors associated with overall and attributable mortality using Cox regression models. Results. Four hundred twenty-one cases were identified between 1986 and 2011. Overall survival at 6 months was 30% (95% confidence interval [CI], 25%-34%). Outcome improved after the year 2000 (all-cause mortality: adjusted hazard ratio [aHR], 0.7 [95% CI,.5-1.0]; P = .06; attributable mortality: aHR, 0.6 [95% CI,.4-.9]; P = .01). Factors independently associated with an increased risk of all-cause and attributable mortality included female sex, elevated bilirubin, lymphopenia, and mechanical ventilation; grade 3/4 acute graft-vs-host disease was associated with all-cause mortality only. An analysis of patients who received transplants in the current preemptive therapy era (n = 233) showed only lymphopenia and mechanical ventilation as significant risk factors for overall and attributable mortality. Antiviral treatment with ganciclovir or foscarnet was associated with improved outcome compared with no antiviral treatment. However, the addition of intravenous pooled or CMV-specific immunoglobulin to antiviral treatment did not seem to improve overall or attributable mortality. Conclusions. Outcome of CMV pneumonia showed a modest improvement over the past 25 years. However, advances seem to be due to antiviral treatment and changes in transplant practices rather than immunoglobulin-based treatments. Novel treatment strategies for CMV pneumonia are needed.
引用
收藏
页码:31 / 39
页数:9
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