ACUTE GRAFT-VERSUS-HOST DISEASE AND THE RISKS FOR IDIOPATHIC PNEUMONIA AFTER MARROW TRANSPLANTATION FOR SEVERE APLASTIC-ANEMIA

Citation
Sw. Crawford et al., ACUTE GRAFT-VERSUS-HOST DISEASE AND THE RISKS FOR IDIOPATHIC PNEUMONIA AFTER MARROW TRANSPLANTATION FOR SEVERE APLASTIC-ANEMIA, Bone marrow transplantation, 12(3), 1993, pp. 225-231
Citations number
32
Categorie Soggetti
Hematology,Oncology,Immunology
Journal title
ISSN journal
02683369
Volume
12
Issue
3
Year of publication
1993
Pages
225 - 231
Database
ISI
SICI code
0268-3369(1993)12:3<225:AGDATR>2.0.ZU;2-8
Abstract
The risks for the development of idiopathic pneumonia after allogeneic BMT were assessed in a case-series review at a single marrow transpla ntation center. All allogeneic marrow recipients (n = 299) (age range 1-60 years) with severe aplastic anemia (SAA) transplanted from family member donors after conditioning with CY were evaluated. Post-graftin g immunosuppression consisted of MTX alone in 205 patients (69%), CY a lone in 16 (5%) and a combination of the two in 78 (26%). The incidenc e estimate for any pneumonia within the first 200 days after transplan t was 18% (95% confidence interval = 14-24%). Of 48 cases of pneumonia , CMV infection was documented in 44%, 21% were idiopathic and the rem ainder were either due to other infections or were not evaluated. The effect of acute GVHD on the incidence of pneumonia was examined using multivariate Cox proportional hazards models which included covariates for potential confounding factors. Consistent with previous reports, acute GVHD was associated with an increased incidence of any pneumonia (relative risk (RR) = 3.5, 95% Cl = 1.9-6.9; p < 0.001). Specifically , acute GVHD also was associated with the largest risk of idiopathic p neumonia (RR = 5.0, 95% Ct = 1.1-22; p = 0.04). In conclusion, recogni tion of acute GVHD as a risk factor for idiopathic pneumonia suggests that mechanisms in addition to chemoradiation damage are responsible f or non-infectious lung injury after BMT.