CYCLOSPORINE AS POSSIBLE PROPHYLAXIS FOR OBSTRUCTIVE AIRWAYS DISEASE AFTER ALLOGENEIC BONE-MARROW TRANSPLANTATION

Citation
L. Payne et al., CYCLOSPORINE AS POSSIBLE PROPHYLAXIS FOR OBSTRUCTIVE AIRWAYS DISEASE AFTER ALLOGENEIC BONE-MARROW TRANSPLANTATION, Chest, 104(1), 1993, pp. 114-118
Citations number
23
Categorie Soggetti
Respiratory System
Journal title
ChestACNP
ISSN journal
00123692
Volume
104
Issue
1
Year of publication
1993
Pages
114 - 118
Database
ISI
SICI code
0012-3692(1993)104:1<114:CAPPFO>2.0.ZU;2-0
Abstract
The objective of this study was to evaluate the impact of cyclosporine (cyclosporin A; CvA) prophylaxis for graft-versus-host disease (GVHD) on the development of obstructive airways disease (OAD) after allogen eic bone marrow transplantation (BMT) in leukemic patients. Patients w ith normal pulmonary function tests (PFTs) prior to BMT were followed with serial PFTs for the development of OAD. Follow-up PFTs were perfo rmed at 3, 6, 9, and 12 months, and thereafter at consecutive yearly i ntervals. Obstructive airways disease was defined as FEV1 less than 80 percent, ratio of FEV1 over the forced vital capacity (FFV1/FVC) less than SO percent of predicted, maximal midexpiratory flow rate at 50 p ercent vital capacity less than 65 percent of predicted, or residual v olume greater than 120 percent of predicted. In the period prior to Cy A prophylaxis for GVHD development (March 1983 to September 1986), 17 (39 percent) of the 44 patients undergoing BMT developed OAD, compared with 2 (4 percent) of 45 in the post-CyA period (September 1986 to Ma rch 1990) (chi2 = 17; p<0.00005). Age, sex, type of leukemia, severity of GVHD, histocompatibility status, presence of acute GVHD, and sex m ismatch between donor and recipient were not associated with developme nt of OAD. Although chronic GVHD was associated with OAD in univariate analysis, a multivariate logistic regression analysis showed that the only significant independent predictor for OAD was the use of CyA. We conclude that CyA is protective against the development of OAD after BMT in leukemic patients.