Non-infectious lung complications are closely associated with chronic graft-versus-host disease: a single center study of incidence, risk factors and outcome

被引:51
作者
Duncker, C
Dohr, D
von Harsdorf, S
Duyster, J
Stefanic, M
Martini, C
Treiber, M
Hertenstein, B
Novotny, J
Arnold, R
Heimpel, H
Bergmann, L
Bunjes, D
机构
[1] Univ Ulm, Dept Haematol Oncol, Ulm, Germany
[2] Zent Klinikum Augsburg, Dept Radiotherapy, Augsburg, Germany
[3] Univ Freiburg, Dept Radiotherapy, Freiburg, Germany
[4] Univ Heidelberg, Dept Radiotherapy, Heidelberg, Germany
[5] Med Hsch Hannover, Dept Haematol Oncol, Hannover, Germany
[6] Univ Hosp Charite Berlin, Dept Internal Med 2, Berlin, Germany
关键词
non-infectious lung complications; allogeneic BMT; chronic GVHD;
D O I
10.1038/sj.bmt.1702429
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Non-infectious lung complications (NILC) are frequent, influencing morbidity and mortality of patients after allogeneic BMT. Although the term NILC encompasses a number of different entities, an association with GVHD has been noted for almost all of them. Our study was directed towards assessing the incidence and risk factors for developing NILC, as well as the response to treatment and long-term outcome. Forty (14.7%) out of 272 patients surviving for more than 3 months after allogeneic BMT, developed lung complications fulfilling the criteria for NILC. The evaluation was based on clinical investigation, radiologic imaging, lung function tests, broncho-alveolar lavage and biopsies. Risk factors were assessed by univariate and multiple statistical regression models, where chronic GVHD proved to be the only significant risk factor for the development of NILC (P = 0.011). In three patients NILC developed in direct association with donor lymphocyte infusions. The majority of patients responded well to treatment with corticosteroids and immunosuppressive drugs, NILC had no adverse effect on survival. The frequency of NILC was low in autologous (5%) as compared with allogeneic transplants (14.7%) but this difference was not statistically significant.
引用
收藏
页码:1263 / 1268
页数:6
相关论文
共 32 条
[1]  
[Anonymous], 1989, Applied Linear Regression Models
[2]   LYMPHOCYTIC BRONCHITIS ASSOCIATED WITH GRAFT VERSUS HOST DISEASE IN RECIPIENTS OF BONE-MARROW TRANSPLANTS [J].
BESCHORNER, WE ;
SARAL, R ;
HUTCHINS, GM ;
TUTSCHKA, PJ ;
SANTOS, GW .
NEW ENGLAND JOURNAL OF MEDICINE, 1978, 299 (19) :1030-1036
[3]   MONONUCLEAR CELL RECONSTITUTION IN THE LUNG AFTER MARROW TRANSPLANTATION - LACK OF INFLUENCE OF CYTOMEGALOVIRUS PNEUMONIA, IRRADIATION, AND GRAFT-VERSUS-HOST DISEASE [J].
BOWDEN, RA ;
MORI, M ;
DOBBS, S ;
HACKMAN, R ;
KOPECKY, K ;
CRAWFORD, S .
TRANSPLANTATION, 1993, 55 (03) :557-561
[4]  
BUNJES D, 1995, BONE MARROW TRANSPL, V15, P563
[5]   CYCLOSPORINE AS AN ALTERNATIVE TO CYCLOPHOSPHAMIDE IN THE TREATMENT OF CHRONIC GRAFT-VERSUS-HOST DISEASE [J].
BUNJES, D ;
HEIT, W ;
ARNOLD, R ;
SCHMEISER, T ;
HEIMPEL, H .
TRANSPLANTATION, 1986, 41 (02) :170-172
[6]   OBSTRUCTIVE LUNG-DISEASE AFTER ALLOGENEIC MARROW TRANSPLANTATION - CLINICAL PRESENTATION AND COURSE [J].
CLARK, JG ;
CRAWFORD, SW ;
MADTES, DK ;
SULLIVAN, KM .
ANNALS OF INTERNAL MEDICINE, 1989, 111 (05) :368-376
[7]   IDIOPATHIC PNEUMONIA SYNDROME AFTER BONE-MARROW TRANSPLANTATION [J].
CLARK, JG ;
HANSEN, JA ;
HERTZ, MI ;
PARKMAN, R ;
JENSEN, L ;
PEAVY, HH .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1993, 147 (06) :1601-1606
[8]   RISK-FACTORS FOR AIR-FLOW OBSTRUCTION IN RECIPIENTS OF BONE-MARROW TRANSPLANTS [J].
CLARK, JG ;
SCHWARTZ, DA ;
FLOURNOY, N ;
SULLIVAN, KM ;
CRAWFORD, SW ;
THOMAS, ED .
ANNALS OF INTERNAL MEDICINE, 1987, 107 (05) :648-656
[9]   An experimental model of idiopathic pneumonia syndrome after bone marrow transplantation .1. The roles of minor H antigens and endotoxin [J].
Cooke, KR ;
Kobzik, L ;
Martin, TR ;
Brewer, J ;
Delmonte, J ;
Crawford, JM ;
Ferrara, JLM .
BLOOD, 1996, 88 (08) :3230-3239
[10]  
CURTIS DJ, 1995, BONE MARROW TRANSPL, V16, P169