CYCLOSPORINE IN SEVERE ULCERATIVE-COLITIS REFRACTORY TO STEROID-THERAPY

被引:1391
作者
LICHTIGER, S
PRESENT, DH
KORNBLUTH, A
GELERNT, I
BAUER, J
GALLER, G
MICHELASSI, F
HANAUER, S
机构
[1] CUNY MT SINAI SCH MED,DEPT MED,DIV GASTROENTEROL,NEW YORK,NY 10029
[2] CUNY MT SINAI SCH MED,DEPT SURG,NEW YORK,NY 10029
[3] UNIV CHICAGO,MED CTR,DEPT MED,DIV GASTROENTEROL,CHICAGO,IL 60637
[4] UNIV CHICAGO,MED CTR,DEPT SURG,CHICAGO,IL 60637
关键词
D O I
10.1056/NEJM199406303302601
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background. There has been no new effective drug therapy for patients with severe ulcerative colitis since corticosteroids were introduced almost 40 years ago. In an uncontrolled study, 80 percent of 32 patients with active ulcerative colitis refractory to corticosteroid therapy had a response to cyclosporine therapy. Methods. We conducted a randomized, double-blind, controlled trial in which cyclosporine (4 mg per kilogram of body weight per day) or placebo was administered by continuous intravenous infusion to 20 patients with severe ulcerative colitis whose condition had not improved after at least seven days of intravenous corticosteroid therapy. A response to therapy was defined as an improvement in a numerical symptom score (0 indicated no symptoms, and 21 severe symptoms) leading to discharge from the hospital and treatment with oral medications. Failure to respond to therapy resulted in colectomy, but some patients in the placebo group who had no response and no urgent need for surgery were subsequently treated with cyclosporine. Results. Nine of 11 patients (82 percent) treated with cyclosporine had a response within a mean of seven days, as compared with 0 of 9 patients who received placebo (P<0.001). The mean clinical-activity score fell from 13 to 6 in the cyclosporine group, as compared with a decrease from 14 to 13 in the placebo group. All five patients in the placebo group who later received cyclosporine therapy had a response. Conclusions. Intravenous cyclosporine therapy is rapidly effective for patients with severe corticosteroid-resistant ulcerative colitis.
引用
收藏
页码:1841 / 1845
页数:5
相关论文
共 22 条
[1]  
ACTIS G C, 1992, Gastroenterology, V102, pA588
[2]  
ATKINSON K, 1983, TRANSPLANT P, V15, P2446
[3]   A PLACEBO-CONTROLLED, DOUBLE-BLIND, RANDOMIZED TRIAL OF CYCLOSPORINE THERAPY IN ACTIVE CHRONIC CROHNS-DISEASE [J].
BRYNSKOV, J ;
FREUND, L ;
RASMUSSEN, SN ;
LAURITSEN, K ;
DEMUCKADELL, OS ;
WILLIAMS, N ;
MACDONALD, AS ;
TANTON, R ;
MOLINA, F ;
CAMPANINI, MC ;
BIANCHI, P ;
RANZI, T ;
DIPALO, FQ ;
MALCHOWMOLLER, A ;
THOMSEN, OO ;
TAGEJENSEN, U ;
BINDER, V ;
RIIS, P .
NEW ENGLAND JOURNAL OF MEDICINE, 1989, 321 (13) :845-850
[4]  
CHALMERS TC, 1982, RANDOMIZED CLIN THER, P235
[5]   THE RISK OF NEOPLASMS IN PATIENTS TREATED WITH CYCLOSPORINE-A [J].
COCKBURN, ITR ;
KRUPP, P .
JOURNAL OF AUTOIMMUNITY, 1989, 2 (05) :723-731
[6]   CENTRAL-NERVOUS-SYSTEM TOXICITY AFTER LIVER-TRANSPLANTATION - THE ROLE OF CYCLOSPORINE AND CHOLESTEROL [J].
DEGROEN, PC ;
AKSAMIT, AJ ;
RAKELA, J ;
FORBES, GS ;
KROM, RAF .
NEW ENGLAND JOURNAL OF MEDICINE, 1987, 317 (14) :861-866
[7]  
EDWARDS FC, 1963, GUT, V4, P300
[8]  
JARNEROT G, 1985, GASTROENTEROLOGY, V89, P1005
[9]  
KORNBLUTH A, 1991, AM J GASTROENTEROL, V86, P1356
[10]  
LICHTIGER S, 1990, MT SINAI J MED, V57, P315