help button home button
AJRCCM
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by WYSER, C. P.
Right arrow Articles by JOUBERT, J. R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by WYSER, C. P.
Right arrow Articles by JOUBERT, J. R.

Am. J. Respir. Crit. Care Med., Volume 156, Number 5, November 1997, 1371-1376

Treatment of Progressive Pulmonary Sarcoidosis with Cyclosporin A
A Randomized Controlled Trial

CHRISTOPH P. WYSER, EMMERENTIA M. van SCHALKWYK, BERTHOLD ALHEIT, PHILIP G. BARDIN, and JAMES R. JOUBERT

Department of Internal Medicine and Stellenbosch University Pulmonary Unit for Research, Cape Town, South Africa

Conventional treatment of sarcoidosis is often only partially effective. We examined the effect of cyclosporin A (CsA) combined with prednisone for the treatment of sarcoidosis. Thirty-seven patients with biopsy-proven sarcoidosis were treated with either prednisone 20 mg/d in a prospectively tapered regimen (P) or with combination therapy consisting of prednisone 20 mg/d in a prospectively tapered regimen and cyclosporin A, 5 to 7 mg/kg/d (P-CsA) for up to 18 mo in an open-label randomized controlled trial. Evaluation was done at baseline and at 3, 9, and 18 mo of the degree of dyspnea, pulmonary function, chest radiographs, bronchoalveolar lavage (BAL), and adverse events. Criteria for a good therapeutic response, improvement, treatment failure, and relapse were defined. Thirty-seven patients were treated for at least 9 mo and 18 for at least 18 mo. Six patients in remission were included in an intention-to-treat-analysis at 18 mo. The groups did not differ significantly with respect to therapeutic response from baseline. A significant (p < 0.05) improvement was observed in dyspnea until 9 mo (P) and 18 mo (P-CsA), and in lung function until 9 mo (P) and 3 mo (P-CsA). BAL results showed a significant decrease in lymphocyte counts at 9 mo for the P group only (p < 0.05). More side effects were observed in the P-CsA group than in the P group, including elevation of the mean serum creatinine concentration at 3 and 9 mo (p < 0.05), and a doubling of the number of infections in this group. Relapse after an initially good therapeutic response occurred in two of nine patients in the P group and five of seven patients in the P-CsA group (p < 0.07). Although CsA may have theoretical benefits in the treatment of sarcoidosis, our results do not support its use in this disease.




This article has been cited by other articles:


Home page
ACCP Pulmonary Med Brd RevHome page
J. P. Lynch III
Idiopathic Pulmonary Fibrosis, Nonspecific Interstitial Pneumonia/Fibrosis, and Sarcoidosis
ACCP Pulmonary Med Brd Rev, January 1, 2009; 25(0): 635 - 686.
[Full Text] [PDF]


Home page
ThoraxHome page
A U Wells, N Hirani, and on behalf of the BTS Interstitial Lung Disease Gui
Interstitial lung disease guideline
Thorax, September 1, 2008; 63(Suppl_5): v1 - v58.
[Full Text] [PDF]


Home page
JAMAHome page
S. E. Weinberger
A 47-year-old woman with sarcoidosis.
JAMA, November 1, 2006; 296(17): 2133 - 2140.
[Abstract] [Full Text] [PDF]


Home page
Eur Respir JHome page
J. C. Grutters and J. M. M. van den Bosch
Corticosteroid treatment in sarcoidosis.
Eur. Respir. J., September 1, 2006; 28(3): 627 - 636.
[Abstract] [Full Text] [PDF]


Home page
Eur Respir JHome page
N. Milman, C. B. Andersen, C. M. Burton, and M. Iversen
Recurrent sarcoid granulomas in a transplanted lung derive from recipient immune cells
Eur. Respir. J., September 1, 2005; 26(3): 549 - 552.
[Abstract] [Full Text] [PDF]


Home page
Rheumatology (Oxford)Home page
V. Majithia, S. Sanders, V. Harisdangkul, and J. G. Wilson
Successful treatment of sarcoidosis with leflunomide
Rheumatology, May 1, 2003; 42(5): 700 - 702.
[Full Text] [PDF]


Home page
Eur Respir JHome page
U. Costabel
Sarcoidosis: clinical update
Eur. Respir. J., July 1, 2001; 18(32_suppl): 56S - 68s.
[Abstract] [Full Text] [PDF]


Home page
ThoraxHome page
G J GIBSON
Sarcoidosis: old and new treatments
Thorax, May 1, 2001; 56(5): 336 - 339.
[Full Text]


Home page
ThoraxHome page
D. M Mitchell and A. Woodcock
Introduction
Thorax, August 1, 1999; 54(90002): S1 - 1.
[PDF]


Home page
Am. J. Respir. Crit. Care Med.Home page
G. W. Hunninghake
Goal of the Treatment for Sarcoidosis . Minimize Harm for the Patient
Am. J. Respir. Crit. Care Med., November 1, 1997; 156(5): 1369 - 1370.
[Full Text]


Home page
ThoraxHome page
B. T. SOCIETY and S. O. C. COMMITTEE
The Diagnosis, Assessment and Treatment of Diffuse Parenchymal Lung Disease in Adults---British Thoracic Society recommendations
Thorax, April 1, 1990; 54(90001): 1S - 28.
[Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Proc. Am. Thorac. Soc. Am. J. Respir. Cell Mol. Biol.
Copyright © 1997 American Thoracic Society
  Work-Life