|
Sign In to gain access to subscriptions and/or personal tools.
|
Oral Cyclophosphamide for Active Scleroderma Lung Disease: A Decision Analysis
Dinesh Khanna, MD, MSc*,
Daniel E. Furst, MD,
Philip J. Clements, MD, MPH,
Donald P. Tashkin, MD,
and
Mark H. Eckman, MD
* To whom correspondence should be addressed. E-mail: dkhanna{at}mednet.ucla.edu.
 |
Abstract |
|---|
Background. Results from the recent Scleroderma Lung Study (SLS) show that oral cyclophosphamide (CYC) is better than placebo in preventing the progression of scleroderma-related interstitial lung disease (SSc-ILD) at 12 mo but is associated with adverse events. Also, the long-term balance of risk and benefit remains unclear. Methods. The authors evaluate the risk-benefit tradeoffs using a Markov decision analytic model to project the quality-adjusted life years (QALYs) for strategies of CYC versus no CYC in SSc-ILD. The base case examined a 50-y-old woman with SSc of 1.5 y, SSc-ILD with moderate ventilatory restriction. The authors analyze the decision to treat with 1 y of daily CYC versus no SSc-ILD–specific therapy. Based on 2-y data from the SLS, the authors assume CYC resulted in no survival benefit and only a transient beneficial impact on pulmonary function. They explore the impact of changes in model parameters through sensitivity analyses, including the efficacy of CYC in preventing progression of lung disease and SSc-ILD–related death. Results. In the base-case analysis, CYC-treated patients fared worse, with a small loss of 0.21 QALYs (16.84 v. 17.15). CYC remained inferior across sensitivity analyses for most variables. In analyses assuming a survival benefit with CYC, CYC resulted in a clinically significant gain (18.17 v. 17.15 QALYs). Conclusions. CYC therapy for 1 y results in a small loss in QALYs compared with no CYC for SSc-ILD. The lack of a beneficial impact on survival and the transience of CYC's impact on decline in pulmonary function drive this conclusion. Key words: Scleroderma Lung Study; scleroderma; cyclophosphamide; interstitial lung disease; pulmonary fibrosis; decision analysis. (Med Decis Making XXXX;XX:xx–xx)
First published on April 28, 2008, doi:10.1177/0272989X08317015
Medical Decision Making 2008;28:926.
A more recent version of this article appeared on November 1, 2008

CiteULike Complore Connotea Del.icio.us Digg Reddit Technorati Twitter What's this?
This article has been cited by other articles:

|
 |

|
 |
 
J. Behr and V. J. Thannickal
Update in Diffuse Parenchymal Lung Disease 2008
Am. J. Respir. Crit. Care Med.,
March 15, 2009;
179(6):
439 - 444.
[Full Text]
[PDF]
|
 |
|
|
|