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Wiley InterScience

British Journal of Dermatology

British Journal of Dermatology

Volume 161 Issue 3, Pages 605 - 616

Published Online: 24 Apr 2009

Journal compilation © 2010 British Association of Dermatologists



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EPIDEMIOLOGY AND HEALTH SERVICES RESEARCH
Using 'number needed to treat' to help conceptualize the magnitude of benefit and risk of tumour necrosis factor-α inhibitors for patients with severe psoriasis
J.W. Dharamsi, M. Bhosle*, R. Balkrishnan*, B.A. Yentzer and S.R. Feldman
 Johns Hopkins University School of Medicine, Baltimore, MD, U.S.A.
  *Department of Pharmacy Practice and Administration, Ohio State University, Columbus, OH, U.S.A.
  Center for Dermatology Research, Departments of Dermatology, Pathology, Public Health Sciences and Internal Medicine, Wake Forest University School of Medicine, Medical Center Boulevard, Winston-Salem, NC 27157-1071, U.S.A.
Correspondence to Steven R. Feldman.
E-mail: sfeldman@wfubmc.edu
 

Conflicts of interest S.R.F. with Astellas, Abbott Labs, Galderma, Genentech, Centocor and Amgen.

Copyright Journal Compilation © 2009 British Association of Dermatologists
KEYWORDS
demyelinating disease • lymphoma • psoriasis • tuberculosis • tumour necrosis factor inhibitor

ABSTRACT

Background Risks and benefits of tumour necrosis factor (TNF) α inhibitors are often presented using statistical descriptions that are difficult to translate directly for patients into a clinically meaningful context.

Objectives To illustrate the risks and benefits of TNFα inhibitors in relation to risks that patients understand.

Methods We performed a number needed to treat analysis for patients with psoriasis on TNFα inhibitors via a Medline and Embase search. We determined the number needed to benefit and the number needed to harm with TNFα inhibitor treatment. We compared the risk of serious adverse events from treatment with a TNFα inhibitor to the risk of death from driving a car. The risk analyses were limited to the risks of tuberculosis, lymphoma and demyelinating disease.

Results The numbers needed to benefit were 2·1 for etanercept, 1·4 for infliximab, and 1·6 for adalimumab. Depending on the adverse event, the numbers needed to harm ranged from 380 to 360 000 treated patients per year. Screening prior to the initiation of TNFα inhibitor therapy reduces risk of tuberculosis. Patients are about as likely to die in a car accident as to have a serious adverse event from treatment with a TNFα inhibitor.

Conclusions All three of the TNFα antagonists have remarkable efficacy in patients with severe psoriasis. The risks of serious adverse events are relatively rare and comparable to the risks patients take on a regular basis such as driving a car. For many patients with severe psoriasis, the benefits of TNFα inhibitors may greatly outweigh the risks.


Accepted for publication 18 January 2009

DIGITAL OBJECT IDENTIFIER (DOI)
10.1111/j.1365-2133.2009.09158.x About DOI

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