S.T.E.P.S.: a comprehensive program for controlling and monitoring access to thalidomide
- PMID: 10211535
- DOI: 10.1016/s0149-2918(00)88289-2
S.T.E.P.S.: a comprehensive program for controlling and monitoring access to thalidomide
Abstract
In July 1998, the US Food and Drug Administration approved the marketing of thalidomide for the treatment of cutaneous manifestations of erythema nodosum leprosum. To ensure that fetal exposure to this teratogenic agent does not occur, the manufacturer has instituted a comprehensive program to control prescribing, dispensing, and use of the drug. This program, known as the System for Thalidomide Education and Prescribing Safety (S.T.E.P.S. [Celgene Corporation, Warren, New Jersey]), is based in part on experience gained with other drugs--specifically isotretinoin and clozapine--that offer important clinical benefits but carry the potential for serious harm. To achieve its goal of the lowest possible incidence of drug-associated teratogenicity, the S.T.E.P.S. program uses a three-pronged approach: (1) controlling access to the drug; (2) educating prescribers, pharmacists, and patients; and (3) monitoring compliance. Clinicians who wish to prescribe thalidomide must be registered in the S.T.E.P.S. Prescriber Registry and agree to prescribe the drug in accordance with S.T.E.P.S. patient eligibility criteria and monitoring procedures. Pharmacies must also register and agree to comply with patient identification and monitoring criteria. Finally, patients receive visual aids, including a videotape, written material, and verbal counseling about the benefits and risks of thalidomide therapy, the importance of not becoming pregnant during therapy, and the types of contraception required (including emergency contraception) and their availability. Women of childbearing potential must agree to undergo pregnancy testing before starting therapy and on a regular schedule during therapy. All patients must agree to complete a confidential survey about their compliance with contraception, testing, and drug therapy. The manufacturer is monitoring survey results and outcome data and is prepared to make whatever modifications to the S.T.E.P.S. program are necessary to ensure its effectiveness. In addition to minimizing the potential risk for fetal harm associated with thalidomide therapy, the S.T.E.P.S. program may provide a model for future cases in which a drug offers compelling benefits but poses profound risks unless its distribution is carefully controlled.
Similar articles
-
Thalidomide use in the US : experience with pregnancy testing in the S.T.E.P.S. programme.Drug Saf. 2006;29(4):321-9. doi: 10.2165/00002018-200629040-00003. Drug Saf. 2006. PMID: 16569081
-
The return of thalidomide: can birth defects be prevented?Drug Saf. 1999 Sep;21(3):161-9. doi: 10.2165/00002018-199921030-00002. Drug Saf. 1999. PMID: 10487395 Review.
-
Challenges of thalidomide distribution in a hospital setting.Am J Health Syst Pharm. 1999 Sep 1;56(17):1721-5. doi: 10.1093/ajhp/56.17.1721. Am J Health Syst Pharm. 1999. PMID: 10512502
-
Thalidomide: current and potential clinical applications.Am J Med. 2000 Apr 15;108(6):487-95. doi: 10.1016/s0002-9343(99)00408-8. Am J Med. 2000. PMID: 10781782 Review.
-
Thalidomide: a review of approved and investigational uses.Clin Ther. 2003 Feb;25(2):342-95. doi: 10.1016/s0149-2918(03)80085-1. Clin Ther. 2003. PMID: 12749503 Review.
Cited by
-
Thalidomide-induced teratogenesis: history and mechanisms.Birth Defects Res C Embryo Today. 2015 Jun;105(2):140-56. doi: 10.1002/bdrc.21096. Epub 2015 Jun 4. Birth Defects Res C Embryo Today. 2015. PMID: 26043938 Free PMC article. Review.
-
Use of thalidomide in the management of three HIV seroreactive children with Kaposi's sarcoma referred for palliative care.Malawi Med J. 2008 Dec;20(4):143-6. doi: 10.4314/mmj.v20i4.10980. Malawi Med J. 2008. PMID: 19537399 Free PMC article. No abstract available.
-
Ligand-mediated protein degradation reveals functional conservation among sequence variants of the CUL4-type E3 ligase substrate receptor cereblon.J Biol Chem. 2018 Apr 20;293(16):6187-6200. doi: 10.1074/jbc.M117.816868. Epub 2018 Feb 15. J Biol Chem. 2018. PMID: 29449372 Free PMC article.
-
Treatment of cutaneous lupus.Curr Rheumatol Rep. 2011 Aug;13(4):300-7. doi: 10.1007/s11926-011-0180-z. Curr Rheumatol Rep. 2011. PMID: 21503694 Free PMC article. Review.
-
Management of thalidomide toxicity.J Support Oncol. 2003 Sep-Oct;1(3):194-205. J Support Oncol. 2003. PMID: 15334875 Free PMC article. Review.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical