Lessons learned from the failure of several recent trials with biologic treatment in systemic lupus erythematosus
Language English Country Great Britain, England Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't, Review
- Keywords
- SLE, biologic treatment, clinical trial, monoclonal antibodies, treatment,
- MeSH
- Biological Factors therapeutic use MeSH
- Biological Products therapeutic use MeSH
- Antibodies, Monoclonal, Humanized therapeutic use MeSH
- Clinical Trials as Topic standards statistics & numerical data MeSH
- Humans MeSH
- Antibodies, Monoclonal therapeutic use MeSH
- Treatment Failure MeSH
- Lupus Erythematosus, Systemic drug therapy epidemiology MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Review MeSH
- Names of Substances
- belimumab MeSH Browser
- Biological Factors MeSH
- Biological Products MeSH
- Antibodies, Monoclonal, Humanized MeSH
- Antibodies, Monoclonal MeSH
INTRODUCTION: Treatment of systemic lupus erythematosus (SLE) represents a challenge due to variable disease manifestations, clinical course, and outcome. Long-term outcome in SLE remain unsatisfactory and a search for new therapeutic options is definitely warranted. Despite expectations, most clinical trials performed in SLE and lupus nephritis in the last decade did not reach primary outcome, and the only drug that has been licensed is belimumab. AREAS COVERED: Results of negative trials testing monoclonal antibodies and other biologic agents in SLE are briefly summarized. Reasons for the failure of the trials are listed and discussed. EXPERT OPINION: Future studies should recruit patients with similar organ involvement, better defined disease manifestations, higher activity, and similar severity. In addition to testing higher efficacy if given as add-on treatment to standard-of-care, the trials should be aimed at reducing dosing, or completely eliminating some parts of the current standard treatment, especially corticosteroids. Median follow-up of the patients should be longer. Moreover, specific biomarkers are needed to help to identify eligible patients and to better define response to treatment. An urgent unmet need is testing these new drugs in patients with severe SLE (including those refractory to current treatment).
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