Abstract
TNF-blocking strategies are widely used in the treatment of rheumatoid arthritis (RA). Three anti-TNF agents are registered for use in RA: etanercept, infliximab and adalimumab. Although anti-TNF therapy is very effective in controlling disease activity and slowing down radiological damage, prolonged response is only seen in approximately 70% of the patients. The causes for nonresponse in the remaining patients have not yet been elucidated. Pharmacogenetic studies focusing on genes involved in RA etiology (and/or progression) and in the pharmacokinetics of TNF-blocking agents have identified markers associated with anti-TNF treatment outcome. In the future, more exhaustive, less hypothesis-driven search strategies are expected to discover additional markers. Identification of these markers might be viewed as the first step towards tailored TNF-blocking therapy for patients with RA. Nevertheless, replication and large prospective studies will be needed to demonstrate the validity of the identified genetic markers before implementation into daily clinical practice.
| Original language | English |
|---|---|
| Pages (from-to) | 761-73 |
| Number of pages | 13 |
| Journal | Pharmacogenomics |
| Volume | 8 |
| Issue number | 7 |
| DOIs | |
| Publication status | Published - Jul 2007 |
| Externally published | Yes |
Keywords
- Adalimumab
- Antibodies, Monoclonal
- Antibodies, Monoclonal, Humanized
- Antirheumatic Agents
- Arthritis, Rheumatoid
- Cohort Studies
- Etanercept
- Humans
- Immunoglobulin G
- Infliximab
- Patient Selection
- Pharmacogenetics
- Receptors, Tumor Necrosis Factor
- Tumor Necrosis Factor-alpha
- Journal Article
- Research Support, Non-U.S. Gov't