Abstract | OBJECTIVE: METHODS: Analysis was based on the long-term follow-up (weeks 24-144) of 10 patients enrolled in a prospective open-label phase II study; etanercept was initially administered subcutaneously 50 mg once weekly for 12 weeks in 10 patients. Disease recurrence and the need to restart etanercept were recorded. RESULTS: Three patients did not report any disease recurrence. A second course of treatment with etanercept was needed in seven patients. Favourable responses were found in five; two patients failed treatment. CONCLUSIONS: The first treatment course achieved long-term disease remission in almost one-third of patients. The remaining needed a second treatment course but even in that case, their disease severity at restart was significantly lower compared with baseline.
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Authors | Aimilia Pelekanou, Theodora Kanni, Athina Savva, Maria Mouktaroudi, Maria Raftogiannis, Antigone Kotsaki, Evangelos J Giamarellos-Bourboulis |
Journal | Experimental dermatology
(Exp Dermatol)
Vol. 19
Issue 6
Pg. 538-40
(Jun 2010)
ISSN: 1600-0625 [Electronic] Denmark |
PMID | 19758320
(Publication Type: Clinical Trial, Phase II, Letter)
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Chemical References |
- Anti-Inflammatory Agents, Non-Steroidal
- Immunoglobulin G
- Receptors, Tumor Necrosis Factor
- Etanercept
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Topics |
- Adolescent
- Adult
- Anti-Inflammatory Agents, Non-Steroidal
(administration & dosage, adverse effects, therapeutic use)
- Etanercept
- Female
- Follow-Up Studies
- Hidradenitis Suppurativa
(diagnosis, drug therapy, pathology)
- Humans
- Immunoglobulin G
(administration & dosage, adverse effects, therapeutic use)
- Male
- Middle Aged
- Receptors, Tumor Necrosis Factor
(administration & dosage, therapeutic use)
- Recurrence
- Remission Induction
- Severity of Illness Index
- Treatment Outcome
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