Evaluation of Thalidomide Treatment of Patients With Chronic Erythema Multiforme: A Multicenter Retrospective Cohort Study.


Journal

JAMA dermatology
ISSN: 2168-6084
Titre abrégé: JAMA Dermatol
Pays: United States
ID NLM: 101589530

Informations de publication

Date de publication:
01 Dec 2021
Historique:
pubmed: 11 11 2021
medline: 26 3 2022
entrez: 10 11 2021
Statut: ppublish

Résumé

Erythema multiforme (EM) may become long term, with a recurrent or persistent course. First-line treatment for chronic EM is valaciclovir. There is no consensus for selection of second-line treatment of chronic EM. The aim of this study was to assess the effectiveness of treatment with thalidomide for patients with chronic EM. In this retrospective national multicenter cohort study, among 68 French hospital dermatology departments contacted by e-mail, 10 reported having eligible cases. All adults aged 18 years or older under dermatology care for chronic EM (including recurrent and persistent forms) who had received thalidomide between 2010 and 2018 were included. Analyses were conducted from June 24, 2019, to December 31, 2019. The primary outcome was the proportion of patients who did not experience an EM flare within 6 months of initiating thalidomide treatment for recurrent EM or with complete clearance at 6 months for persistent EM (complete remission). Overall, 35 patients with chronic EM (median [range] age, 33 [15-65] years; 20 [57%] female) experienced failure of at least 1 previous treatment prior to initiating treatment with thalidomide. After 6 months of continuous thalidomide treatment, 23 (66%) were in complete remission, 5 (14%) had stopped the treatment, and 7 (20%) experienced at least 1 flare. The median (IQR) initial dose followed by remission was 50 (50-100) mg/d. Main adverse effects were asthenia (16 [46%]) and neuropathy (14 [40%]). Twenty-five (71%) of patients stopped thalidomide treatment after a median (IQR) of 12 (8-20) months owing to lack of effect (7/25 [28%]), neuropathy or another adverse effect (14/25 [56%]), or long-term complete remission (4/25 [16%]). Low-dose thalidomide, less than 50 mg every other day was sufficient in 9 of 23 (39%) of responders and was associated with less neuropathy and longer treatment duration. In this cohort study, second-line therapy with thalidomide was associated with complete remission in two-thirds of the 35 patients with chronic EM. However, adverse events were a common cause of thalidomide withdrawal. In the long term, dose reduction when possible may allow for continuation by improving tolerance.

Identifiants

pubmed: 34757396
pii: 2785842
doi: 10.1001/jamadermatol.2021.4083
pmc: PMC8581790
doi:

Substances chimiques

Thalidomide 4Z8R6ORS6L

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1472-1476

Commentaires et corrections

Type : CommentIn

Auteurs

Camille Roux (C)

Department of Dermatology, Henri Mondor Hospital, AP-HP, Créteil, France.

Emilie Sbidian (E)

Department of Dermatology, Henri Mondor Hospital, AP-HP, Créteil, France.
Université Paris Est Créteil EpiDermE, Créteil, France.

Jean-David Bouaziz (JD)

Department of Dermatology, Saint-Louis Hospital, AP-HP, Université de Paris, Paris, France.

Diane Kottler (D)

Department of Dermatology, Bichat Hospital, AP-HP, Université de Paris, Paris, France.
Department of Dermatology, Caen University Hospital, Caen, France.

Pascal Joly (P)

Department of Dermatology, Rouen University Hospital and INSERM 1234, Normandie University, Rouen, France.

Vincent Descamps (V)

Department of Dermatology, Bichat Hospital, AP-HP, Université de Paris, Paris, France.
Department of Dermatology, Caen University Hospital, Caen, France.

Catherine Prost (C)

Department of Dermatology, Avicenne Hospital, AP-HP, Bobigny, France.

Mahtab Samimi (M)

Department of Dermatology, University Hospital of Tours, Tours, France.

Julien Seneschal (J)

Department of Dermatology, National Reference Center for Rare Skin Diseases, Université Bordeaux, Bordeaux, France.

Nicolas Dupin (N)

Department of Dermatology, Cochin Hospital, AP-HP, Paris, France.

Céline Girard (C)

Department of Dermatology, Montpellier University Hospital, Montpellier, France.

Muriel Paul (M)

Université Paris Est Créteil EpiDermE, Créteil, France.
Department of Hospital Pharmacy, Henri Mondor Hospital, AP-HP, Créteil, France.

Laurence Le Cleach (L)

Department of Dermatology, Henri Mondor Hospital, AP-HP, Créteil, France.
Université Paris Est Créteil EpiDermE, Créteil, France.

Saskia Ingen-Housz-Oro (S)

Department of Dermatology, Henri Mondor Hospital, AP-HP, Créteil, France.
Université Paris Est Créteil EpiDermE, Créteil, France.
Reference Center for toxic bullous dermatoses and severe drug reactions TOXIBUL, Créteil, France.

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Classifications MeSH