Management of Kaposi sarcoma after solid organ transplantation: A European retrospective study.


Journal

Journal of the American Academy of Dermatology
ISSN: 1097-6787
Titre abrégé: J Am Acad Dermatol
Pays: United States
ID NLM: 7907132

Informations de publication

Date de publication:
Aug 2019
Historique:
received: 13 08 2018
revised: 14 02 2019
accepted: 12 03 2019
pubmed: 25 3 2019
medline: 21 12 2019
entrez: 24 3 2019
Statut: ppublish

Résumé

Systemic therapeutic management of post-transplant Kaposi sarcoma (KS) is mainly based on 3 axes: reduction of immunosuppression, conversion to mammalian target of rapamycin (mTOR) inhibitors, chemotherapy, or a combination of these. To obtain an overview of clinical strategies about the current treatment of KS. We conducted a multicenter retrospective cohort study including 145 solid organ transplant recipients diagnosed with KS between 1985 and 2011 to collect data regarding first-line treatment and response at 6 months. Overall, 95%, 28%, and 16% of patients had reduction of immunosuppression, conversion to mTOR inhibitor, and chemotherapy, respectively. Patients treated with chemotherapy or mTOR inhibitor conversion were more likely to have visceral KS. At 6 months, 83% of patients had response, including 40% complete responses. The retrospective design of the study. Currently available therapeutic options seem to be effective to control KS in most patients. Tapering down the immunosuppressive regimen remains the cornerstone of KS management.

Sections du résumé

BACKGROUND BACKGROUND
Systemic therapeutic management of post-transplant Kaposi sarcoma (KS) is mainly based on 3 axes: reduction of immunosuppression, conversion to mammalian target of rapamycin (mTOR) inhibitors, chemotherapy, or a combination of these.
OBJECTIVE OBJECTIVE
To obtain an overview of clinical strategies about the current treatment of KS.
METHODS METHODS
We conducted a multicenter retrospective cohort study including 145 solid organ transplant recipients diagnosed with KS between 1985 and 2011 to collect data regarding first-line treatment and response at 6 months.
RESULTS RESULTS
Overall, 95%, 28%, and 16% of patients had reduction of immunosuppression, conversion to mTOR inhibitor, and chemotherapy, respectively. Patients treated with chemotherapy or mTOR inhibitor conversion were more likely to have visceral KS. At 6 months, 83% of patients had response, including 40% complete responses.
LIMITATIONS CONCLUSIONS
The retrospective design of the study.
CONCLUSION CONCLUSIONS
Currently available therapeutic options seem to be effective to control KS in most patients. Tapering down the immunosuppressive regimen remains the cornerstone of KS management.

Identifiants

pubmed: 30902727
pii: S0190-9622(19)30442-6
doi: 10.1016/j.jaad.2019.03.028
pii:
doi:

Substances chimiques

Antineoplastic Agents 0
Immunosuppressive Agents 0
TOR Serine-Threonine Kinases EC 2.7.11.1
Sirolimus W36ZG6FT64
Tacrolimus WM0HAQ4WNM

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

448-455

Informations de copyright

Copyright © 2019 American Academy of Dermatology, Inc. Published by Elsevier Inc. All rights reserved.

Auteurs

Julie Delyon (J)

Department of Dermatology, Assistance Publique-Hôpitaux de Paris (AP-HP) Hôpital Saint Louis, Institut National de la Santé et de la Recherche Médicale U976, Université Paris Diderot, Sorbonne Paris Cité, Paris, France. Electronic address: julie.delyon@aphp.fr.

Clementine Rabate (C)

Service de Néphrologie-Transplantation Adultes, Hôpital Necker, AP-HP, and Université Paris Descartes, Paris, France.

Sylvie Euvrard (S)

Department of Dermatology, Edouard Herriot Hospital, Hospices Civils de Lyon, Lyon, France.

Catherine A Harwood (CA)

Centre for Cell Biology and Cutaneous Research, Blizard Institute, Barts, and the London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom.

Charlotte Proby (C)

Dermatology, School of Medicine, University of Dundee, Dundee, United Kingdom.

A Tülin Güleç (AT)

Department of Dermatology, Başkent University Faculty of Medicine, Ankara, Turkey.

Deniz Seçkin (D)

Department of Dermatology, Başkent University Faculty of Medicine, Ankara, Turkey.

Veronique Del Marmol (V)

Dermatology, Erasme Hospital, Université Libre de Bruxelles, Brussels, Belgium.

Jan Nico Bouwes-Bavinck (JN)

Department of Dermatology, Leiden University Medical Center, Leiden, The Netherlands.

Carla Ferrándiz-Pulido (C)

Department of Dermatology, Hospital Universitari Vall d'Hebron, Barcelona, Spain.

Maria Andrea Ocampo (MA)

Department of Dermatology, Edouard Herriot Hospital, Hospices Civils de Lyon, Lyon, France.

Stephane Barete (S)

Sorbonne Université, Unit of Dermatology, AP-HP Pitié-Salpêtrière Hospital, Paris, France.

Christophe Legendre (C)

Service de Néphrologie-Transplantation Adultes, Hôpital Necker, AP-HP, and Université Paris Descartes, Paris, France.

Camille Francès (C)

Sorbonne Université, Service de Dermatologie et Allergologie, AP-HP Hôpital Tenon, Paris, France.

Raphael Porcher (R)

AP-HP, Centre d'Épidémiologie Clinique, Hôpital Hôtel-Dieu, and Centre of Research in Epidemiology and StatisticS (CRESS) Institut National de la Santé et de la Recherche Médicale U1153; Université Paris Descartes, Sorbonne Paris Cité, Paris, France.

Celeste Lebbe (C)

Department of Dermatology, Assistance Publique-Hôpitaux de Paris (AP-HP) Hôpital Saint Louis, Institut National de la Santé et de la Recherche Médicale U976, Université Paris Diderot, Sorbonne Paris Cité, Paris, France.

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Classifications MeSH