Kaposi Sarcoma in HIV-positive Solid-Organ Transplant Recipients: A French Multicentric National Study and Literature Review.


Journal

Transplantation
ISSN: 1534-6080
Titre abrégé: Transplantation
Pays: United States
ID NLM: 0132144

Informations de publication

Date de publication:
01 2019
Historique:
pubmed: 3 10 2018
medline: 29 5 2019
entrez: 2 10 2018
Statut: ppublish

Résumé

Kaposi sarcoma is a vascular tumor related to herpesvirus-8 and is promoted by immunosuppression. For the last 15 years, human immunodeficiency virus (HIV) patients have had access to organ transplantation. The dual immunosuppression of HIV and immunosuppressive treatments might increase the risk and severity of Kaposi sarcoma. We conducted a multicentric retrospective study by collecting cases from French databases and society members of transplanted patients, among which 7 HIV-infected patients who subsequently developed Kaposi sarcoma were included. In the CRISTAL database (114 511 patients) and the DIVAT (Données Informatisées et VAlidées en Transplantation) database (19 077 patients), the prevalence of Kaposi sarcoma was 0.18% and 0.46%, respectively, in transplanted patients; these values compare with 0.66% and 0.50%, respectively, in transplanted patients with HIV. The median time from HIV infection to Kaposi sarcoma was 20 years. Kaposi sarcoma occurred during the first year after transplantation in most cases, whereas HIV viral load was undetectable. Only 2 patients had visceral involvement. Five patients were treated with conversion of calcineurin inhibitor to mammalian target of rapamycin inhibitor, and 5 patients were managed by decreasing immunosuppressive therapies. At 1 year, 4 patients had a complete response, and 3 had a partial response. In our study, Kaposi sarcoma in transplanted patients with HIV did not show any aggressive features and was treated with the usual posttransplant Kaposi sarcoma management protocol.

Sections du résumé

BACKGROUND
Kaposi sarcoma is a vascular tumor related to herpesvirus-8 and is promoted by immunosuppression. For the last 15 years, human immunodeficiency virus (HIV) patients have had access to organ transplantation. The dual immunosuppression of HIV and immunosuppressive treatments might increase the risk and severity of Kaposi sarcoma.
METHODS
We conducted a multicentric retrospective study by collecting cases from French databases and society members of transplanted patients, among which 7 HIV-infected patients who subsequently developed Kaposi sarcoma were included.
RESULTS
In the CRISTAL database (114 511 patients) and the DIVAT (Données Informatisées et VAlidées en Transplantation) database (19 077 patients), the prevalence of Kaposi sarcoma was 0.18% and 0.46%, respectively, in transplanted patients; these values compare with 0.66% and 0.50%, respectively, in transplanted patients with HIV. The median time from HIV infection to Kaposi sarcoma was 20 years. Kaposi sarcoma occurred during the first year after transplantation in most cases, whereas HIV viral load was undetectable. Only 2 patients had visceral involvement. Five patients were treated with conversion of calcineurin inhibitor to mammalian target of rapamycin inhibitor, and 5 patients were managed by decreasing immunosuppressive therapies. At 1 year, 4 patients had a complete response, and 3 had a partial response.
CONCLUSIONS
In our study, Kaposi sarcoma in transplanted patients with HIV did not show any aggressive features and was treated with the usual posttransplant Kaposi sarcoma management protocol.

Identifiants

pubmed: 30273235
doi: 10.1097/TP.0000000000002468
doi:

Substances chimiques

Anti-HIV Agents 0
Immunosuppressive Agents 0

Types de publication

Journal Article Multicenter Study Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

e22-e28

Auteurs

Chloé Charpentier (C)

APHP Department of Dermatology, Saint Louis Hospital, Paris, France.

Julie Delyon (J)

APHP Department of Dermatology, Saint Louis Hospital, Paris, France.
INSERM U976, France.
Paris Diderot University, Sorbonne Paris Cité, France.

Denis Glotz (D)

Paris Diderot University, Sorbonne Paris Cité, France.
Department of Nephrology, Saint Louis Hospital, Paris, France.

Marie-Noelle Peraldi (MN)

Paris Diderot University, Sorbonne Paris Cité, France.
Department of Nephrology, Saint Louis Hospital, Paris, France.

Jean-Philippe Rerolle (JP)

Department of Nephrology, Dupuytren Hospital, Limoges, France.

Benoît Barrou (B)

UPMC, Department of Urology, Nephrology and Transplantation, Pitié-Salpêtrière Hospital, Sorbonne University, Paris, France.

Emilie Ducroux (E)

Department of Dermatology, Edouard Herriot Hospital, Lyon, France.

Audrey Coilly (A)

Department of Hepatology and Gastrology, Paul Brousse Hospital, Villejuif, France.

Camille Legeai (C)

Biomedicine Agency. Saint-Denis La Plaine, France.

Stéphane Barete (S)

UPMC, Unit of Dermatology, Pitié-Salpêtrière Hospital, Sorbonne University, Paris, France.

Céleste Lebbé (C)

APHP Department of Dermatology, Saint Louis Hospital, Paris, France.
INSERM U976, France.
Paris Diderot University, Sorbonne Paris Cité, France.

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