Successful sirolimus treatment of patients with pure red cell aplasia complicated with renal insufficiency.


Journal

Annals of hematology
ISSN: 1432-0584
Titre abrégé: Ann Hematol
Pays: Germany
ID NLM: 9107334

Informations de publication

Date de publication:
Apr 2020
Historique:
received: 06 08 2019
accepted: 27 01 2020
pubmed: 8 2 2020
medline: 10 4 2020
entrez: 8 2 2020
Statut: ppublish

Résumé

For patients with pure red cell aplasia (PRCA), cyclosporine (CsA) is the first line therapy. Occasionally, some patients who suffer from renal insufficiency cannot tolerate CsA. To explore the efficacy and tolerance of sirolimus treatment for those patients, twelve PRCA patients with renal insufficiency from May 2014 to May 2018 in Peking Union Medical College Hospital were enrolled, treated with sirolimus, and followed up at the median time of 16 (10-50) months. Eleven patients (91.7%) responded to sirolimus, with 58.3% complete response (CR) and 41.7% partial response (PR). The median time to achieve the optimum effect was 4 (1-7) months. The serum creatinine level remained stable or even reduced during the treatment period for eleven patients. Seven patients (58.3%) reported adverse events during sirolimus therapy, including increased blood glucose, infection, skin rash, elevated triglyceride or total cholesterol, and elevated serum creatinine compared with baseline. No treatment-related death was noticed during the follow-up time. Three patients relapsed with an overall response rate of 75.0% at 1 year. These results suggested that sirolimus was effective and tolerable for patients with PRCA complicated with renal insufficiency.

Identifiants

pubmed: 32030447
doi: 10.1007/s00277-020-03946-2
pii: 10.1007/s00277-020-03946-2
doi:

Substances chimiques

Immunosuppressive Agents 0
Cyclosporine 83HN0GTJ6D
Creatinine AYI8EX34EU
Sirolimus W36ZG6FT64

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

737-741

Subventions

Organisme : Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences and Peking Union Medical College
ID : 2016-I2M-3-004
Organisme : The National Key Research and Development Program of China
ID : 2016YFC0901500
Organisme : Beijing Natural Science Foundation
ID : 7192168

Auteurs

Zesong Chen (Z)

Department of Hematology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100730, China.

Xinjian Liu (X)

Department of Hematology, Institute of Hematology of Henan Province, Affiliated Cancer Hospital of Zhengzhou University, Henan Cancer Hospital, 127 Dongming Road, Zhengzhou, China.

Miao Chen (M)

Department of Hematology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100730, China.

Chen Yang (C)

Department of Hematology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100730, China.

Bing Han (B)

Department of Hematology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100730, China. hanbing_li@sina.com.

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Classifications MeSH