P.1521 Efficacy and Safety of Enteric-Coated Mycophenolate Sodium in Chinese Living-Donor Kidney Transplant Recipients: A Multicenter Prospective Cohort Study
Saturday August 20, 2016 from 17:00 to 18:30
Hall 5FG-Level 5
Presenter

Chunbai Mo Sr., People's Republic of China

Tianjin First Center Hospital

Department of transplantation

Tianjin First Center Hospital

Abstract

Efficacy and safety of enteric-coated mycophenolate sodium in Chinese living-donor kidney transplant recipients: A multicenter prospective cohort study

chunbai mo1, Changxi Wang2, Tongyi Men3, Jinliang Xie4, Aiming Zhang5.

1Organ transplantation center, Tianjin First Center Hospital, Tianjin, People's Republic of China; 2Organ transplantation center, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, People's Republic of China; 3Organ transplantation center, Qian Fo-shan Hospital, Jinan, People's Republic of China; 4Organ transplantation center, Xiang Ya Hospital Central South University, Changsha, People's Republic of China; 5Organ transplantation center, Ji Nan Military General Hospital, Jinan, People's Republic of China

Objective: To investigate the efficacy and safety of enteric-coated mycophenolate sodium (EC-MPS) in Chinese living-donor kidney transplant recipients.

Methods: Twenty-eight cases of living donor kidney transplant recipients from five centers were enrolled in this prospective cohort study. Maintenance immunosuppressive therapy was EC-MPS and calcineurin inhibitor (CNI) plus corticosteroids. The study was conducted according to the Declaration of Helsinki, and informed consent was obtained from all patients. The patients were followed up for 24 months. Biopsy-proven acute rejection (BPAR), patient / graft survival and adverse events were observed.

Results: All patients completed the follow-up. The patient and graft survival rates were both 100%, respectively. No biopsy-proven acute rejection was observed. The gastrointestinal adverse effects were assessed by using Gastrointestinal Symptom Rating Scale (GSRS) and the scores were 0 at 12, 15 and 21 months post-transplant, respectively. The scores were 0.1 ± 0.64 at 18 months and 0.0 ± 0.19 at 24 months. The medication adherence categories of ‘excellent’ and ‘good’ were 74.1% and 25.9% at 22-24 months, respectively. As to complete blood cell counts, one patient had significantly abnormal white blood cell counts and another had abnormal absolute neutrophil count at the visit of 24 months, respectively. No significantly abnormal variables of complete blood cell counts were found at other visits.

Conclusion: The triple therapy with EC-MPS and CNI plus corticosteroids for living-donor kidney transplant recipients has favorable clinical outcomes in a moderately long term. The combination regimen also demonstrated good gastrointestinal tolerance according to GSRS, which may contribute to good medication adherence.

Author Disclosure: The authors have declared no conflict of interest.


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