Risk Factors of Chinese Kidney Transplant Recipients DSA Based on MPA Immunosuppressive Regimen

Sponsor

First Affiliated Hospital Xi'an Jiaotong University (Other)

Overall Status

Recruiting

CT.gov ID

NCT04444843

Collaborator

(none)

300

Enrollment

Location

Arm

35.3

Anticipated Duration (Months)

8.5

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

THE INCIDENCE AND INFLUENTIAL FACTORS OF DSA IN CHINESE RENAL TRANSPLANT RECIPIENTS WITH MPA-BASED IMMUNOSUPPRESSIVE REGIMEN： A MULTI-CENTER CLINICAL STUDY (TIAIFOD STUDY)

Study procedure Investigators at participating centers will identify patients fulfilling inclusion criteria and do not violate any exclusion criteria. Informed consent will be obtained upon entry into the study according to national regulations. Patients will be enrolled into the study and clinical data of patient history will be collected. Clinical data will be collected prospectively up to a total period of 12 months.

Condition or Disease	Intervention/Treatment	Phase
Kidney Transplant Recipients	Drug: Mycophenolate Mofetil Capsules	Phase 4

Detailed Description

Medical history and Kidney transplantation This will include age at transplantation, gender, race, weight, height of both recipient and donor; Recipients: previous history ,BMI ,primary kidney disease including biopsy proven diagnosis (if present), historic dialysis，pregnancy history (female). Donor: the catalogue (DCD,DBD,DBCD), ECD or not，the cause of death, received CPR or not; zero biopsy results if done, ABO blood type match, HLA-MM, cold and warm ischemic time.

Clinical data at baseline and 12months follow up period:

Clinical assessments, laboratory, comorbidity, immunosuppressive therapy, and selected concomitant therapy (anti-hypertension anti-hyperlipidemics, anti-diabetics and drugs known to affect renal function) will be collected at transplant day（Day 0, visit 0）and 8 subsequent visits scheduled Day 3, Week1, Week2, Week 4，Week 12，Week 26，Week 40，Week 52 post transplantation. MPA-AUC, acute rejection episodes and graft loss will be collected at visits scheduled Day 3, Week 1，Week 2, Week 4，Week 12， Week 26(6 month)，Week 40，Week 52 (12 month) post transplantation. On day 3, MPA-AUC will be tested by full time sample (0h,0.5h,1h,2h,3h,4h,6h,8h,10h,12h post receiving MMF). LSS (0h, 0.5h, 2h post receiving MMF) will be used for testing MPA-AUC on other visits. PRA will be tested on week 4, week 12, week 26, week 52. If PRA is positive, DSA will be tested following once. All the PRA and DSA MFI and phenotype will be collected（including the clinical-drive test）.

Statistical analysis:

The primary endpoint in this study is the incidence of DSA formation in 12-months post-transplantation in Chinese kidney transplant recipients with MMF-based IS regimen. The proportion and its 95% CI will be provided.

The influential factors of DSA formation will be estimated using logistic regression including relevant influential factors, where the influential factors are defined as {age, gender of donor / recipients recipient: BMI, blood transfusion, previous AR （before DSA appears）, ECD , cold ischemia time, HLA-MM, Tac trough concentration, MPA-AUC, DGF, introduction therapy (including use or not and the drugs )}. .

The full MPA-AUC0-12h will be calculated using the trapezoidal rule. The calculated formula with Limited Sample Strategy (LSS) will be established to predict the MPA-AUC0-12h in the Chinese patients. Correlation coefficients will be calculated and multiple stepwise regression analysis will be used to determine the time points and best equation for evaluating MPA-AUC0-12h.

Estimates for the time-to-event variable(s), such as Overall Survival(OS), will be obtained by using the Kaplan-Meier (KM) approach together with associated 95% CI.

The other secondary endpoints will be summarized descriptively depended on the variable type. The comparison between patients with and without DSA-positive will be performed according to the variable type.

Study Design

Study Type:

Interventional

Anticipated Enrollment :

300 participants

Allocation:

N/A

Intervention Model:

Single Group Assignment

Intervention Model Description:

To estimate the incidence of DSA formation during 12-months post-transplantationTo estimate the incidence of DSA formation during 12-months post-transplantation

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

A Multicenter Clinical Trial: Risk Factors of Chinese Kidney Transplant Recipients DSA Based on MPA Immunosuppressive Regimen

Actual Study Start Date :

Jan 22, 2021

Anticipated Primary Completion Date :

Dec 21, 2022

Anticipated Study Completion Date :

Dec 31, 2023

Arms and Interventions

Arm	Intervention/Treatment
Other: Mycophenolate Mofetil Capsules The dosage of mycophenolate mofetil (CellCept) will be decided by the investigator and should be adjusted according to clinical response or therapeutic drug monitoring. It is not allowed to switch to other MPAs. When MMF is discontinued but is not switched to other MPA, the patients will be followed until the end of study.	Drug: Mycophenolate Mofetil Capsules Patients who received MMF+TAC+ Corticosteroids immunosuppressive regimen as first choice post transplantation Other Names: Other MPAs

Arm

Intervention/Treatment

Other: Mycophenolate Mofetil Capsules

The dosage of mycophenolate mofetil (CellCept) will be decided by the investigator and should be adjusted according to clinical response or therapeutic drug monitoring. It is not allowed to switch to other MPAs. When MMF is discontinued but is not switched to other MPA, the patients will be followed until the end of study.

Drug: Mycophenolate Mofetil Capsules

Patients who received MMF+TAC+ Corticosteroids immunosuppressive regimen as first choice post transplantation

Other Names:

Other MPAs

Outcome Measures

Primary Outcome Measures

the incidence of Donor specific antibody(DSA) formation during 12-months post-transplantation [12-months]
the incidence of DSA formation during 12-months post-transplantation

Secondary Outcome Measures

the incidence of DSA formation during 6-months post-transplantation [6 months]
the incidence of DSA formation during 6-months post-transplantation
the influential factors of DSA formation [12 months]
the influential factors of DSA formation
the association between DSA and MPA AUC [12 months]
the association between DSA and MPA AUC
the calculation formula for MPA-AUC with ISS using multiple regression analysis [12 months]
the calculation formula for MPA-AUC with ISS using multiple regression analysis
the proportion of patients experiencing Acute Rejection(AR), Biopsy proven acute rejection(BPAR), Antibody mediated rejection(ABMR) and the association with Donor specific antibody(DSA) [12 months]
the proportion of patients experiencing AR, BPAR, ABMR and the association with DSA
the renal function (Calculated creatinine clearance) at 12 month and association with DSA [12 months]
the renal function (Calculated creatinine clearance) at 12 month and association with DSA
the death-censored graft survival rate at 12 month post transplantation and association with Donor specific antibody(DSA) [12 months]
the death-censored graft survival rate and association with Donor specific antibody(DSA)

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years to 65 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Male or female kidney transplant recipients from 18 to 65 years of age (including 18 & 65 years old patients)
Single organ and first kidney transplant recipients from donation after citizen's death
Patients who received MMF+TAC+ Corticosteroids immunosuppressive regimen as first choice post transplantation
Pre-transplant PRA is negative (0%)
One serum pregnancy test with a sensitivity of at least 25mlU/Ml for patients of childbearing potential before enrolled. A second test should be performed 8-10 days later. Repeat pregnancy tests should be performed during routine follow-up visits. Results of all pregnancy tests should be discussed with the patient. Patients should be instructed to consult their physician immediately should pregnancy occur. For patients to be included in the study, negative result must be obtained. And highly effective contraception for women of childbearing potential. Contraception must be taken before beginning study drug therapy, during therapy and for 6 weeks after the last dose of study medication

Exclusion criteria:

Patients who do not receive MMF
Patients who are re-transplantation or multiple organ transplantation recipients
Female patients who are pregnant or lactating
Patients who have any form of substance abuse, psychological illness or any other condition, which, in the opinion of the investigator, may interfere with the patient's ability to understand the requirements of the study.
Patients who would have received another investigational drug within 30 days preceding the enrollment, received prohibited immunosuppressant medications prior to transplant
Patients who are using AZA, MTX, CTX or will use these drugs post-transplantation
Known contraindications to TAC , corticosteroids, MMF
Patients who have active peptic ulcer
Patients who have severe cardiac or lung disease
Patient who have active hepatica disease
Patients who have a history of cancer, except successfully treated localized nonmelanocytic skin cancer
Patients who would not be available for routine study visits or follow-up, or not being followed by an accredited laboratory.