Low-dose Cyclophosphamide or CNI in the Prevention of Acute Graft-versus-host Disease After gDLI

NCT ID: NCT06490562

Last Updated: 2024-07-08

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: NA
• Total Enrollment: 66 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-07-31
• Study Completion Date: 2028-12-31

Brief Summary

Assess the cumulative incidence of severe (III-IV) aGVHD after low-dose cyclophosphamide or CNI is used to after gDLI. Evaluate the overall survival rate (OS), non recurrent mortality rate (NRM), and recurrence rate (CIR) of two groups of patients; The complete response rate (CR) and partial response rate (PR) of patients with morphological/extramedullary recurrence, as well as the complete response rate and MRD response rate of patients with molecular recurrence. The incidence of adverse events such as infection, hemorrhagic cystitis, and cardiac events in two groups.

Detailed Description

Assess the cumulative incidence of severe (III-IV) aGVHD after low-dose cyclophosphamide or CNI is used to after gDLI. Evaluate the overall survival rate (OS), non recurrent mortality rate (NRM), and recurrence rate (CIR) of two groups of patients; The complete response rate (CR) and partial response rate (PR) of patients with morphological/extramedullary recurrence, as well as the complete response rate and MRD response rate of patients with molecular recurrence. The incidence of adverse events such as infection, hemorrhagic cystitis, and cardiac events in two groups.

Efficacy Evaluation: Follow up observation of the difference in efficacy and safety between two groups in preventing severe (III-IV) aGVHD.

Primary Exploratory Endpoint: Assess the cumulative incidence of severe (III-IV) aGVHD after low-dose cyclophosphamide or CNI is used after gDLI.

Secondary Exploratory Endpoints:

1. 1-year overall survival rate (OS);

2. 1-year recurrence rate (CIR);

3. 1-year non recurrent mortality rate (NRM);

4. The complete response rate (CR) and partial response rate (PR) of patients with morphological/extramedullary recurrence, as well as the complete response rate and MRD response rate of patients with molecular recurrent minimal residual disease (MRD);

5. The incidence of adverse events such as infection, hemorrhagic cystitis, and cardiac events in two groups.

Conditions

Acute Graft-versus-host Disease

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: PREVENTION
• Blinding Strategy: NONE

Study Groups

PDCy group

Low dose Cy 30 mg/kg/d was administered on the 3rd and 4th day after gDLI to prevent GVHD

Group Type: OTHER

PDCy

Intervention Type: DRUG

Low dose Cy 30 mg/kg/d was administered on the 3rd and 4th day after gDLI to prevent GVHD

Non Cy group

Oral administration of low-dose CNI (CSA 25mg Q12H or FK506 0.25mg Q12H combined with azole fungal drugs) for 2 weeks to prevent GVHD at 0 days after gDLI

Group Type: OTHER

Non Cy

Intervention Type: DRUG

Oral administration of low-dose CNI (CSA 25mg Q12H or FK506 0.25mg Q12H combined with azole fungal drugs) for 2 weeks to prevent GVHD at 0 days after gDLI

Interventions

PDCy

Low dose Cy 30 mg/kg/d was administered on the 3rd and 4th day after gDLI to prevent GVHD

Intervention Type: DRUG

Non Cy

Oral administration of low-dose CNI (CSA 25mg Q12H or FK506 0.25mg Q12H combined with azole fungal drugs) for 2 weeks to prevent GVHD at 0 days after gDLI

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Subjects eligible for inclusion in this study must meet all of the following criteria:

1. Patients with malignant hematological diseases undergo haploid/sibling incomplete matching/unrelated donor transplantation;

2. Recurrence after transplantation (morphological, extramedullary, or molecular recurrence);

3. Plan to administer granulocyte colony-stimulating factor mobilization donor lymphocyte infusion (gDLI) for treatment;

4. No age, gender, or race restrictions;

5. The physical condition assessment (ECOG-PS) of the Eastern Oncology Collaborative Group is 0-2 points;

6. The patient or their authorized representative agrees to participate in the clinical trial and signs an informed consent form.

Exclusion Criteria

• Subjects meeting any of the following criteria are not eligible for inclusion in this study:

1. Siblings of matched donor transplant;

2. Patients with other malignant tumors that require treatment;

3. There are active infections, such as hepatitis B, hepatitis C, tuberculosis, etc;

4. HIV serological reaction was positive;

5. Suffering from mental illness or other conditions that cannot comply with research, treatment, and monitoring requirements;

6. Pregnant patients or patients who are unable to take appropriate contraceptive measures during treatment;

7. Active heart disease is defined as one or more of the following:

1. Have a history of uncontrolled or symptomatic angina pectoris;

2. Myocardial infarction less than 6 months prior to enrollment in the study;

3. A history of arrhythmia requiring medication treatment or severe clinical symptoms;

4. Uncontrolled or symptomatic congestive heart failure (>NYHA level 2);

5. The ejection fraction is below the lower limit of the normal range.

8. Individuals who are allergic to any medication or component such as Cy, CNI, etc;

9. The researchers believe that it is not suitable for participants.

• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Institute of Hematology & Blood Diseases Hospital, China

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Central Contacts

erlie jiang, MD

Role: CONTACT

jiangerlie@ihcams.ac.cn

+86-15122538106

Other Identifiers

IIT2024034

Identifier Type: -

Identifier Source: org_study_id