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MTX and Steroid for aGVHD Treatment

A Single-cohort, Phase II Study of Methotrexate Combined Corticosteroid in Chinese Patients With Acute Graft vs. Host Disease After Allogeneic Hematopoietic Stem Cell Transplantation

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04677868
Enrollment
30
Registered
2020-12-21
Start date
2020-12-23
Completion date
2022-06-30
Last updated
2021-09-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute GVH Disease

Keywords

acute GVHD, MTX, Corticosteroid

Brief summary

The aim of the study is to identify the efficacy and safety of methotrexate (MTX) combined corticosteroid treatment for acute graft-versus-host disease (aGVHD) after allogeneic hematopoietic stem cell transplantation (allo-HSCT).

Detailed description

Allo-HSCT is an effective treatment of malignant hematopoietic diseases. However, aGVHD remains a major complication after allo-HSCT and the destruction of recipient tissues by alloantigen-activated T cells is a key event in the development of aGVHD. Corticosteroid is the standard first-line therapy for aGVHD due to their roles in suppressing T cell responses. However, the response rate of corticosteroid was approximate 50%, and the clinical outcomes of patients with corticosteroid refractory GVHD were poor. Thus far, no combination therapy had been prove to be superior to corticosteroid alone as initial therapy for aGVHD. The study hypothesis: MTX combined corticosteroid treatment could help to further ameliorate the activity of T cells and control aGVHD.

Interventions

DRUGMethotrexate

Methylprednisolone 1 mg/kg/day MTX (10 mg/day) was given on days 1, 3, and 8, and repeated weekly until aGVHD was less than grade II;

Sponsors

Peking University People's Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
16 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

1. Patients who are fully informed and sign informed consent by themselves or their guardians; 2. Patients receiving allogeneic hematopoietic stem cell transplantation; 3. Patients with acute graft-versus-host disease of grade II-IV were diagnosed after transplantation; 4. Patients with stable implantation of granulocytes and platelets.

Exclusion criteria

1. Patients who have received more than one transplant; 2. Patients with overlap syndrome; 3. Patients within six months after the failure of the first transplantation; 4. Patients with uncontrollable active infection; 5. Patients with recurrence of primary malignant hematopathy; 6. Patients with DLI or induced graft-versus-host disease after first intervention; 7. Patients with serious respiratory diseases; 8. Patients with severe renal insufficiency; 9. Patients with serious and uncontrolled heart disease; 10. Patients with severe hepatobiliary diseases unrelated to graft-versus-host disease; 11. Within one week patients who need to use more than 1mg/kg/d methylprednisolone for reasons other than graft-versus-host disease; 12. patients who have participated in other clinical trials within 1 month; 13. The researcher judges that there are other factors that are not suitable for participating

Design outcomes

Primary

MeasureTime frameDescription
Overall response rate (ORR) for GVHD treatment at 7 days after treatment7 daysOverall response rate is defined as the proportion of patients demonstrating a complete response or partial response without requirement for additional systemic therapies for an earlier progression, mixed response or non-response.

Secondary

MeasureTime frameDescription
Non-relapse mortality1 yearNon-relapse mortality
Overall survival1 yearOverall survival
Disease free survival1 yearDisease free survival
Relapse1 yearRelapse
Chronic GVHD1 yearChronic GVHD
Overall response rate (ORR) at 28 days after treatment28 daysOverall response rate is defined as the proportion of patients demonstrating a complete response or partial response without requirement for additional systemic therapies for an earlier progression, mixed response or non-response.
Failure free survival1 yearFailure free survival

Other

MeasureTime frameDescription
Safety data1 yearSafety data

Countries

China

Contacts

Primary ContactXiao-Dong Mo, Dr
mxd453@163.com86-10-88326001

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026