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NCT Number: NCT05921305

Mini-dose MTX Plus Standard-dose Steroid for the Initial Treatment of Acute GVHD

This trial is a randomized (1:1) phase III open label study of frontline mini-MTX plus methylprednisolone 2mg/kg/day compared to methylprednisolone 2mg/kg in allogeneic stem cell transplant recipients with grade 2-4 aGVHD.

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Key information

Age range

15 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Peking University Institute of Hematology,, Beijing, Beijing Municipality, China

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About this study

Allo-HSCT is an effective treatment of malignant hematopoietic diseases. However, aGVHD remains a major complication after allo-HSCT. Corticosteroid is the standard first-line therapy for aGVHD. 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 control aGVHD.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients who are fully informed and sign informed consent by themselves or their guardians;
  • Patients receiving first allogeneic hematopoietic stem cell transplantation;
  • Patients with acute graft-versus-host disease of grade II-IV were diagnosed after transplantation;
  • KPS>60, Estimated survival >3 months;
  • No serious organ damage:
  • ANC in peripheral blood is greater than 0.5×109/l
  • Creatinine < 1.5mg/dl
  • Cardiac ejection index > 55%

Exclusion criteria

  • Patients with severe brain, heart, kidney or liver dysfunction unrelated to graft-versus host disease;
  • Patients with uncontrollable active infection;
  • Patients with recurrence of primary malignant hematopathy;
  • Expected survival is less than 3 months
  • Patients who have histories of severe allergic reactions
  • Pregnant or lactating women
  • The researcher judges that there are other factors that are not suitable for participating
  • Patients who received donor lymphocyte infusion

Treatment and study plan

MTX

Drug

MTX (5mg/m^2/day) was given on days 1, 3, and 8, and repeated weekly until aGVHD was CR

Corticosteroid

Drug

Corticosteroid Methylprednisolone 2 mg/kg/day was given for 3 days, and for responding patients, the dose of prednisone must be at least 0.25mg/kg/day prednisone (or 0.2mg/kg/day methylprednisolone).

Primary outcomes

  1. Overall response rate (ORR) for aGVHD treatment after treatment

    Time frame: 14 days

    Overall 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 outcomes

  1. Overall response rate (ORR) for aGVHD treatment at 28 days after treatment

    Time frame: 28 days

    Overall 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

  2. Overall response rate (ORR) for aGVHD treatment at 42 days after treatment

    Time frame: 42 days

    Overall 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

  3. Number of participants with treatment-related adverse events as assessed by CTCAE v4.0

    Time frame: 42 days

    Data collection including questionnaires at individual and group visits and physician interviews at individual visits will be used to assess participants for treatment-related adverse events.

  4. cGVHD

    Time frame: 1 years

    The cumulative incidence of chronic GVHD

  5. Infection and poor graft function

    Time frame: 1 year

    The cumulative incidence of severe infection and poor graft function

  6. Relapse

    Time frame: 1 year

    The cumulative incidence of relapse

  7. Non-relapse mortality

    Time frame: 1 year

    The cumulative incidence of non-relapse mortality

  8. Overall survival

    Time frame: 1 year

    The cumulative incidence of overall survival

  9. Disease free survival

    Time frame: 1 year

    The cumulative incidence of disease free survival

Study contacts

Contact information is provided by the study sponsor or research team.

Xiao-Jun Huang, M.D.

CONTACT

Yu Wang, M.D.

CONTACT

[email protected]

86-13552647384

Sponsors and collaborators

Lead sponsor

Peking University People's Hospital

Other

Registry information

Official study title

Randomized Trial of Mini-dose Methotrexate Plus Standard-dose Steroid vs Steroids for the Initial Treatment of Acute Graft Versus Host Disease

Important dates

Study start
2023
Primary completion
2026
Study completion
2026
First posted
Jun 27, 2023
Registry last updated
Jun 3, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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