Sitagliptin for Prevention of aGVHD After Alternative Donor Transplantation

Last updated: March 28, 2023
Sponsor: The First Affiliated Hospital of Soochow University
Overall Status: Active - Recruiting

Phase

3

Condition

Allo-hematopoietic Stem Cell Transplant

Allogeneic Hematopoietic Stem Cell Transplant

Treatment

N/A

Clinical Study ID

NCT05149365
SZ-GVHD 06
  • Ages 18-60
  • All Genders

Study Summary

Primary Objective:

It is hypothesized that the efficacy of Sitagliptin would reduce the incidence of grade II-IV acute Graft Versus Host Disease (GVHD) by day +100 post-transplant in patients undergoing alternative donor (related haploid or unrelated donor ) allogeneic Hematopoietic Stem Cell Transplantation (HSCT) and receiving standard GVHD prophylaxis.

Secondary Objectives

The following descriptive secondary objectives will be studied:

  1. Determine the tolerability and potential toxicity of sitagliptin in patients undergoing allogeneic HSCT.

  2. Determine the cumulative incidence of grades II-IV acute GVHD by day +100.

  3. To investigate the cumulative incidence of grades III-IV acute GVHD.

  4. To investigate the engraftment kinetics of absolute neutrophil count and platelets.

  5. To evaluate the incidence of Cytomegalovirus (CMV), Epstein-Barr virus (EBV) and other infections occurring during the 100 days post-transplant.

  6. To study non-relapse mortality (NRM) at day +100, and 1 year post-transplant.

  7. Determine the overall survival at 1 year post-transplant.

  8. Determine the incidence of chronic GVHD.

  9. Determine the cumulative incidence of relapse of the primary hematological malignancy.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Patient age ≥ 18 to ≤ 60 years
  2. Eastern Cooperative Oncology Group (ECOG）score 0-2 points / Karnofsky score ≧80
  3. To receive allogeneic hematopoietic stem cell transplantation from related haploid orunrelated donor
  4. The pretreatment of modified Bu/Cy+ATG scheme was planned.
  5. Patients with malignant hematological diseases indicated by transplantation and incomplete remission (CR) state.
  6. Expected survival ≥ 3 months
  7. Signed written informed consent (Patient must be capable of understanding theinvestigational nature, potential risks and benefits of the study, and able to providevalid informed consent)
  8. Agree to use effective contraception

Exclusion

Exclusion Criteria:

  1. Prior allogeneic hematopoietic stem cell transplant
  2. Allergy/intolerance to Sitagliptin
  3. There are contraindications for Sitagliptin use.
  4. Moderate or severe renal insufficiency
  5. Patients with diabetes mellitus requiring insulin secretagogues and/or insulin
  6. Human immunodeficiency virus or active hepatitis C virus or active hepatitis B virusinfection
  7. Active infection that is difficult to control
  8. Vital organ function cannot tolerate transplantation
  9. Other malignant tumors outside the blood system, except the following diseases:malignant tumors that have been cured for 3 years without active lesions; Adequatetreatment of non-melanoma skin cancer without active foci of malignant amygdala andcarcinoma in situ
  10. There is evidence that may interfere with the study or make patients at risk ofserious complications or medical conditions, including but not limited to seriouscardiovascular diseases (such as New York heart association class III or IV heartdisease over the past six months of myocardial infarction, unstable type of cardiacarrhythmias) or unstable angina and/or severe lung disease (e.g. History of severeobstructive pulmonary disease and symptomatic bronchospasm)
  11. Pregnant or lactating women
  12. Any life-threatening medical condition or organ system dysfunction considered by theinvestigator may endanger the patient's safety by interfering with the absorption ormetabolism of sitagliptin or putting study results at unnecessary risk

Study Design

Total Participants: 190
Study Start date:
December 22, 2021
Estimated Completion Date:
February 29, 2024

Study Description

This is a Prospective, Multi-center, Open-label, Randomized, Controlled clinical trial of Sitagliptin for the prevention and safety of aGVHD after Alternative Donor hematopoietic stem cell transplantation.

190 adult patients with hematologic malignancies receiving haploid or unrelated donor sourced HSCT are planned to be enrolled competitively in this study from 5 clinical centers in China. These patients will be randomly assigned to two groups of 95 patients each, which one is experimental group and the other is control group. 95 patients in experimental group will receive Sitagliptin combined with Standard prophylaxis for GVHD. 95 patients in the control group will receive Standard prophylaxis regimen for GVHD of Alternative Donor HSCT.

Control group uses antithymocyte immunoglobulin (ATG)+cyclosporin A (CSA)+MMF+MTX for GVHD prophylaxis with the details as follows: CSA 3mg/kg continuous i.v. drip, start before Day -7, change to p.o. when gastrointestinal function recovers with a dose of 5mg/kg as two divided doses, maintaining CSA within 150-250ng/ml（If CsA cannot be tolerated, tacrolimus may be used as an alternative.）; MTX 15mg/m2,Day +1, 10mg/m2,Days +3, +6, and +11; MMF 0.5g bid, starting from Day -7 to day +30 for one month; ATG 2.5mg/kg/d, Day -4 to Day -1.

Experimental group will take Sitagliptin orally from d-1 to d+14 in addition to Standard Prophylaxis Regimen.

With regard to the content of dose reduction of CSA (including time and reduction rate), it is recommended for patients with hematologic malignancies in standard risk group to start to reduce dose after 3-6 months in the absence of GVHD and reoccurrence. The specific reduction rate can be determined at each site; the patients with GVHD will be managed by routine practice in this site.

Connect with a study center

  • The First Affiliated Hospital of Soochow University, Jiangsu Institute of Hematology

    Suzhou, Jiangsu 215000
    China

    Active - Recruiting

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