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MSC for Treatment of cGVHD After Allo-HSCT

NCT04692376 — Phase 2, Unknown, 152 participants, Nanfang Hospital, Southern Medical University

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Mesenchymal Stem Cell for Treatment of Chronic Graft-versus-host Disease After Allogenetic Hematopoietic Stem Cell Transplantation

RegistryNCT04692376
StatusUnknown
PhasePhase 2
Study typeInterventional; randomized, parallel, masking: none, treatment
Enrollment152 (Estimated)
SponsorNanfang Hospital, Southern Medical University (Other); collaborators: Sun Yat-sen University, Army Medical University, China, Peking University People's Hospital
ConditionsChronic Graft-versus-host Disease
InterventionsMesenchymal stem cells, Glucocorticoids, cyclosporine (Biological, drug)
Datesstart 2021-01-10 (estimated), primary completion 2022-12-31 (estimated), completion 2023-06-30 (estimated), first posted 2020-12-31, last updated 2020-12-31
Locations1 site in China

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-Summary

The purpose of this study is to evaluate the efficacy of mesenchymal stem cells in patients with chronic graft-versus-host disease.

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+Detailed description

Allogeneic hematopoietic stem cell transplantation(allo-HSCT) can cure many hematologic diseases. Although great progress has been made in the prevention and treatment of side effects associated with transplantation,chronic graft-versus-host disease(cGVHD) remains an important complication that occurs in about 50% patients. The mortality of cGVHD and its complication could reach up to 50%,and cGVHD seriously influence the quality of life. At present, the first line treatment of cGVHD remains in discussion.

Mesenchymal stem cells (MSCs) are a form of multipotent adult stem cells that can be isolated from bone marrow (BM), adipose tissue, and cord blood. Clinical applications of human MSCs are evolving rapidly with goals of improving hematopoietic engraftment, preventing and treating GVHD after allo-HSCT and so on. However, the efficacy of treatment of cGVHD remains undetermined.

In the present study, the investigators will prospectively evaluate the efficacy and safety of ex-vivo-expanded MSCs in treating patients with cGVHD.

+Arms and interventions

ArmTypeInterventionsDescription
MSCs groupExperimentalBiological: Mesenchymal stem cells; Drug: Glucocorticoids; Drug: cyclosporineMSCs group refers to treatment with mesenchymal stem cells (1×10\^6 cells/kg, intravenously) weekly for 8 doses. Besides, glucocorticoids and cyclosporine (CsA) will be used for treatment concurrently.
Control groupActive comparatorDrug: Glucocorticoids; Drug: cyclosporineGlucocorticoids and CsA will be used for treatment.
  • Mesenchymal stem cells (Biological): Mesenchymal stem cells (MSCs) will be intravenously infused via a central venous catheter(at a dose of 1×10\^6 cells/kg, over 15 mins) weekly. MSCs will be administrated for 8 doses.
  • Glucocorticoids (Drug): Glucocorticoids (i.e. Methylprednisolone) will be used with an initial dose of 1mg/kg.
  • cyclosporine (Drug): Cyclosporine (CsA) will be used with an initial dose of 2.5mg/kg/d and adjusted according to the concentration of CsA. The targeted concentration is 200-300 ng/Ml.

+Outcome measures

Primary outcomes

  • ORR [12 weeks after the first dose of MSCs]: Overall response rate (ORR)includes complete response (CR) and part response (PR).

Secondary outcomes

  • OS [1 year after the first dose of MSCs]: Overall survival (OS)
  • DFS [1 year after the first dose of MSCs]: Disease-free survival (DFS)
  • Response rate [4 weeks after the first dose of MSCs]
  • EBV DNA-emia [1 year after the first dose of MSCs]: EBV DNA-emia refers to detection of EBV DNA in peripheral blood via PCR.
  • CMV DNA-emia [1 year after the first dose of MSCs]: CMV DNA-emia refers to detection of CMV DNA in peripheral blood via PCR.
  • PGF [1 year after the first dose of MSCs]: Poor graft function (PGF) refers to a slow or incomplete recovery of blood cell counts (ANC ≤0.5x10\^9/L and PLT ≤20x10\^9/L) by +28 days after allo-HSCT or a fall in blood cell counts to levels fulfilling the diagnostic criteria for PGF after successful and prompt hematopoietic engraftment.

+Eligibility

Sex: All, ages: 18 Years to 65 Years

Inclusion Criteria:

* A patient age of 18-65 years
* Recipients of allogeneic hematopoietic stem cell transplantation Patients with moderate/ severe cGVHD without systemic treatment
* Subjects (or their legally acceptable representatives) must have signed an informed consent document indicating that they understand the purpose of and procedures required for the study and are willing to participate in the study

Exclusion Criteria:

* Any abnormality in a vital sign (e.g., heart rate, respiratory rate, or blood pressure)
* Primary disease relapse
* Expected lifetime less than 3 months
* Patients with any conditions not suitable for the trial (investigators' decision)

+Locations (1)

FacilityCityCountryStatus
Department of Hematology,Nanfang Hospital, Southern Medical UniversityGuangzhou, GuangdongChinaRecruiting

+Investigators

  • Qi-fa Liu, MD, Principal investigator, Nanfang Hospital, Southern Medical University

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