drugset / Trial / NCT02487563

Summary

Isolated thrombocytopenia is a common and severe complication of HSCT, which often leads to an increased risk of life-threatening hemorrhage, frequent requirement of platelet transfusions and extended hospital stays, representing a challenging clinical problem. Current treatments for thrombocytopenia after HSCT are frequently unsatisfactory in platelet recovery and for preventing potentially fatal bleeding complications. Therefore, it is urgent to explore an effective therapy to improve the outcomes of thrombocytopenia after HSCT. Previous studies have demonstrated that decitabine, a hypomethylating agent, may reduce platelet transfusions in myelodysplastic syndrome (MDS) patients. The investigators conducted an prospective clinical trial to evaluate the safety and efficiency of rhTPO and decitabine in the treatment of thrombocytopenia following HSCT.

Timeline

Start
2015-10
Primary completion
2019-04-12
Completion
2019-04-12

Outcome

Met primary endpoint

paper Among the 91 evaluable patients, response rates were 66.7%, 73.3%, and 19.4% for the 3 arms, respectively (P < .001). PMID 33646303 ↗

paper This study showed low-dose decitabine improved platelet recovery as well as overall survival in RPIT patients after transplantation. PMID 33646303 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Decitabine Small molecule 15 mg/m2 Intravenous
Subject rhTPO Protein / enzyme biologic 300 iu/kg —

Indications