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Study on the efficacy and safety of flumatinib versus dasatinib for maintenance therapy after allogeneic hematopoietic stem cell transplantation in adult Ph+ acute lymphoblastic leukemia

Study on the efficacy and safety of flumatinib versus dasatinib for maintenance therapy after allogeneic hematopoietic stem cell transplantation in adult Ph+ acute lymphoblastic leukemia

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100046563
Enrollment
Unknown
Registered
2021-05-22
Start date
2021-06-01
Completion date
Unknown
Last updated
2023-01-09

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

Conditions

Ph+ acute lymphoblastic leukemia

Interventions

Group 1:Flumatinib maintenance treatment
Group 2:Dasatinib maintenance therapy

Sponsors

University of Electronic Science and Technology Affiliated Hospital·Sichuan Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Ph+ acute lymphoblastic leukemia patients receiving allogeneic hematopoietic stem cell transplantation in our department from June 2021 to June 2023; 2. Aged 14 to 60 years, no gender limit; 3. ECOG score 0-3 points; 4. The patient must be able to understand and be willing to participate in this study, and sign an informed consent form at the same time.

Exclusion criteria

Exclusion criteria: 1. Women who are pregnant, preparing to become pregnant or breast-feeding; 2. Patients secondary to myelodysplastic syndrome (MDS), chronic myeloproliferative disease (MPN) and lymphatic system proliferative disease; 3. Patients with severe liver, kidney and other important organ dysfunctions or diseases that affect the prognosis of treatment; 4. Combine other diseases that cannot be controlled and may restrict patients from participating in this trial. 5. The investigator believes that it is not suitable to join, and any situation that the investigator believes may increase the risk of the subject or interfere with the test results.

Design outcomes

Primary

MeasureTime frame
Recurrence-free survival;Residual disease;Cumulative recurrence rate;Proportion of interrupted treatment due to adverse reactions;

Secondary

MeasureTime frame
Overall survival rate;Recurrence-free survival of graft-versus-host disease;

Countries

China

Contacts

Public ContactYang Xi

University of Electronic Science and Technology Affiliated Hospital·Sichuan Provincial People's Hospital

yangxi2017@aliyun.com+86 15390030986

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026