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A prospective clinical control study on the treatment of molecular biological recurrence after transplantation of myeloid tumor by donor lymphocyte infusion combined with desetabine or azacytidine

A prospective clinical control study on the treatment of molecular biological recurrence after transplantation of myeloid tumor by donor lymphocyte infusion combined with desetabine or azacytidine

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000031733
Enrollment
Unknown
Registered
2020-04-08
Start date
2020-04-01
Completion date
Unknown
Last updated
2020-04-13

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

Conditions

hematologic disease

Interventions

Group 1 vs Group 2:donor lymphocyte infusion combined with desetabine or azacytidine

Sponsors

Institute of Hematology and Blood Diseases Hospital, CAMS & PUMC
Lead Sponsor

Eligibility

Sex/Gender
All
Age
14 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Age: 14-70 years old (including 14, 70 years old), gender unlimited; 2. Myeloid tumor patients who have undergone allogeneic hematopoietic stem cell transplantation (allo HSCT), including but not limited to acute myeloid leukemia (AML), myelodysplastic syndrome (MDS), chronic myelomonocytic leukemia (CMML), etc; 3. Patients diagnosed as relapse of molecular biology after transplantation within 1 month should be reexamined within 2 weeks; 4. Patients who voluntarily participate in the trial and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with ECoG physical condition score >= 3; 2. Patients whose estimated survival time is less than 3 months; 3. Patients with hematological recurrence after transplantation; 4. Patients who are in the process of 3-4 degrees of severe GVHD without DLI; 5. Patients who are known to be allergic to azacytidine or dicithabine; 6. Patients who may not be able to complete the study due to other reasons or who are considered unsuitable by the investigator.

Design outcomes

Primary

MeasureTime frame
Response rate to treatment;Treatment-emergent adverse events;median OS;

Secondary

MeasureTime frame
quantification of immunoglobulin;lymphocyte subpopulations;whole transcriptomeanalysis of lymphocytes;

Countries

China

Contacts

Public ContactYang Donglin

Institute of Hematology and Blood Diseases Hospital, CAMS & PUMC

yangdonglin@ihcams.ac.cn+86 13902087176

Outcome results

None listed

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