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Multicenter prospective observational study on minimal residual disease of ALL after allogeneic transplantation using circulating cell-free tumor DNA KSGCT1901(ctALL)

Multicenter prospective observational study on minimal residual disease of ALL after allogeneic transplantation using circulating cell-free tumor DNA KSGCT1901(ctALL) - Prospective study on MRD of ALL after transplant using ctDNA, KSGCT1901(ctALL)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000039899
Enrollment
55
Registered
2020-03-23
Start date
2020-07-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Acute lymphocytic leukemia

Interventions

None listed

Sponsors

Kanto Study Group for Cell Therapy
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Patients age >= 16 years 2) Precursor Lymphoid neoplasms, Chronic myeloid leukeamia, BCR-ABL1-positive in blastic phase (not including myeloid crisis), and mixed-phenotype acute leukeamia with t(9;22) 3) No limit on the disease stage or chemosensitivity at the time of transplant 4) Patients in which a high-quality sample with a tumor volume of 20% or more (at the time of initial diagnosis or relapse) is available. 5) Patients who may undergo allogeneic transplantation at the time of registration. 6)Patients who were informed and concented

Exclusion criteria

Exclusion criteria: Patients who are otherwise classified as unfit by the attending physicians for this research.

Design outcomes

Primary

MeasureTime frame
One-year cumulative incidence of ALL relapse

Secondary

MeasureTime frame
One-year overall survival, Somatic gene mutation, gene expression and immune cell profile at initial diagnosis and relapse

Countries

Japan

Contacts

Public ContactHiroto Ishii

Jikei University School of Medicine Division of Clinical Oncology and Hematology

ksgctdc@ksgct.net03-3433-1111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026