Skip to content

Imatinib combined with oncovin and dexamethasone for Ph1 positive ALL, and comparison of two treatment methods after first remission

Imatinib combined with oncovin and dexamethasone for Ph1 positive ALL, and comparison of two treatment methods after first remission

Status
Active, not recruiting
Phases
Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-TNRC-09000309
Enrollment
Unknown
Registered
2009-01-01
Start date
2008-08-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Newly diagnosed adult with Ph1 positive acute lymphoblastic leukemia

Interventions

Phase 1 Induction:Induction Therapy: all patients recieve the same induction therapy with Imatinib,vindesine and dexamethasone
Phase 2: Intensify Chemotherapy :Patients achieve CR, will recieve 3 courses of intensified chemotherapy
Phase 3 Allo-SCT Group :Patient as a candidate for Allo stem cell transplantation will receive transplantation as soon as he/she complete intensify chemotherapy. Otherwise, chemotherapy as maintenanc
Phase 3 Maintenance Group :Maintenance Therapy: imatinib plus oncovin and dexamethasone, and intrathecal prevention of CNS leukemia.Maintennance therapy will continue for 2 years.

Sponsors

Department of Hematology of West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Newly diagnosed acute lymphoblastic leukemia with positive BCR/ABL fusion gene or positive Ph1 chromosome; 2. HBV surface antigen negative, or HBV-DNA<1*10^3 copy/ml for the HBsAg positive patients; 3. Total bilirubin <2 times of upper limit, ALT <3 times of upper limit, AST <3 times of upper limit.

Exclusion criteria

Exclusion criteria: 1. ECOG>2; 2. previous history of small molecular target drug for BCR/ABL gene(e.g. Imatinib, Dasatinib etc); 3. previous history of allo stem cell transplantation; 4. severe underlying disease of vital organs(e.g. heart, lung, liver, kidney, pancrea); 5. active GI or Urinary Hemorrhage; 6. previous history of chronic myelogenous leukemia; 7. complicated other malignancies, not including cured cervix cancer; 8. woman with pregnancy or lactation.

Design outcomes

Primary

MeasureTime frame
disease free survival;overall survival;CR rate;

Countries

China

Contacts

Public ContactTing Liu
liuting@scu.edu.cn+86 028 85422364

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 25, 2026