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Dasatinib for Treatment of de novo Ph-Positive Acute Lymphoblastic Leukemia

Dasatinib Combined with Reduced-Intensive Chemotherapy and IFN-a for Ph-Positive Acute Lymphoblastic Leukemia

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800015763
Enrollment
Unknown
Registered
2018-04-19
Start date
2016-01-01
Completion date
Unknown
Last updated
2018-04-30

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

Conditions

Ph-positive acute lymphoblastic leukemia

Interventions

Case series:dasatinib

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 70 years old male and female; 2. Confirmed Ph positive acute lymphoblastic leukemia (see WHO Hematopoietic and Lymphatic Tumor Pathology and Genetics) requiring positive BCR/ABL fusion gene and / or Ph1 chromosome t(9; 22) (q34; q11) ; 3. Hepatitis B surface antigen negative, HBsAg positive patients need HBV-DNA <1×10^3 copy/ml; 4. Liver function: ALT < 2 times the upper limit of normal, AST < 2 times the upper limit of normal; 5. normal renal function; 6. Hepatitis B virus surface antigen is negative, positive surface antigen or HBV-DNA replication are active, need antiviral therapy.

Exclusion criteria

Exclusion criteria: 1. ECOG score> 2; 2. Previous history of drugs (dasatinib, dasatinib, and nilotinib) targeting at BCR/ABL fusion genes; 3. Serious heart, lung, kidney disease, or the any other life threatening condition; 4. Active gastrointestinal bleeding; 5. Lymphoblastic crisis of chronic myelogenous leukemia;; 6. Other coexisting malignancies other than cured cervical cancer; 7. Pregnant or breastfeeding patients.

Design outcomes

Primary

MeasureTime frame
completer remission rate;overall survival;relaspe free survival;

Secondary

MeasureTime frame
treament related mortality;

Countries

China

Contacts

Public ContactTing Liu

Department of Hematology, West China Hospital, Sichuan University

liuting@scu.edu.cn+86 18980601240

Outcome results

None listed

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