Selinexor Combined With Induction Chemotherapy for Children With NUP98-positive AML
- Sponsor
- The Children's Hospital of Zhejiang University School of Medicine
- Study ID
- NCT07437170
- Phase
- PHASE2
- Status
- Active Not Recruiting
Conditions
- Acute Myeloid Leukemia
- NUP98 Fusion-positive Acute Myeloid Leukemia
- Pediatric Acute Myeloid Leukemia
Eligibility Criteria
- Sex
- ALL
- Age
- 1 Year - 18 Years
- Healthy Volunteers
- Not accepted
Interventions
- Selinexor — DRUGInduction Course 1: 40mg/m² orally on Days 1, 3, 8, and 10. Induction Course 2: 40mg/m² orally on Days 1 and 3.
- ZJCH-AML Standardized Chemotherapy — DRUGCourse 1 (HAG): Homoharringtonine (HHT) 2mg/m²/d, Cytarabine (Ara-C) 10mg/m² q12h, and G-CSF 200μg/m²/d for 14 days. Course 2 (Risk-stratified): Based on the response to Course 1, patients receive HDA (for CR), DAC+HDA (for PR), or CLAG (for NR).
Study Details
This is a prospective, single-arm, open-label clinical study to evaluate the efficacy and safety of Selinexor combined with a standardized induction chemotherapy regimen (ZJCH-AML) for children with NUP98-fusion positive Acute Myeloid Leukemia (AML). NUP98-fusion positive AML is a high-risk subtype in pediatric patients, characterized by poor prognosis and high relapse rates under traditional chemotherapy. Preliminary research suggests that Selinexor, an XPO1 inhibitor, can selectively inhibit NUP98-driven leukemia cells. This study aims to determine if adding Selinexor to standardized chemotherapy can increase the complete remission rate and improve the overall survival for these specific high-risk patients.
Key Dates
- Start date
- Jan 1, 2024
- Status verified
- Feb 2026
- Primary completion
- Dec 31, 2027
- Completion
- Dec 31, 2027
Study Design
- Enrollment
- 10 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Selinexor + ZJCH-AMLAll enrolled patients receive Selinexor combined with the Zhejiang Children's Hospital (ZJCH) AML induction chemotherapy protocol.
Primary Outcome Measure
Complete Remission (CR) Rate [ Time Frame: Day 14 of Induction Course 2 (approximately 2 months). ]
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