Newly-diagnosed Pediatric T-cell ALL Protocol

Trial statusRecruiting
Trial phasePhase 2, Phase 3
Trial typeInterventional
Biological sexAll
Age1-18
SponsorInstitute of Hematology & Blood Diseases Hospital, China

About this trial

This is a prospective, multicenter study conducted within the Chinese Children's Cancer Group (CCCG). The study aims to evaluate whether the addition of three novel agents, dasatinib, venetoclax and homoharringtonine, can improve the minimal residual disease (MRD)-negative remission rate, enhance event-free survival (EFS), and reduce the cumulative incidence of relapse (CIR) in pediatric patients with newly diagnosed T-cell acute lymphoblastic leukemia (T-ALL).

Eligibility criteria

Qualifiers

Age older than 1 month to younger than 18 years.

Diagnosis of acute lymphoblastic leukemia by bone marrow morphology.

Diagnosis of T-ALL by immunophenotyping.

Disqualifiers

B-ALL

AML

Acute leukemias of ambiguous lineage diagnosed according to WHO or EGIL criteria.

ALL evolved from chronic myeloid leukemia (CML).

Trial design

Treatments tested in this trial

  • Venetoclax
  • Dasatinib
  • homoharringtonine

Treatment groups

610 Participants
are divided into 3 treatment groups