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In children with Ph+ ALL, TKI-based therapy reduced HSCT use while maintaining comparable outcomes versus Ph+ALL04.

In children with Ph+ ALL, TKI-based therapy reduced HSCT use while maintaining comparable outcomes v…
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Key Takeaway
Consider that TKI-based therapy may reduce HSCT use in Ph+ ALL while maintaining comparable 3-year outcomes.

This single-arm Phase 2 trial enrolled 43 patients, with 41 eligible, who had Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ ALL) aged 1 to 19 years. The intervention involved chemotherapy with tyrosine kinase inhibitors (TKIs) guided by minimal residual disease (MRD). The comparator was the Ph+ALL04 regimen, which utilized allogeneic hematopoietic stem cell transplantation (HSCT) in first complete remission. The primary outcome was the 3-year event-free survival (EFS) rate, with secondary outcomes including 3-year and 5-year overall survival (OS) rates. Follow-up averaged 48.0 months.

At 3 years, the 3-year EFS rate was 65% (95% CI: 48%-78%), and the 3-year OS rate was 85% (95% CI: 70%-93%). By 5 years, EFS decreased to 48% (95% CI: 30%-64%), while OS remained at 85% (95% CI: 70%-93%). These results indicate that HSCT was substantially reduced in this cohort while maintaining outcomes comparable to the historical Ph+ALL04 control.

Safety data reported nonhematological adverse events leading to temporary discontinuations. Four sepsis-related deaths occurred during the study. Tolerability was managed through resumption at 80% of the original dose for some patients. Several relapses occurred beyond the 3-year follow-up period.

Key limitations include the single-arm design and the occurrence of late relapses. Further optimization of treatment, particularly the duration of TKI administration, is needed to maintain long-term EFS. The study was conducted in a multicenter setting, though funding or conflicts of interest were not reported.

Study Details

Study typePhase2
EvidenceLevel 3
Follow-up48.0 mo
PublishedApr 2026
View Original Abstract ↓
BACKGROUND: Patients with Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph ALL) have a poor prognosis. In Ph+ALL04, allogeneic hematopoietic stem cell transplantation (HSCT) in first complete remission (CR) was indicated for all patients, and was performed in those who remained in CR at the scheduled time of transplantation, with 4-year event-free survival (EFS) and overall survival (OS) rates of 54% (95% confidence interval [CI]: 38%-68%) and 78% (95% CI: 62%-88%), respectively. PROCEDURE: The Japan Children's Cancer Group conducted ALL-Ph13, a multicenter single-arm Phase 2 clinical trial, to improve outcomes and reduce HSCTs by using chemotherapy with tyrosine kinase inhibitors (TKIs) guided by minimal residual disease (MRD). The primary endpoint was the 3-year EFS rate. RESULTS: Between 2013 and 2017, 41 of 43 enrolled patients with Ph ALL aged 1-19 years were eligible. Imatinib was started on Day 15 of induction and switched to dasatinib if MRD-positive after consolidation IB. TKIs were administered until the end of maintenance treatment (Week 104), with temporary discontinuation due to the severity of nonhematological adverse events and resumption at 80% of the original dose. When MRD was positive after the three HR blocks, HSCT was performed. Following four sepsis-related deaths, the protocol was amended in 2016, after which no such deaths occurred. Six patients (15%) underwent HSCT in the first CR, one per protocol indication and five without. The 3-year EFS and OS rates were 65% (95% CI: 48%-78%) and 85% (95% CI: 70%-93%), respectively. As several relapses occurred beyond 3 years, the 5-year EFS and OS rates were also calculated: 48% (95% CI: 30%-64%) and 85% (95% CI: 70%-93%), respectively. CONCLUSIONS: Compared with Ph+ALL04, HSCT was substantially reduced in ALL-Ph13 while maintaining comparable outcomes. Further optimization of treatment, particularly the duration of TKI administration, is needed to maintain long-term EFS.
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