Outcomes of children with T-cell acute lymphoblastic leukemia treated with the JACLS T-02 protocol

Hisashi Ishida1, Souichi Suenobu2, Toshihiko Imamura3

  • 1Department of Pediatrics, Okayama University Hospital, Okayama, Japan.

PubMed

Insights

Intensive chemotherapy for T-cell acute lymphoblastic leukemia (T-ALL) improved outcomes. The T-02 protocol showed a 70.9% event-free survival, but female patients with rapid response may benefit from tailored therapy.

Area of Science:

  • Pediatric Oncology
  • Hematology
  • Clinical Trials

Background:

  • T-cell acute lymphoblastic leukemia (T-ALL) historically had poorer outcomes than B-cell ALL.
  • Intensive chemotherapy regimens have narrowed the outcome gap between T-ALL and B-cell ALL.
  • The Japan Association of Childhood Leukemia Study (JACLS) ALL-02 study investigated a specific T-ALL protocol (T-02).

Purpose of the Study:

  • To evaluate the efficacy and safety of the T-02 protocol for T-ALL patients.
  • To determine the 2-year event-free survival (EFS) as the primary outcome.
  • To identify prognostic factors influencing T-ALL patient outcomes.

Main Methods:

  • Prospective study (ALL-02) involving 107 T-ALL patients from 2002-2008.
  • All patients received uniform induction therapy; those with <25% bone marrow blasts at day 15 proceeded with the T-02 protocol.
  • Event-free survival (EFS) and cumulative incidence of relapse were analyzed.

Main Results:

  • 98% of enrolled T-ALL patients achieved complete remission (CR) after induction.
  • Among 79 patients on the T-02 protocol, the 2-year EFS was 70.9%.
  • A cumulative incidence of relapse was 29.1%, with no nonrelapse mortality observed. Female sex was a significant predictor of better EFS.

Conclusions:

  • The T-02 protocol demonstrated acceptable outcomes for T-ALL, but excessive treatment reduction might negatively impact results.
  • Female patients with a rapid early response to therapy may tolerate less intensive treatment.
  • Further investigation in larger studies is warranted to explore tailored therapeutic approaches for specific T-ALL patient subgroups.