Preserved High Probability of Overall Survival with Significant Reduction of Chemotherapy for Myeloid Leukemia in Down Syndrome: A Nationwide Prospective Study in Japan

  • Takashi Taga
  • , Tomoyuki Watanabe
  • , Daisuke Tomizawa
  • , Kazuko Kudo
  • , Kiminori Terui
  • , Hiroshi Moritake
  • , Akitoshi Kinoshita
  • , Shotaro Iwamoto
  • , Hideki Nakayama
  • , Hiroyuki Takahashi
  • , Akira Shimada
  • , Tomohiko Taki
  • , Tsutomu Toki
  • , Etsuro Ito
  • , Hiroaki Goto
  • , Katsuyoshi Koh
  • , Akiko M. Saito
  • , Keizo Horibe
  • , Tatsutoshi Nakahata
  • , Akio Tawa
  • Souichi Adachi

Research output: Contribution to journalArticlepeer-review

Abstract

Background: On the basis of results of previous Japanese trials for myeloid leukemia in Down syndrome (ML-DS), the efficacy of risk-oriented therapy was evaluated in the Japanese Pediatric Leukemia/Lymphoma Study Group AML-D05 study. Procedure: All patients received induction chemotherapy that consisted of pirarubicin, intermediate-dose cytarabine, and etoposide. Patients who achieved complete remission (CR) after initial induction therapy were stratified to the standard risk (SR) group and received four courses of reduced-dose intensification therapy. Patients who did not achieve CR were stratified to the high risk (HR) group and received intensified therapy that consisted of continuous or high-dose cytarabine. Results: A total of 72 patients were eligible and evaluated. One patient died of sepsis during initial induction therapy. Sixty-nine patients were stratified to SR and two patients to HR. No therapy-related deaths were observed during intensification therapy. The 3-year event-free and overall survival rates were 83.3% ± 4.4% and 87.5% ± 3.9 %, respectively. Age at diagnosis less than 2 years was a significant favorable prognostic factor for risk of relapse (P = 0.009). Conclusions: The attempt of risk-oriented prospective study for ML-DS was unsuccessful, but despite the dose reduction of chemotherapeutic agents, the overall outcome was good, and further dose reduction might be possible for specific subgroups.

Original languageEnglish
Pages (from-to)248-254
Number of pages7
JournalPediatric Blood and Cancer
Volume63
Issue number2
DOIs
Publication statusPublished - 01-02-2016
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • Pediatrics, Perinatology, and Child Health
  • Hematology
  • Oncology

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