Toru Sakura

Toru Sakura


Research Focus & Metrics

Academic Career Length

8Years (2019-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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31 August 2019 in International Journal of Hematology
Verified
Journal Article
Closed access
PDF file
TTTakeshi Takahashi
Takeshi Takahashi
KUKensuke Usuki
Kensuke Usuki
KMKosei Matsue
Kosei Matsue
HOHitoshi Ohno
Hitoshi Ohno
TSToru Sakura
Toru Sakura
SSSakura Sakajiri
Sakura Sakajiri

1 June 2020 in Cancers
Verified
Journal Article
Open access
PDF file
ATAkihiro Takeshita
Akihiro Takeshita
NANorio Asou
Norio Asou
YAYoshiko Atsuta
Yoshiko Atsuta
HFHiroaki Furumaki
Hiroaki Furumaki
TSToru Sakura
Toru Sakura
TGthe Japan Adult Leukemia Study Group
the Japan Adult Leukemia Study Group
Background: After long-term analysis of the JALSG-APL204 study we recently reported that maintenance therapy with tamibarotene was more effective than all-trans retinoic acid (ATRA) by reducing relapse in APL patients. Here, the clinical significance of other important prognostic factors was evaluated with multivariate analyses. Patients and Methods: Newly diagnosed acute promyelocytic leukemia (APL) patients were registered with the study. Induction was composed of ATRA and chemotherapy. Patients who achieved molecular remission after consolidation were randomly assigned to maintenance with tamibarotene or ATRA. Results: Of the 344 eligible patients, 319 (93%) achieved complete remission (CR). After completing consolidation, 269 patients underwent maintenance random assignment—135 to ATRA, and 134 to tamibarotene. By multivariate analysis, overexpression of CD56 in blast was an independent unfavorable prognostic factor for relapse-free survival (RFS) (p = 0.006) together with more than 10.0 × 109/L WBC counts (p = 0.001) and the ATRA arm in maintenance (p = 0.028). Of all phenotypes, CD56 was related most clearly to an unfavorable prognosis. The CR rate, mortality rate during induction and overall survival of CD56+ APL were not significantly different compared with CD56− APL. CD56 is continuously an independent unfavorable prognostic factor for RFS in APL patients treated with ATRA and chemotherapy followed by ATRA or tamibarotene maintenance therapy.