TY - JOUR
T1 - Impact of CD56 continuously recognizable as prognostic value of acute promyelocytic leukemia
T2 - Results of multivariate analyses in the Japan adult leukemia study group (JALSG)-APL204 study and a review of the literature
AU - The Japan Adult Leukemia Study Group
AU - Takeshita, Akihiro
AU - Asou, Norio
AU - Atsuta, Yoshiko
AU - Furumaki, Hiroaki
AU - Sakura, Toru
AU - Ueda, Yasunori
AU - Sawa, Masashi
AU - Dobashi, Nobuaki
AU - Taniguchi, Yasuhiro
AU - Suzuki, Rikio
AU - Nakagawa, Masaru
AU - Tamaki, Shigehisa
AU - Hagihara, Maki
AU - Fujimaki, Katsumichi
AU - Minamiguchi, Hitoshi
AU - Fujita, Hiroyuki
AU - Yanada, Masamitsu
AU - Maeda, Yoshinobu
AU - Usui, Noriko
AU - Kobayashi, Yukio
AU - Kiyoi, Hitoshi
AU - Ohtake, Shigeki
AU - Matsumura, Itaru
AU - Naoe, Tomoki
AU - Miyazaki, Yasushi
N1 - Publisher Copyright:
© 2020 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2020/6
Y1 - 2020/6
N2 - 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.
AB - 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.
KW - Acute promyelocytic leukemia
KW - CD56
KW - Multivariate analysis
KW - Prognosis
KW - Tamibarotene
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U2 - 10.3390/cancers12061444
DO - 10.3390/cancers12061444
M3 - Article
AN - SCOPUS:85086006792
SN - 2072-6694
VL - 12
JO - Cancers
JF - Cancers
IS - 6
M1 - 1444
ER -