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Impact of CD56 Continuously Recognizable as Prognostic Value of Acute Promyelocytic Leukemia: Results of Multivariate Analyses in the Japan Adult Leukemia Study Group (JALSG)-APL204 Study and a Review of the Literature

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 evaluat...

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Autores principales: Takeshita, Akihiro, Asou, Norio, Atsuta, Yoshiko, Furumaki, Hiroaki, Sakura, Toru, Ueda, Yasunori, Sawa, Masashi, Dobashi, Nobuaki, Taniguchi, Yasuhiro, Suzuki, Rikio, Nakagawa, Masaru, Tamaki, Shigehisa, Hagihara, Maki, Fujimaki, Katsumichi, Minamiguchi, Hitoshi, Fujita, Hiroyuki, Yanada, Masamitsu, Maeda, Yoshinobu, Usui, Noriko, Kobayashi, Yukio, Kiyoi, Hitoshi, Ohtake, Shigeki, Matsumura, Itaru, Naoe, Tomoki, Miyazaki, Yasushi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7352829/
https://www.ncbi.nlm.nih.gov/pubmed/32492981
http://dx.doi.org/10.3390/cancers12061444
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author Takeshita, Akihiro
Asou, Norio
Atsuta, Yoshiko
Furumaki, Hiroaki
Sakura, Toru
Ueda, Yasunori
Sawa, Masashi
Dobashi, Nobuaki
Taniguchi, Yasuhiro
Suzuki, Rikio
Nakagawa, Masaru
Tamaki, Shigehisa
Hagihara, Maki
Fujimaki, Katsumichi
Minamiguchi, Hitoshi
Fujita, Hiroyuki
Yanada, Masamitsu
Maeda, Yoshinobu
Usui, Noriko
Kobayashi, Yukio
Kiyoi, Hitoshi
Ohtake, Shigeki
Matsumura, Itaru
Naoe, Tomoki
Miyazaki, Yasushi
author_facet Takeshita, Akihiro
Asou, Norio
Atsuta, Yoshiko
Furumaki, Hiroaki
Sakura, Toru
Ueda, Yasunori
Sawa, Masashi
Dobashi, Nobuaki
Taniguchi, Yasuhiro
Suzuki, Rikio
Nakagawa, Masaru
Tamaki, Shigehisa
Hagihara, Maki
Fujimaki, Katsumichi
Minamiguchi, Hitoshi
Fujita, Hiroyuki
Yanada, Masamitsu
Maeda, Yoshinobu
Usui, Noriko
Kobayashi, Yukio
Kiyoi, Hitoshi
Ohtake, Shigeki
Matsumura, Itaru
Naoe, Tomoki
Miyazaki, Yasushi
author_sort Takeshita, Akihiro
collection PubMed
description 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 × 10(9)/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.
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spelling pubmed-73528292020-07-15 Impact of CD56 Continuously Recognizable as Prognostic Value of Acute Promyelocytic Leukemia: Results of Multivariate Analyses in the Japan Adult Leukemia Study Group (JALSG)-APL204 Study and a Review of the Literature Takeshita, Akihiro Asou, Norio Atsuta, Yoshiko Furumaki, Hiroaki Sakura, Toru Ueda, Yasunori Sawa, Masashi Dobashi, Nobuaki Taniguchi, Yasuhiro Suzuki, Rikio Nakagawa, Masaru Tamaki, Shigehisa Hagihara, Maki Fujimaki, Katsumichi Minamiguchi, Hitoshi Fujita, Hiroyuki Yanada, Masamitsu Maeda, Yoshinobu Usui, Noriko Kobayashi, Yukio Kiyoi, Hitoshi Ohtake, Shigeki Matsumura, Itaru Naoe, Tomoki Miyazaki, Yasushi Cancers (Basel) Article 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 × 10(9)/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. MDPI 2020-06-01 /pmc/articles/PMC7352829/ /pubmed/32492981 http://dx.doi.org/10.3390/cancers12061444 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Takeshita, Akihiro
Asou, Norio
Atsuta, Yoshiko
Furumaki, Hiroaki
Sakura, Toru
Ueda, Yasunori
Sawa, Masashi
Dobashi, Nobuaki
Taniguchi, Yasuhiro
Suzuki, Rikio
Nakagawa, Masaru
Tamaki, Shigehisa
Hagihara, Maki
Fujimaki, Katsumichi
Minamiguchi, Hitoshi
Fujita, Hiroyuki
Yanada, Masamitsu
Maeda, Yoshinobu
Usui, Noriko
Kobayashi, Yukio
Kiyoi, Hitoshi
Ohtake, Shigeki
Matsumura, Itaru
Naoe, Tomoki
Miyazaki, Yasushi
Impact of CD56 Continuously Recognizable as Prognostic Value of Acute Promyelocytic Leukemia: Results of Multivariate Analyses in the Japan Adult Leukemia Study Group (JALSG)-APL204 Study and a Review of the Literature
title Impact of CD56 Continuously Recognizable as Prognostic Value of Acute Promyelocytic Leukemia: Results of Multivariate Analyses in the Japan Adult Leukemia Study Group (JALSG)-APL204 Study and a Review of the Literature
title_full Impact of CD56 Continuously Recognizable as Prognostic Value of Acute Promyelocytic Leukemia: Results of Multivariate Analyses in the Japan Adult Leukemia Study Group (JALSG)-APL204 Study and a Review of the Literature
title_fullStr Impact of CD56 Continuously Recognizable as Prognostic Value of Acute Promyelocytic Leukemia: Results of Multivariate Analyses in the Japan Adult Leukemia Study Group (JALSG)-APL204 Study and a Review of the Literature
title_full_unstemmed Impact of CD56 Continuously Recognizable as Prognostic Value of Acute Promyelocytic Leukemia: Results of Multivariate Analyses in the Japan Adult Leukemia Study Group (JALSG)-APL204 Study and a Review of the Literature
title_short Impact of CD56 Continuously Recognizable as Prognostic Value of Acute Promyelocytic Leukemia: Results of Multivariate Analyses in the Japan Adult Leukemia Study Group (JALSG)-APL204 Study and a Review of the Literature
title_sort impact of cd56 continuously recognizable as prognostic value of acute promyelocytic leukemia: results of multivariate analyses in the japan adult leukemia study group (jalsg)-apl204 study and a review of the literature
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7352829/
https://www.ncbi.nlm.nih.gov/pubmed/32492981
http://dx.doi.org/10.3390/cancers12061444
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