Cargando…
全反式维甲酸联合三氧化二砷治疗177例急性早幼粒细胞白血病患者的临床观察
OBJECTIVE: To investigate the clinical efficacy of all-trans retinoic acid (ATRA) plus arsenic trioxide (ATO) in induction and maintenance therapy in newly diagnosed acute promyelocytic leukemia (APL). METHODS: A retrospective analysis of 298 newly diagnosed APL patients from the department of hemat...
Formato: | Online Artículo Texto |
---|---|
Lenguaje: | English |
Publicado: |
Editorial office of Chinese Journal of Hematology
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7342586/ https://www.ncbi.nlm.nih.gov/pubmed/26031521 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2015.05.004 |
_version_ | 1783555532849676288 |
---|---|
collection | PubMed |
description | OBJECTIVE: To investigate the clinical efficacy of all-trans retinoic acid (ATRA) plus arsenic trioxide (ATO) in induction and maintenance therapy in newly diagnosed acute promyelocytic leukemia (APL). METHODS: A retrospective analysis of 298 newly diagnosed APL patients from the department of hematology, First Affiliated Hospital of Zhejiang University since September 2004 to December 2013, including 177 cases with ATRA plus ATO and 116 ATRA plus chemotherapy (CT), was performed to investigate the clinical efficacy between the low-intermediate (WBC≤10 × 10(9)/L) and high (WBC >10 × 10(9)/L) risk APL patients, respectively. RESULTS: For the low-intermediate risk patients, the relapse rate in ATRA plus CT and ATRA plus ATO are 22.0% and 6.1% (P=0.004), respectively; the 3 years estimated relapse-free survival (RFS) are 78.0% and 92.9% (P=0.021), respectively. For the high risk patients, the relapse rate in ATRA plus CT and ATRA plus ATO are 25.0% and 5.2% (P=0.035), respectively; the 3 years estimated RFS rate were 80.8% and 93.0% (P=0.021), respectively. But the rate of early death (ED), complete remission (CR) and overall survival (OS) between the two therapy protocols had no statistical difference (P>0.05). CONCLUSION: ATRA plus ATO in induction and maintenance therapy might prolong the RFS time of the low-intermediate risk APL patients and decrease the relapse rate of the low, intermediate and high risk APL patients. |
format | Online Article Text |
id | pubmed-7342586 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Editorial office of Chinese Journal of Hematology |
record_format | MEDLINE/PubMed |
spelling | pubmed-73425862020-07-16 全反式维甲酸联合三氧化二砷治疗177例急性早幼粒细胞白血病患者的临床观察 Zhonghua Xue Ye Xue Za Zhi 论著 OBJECTIVE: To investigate the clinical efficacy of all-trans retinoic acid (ATRA) plus arsenic trioxide (ATO) in induction and maintenance therapy in newly diagnosed acute promyelocytic leukemia (APL). METHODS: A retrospective analysis of 298 newly diagnosed APL patients from the department of hematology, First Affiliated Hospital of Zhejiang University since September 2004 to December 2013, including 177 cases with ATRA plus ATO and 116 ATRA plus chemotherapy (CT), was performed to investigate the clinical efficacy between the low-intermediate (WBC≤10 × 10(9)/L) and high (WBC >10 × 10(9)/L) risk APL patients, respectively. RESULTS: For the low-intermediate risk patients, the relapse rate in ATRA plus CT and ATRA plus ATO are 22.0% and 6.1% (P=0.004), respectively; the 3 years estimated relapse-free survival (RFS) are 78.0% and 92.9% (P=0.021), respectively. For the high risk patients, the relapse rate in ATRA plus CT and ATRA plus ATO are 25.0% and 5.2% (P=0.035), respectively; the 3 years estimated RFS rate were 80.8% and 93.0% (P=0.021), respectively. But the rate of early death (ED), complete remission (CR) and overall survival (OS) between the two therapy protocols had no statistical difference (P>0.05). CONCLUSION: ATRA plus ATO in induction and maintenance therapy might prolong the RFS time of the low-intermediate risk APL patients and decrease the relapse rate of the low, intermediate and high risk APL patients. Editorial office of Chinese Journal of Hematology 2015-05 /pmc/articles/PMC7342586/ /pubmed/26031521 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2015.05.004 Text en 2015年版权归中华医学会所有 http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution 3.0 License (CC-BY-NC). The Copyright own by Publisher. Without authorization, shall not reprint, except this publication article, shall not use this publication format design. Unless otherwise stated, all articles published in this journal do not represent the views of the Chinese Medical Association or the editorial board of this journal. |
spellingShingle | 论著 全反式维甲酸联合三氧化二砷治疗177例急性早幼粒细胞白血病患者的临床观察 |
title | 全反式维甲酸联合三氧化二砷治疗177例急性早幼粒细胞白血病患者的临床观察 |
title_full | 全反式维甲酸联合三氧化二砷治疗177例急性早幼粒细胞白血病患者的临床观察 |
title_fullStr | 全反式维甲酸联合三氧化二砷治疗177例急性早幼粒细胞白血病患者的临床观察 |
title_full_unstemmed | 全反式维甲酸联合三氧化二砷治疗177例急性早幼粒细胞白血病患者的临床观察 |
title_short | 全反式维甲酸联合三氧化二砷治疗177例急性早幼粒细胞白血病患者的临床观察 |
title_sort | 全反式维甲酸联合三氧化二砷治疗177例急性早幼粒细胞白血病患者的临床观察 |
topic | 论著 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7342586/ https://www.ncbi.nlm.nih.gov/pubmed/26031521 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2015.05.004 |
work_keys_str_mv | AT quánfǎnshìwéijiǎsuānliánhésānyǎnghuàèrshēnzhìliáo177lìjíxìngzǎoyòulìxìbāobáixuèbìnghuànzhědelínchuángguānchá AT quánfǎnshìwéijiǎsuānliánhésānyǎnghuàèrshēnzhìliáo177lìjíxìngzǎoyòulìxìbāobáixuèbìnghuànzhědelínchuángguānchá AT quánfǎnshìwéijiǎsuānliánhésānyǎnghuàèrshēnzhìliáo177lìjíxìngzǎoyòulìxìbāobáixuèbìnghuànzhědelínchuángguānchá AT quánfǎnshìwéijiǎsuānliánhésānyǎnghuàèrshēnzhìliáo177lìjíxìngzǎoyòulìxìbāobáixuèbìnghuànzhědelínchuángguānchá AT quánfǎnshìwéijiǎsuānliánhésānyǎnghuàèrshēnzhìliáo177lìjíxìngzǎoyòulìxìbāobáixuèbìnghuànzhědelínchuángguānchá AT quánfǎnshìwéijiǎsuānliánhésānyǎnghuàèrshēnzhìliáo177lìjíxìngzǎoyòulìxìbāobáixuèbìnghuànzhědelínchuángguānchá AT quánfǎnshìwéijiǎsuānliánhésānyǎnghuàèrshēnzhìliáo177lìjíxìngzǎoyòulìxìbāobáixuèbìnghuànzhědelínchuángguānchá AT quánfǎnshìwéijiǎsuānliánhésānyǎnghuàèrshēnzhìliáo177lìjíxìngzǎoyòulìxìbāobáixuèbìnghuànzhědelínchuángguānchá AT quánfǎnshìwéijiǎsuānliánhésānyǎnghuàèrshēnzhìliáo177lìjíxìngzǎoyòulìxìbāobáixuèbìnghuànzhědelínchuángguānchá AT quánfǎnshìwéijiǎsuānliánhésānyǎnghuàèrshēnzhìliáo177lìjíxìngzǎoyòulìxìbāobáixuèbìnghuànzhědelínchuángguānchá AT quánfǎnshìwéijiǎsuānliánhésānyǎnghuàèrshēnzhìliáo177lìjíxìngzǎoyòulìxìbāobáixuèbìnghuànzhědelínchuángguānchá |