[急性髓性白血病中的 CEBPA 突变类型及其对预后的影响]。

Q3 Medicine
Y Y Mao, H Cai, X X Cao, J Feng, L Zhang, D B Zhou, J Li
{"title":"[急性髓性白血病中的 CEBPA 突变类型及其对预后的影响]。","authors":"Y Y Mao, H Cai, X X Cao, J Feng, L Zhang, D B Zhou, J Li","doi":"10.3760/cma.j.cn121090-20240316-00098","DOIUrl":null,"url":null,"abstract":"<p><p><b>Objective:</b> To demonstrate the type of CEBPA gene mutations among patients with acute myeloid leukemia (AML), clinical characteristics, and prognostic effect on patient outcomes. <b>Methods:</b> Demographic data, clinical features, laboratory characteristics, and data about treatment and follow-up of 57 patients with CEBPA mutated AML diagnosed at Peking Union Medical College Hospital between April 2016 and November 2022 were collected and analyzed. <b>Results:</b> In total, 57 patients with CEBPA mutation accounted for 16.1% of all the 353 patients with AML, among which 28 patients had CEBPA-bZIPinf and 29 had CEBPA-other. Compared with the CEBPA-other group, the CEBPA-bZIPinf group was younger (54 <i>vs</i> 64 years, <i>P</i>=0.010), de novo AML was more common (<i>P</i>=0.001), and the level of bone marrow blast was higher (68.0% <i>vs</i> 36.3%, <i>P</i>=0.001). Moreover, 24 patients from the CEBPA-bZIPinf group and 19 from the CEBPA-other group received chemotherapy. The one-course complete remission (CR) rate of the CEBPA-bZIPinf group was significantly higher than that of the CEBPA-other (87.5% <i>vs</i> 47.4%, <i>P</i>=0.010) and CEBPA-wt (87.5% <i>vs</i> 50.3%, <i>P</i>=0.002) groups. After a median follow-up of 11 months, the median OS of the CEBPA-bZIPinf group was significantly longer than that of the CEBPA-wt group (not reached <i>vs</i> 22.1 months, <i>P</i>=0.012) . <b>Conclusion:</b> CEBPA-bZIPinf mutated AML is a unique clinical entity, with a younger age of diagnosis, better response to chemotherapy, and better prognosis.</p>","PeriodicalId":24016,"journal":{"name":"Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi","volume":"45 6","pages":"556-560"},"PeriodicalIF":0.0000,"publicationDate":"2024-06-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11310808/pdf/","citationCount":"0","resultStr":"{\"title\":\"[Type of CEBPA mutations in acute myeloid leukemia and their effect on prognosis].\",\"authors\":\"Y Y Mao, H Cai, X X Cao, J Feng, L Zhang, D B Zhou, J Li\",\"doi\":\"10.3760/cma.j.cn121090-20240316-00098\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><b>Objective:</b> To demonstrate the type of CEBPA gene mutations among patients with acute myeloid leukemia (AML), clinical characteristics, and prognostic effect on patient outcomes. <b>Methods:</b> Demographic data, clinical features, laboratory characteristics, and data about treatment and follow-up of 57 patients with CEBPA mutated AML diagnosed at Peking Union Medical College Hospital between April 2016 and November 2022 were collected and analyzed. <b>Results:</b> In total, 57 patients with CEBPA mutation accounted for 16.1% of all the 353 patients with AML, among which 28 patients had CEBPA-bZIPinf and 29 had CEBPA-other. Compared with the CEBPA-other group, the CEBPA-bZIPinf group was younger (54 <i>vs</i> 64 years, <i>P</i>=0.010), de novo AML was more common (<i>P</i>=0.001), and the level of bone marrow blast was higher (68.0% <i>vs</i> 36.3%, <i>P</i>=0.001). Moreover, 24 patients from the CEBPA-bZIPinf group and 19 from the CEBPA-other group received chemotherapy. The one-course complete remission (CR) rate of the CEBPA-bZIPinf group was significantly higher than that of the CEBPA-other (87.5% <i>vs</i> 47.4%, <i>P</i>=0.010) and CEBPA-wt (87.5% <i>vs</i> 50.3%, <i>P</i>=0.002) groups. After a median follow-up of 11 months, the median OS of the CEBPA-bZIPinf group was significantly longer than that of the CEBPA-wt group (not reached <i>vs</i> 22.1 months, <i>P</i>=0.012) . <b>Conclusion:</b> CEBPA-bZIPinf mutated AML is a unique clinical entity, with a younger age of diagnosis, better response to chemotherapy, and better prognosis.</p>\",\"PeriodicalId\":24016,\"journal\":{\"name\":\"Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi\",\"volume\":\"45 6\",\"pages\":\"556-560\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-06-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11310808/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3760/cma.j.cn121090-20240316-00098\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3760/cma.j.cn121090-20240316-00098","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

摘要

目的研究急性髓性白血病(AML)患者中 CEBPA 基因突变的类型、临床特征以及对患者预后的影响。研究方法:通过人口统计学数据、临床特征、实验室检查结果和患者预后等方面的信息,对急性髓性白血病患者的CEBPA基因突变类型进行分析:收集并分析2016年4月至2022年11月期间北京协和医院确诊的57例CEBPA基因突变AML患者的人口统计学数据、临床特征、实验室特征以及治疗和随访数据。结果在353例AML患者中,CEBPA突变患者共57例,占16.1%,其中CEBPA-bZIPinf患者28例,CEBPA-other患者29例。与CEBPA-其他组相比,CEBPA-bZIPinf组更年轻(54岁对64岁,P=0.010),新发AML更常见(P=0.001),骨髓造血水平更高(68.0%对36.3%,P=0.001)。此外,CEBPA-bZIPinf 组有 24 名患者接受了化疗,CEBPA-其他组有 19 名患者接受了化疗。CEBPA-bZIPinf组的一疗程完全缓解率(CR)明显高于CEBPA-其他组(87.5% vs 47.4%,P=0.010)和CEBPA-wt组(87.5% vs 50.3%,P=0.002)。中位随访11个月后,CEBPA-bZIPinf组的中位OS明显长于CEBPA-wt组(未达到vs 22.1个月,P=0.012)。结论CEBPA-bZIPinf突变型急性髓细胞白血病是一种独特的临床实体,其确诊年龄较小,对化疗的反应较好,预后较佳。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Type of CEBPA mutations in acute myeloid leukemia and their effect on prognosis].

Objective: To demonstrate the type of CEBPA gene mutations among patients with acute myeloid leukemia (AML), clinical characteristics, and prognostic effect on patient outcomes. Methods: Demographic data, clinical features, laboratory characteristics, and data about treatment and follow-up of 57 patients with CEBPA mutated AML diagnosed at Peking Union Medical College Hospital between April 2016 and November 2022 were collected and analyzed. Results: In total, 57 patients with CEBPA mutation accounted for 16.1% of all the 353 patients with AML, among which 28 patients had CEBPA-bZIPinf and 29 had CEBPA-other. Compared with the CEBPA-other group, the CEBPA-bZIPinf group was younger (54 vs 64 years, P=0.010), de novo AML was more common (P=0.001), and the level of bone marrow blast was higher (68.0% vs 36.3%, P=0.001). Moreover, 24 patients from the CEBPA-bZIPinf group and 19 from the CEBPA-other group received chemotherapy. The one-course complete remission (CR) rate of the CEBPA-bZIPinf group was significantly higher than that of the CEBPA-other (87.5% vs 47.4%, P=0.010) and CEBPA-wt (87.5% vs 50.3%, P=0.002) groups. After a median follow-up of 11 months, the median OS of the CEBPA-bZIPinf group was significantly longer than that of the CEBPA-wt group (not reached vs 22.1 months, P=0.012) . Conclusion: CEBPA-bZIPinf mutated AML is a unique clinical entity, with a younger age of diagnosis, better response to chemotherapy, and better prognosis.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
0.80
自引率
0.00%
发文量
100
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信