Q Y He, A L Lai, A Zhang, L N Wang, X M Chen, S W Qiu, H Wei, J X Wang, G J Zhang
{"title":"高原地区新发急性白血病临床特点及治疗效果分析","authors":"Q Y He, A L Lai, A Zhang, L N Wang, X M Chen, S W Qiu, H Wei, J X Wang, G J Zhang","doi":"10.3760/cma.j.cn121090-20240514-00182","DOIUrl":null,"url":null,"abstract":"<p><p><b>Objective:</b> This study aimed to retrospectively analyze the clinical characteristics and prognosis of patients with acute leukemia in the plateau. <b>Methods:</b> The clinical information of patients diagnosed with acute leukemia from February 2010 to April 2023 at the People's Hospital of Tibet Autonomous Region was reviewed and collected, including blood cell count, morphology, immunophenotype, cytogenetics, and molecular data. Survival analysis was conducted to analyze the outcome of patients with acute leukemia. <b>Results:</b> This study enrolled 105 patients with acute leukemia, including 24 with acute lymphoblastic leukemia (ALL), 62 with acute myeloid leukemia (AML), and 19 with acute leukemia without baseline data. Of the patients with ALL, 11 underwent bone marrow testing for immunophenotype, all of whom were B-cell lineage. The main FAB subtype of patients with AML was M(2) (25/57), followed by M(3) (12/57), M(5) (6/57), M(4EO) (5/57), M(1) (4/57), M(4) (4/57), and M(0) (1/57). The complete remission rates of patients with ALL, acute promyelocytic leukemia (APL), and AML (non-APL) after one course of induction therapy were 57.1% (8/14), 100% (6/6), and 53.6% (15/28), respectively. The median event-free survival (EFS) and overall survival (OS) for patients with ALL were 2 (95% <i>CI</i> 0-9) and 3 (95% <i>CI</i> 0-9) months, respectively, with a median followup of 37 (95% <i>CI</i> 17-57) months. Patients with APL did not reach median EFS or OS, whereas the median EFS and OS for core binding factor AML (CBF-AML) cases were 10 (95% <i>CI</i> 0-21) months and 13 (95% <i>CI</i> 3-23) months, respectively, and patients with non-CBF-AML had inferior median EFS (2 months, 95% <i>CI</i> 1-3) and OS (2 months, 95% <i>CI</i> 1-3) (<i>P</i><0.01). Patients with ALL treated from 2020 to 2023 demonstrated trends toward better EFS (<i>P</i>=0.16) and OS (<i>P</i>=0.10) than those treated from 2010 to 2019. Similarly, trends toward superior EFS (<i>P</i>=0.27) and OS (<i>P</i>=0.12) were observed in patients with AML treated from 2016 to 2023, in comparison with those treated from 2010 to 2015. <b>Conclusion:</b> Progress in the treatment and prognosis of patients with acute leukemia in the plateau has been observed in recent years, which can be further promoted by precision diagnosis and tailored regimens.</p>","PeriodicalId":24016,"journal":{"name":"Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi","volume":"45 12","pages":"1106-1112"},"PeriodicalIF":0.0000,"publicationDate":"2024-12-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11886690/pdf/","citationCount":"0","resultStr":"{\"title\":\"[Clinical characteristics and treatment efficacy of newly diagnosed acute leukemia in the plateau].\",\"authors\":\"Q Y He, A L Lai, A Zhang, L N Wang, X M Chen, S W Qiu, H Wei, J X Wang, G J Zhang\",\"doi\":\"10.3760/cma.j.cn121090-20240514-00182\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><b>Objective:</b> This study aimed to retrospectively analyze the clinical characteristics and prognosis of patients with acute leukemia in the plateau. <b>Methods:</b> The clinical information of patients diagnosed with acute leukemia from February 2010 to April 2023 at the People's Hospital of Tibet Autonomous Region was reviewed and collected, including blood cell count, morphology, immunophenotype, cytogenetics, and molecular data. Survival analysis was conducted to analyze the outcome of patients with acute leukemia. <b>Results:</b> This study enrolled 105 patients with acute leukemia, including 24 with acute lymphoblastic leukemia (ALL), 62 with acute myeloid leukemia (AML), and 19 with acute leukemia without baseline data. Of the patients with ALL, 11 underwent bone marrow testing for immunophenotype, all of whom were B-cell lineage. The main FAB subtype of patients with AML was M(2) (25/57), followed by M(3) (12/57), M(5) (6/57), M(4EO) (5/57), M(1) (4/57), M(4) (4/57), and M(0) (1/57). The complete remission rates of patients with ALL, acute promyelocytic leukemia (APL), and AML (non-APL) after one course of induction therapy were 57.1% (8/14), 100% (6/6), and 53.6% (15/28), respectively. The median event-free survival (EFS) and overall survival (OS) for patients with ALL were 2 (95% <i>CI</i> 0-9) and 3 (95% <i>CI</i> 0-9) months, respectively, with a median followup of 37 (95% <i>CI</i> 17-57) months. Patients with APL did not reach median EFS or OS, whereas the median EFS and OS for core binding factor AML (CBF-AML) cases were 10 (95% <i>CI</i> 0-21) months and 13 (95% <i>CI</i> 3-23) months, respectively, and patients with non-CBF-AML had inferior median EFS (2 months, 95% <i>CI</i> 1-3) and OS (2 months, 95% <i>CI</i> 1-3) (<i>P</i><0.01). Patients with ALL treated from 2020 to 2023 demonstrated trends toward better EFS (<i>P</i>=0.16) and OS (<i>P</i>=0.10) than those treated from 2010 to 2019. Similarly, trends toward superior EFS (<i>P</i>=0.27) and OS (<i>P</i>=0.12) were observed in patients with AML treated from 2016 to 2023, in comparison with those treated from 2010 to 2015. <b>Conclusion:</b> Progress in the treatment and prognosis of patients with acute leukemia in the plateau has been observed in recent years, which can be further promoted by precision diagnosis and tailored regimens.</p>\",\"PeriodicalId\":24016,\"journal\":{\"name\":\"Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi\",\"volume\":\"45 12\",\"pages\":\"1106-1112\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-12-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11886690/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.cn121090-20240514-00182\",\"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.cn121090-20240514-00182","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:回顾性分析高原急性白血病患者的临床特点及预后。方法:收集2010年2月至2023年4月西藏自治区人民医院诊断为急性白血病患者的临床资料,包括血细胞计数、形态学、免疫表型、细胞遗传学和分子数据。采用生存分析分析急性白血病患者的预后。结果:本研究纳入105例急性白血病患者,包括24例急性淋巴细胞白血病(ALL), 62例急性髓系白血病(AML), 19例急性白血病,无基线数据。在ALL患者中,11例接受骨髓免疫表型检测,均为b细胞谱系。AML患者FAB亚型主要为M(2)(25/57),其次为M(3)(12/57)、M(5)(6/57)、M(4EO)(5/57)、M(1)(4/57)、M(4)(4/57)、M(0)(1/57)。ALL、急性早幼粒细胞白血病(APL)和AML(非APL)患者经过1个疗程诱导治疗后完全缓解率分别为57.1%(8/14)、100%(6/6)和53.6%(15/28)。ALL患者的中位无事件生存期(EFS)和总生存期(OS)分别为2个月(95% CI 0-9)和3个月(95% CI 0-9),中位随访期为37个月(95% CI 17-57)。APL患者未达到中位EFS或OS,而核心结合因子AML (CBF-AML)病例的中位EFS和OS分别为10 (95% CI 0-21)个月和13 (95% CI 3-23)个月,非CBF-AML患者的中位EFS(2个月,95% CI 1-3)和OS(2个月,95% CI 1-3) (PP=0.16)和OS (P=0.10)低于2010年至2019年治疗的患者。同样,与2010年至2015年治疗的AML患者相比,2016年至2023年治疗的AML患者有更优越的EFS (P=0.27)和OS (P=0.12)的趋势。结论:近年来,高原急性白血病患者的治疗和预后有了一定的进展,通过精准诊断和量身定制的治疗方案可以进一步促进这一进展。
[Clinical characteristics and treatment efficacy of newly diagnosed acute leukemia in the plateau].
Objective: This study aimed to retrospectively analyze the clinical characteristics and prognosis of patients with acute leukemia in the plateau. Methods: The clinical information of patients diagnosed with acute leukemia from February 2010 to April 2023 at the People's Hospital of Tibet Autonomous Region was reviewed and collected, including blood cell count, morphology, immunophenotype, cytogenetics, and molecular data. Survival analysis was conducted to analyze the outcome of patients with acute leukemia. Results: This study enrolled 105 patients with acute leukemia, including 24 with acute lymphoblastic leukemia (ALL), 62 with acute myeloid leukemia (AML), and 19 with acute leukemia without baseline data. Of the patients with ALL, 11 underwent bone marrow testing for immunophenotype, all of whom were B-cell lineage. The main FAB subtype of patients with AML was M(2) (25/57), followed by M(3) (12/57), M(5) (6/57), M(4EO) (5/57), M(1) (4/57), M(4) (4/57), and M(0) (1/57). The complete remission rates of patients with ALL, acute promyelocytic leukemia (APL), and AML (non-APL) after one course of induction therapy were 57.1% (8/14), 100% (6/6), and 53.6% (15/28), respectively. The median event-free survival (EFS) and overall survival (OS) for patients with ALL were 2 (95% CI 0-9) and 3 (95% CI 0-9) months, respectively, with a median followup of 37 (95% CI 17-57) months. Patients with APL did not reach median EFS or OS, whereas the median EFS and OS for core binding factor AML (CBF-AML) cases were 10 (95% CI 0-21) months and 13 (95% CI 3-23) months, respectively, and patients with non-CBF-AML had inferior median EFS (2 months, 95% CI 1-3) and OS (2 months, 95% CI 1-3) (P<0.01). Patients with ALL treated from 2020 to 2023 demonstrated trends toward better EFS (P=0.16) and OS (P=0.10) than those treated from 2010 to 2019. Similarly, trends toward superior EFS (P=0.27) and OS (P=0.12) were observed in patients with AML treated from 2016 to 2023, in comparison with those treated from 2010 to 2015. Conclusion: Progress in the treatment and prognosis of patients with acute leukemia in the plateau has been observed in recent years, which can be further promoted by precision diagnosis and tailored regimens.