Epidemiological and clinical characteristics of adult acute lymphoblastic leukemia patients in Chile: A single-center analysis

IF 0.7 Q4 HEMATOLOGY
Joaquín Jerez , Valentina Goldschmidt , María Carolina Guerra , José Luis Briones , Carlos Torres , Sebastián Hidalgo , Raimundo Gazitúa
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引用次数: 0

Abstract

Background

Acute lymphoblastic leukemia represents 20% of acute leukemias in adults. Currently, there is limited data in Chile regarding the clinical, cytogenetic, and prognostic characteristics of this condition.

Methods

This is a retrospective, observational, and descriptive study of 67 patients treated for acute lymphoblastic leukemia at the Arturo Lopez Perez Foundation between 2018 and 2021. The main objective is to evaluate epidemiological and clinical characteristics, as well as identifying factors associated with improved overall survival and/or progression-free survival.

Results

88% of the cases were B-lineage, mainly the common B phenotype. Cytogenetic analysis was performed in less than 50% of the patients, with lower yield than expected according to the literature. Molecular testing was performed in 86.5% of the patients, with the most frequent alteration being BCR-ABL. No study was performed to search for Ph-like abnormalities. The rate of complete response after induction was 83.3%, the majority of patients having negative minimal residual disease. Only 12% of the patients received consolidation with allogenic bone marrow transplant. At 2 years, the overall survival was 69% and the progression-free survival was 59%.

Conclusion

The results in terms of overall survival and progression-free survival are similar to those reported in the literature. Important diagnostic gaps prevent adequate prognostic characterization. Allogeneic consolidation transplantation was performed in a lower percentage than expected, highlighting the national deficit in access to this treatment.

智利成人急性淋巴细胞白血病患者的流行病学和临床特征:单中心分析
背景:急性淋巴细胞白血病占成人急性白血病的20%。目前,智利关于该疾病的临床、细胞遗传学和预后特征的数据有限。方法:这是一项回顾性、观察性和描述性研究,纳入了2018年至2021年间在Arturo Lopez Perez基金会接受急性淋巴细胞白血病治疗的67例患者。主要目的是评估流行病学和临床特征,以及确定与改善总生存期和/或无进展生存期相关的因素。结果88%的病例为B系,以普通B型为主。不到50%的患者进行了细胞遗传学分析,产量低于文献预期。86.5%的患者进行了分子检测,最常见的改变是BCR-ABL。没有研究进行寻找ph样异常。诱导后的完全缓解率为83.3%,大多数患者为阴性微小残留病。只有12%的患者接受同种异体骨髓移植巩固。2年时,总生存率为69%,无进展生存率为59%。结论总生存期和无进展生存期与文献报道相似。重要的诊断差距妨碍了充分的预后表征。同种异体巩固移植的实施比例低于预期,这凸显了国家在获得这种治疗方面的不足。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Leukemia Research Reports
Leukemia Research Reports Medicine-Oncology
CiteScore
1.70
自引率
0.00%
发文量
70
审稿时长
23 weeks
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