The feasibility of PETHEMA ALL-96 regimen on treatment of patients with acute lymphoid leukemia.

IF 1.5 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL
Farzaneh Ashrafi, Alireza Sadeghi, Ali Derakhshandeh, Padideh Oghab
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引用次数: 0

Abstract

Background: Asparaginase-based treatment regimen for acute lymphocytic leukemia (ALL) is considered as feasible, but there is still a lack of data. In this study, considering the results of other regimen that were not optimum in previous studies. Here, we aimed to investigate the feasibility of PETHEMA ALL-96 treatment regimen.

Materials and methods: This is a retrospective feasibility study that was performed in 2019-2021 on 13 patients diagnosed with B-cell ALL. Patients were treated by PETHEMA ALL-96 regimen during induction, consolidation, reinduction, and maintenance phases. Patients were followed for 2 years after initiation of PETHEMA ALL-96 regimen for disease-free survival (DFS) and overall survival (OS) of all patients were evaluated after 2 years.

Results: Data of 11 patients were analyzed. Within 28 days after treatments, all patients (100%) had no blasts in the bone marrow that was considered as complete remission (CR). The CR rate was 100% within 6 months and 12 months and 81.8% within 2 years after the treatments. Evaluation of OS, CR, and DFS regarding 6, 12, and 24 months showed 100% for all items after 6 and 12 months. After 24 months, the CR was 90.9%, the OS was 81.8% and the DFS was 90.9%. None of the patients died during the induction phase and during the 12 months study. No side effects were observed.

Conclusion: The PETHEMA ALL-96 had high feasibility and survival rates with no side effects during the study course. It is believed that PETHEMA ALL-96 regimen has beneficial outcomes in young patients with ALL.

PETHEMA ALL-96方案治疗急性淋巴细胞白血病的可行性。
背景:基于天冬酰胺酶的急性淋巴细胞白血病(ALL)治疗方案被认为是可行的,但仍缺乏相关数据。在本研究中,考虑到其他方案在以往的研究中并不理想的结果。在这里,我们旨在探讨PETHEMA ALL-96治疗方案的可行性。材料和方法:这是一项回顾性可行性研究,于2019-2021年对13例诊断为b细胞ALL的患者进行了研究。患者在诱导、巩固、再诱导和维持阶段接受PETHEMA ALL-96方案治疗。开始PETHEMA all -96方案后随访2年,观察无病生存期(DFS), 2年后评估所有患者的总生存期(OS)。结果:对11例患者资料进行分析。在治疗后28天内,所有患者(100%)骨髓中没有母细胞,被认为是完全缓解(CR)。治疗后6个月和12个月的CR为100%,2年内CR为81.8%。6个月、12个月和24个月的OS、CR和DFS评估显示,6个月和12个月后所有项目均达到100%。24个月后,CR为90.9%,OS为81.8%,DFS为90.9%。在诱导期和12个月的研究期间,没有患者死亡。未观察到任何副作用。结论:PETHEMA ALL-96具有较高的可行性和生存率,在研究过程中无不良反应。相信PETHEMA ALL-96方案对年轻ALL患者有有益的结果。
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
Journal of Research in Medical Sciences
Journal of Research in Medical Sciences MEDICINE, GENERAL & INTERNAL-
CiteScore
2.60
自引率
6.20%
发文量
75
审稿时长
3-6 weeks
期刊介绍: Journal of Research in Medical Sciences, a publication of Isfahan University of Medical Sciences, is a peer-reviewed online continuous journal with print on demand compilation of issues published. The journal’s full text is available online at http://www.jmsjournal.net. The journal allows free access (Open Access) to its contents and permits authors to self-archive final accepted version of the articles on any OAI-compliant institutional / subject-based repository.
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