在印度,按照修改后的 BFM 95 方案治疗小儿急性淋巴细胞白血病,并进行最小残留病监测。

IF 2 4区 医学 Q3 HEMATOLOGY
Hematology Pub Date : 2025-12-01 Epub Date: 2024-12-15 DOI:10.1080/16078454.2024.2439733
Dhwanee Thakkar, K Upasana, D S Udayakumar, Neha Rastogi, Ritu Chadha, Sunisha Arora, Bhawna Jha, Anjali Yadav, Shalini Goel, Renu Saxena, Satya Prakash Yadav
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引用次数: 0

摘要

背景:发展中国家小儿急性淋巴细胞白血病(ALL)的生存率较低。在此,我们报告了印度小儿急性淋巴细胞白血病治疗效果的改善情况:我们分析了2016年至2021年间在本中心接受治疗的ALL患儿的疗效。他们按照改良的BFM 95方案接受治疗,并通过流式细胞术(FCM)监测最小残留病(MRD):我们诊断并治疗了68例患者,其中57例为前体B(Pre B)细胞ALL,其余为T细胞ALL。根据 BFM 95 方案进行风险分层后,19/68、44/68 和 3/68 患者分别属于标准风险 (SR)、中度风险 (MR) 和高度风险 (HR),2/68 患者因诱导死亡而未进行分层。根据MRD进行风险分层后,52/68、11/68和2/68的患者分别属于SR、MR和HR类别,3/68的患者无法根据MRD进行分类(2例诱导死亡和1例难治性疾病),65/68的患者在诱导结束时实现了形态学完全缓解(CR)。68名ALL患者中有5名在CR1时接受了异基因造血干细胞移植(HSCT)。68名患者中有10人复发,其中6人存活并在最后一次随访中达到CR2。平均随访时间为 1150 天(中位数为 1219 天)。治疗相关死亡率为4.4%。中位随访时间为1219天,无事件生存期(EFS)为79.4%,总生存期(OS)为88.2%:结论:随着BFM 95方案的修改和MRD评估的纳入,ALL患儿的生存率有所提高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Treatment of Pediatric Acute Lymphoblastic Leukemia in India as per modified BFM 95 protocol with Minimal Residual Disease monitoring.

Background: Survival outcomes of Pediatric Acute Lymphoblastic Leukemia (ALL) in the developing world have lagged. Here we report improved outcomes of pediatric ALL from India.Methods: We analyzed outcomes of children with ALL treated at our center between 2016 and 2021. They were treated as per the modified BFM 95 protocol with Minimal Residual Disease (MRD) monitoring by flow cytometry (FCM).Results: We diagnosed and managed 68 patients, 57 being Precursor B (Pre B) cell ALL and the rest of T cell ALL. With BFM 95 protocol-based risk stratification, 19/68, 44/68 and 3/68 patients were Standard risk (SR), Medium risk (MR) and High risk (HR), respectively and 2/68 were not stratified due to Induction mortality. With MRD-based risk stratification, 52/68, 11/68 and 2/68 patients fell in the SR, MR and HR category, respectively and 3/68 patients were not classifiable by MRD (2 Induction deaths and 1 refractory disease) and 65/68 patients achieved morphological complete remission (CR) at the end of Induction. Five out of 68 ALL patients underwent allogeneic hematopoietic stem cell transplant (HSCT) in CR1. Ten out of 68 patients had a relapse, 6 of whom are alive and in CR2 till the last follow-up. The mean duration of follow-up was 1150 days (median 1219 days). Treatment-related mortality was 4.4% in our cohort. The Event Free Survival (EFS) of our cohort was 79.4% and Overall Survival (OS) was 88.2% at a median follow-up of 1219 days.Conclusion: Survival outcomes have improved for children with ALL with modifications in BFM 95 protocol and incorporation of MRD assessment.

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来源期刊
Hematology
Hematology 医学-血液学
CiteScore
2.60
自引率
5.30%
发文量
140
审稿时长
3 months
期刊介绍: Hematology is an international journal publishing original and review articles in the field of general hematology, including oncology, pathology, biology, clinical research and epidemiology. Of the fixed sections, annotations are accepted on any general or scientific field: technical annotations covering current laboratory practice in general hematology, blood transfusion and clinical trials, and current clinical practice reviews the consensus driven areas of care and management.
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