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诱导治疗开始时单次注射聚乙二醇化天冬酰胺酶不仅能加速微小残留病清除,还能改善B系急性淋巴细胞白血病患儿的长期预后。

A Single Dose of PEG-Asparaginase at the Beginning of Induction Not Only Accelerates MRD Clearance but Also Improves Long-Term Outcome in Children with B-Lineage ALL.

作者信息

Popov Alexander, Henze Günter, Roumiantseva Julia, Bydanov Oleh, Belevtsev Mikhail, Verzhbitskaya Tatiana, Movchan Liudmila, Tsaur Grigory, Lagoyko Svetlana, Zharikova Liudmila, Myakova Natalia, Litvinov Dmitry, Khlebnikova Olga, Streneva Olga, Stolyarova Elena, Ponomareva Natalia, Novichkova Galina, Fechina Larisa, Aleinikova Olga, Karachunskiy Alexander

机构信息

Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology, 1, S. Mashela St., Moscow 117998, Russia.

Department of Pediatric Oncology Hematology, Charité-Universitätsmedizin Berlin, 10117 Berlin, Germany.

出版信息

Cancers (Basel). 2023 Nov 23;15(23):5547. doi: 10.3390/cancers15235547.


DOI:10.3390/cancers15235547
PMID:38067249
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10705323/
Abstract

UNLABELLED: This report presents the results of the assessment of MRD response by multicolor flow cytometry (MFC) with regard to the randomized use of pegylated asparaginase (PEG). In this study, PEG was randomly administered at a dose of 1000 U/m on day 3 of induction therapy in children with B-lineage ALL. METHODS: Conventional induction therapy consisted of dexamethasone, vincristine, and daunorubicin. MRD data was available in 502 patients who were randomized at the start of induction therapy, standard-risk (SR) patients into three (conventional induction without PEG, induction with additional PEG and with PEG but without daunorubicin) and intermediate-risk (ImR) patients into two groups (with additional PEG and without PEG). RESULTS: The single administration of PEG resulted in a significantly higher proportion of rapid responders, in SR patients even when no anthracyclines were used for induction. In the SR group, the event-free survival of the MFC-MRD fast responders was similar in the PEG- and PEG+ arms (92.0 ± 3.1% vs. 96.2 ± 1.5%, respectively), and the same unfavorable trend was observed for MFC-MRD slow responders (57.5 ± 12.3% vs. 66.7 ± 15.7%, respectively). Results were similar in ImR patients: (94.3 ± 3.2% vs. 95.1 ± 2.4%, for fast responders and 63.3 ± 7.6% vs. 78.1 ± 7.9%, for slow responders in PEG- and PEG+ arms, respectively). However, there is a large difference between the proportion of MFC-MRD slow responders in the PEG- and PEG+ groups (18.3% vs. 5.2% for the SR group and 44.2% vs. 25.0% for the ImR group). CONCLUSIONS: Therefore, early use of PEG-ASP not only leads to an accelerated reduction of blasts, but also to an excellent outcome in a significantly larger proportion of patients in both risk groups.

摘要

未标注:本报告展示了关于聚乙二醇化天冬酰胺酶(PEG)随机使用情况的多色流式细胞术(MFC)评估微小残留病(MRD)反应的结果。在本研究中,PEG在B系急性淋巴细胞白血病(ALL)儿童诱导治疗的第3天以1000 U/m²的剂量随机给药。 方法:传统诱导治疗包括地塞米松、长春新碱和柔红霉素。502例在诱导治疗开始时随机分组的患者可获得MRD数据,标准风险(SR)患者分为三组(无PEG的传统诱导治疗组、额外使用PEG的诱导治疗组和使用PEG但不使用柔红霉素的诱导治疗组),中危(ImR)患者分为两组(额外使用PEG组和不使用PEG组)。 结果:单次使用PEG导致快速反应者比例显著更高,在SR患者中,即使诱导治疗不使用蒽环类药物也是如此。在SR组中,MFC-MRD快速反应者的无事件生存率在PEG组和PEG+组中相似(分别为92.0±3.1%和96.2±1.5%),MFC-MRD缓慢反应者也观察到相同的不利趋势(分别为57.5±12.3%和66.7±15.7%)。ImR患者的结果相似:PEG组和PEG+组中快速反应者分别为94.3±3.2%和95.1±2.4%,缓慢反应者分别为63.3±7.6%和78.1±7.9%。然而,PEG组和PEG+组中MFC-MRD缓慢反应者的比例存在很大差异(SR组为18.3%对5.2%,ImR组为44.2%对25.0%)。 结论:因此,早期使用PEG-ASP不仅能加速原始细胞的减少,而且在两个风险组中,能使显著更多比例的患者获得良好结局。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5f3/10705323/0bed3dc267de/cancers-15-05547-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5f3/10705323/36eed3a967bc/cancers-15-05547-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5f3/10705323/4d092ca5b4e2/cancers-15-05547-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5f3/10705323/cab7f2b0e810/cancers-15-05547-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5f3/10705323/749818b4f7e2/cancers-15-05547-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5f3/10705323/0bed3dc267de/cancers-15-05547-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5f3/10705323/36eed3a967bc/cancers-15-05547-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5f3/10705323/4d092ca5b4e2/cancers-15-05547-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5f3/10705323/cab7f2b0e810/cancers-15-05547-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5f3/10705323/749818b4f7e2/cancers-15-05547-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5f3/10705323/0bed3dc267de/cancers-15-05547-g005.jpg

相似文献

[1]
A Single Dose of PEG-Asparaginase at the Beginning of Induction Not Only Accelerates MRD Clearance but Also Improves Long-Term Outcome in Children with B-Lineage ALL.

Cancers (Basel). 2023-11-23

[2]
A simple procedure to identify children with B-lineage acute lymphoblastic leukemia who can be successfully treated with low or moderate intensity: Sequential versus single-point minimal residual disease measurement.

Pediatr Blood Cancer. 2023-6

[3]
Augmented post-remission therapy for a minimal residual disease-defined high-risk subgroup of children and young people with clinical standard-risk and intermediate-risk acute lymphoblastic leukaemia (UKALL 2003): a randomised controlled trial.

Lancet Oncol. 2014-6-9

[4]
One-point flow cytometric MRD measurement to identify children with excellent outcome after intermediate-risk BCP-ALL: results of the ALL-MB 2008 study.

J Cancer Res Clin Oncol. 2023-7

[5]
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Lancet Oncol. 2013-2-7

[6]
Methodological aspects of minimal residual disease assessment by flow cytometry in acute lymphoblastic leukemia: A French multicenter study.

Cytometry B Clin Cytom. 2015-1

[7]
[Minimal residual disease analysis in acute lymphoblastic leukemia of childhood within the framework of COALL Study: results of an induction therapy without asparaginase].

Klin Padiatr. 2000

[8]
Post-induction Measurable Residual Disease Using Multicolor Flow Cytometry Is Strongly Predictive of Inferior Clinical Outcome in the Real-Life Management of Childhood T-Cell Acute Lymphoblastic Leukemia: A Study of 256 Patients.

Front Oncol. 2020-4-24

[9]
Minimal residual disease (MRD) measurement as a tool to compare the efficacy of chemotherapeutic drug regimens using Escherichia Coli-asparaginase or Erwinia-asparaginase in childhood acute lymphoblastic leukemia (ALL).

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[10]
Prognostic significance of minimal residual disease in high risk B-ALL: a report from Children's Oncology Group study AALL0232.

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引用本文的文献

[1]
Efficacy and Safety Profile of Biosimilar Polyethylene Glycol (PEG)-Asparaginase (Asviia) in Patients With Acute Leukemia: A Retrospective Study From Kashmir.

Cureus. 2024-11-15

[2]
Exploration of the intracellular chiral metabolome in pediatric BCP-ALL: a pilot study investigating the metabolic phenotype of IgH locus aberrations.

Front Oncol. 2024-8-5

本文引用的文献

[1]
A simple procedure to identify children with B-lineage acute lymphoblastic leukemia who can be successfully treated with low or moderate intensity: Sequential versus single-point minimal residual disease measurement.

Pediatr Blood Cancer. 2023-6

[2]
Outstanding outcomes with two low intensity regimens in children with low-risk B-ALL: a report from COG AALL0932.

Leukemia. 2023-6

[3]
A single flow cytometric MRD measurement in children with B-lineage acute lymphocytic leukemia and hyperleukocytosis redefines the requirements of high-risk treatment: Results of the study ALL-MB 2008.

Leuk Res. 2022-12

[4]
One-point flow cytometric MRD measurement to identify children with excellent outcome after intermediate-risk BCP-ALL: results of the ALL-MB 2008 study.

J Cancer Res Clin Oncol. 2023-7

[5]
A simple algorithm with one flow cytometric MRD measurement identifies more than 40% of children with ALL who can be cured with low-intensity therapy. The ALL-MB 2008 trial results.

Leukemia. 2022-5

[6]
An Extensive Quality Control and Quality Assurance (QC/QA) Program Significantly Improves Inter-Laboratory Concordance Rates of Flow-Cytometric Minimal Residual Disease Assessment in Acute Lymphoblastic Leukemia: An I-BFM-FLOW-Network Report.

Cancers (Basel). 2021-12-6

[7]
How much asparaginase is needed for optimal outcome in childhood acute lymphoblastic leukaemia? A systematic review.

Eur J Cancer. 2021-11

[8]
Blinatumomab in Pediatric Acute Lymphoblastic Leukemia-From Salvage to First Line Therapy (A Systematic Review).

J Clin Med. 2021-6-8

[9]
Pegaspargase in Practice: Minimizing Toxicity, Maximizing Benefit.

Curr Hematol Malig Rep. 2021-6

[10]
Advances in the Diagnosis and Treatment of Pediatric Acute Lymphoblastic Leukemia.

J Clin Med. 2021-4-29

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