Go with the Flow-Early Assessment of Measurable Residual Disease in Children with Acute Lymphoblastic Leukemia Treated According to ALL IC-BFM2009.

acute lymphoblastic leukemia blast cell clearance children flow cytometry minimal or measurable residual disease

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
30 Oct 2022
Historique:
received: 18 08 2022
revised: 25 10 2022
accepted: 28 10 2022
entrez: 11 11 2022
pubmed: 12 11 2022
medline: 12 11 2022
Statut: epublish

Résumé

Measurable residual disease (MRD) is a well-known tool for the evaluation of the early response to treatment in patients with acute lymphoblastic leukemia (ALL). In respect to predicting the relapse the most informative cut-off and time point of MRD measurement during therapy were evaluated in our study. Between 1 January 2013 and 31 December 2019, multiparametric flow cytometry (MFC) MRD was measured in the bone marrow of 140 children with ALL treated according to the ALL IC-BFM2009 protocol. The MRD cut-off of 0.1% and day 33, end of induction, were the most discriminatory for all patients. Patients with negative MRD on day 15 and 33 had a higher 5-year overall survival-OS (100%) and a higher relapse-free survival-RFS rate (97.6%) than those with positive levels of MRD (≥0.01%) at both time points (77.8% and 55.6%,

Identifiants

pubmed: 36358778
pii: cancers14215359
doi: 10.3390/cancers14215359
pmc: PMC9653819
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Katarzyna Pawinska-Wasikowska (K)

Department of Pediatric Oncology and Hematology, Institute of Pediatrics, Jagiellonian University Medical College, 30-663 Krakow, Poland.
Department of Pediatric Oncology and Hematology, University Children's Hospital, 30-663 Krakow, Poland.

Karolina Bukowska-Strakova (K)

Department of Clinical Immunology and Transplantation, Faculty of Medicine, Institute of Pediatrics, Jagiellonian University Medical College, 30-663 Krakow, Poland.

Marta Surman (M)

Department of Clinical Immunology and Transplantation, Faculty of Medicine, Institute of Pediatrics, Jagiellonian University Medical College, 30-663 Krakow, Poland.

Monika Rygielska (M)

Hematology Laboratory, Department of Pediatric Oncology and Hematology, University Children's Hospital, 30-663 Krakow, Poland.

Beata Sadowska (B)

Department of Pediatric Oncology and Hematology, Cytogenetics and Molecular Genetics Laboratory, University Children's Hospital, 30-663 Krakow, Poland.

Teofila Ksiazek (T)

Department of Pediatric Oncology and Hematology, Cytogenetics and Molecular Genetics Laboratory, University Children's Hospital, 30-663 Krakow, Poland.
Department of Medical Genetics, Faculty of Medicine, Jagiellonian University Medical College, 30-663 Krakow, Poland.

Tomasz Klekawka (T)

Department of Pediatric Oncology and Hematology, University Children's Hospital, 30-663 Krakow, Poland.

Aleksandra Wieczorek (A)

Department of Pediatric Oncology and Hematology, Institute of Pediatrics, Jagiellonian University Medical College, 30-663 Krakow, Poland.
Department of Pediatric Oncology and Hematology, University Children's Hospital, 30-663 Krakow, Poland.

Szymon Skoczen (S)

Department of Pediatric Oncology and Hematology, Institute of Pediatrics, Jagiellonian University Medical College, 30-663 Krakow, Poland.
Department of Pediatric Oncology and Hematology, University Children's Hospital, 30-663 Krakow, Poland.

Walentyna Balwierz (W)

Department of Pediatric Oncology and Hematology, Institute of Pediatrics, Jagiellonian University Medical College, 30-663 Krakow, Poland.
Department of Pediatric Oncology and Hematology, University Children's Hospital, 30-663 Krakow, Poland.

Classifications MeSH