Analysis of early and treatment related deaths among children and adolescents with acute myeloid leukemia in Poland: 2005-2023.

acute myeloid leukemia adolescents children early death treatment related death

Journal

Frontiers in pediatrics
ISSN: 2296-2360
Titre abrégé: Front Pediatr
Pays: Switzerland
ID NLM: 101615492

Informations de publication

Date de publication:
2024
Historique:
received: 18 08 2024
accepted: 30 09 2024
medline: 1 11 2024
pubmed: 1 11 2024
entrez: 1 11 2024
Statut: epublish

Résumé

A personalised approach to the treatment of acute myeloid leukemia (AML) in children and adolescents, as well as the development of supportive therapies, has significantly improved survival. Despite this, some patients still die before starting treatment or in an early phase of therapy before achieving remission. The study analysed the frequency, clinical features and risk factors for early deaths (ED) and treatment related deaths (TRD) of children and adolescents with AML. From January 2005 to November 2023, 646 children with AML treated in the centers of the Polish Pediatric Leukemia and Lymphoma Study Group according to three subsequent therapeutic protocols were evaluated: AML-BFM 2004 Interim (385 children), AML-BFM 2012 Registry (131 children) and AML-BFM 2019 (130 children). Out of 646 children, early death occurred in 30 children, including 15 girls. The median age was 10.7 years (1 day to 18 years). More than half of the patients (53%) were diagnosed with acute myelomonocytic leukemia (M5) and 13% with acute promyelocytic leukemia (M3). The ED rate for the three consecutive AML-BFM protocols was 4.9% vs. 5.3% vs. 3.1%, respectively. In 19 patients, death occurred before the 15th day of treatment, in 11 between the 15th and 42nd day. The most common cause of death before the 15th day (ED15) was leukostasis and bleeding, whereas between the 15th and 42nd day (ED15-42), infections, mainly bacterial sepsis. A significant association was found between ED15 and high leukocyte count (>10 × 10 Hyperleukocytosis remains significant factor of early mortality in patients with AML, despite the introduction of various cytoreductive methods. Infections are still the main cause of treatment related deaths. A more individualized approach by using new targeted drugs may be the therapeutic option of choice in the future.

Sections du résumé

Background UNASSIGNED
A personalised approach to the treatment of acute myeloid leukemia (AML) in children and adolescents, as well as the development of supportive therapies, has significantly improved survival. Despite this, some patients still die before starting treatment or in an early phase of therapy before achieving remission. The study analysed the frequency, clinical features and risk factors for early deaths (ED) and treatment related deaths (TRD) of children and adolescents with AML.
Methods UNASSIGNED
From January 2005 to November 2023, 646 children with AML treated in the centers of the Polish Pediatric Leukemia and Lymphoma Study Group according to three subsequent therapeutic protocols were evaluated: AML-BFM 2004 Interim (385 children), AML-BFM 2012 Registry (131 children) and AML-BFM 2019 (130 children).
Results UNASSIGNED
Out of 646 children, early death occurred in 30 children, including 15 girls. The median age was 10.7 years (1 day to 18 years). More than half of the patients (53%) were diagnosed with acute myelomonocytic leukemia (M5) and 13% with acute promyelocytic leukemia (M3). The ED rate for the three consecutive AML-BFM protocols was 4.9% vs. 5.3% vs. 3.1%, respectively. In 19 patients, death occurred before the 15th day of treatment, in 11 between the 15th and 42nd day. The most common cause of death before the 15th day (ED15) was leukostasis and bleeding, whereas between the 15th and 42nd day (ED15-42), infections, mainly bacterial sepsis. A significant association was found between ED15 and high leukocyte count (>10 × 10
Conclusions UNASSIGNED
Hyperleukocytosis remains significant factor of early mortality in patients with AML, despite the introduction of various cytoreductive methods. Infections are still the main cause of treatment related deaths. A more individualized approach by using new targeted drugs may be the therapeutic option of choice in the future.

Identifiants

pubmed: 39483533
doi: 10.3389/fped.2024.1482720
pmc: PMC11524810
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1482720

Informations de copyright

© 2024 Pawińska-Wąsikowska, Czogała, Bukowska-Strakova, Surman, Rygielska, Książek, Sadowska, Pac, Skalska-Sadowska, Samborska, Wachowiak, Ciebiera, Chaber, Tomaszewska, Szczepański, Zielezińska, Urasiński, Rodziewicz-Konarska, Kałwak, Kozłowska, Irga-jaworska, Sikorska-Fic, Chyżyński, Łaguna, Muszyńska-Rosłan, Krawczuk-Rybak, Deleszkiewicz, Drabko, Bobeff, Młynarski, Chodała-Grzywacz, Karolczyk, Mycko, Badowska, Bartoszewicz, Styczyński, Machnik, Stolpa, Mizia-Malarz, Balwierz and Skoczeń.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The author(s) declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision.

Auteurs

Katarzyna Pawińska-Wąsikowska (K)

Department of Pediatric Oncology and Hematology, Institute of Pediatrics, Jagiellonian University Medical College, Krakow, Poland.
Department of Pediatric Oncology and Hematology, University Children Hospital of Krakow, Krakow, Poland.

Małgorzata Czogała (M)

Department of Pediatric Oncology and Hematology, Institute of Pediatrics, Jagiellonian University Medical College, Krakow, Poland.
Department of Pediatric Oncology and Hematology, University Children Hospital of Krakow, Krakow, Poland.

Karolina Bukowska-Strakova (K)

Department of Clinical Immunology, Institute of Pediatrics, Jagiellonian University Medical College, Krakow, Poland.

Marta Surman (M)

Department of Clinical Immunology, Institute of Pediatrics, Jagiellonian University Medical College, Krakow, Poland.

Monika Rygielska (M)

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

Teofila Książek (T)

Department of Molecular Genetics, Institute of Pediatrics, Jagiellonian University Medical College, Krakow, Poland.

Beata Sadowska (B)

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

Agnieszka Pac (A)

Department of Epidemiology and Preventive Medicine, Faculty of Medicine, Jagiellonian University Medical College, Kraków, Poland.

Jolanta Skalska-Sadowska (J)

Department of Pediatric Oncology, Hematology and Transplantology, Poznan University of Medical Sciences, Poznan, Poland.

Magdalena Samborska (M)

Department of Pediatric Oncology, Hematology and Transplantology, Poznan University of Medical Sciences, Poznan, Poland.

Jacek Wachowiak (J)

Department of Pediatric Oncology, Hematology and Transplantology, Poznan University of Medical Sciences, Poznan, Poland.

Małgorzata Ciebiera (M)

Department of Pediatric Oncohematology, Clinical Province Hospital of Rzeszow, Rzeszow, Poland.
Department of Pediatrics, Institute of Medical Sciences, Medical College, University of Rzeszow, Rzeszow, Poland.

Radosław Chaber (R)

Department of Pediatric Oncohematology, Clinical Province Hospital of Rzeszow, Rzeszow, Poland.
Department of Pediatrics, Institute of Medical Sciences, Medical College, University of Rzeszow, Rzeszow, Poland.

Renata Tomaszewska (R)

Department of Pediatric Hematology and Oncology, Zabrze, Medical University of Silesia, Katowice, Poland.

Tomasz Szczepański (T)

Department of Pediatric Hematology and Oncology, Zabrze, Medical University of Silesia, Katowice, Poland.

Karolina Zielezińska (K)

Department of Pediatrics, Hemato-Oncology and Gastroenterology, Pomeranian Medical University in Szczecin, Szczecin, Poland.

Tomasz Urasiński (T)

Department of Pediatrics, Hemato-Oncology and Gastroenterology, Pomeranian Medical University in Szczecin, Szczecin, Poland.

Anna Rodziewicz-Konarska (A)

Clinical Department of Pediatric Bone Marrow Transplantation, Oncology and Hematology, Wroclaw Medical University, Wroclaw, Poland.

Krzysztof Kałwak (K)

Clinical Department of Pediatric Bone Marrow Transplantation, Oncology and Hematology, Wroclaw Medical University, Wroclaw, Poland.

Marta Kozłowska (M)

Department of Pediatrics, Hematology and Oncology, Medical University of Gdansk, Gdansk, Poland.

Ninela Irga-Jaworska (N)

Department of Pediatrics, Hematology and Oncology, Medical University of Gdansk, Gdansk, Poland.

Barbara Sikorska-Fic (B)

Department of Oncology, Pediatric Hematology, Transplantology and Pediatrics, Medical University of Warsaw, Warsaw, Poland.

Bartosz Chyżyński (B)

Department of Oncology, Pediatric Hematology, Transplantology and Pediatrics, Medical University of Warsaw, Warsaw, Poland.

Paweł Łaguna (P)

Department of Oncology, Pediatric Hematology, Transplantology and Pediatrics, Medical University of Warsaw, Warsaw, Poland.

Katarzyna Muszyńska-Rosłan (K)

Departament of Pediatrics, Oncology and Hematology Medical University of Bialystok, Bialystok, Poland.

Maryna Krawczuk-Rybak (M)

Departament of Pediatrics, Oncology and Hematology Medical University of Bialystok, Bialystok, Poland.

Paulina Deleszkiewicz (P)

Department of Pediatric Hematology, Oncology and Transplantology, Medical University of Lublin, Lublin, Poland.

Katarzyna Drabko (K)

Department of Pediatric Hematology, Oncology and Transplantology, Medical University of Lublin, Lublin, Poland.

Katarzyna Bobeff (K)

Department of Pediatrics, Oncology and Hematology, Medical University of Lodz, Lodz, Poland.

Wojciech Młynarski (W)

Department of Pediatrics, Oncology and Hematology, Medical University of Lodz, Lodz, Poland.

Agnieszka Chodała-Grzywacz (A)

Department of Pediatric Hematology and Oncology, Regional Polyclinic Hospital in Kielce, Kielce, Poland.

Grażyna Karolczyk (G)

Department of Pediatric Hematology and Oncology, Regional Polyclinic Hospital in Kielce, Kielce, Poland.

Katarzyna Mycko (K)

Department of Pediatrics and Hematology and Oncology, Province Children's Hospital, Olsztyn, Poland.

Wanda Badowska (W)

Department of Pediatrics and Hematology and Oncology, Province Children's Hospital, Olsztyn, Poland.

Natalia Bartoszewicz (N)

Department of Pediatric Hematology and Oncology, Collegium Medicum, Nicolaus Copernicus University Torun, Bydgoszcz, Poland.

Jan Styczyński (J)

Department of Pediatric Hematology and Oncology, Collegium Medicum, Nicolaus Copernicus University Torun, Bydgoszcz, Poland.

Katarzyna Machnik (K)

Department of Pediatrics, Hematology and Oncology, City Hospital, Chorzow, Poland.

Weronika Stolpa (W)

Department of Pediatrics, Upper Silesia Children's Care Health Centre, Medical University of Silesia, Katowice, Poland.

Agnieszka Mizia-Malarz (A)

Department of Pediatrics, Upper Silesia Children's Care Health Centre, Medical University of Silesia, Katowice, Poland.

Walentyna Balwierz (W)

Department of Pediatric Oncology and Hematology, Institute of Pediatrics, Jagiellonian University Medical College, Krakow, Poland.
Department of Pediatric Oncology and Hematology, University Children Hospital of Krakow, Krakow, Poland.

Szymon Skoczeń (S)

Department of Pediatric Oncology and Hematology, Institute of Pediatrics, Jagiellonian University Medical College, Krakow, Poland.
Department of Pediatric Oncology and Hematology, University Children Hospital of Krakow, Krakow, Poland.

Classifications MeSH