Prognostic significance of chromosomal abnormalities at relapse in children with relapsed acute myeloid leukemia: A retrospective cohort study of the Relapsed AML 2001/01 Study.

chromosomal instability clonal evolution core-binding factor leukemia cytogenetics karyotypic change(s) pediatric acute myeloid leukemia/pediatric AML relapsed AML

Journal

Pediatric blood & cancer
ISSN: 1545-5017
Titre abrégé: Pediatr Blood Cancer
Pays: United States
ID NLM: 101186624

Informations de publication

Date de publication:
01 2022
Historique:
revised: 30 07 2021
received: 15 02 2021
accepted: 18 08 2021
pubmed: 18 9 2021
medline: 4 3 2022
entrez: 17 9 2021
Statut: ppublish

Résumé

In addition to treatment response, cytogenetic and molecular aberrations are the most important prognostic factors in children with de novo acute myeloid leukemia (AML). However, little is known about cytogenetics at the time of relapse. This international study analyzed the prognostic value of cytogenetic profiles and karyotypic changes in pediatric relapsed AML in relation to the probability of event-free (pEFS) and overall survival (pOS). For this purpose, cytogenetic reports from all patients registered on the Relapsed AML 2001/01 Study were reviewed and classified. Cytogenetic information at relapse was available for 403 (71%) of 569 registered patients. Frequently detected aberrations at relapse were t(8;21)(q22;q22) (n = 60) and inv(16)(p13.1q22)/t(16;16)(p13.1;q22) (n = 24), both associated with relatively good outcome (4-year pOS 59% and 71%, respectively). Monosomy 7/7q-, t(9;11)(p22;q23), t(10;11)(p12;q23), and complex karyotypes were associated with poor outcomes (4-year pOS 17%, 19%, 22%, and 22%, respectively). Of 261 (65%) patients for whom cytogenetic data were reliable at both diagnosis and relapse, pEFS was inferior for patients with karyotypic instability (n = 128, 49%), but pOS was similar. Unstable karyotypes with both gain and loss of aberrations were associated with inferior outcome. Early treatment response, time to relapse, and cytogenetic profile at time of relapse were the most important prognostic factors, both outweighing karytoypic instability per se. The cytogenetic subgroup at relapse is an independent risk factor for (event-free) survival. Cytogenetic assessment at the time of relapse is of high importance and may contribute to improved risk-adapted treatment for children with relapsed AML.

Sections du résumé

BACKGROUND
In addition to treatment response, cytogenetic and molecular aberrations are the most important prognostic factors in children with de novo acute myeloid leukemia (AML). However, little is known about cytogenetics at the time of relapse.
METHODS
This international study analyzed the prognostic value of cytogenetic profiles and karyotypic changes in pediatric relapsed AML in relation to the probability of event-free (pEFS) and overall survival (pOS). For this purpose, cytogenetic reports from all patients registered on the Relapsed AML 2001/01 Study were reviewed and classified.
RESULTS
Cytogenetic information at relapse was available for 403 (71%) of 569 registered patients. Frequently detected aberrations at relapse were t(8;21)(q22;q22) (n = 60) and inv(16)(p13.1q22)/t(16;16)(p13.1;q22) (n = 24), both associated with relatively good outcome (4-year pOS 59% and 71%, respectively). Monosomy 7/7q-, t(9;11)(p22;q23), t(10;11)(p12;q23), and complex karyotypes were associated with poor outcomes (4-year pOS 17%, 19%, 22%, and 22%, respectively). Of 261 (65%) patients for whom cytogenetic data were reliable at both diagnosis and relapse, pEFS was inferior for patients with karyotypic instability (n = 128, 49%), but pOS was similar. Unstable karyotypes with both gain and loss of aberrations were associated with inferior outcome. Early treatment response, time to relapse, and cytogenetic profile at time of relapse were the most important prognostic factors, both outweighing karytoypic instability per se.
CONCLUSION
The cytogenetic subgroup at relapse is an independent risk factor for (event-free) survival. Cytogenetic assessment at the time of relapse is of high importance and may contribute to improved risk-adapted treatment for children with relapsed AML.

Identifiants

pubmed: 34532968
doi: 10.1002/pbc.29341
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e29341

Informations de copyright

© 2021 Wiley Periodicals LLC.

Références

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Auteurs

Kim Klein (K)

Pediatric Oncology, Cancer Center Amsterdam, Emma Children's Hospital, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Department of Pediatric Hematology, Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.

H Berna Beverloo (HB)

Department of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, The Netherlands.

Martin Zimmermann (M)

Pediatric Hematology/Oncology, Hannover Medical School, Hannover, Germany.

Susana C Raimondi (SC)

Department of Pathology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.

Christine von Neuhoff (C)

Department of Pediatric Hematology-Oncology, University Hospital Essen, Essen, Germany.

Valérie de Haas (V)

Clinical laboratory, Dutch Childhood Oncology Group, The Hague, The Netherlands.
Department of Pediatric Hematology, Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.

Romy van Weelderen (R)

Pediatric Oncology, Cancer Center Amsterdam, Emma Children's Hospital, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Department of Pediatric Hematology, Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.

Jacqueline Cloos (J)

Pediatric Oncology, Cancer Center Amsterdam, Emma Children's Hospital, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.

Jonas Abrahamsson (J)

Department of Pediatrics, Queen Silvia Children's Hospital, Gothenburg, Sweden.

Yves Bertrand (Y)

Children's Leukemia Cooperative Group/European Organisation for Research and Treatment of Cancer, Institut d'Hématologie et d'Oncologie Pédiatrique, Lyon, France.

Michael Dworzak (M)

St. Anna Children's Hospital and Children's Cancer Research Institute, Medical University of Vienna, Vienna, Austria.

Alcira Fynn (A)

Grupo Argentino de Tratamiento de la Leucemia Aguda, Children's Hospital La Plata, La Plata, Buenos Aires, Argentina.

Brenda Gibson (B)

Department of Paediatric Haematology, United Kingdom Childhood Leukaemia Study Group, Royal Hospital for Children, Glasgow, UK.

Shau-Yin Ha (SY)

Department of Pediatrics/Pediatric oncology, Hong Kong Children's Hospital, Hong Kong, China.

Christine J Harrison (CJ)

Leukaemia Research Cytogenetics Group, Translational and Clinical Research Institute, Newcastle University Centre for Cancer, Newcastle upon Tyne, UK.

Henrik Hasle (H)

Department of Pediatrics, Aarhus University Hospital Skejby, Aarhus, Denmark.

Sarah Elitzur (S)

Schneider Children's Medical Center, Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel.

Guy Leverger (G)

Hematopathology Department, Assistance Publique Hopitaux de Paris, Paris, France.

Alexei Maschan (A)

Oncology and Immunology, Dmitriy Rogachev Federal Center for Pediatric Hematology, Moscow, Russia.

Bassem Razzouk (B)

Children's Center for Cancer and Blood Diseases, Peyton Manning Children's Hospital at St. Vincent, Indianapolis, Indiana, USA.

Dirk Reinhardt (D)

Department of Pediatric Hematology-Oncology, University Hospital Essen, Essen, Germany.

Carmelo Rizzari (C)

Pediatric Hematology-Oncology Unit, Department of Pediatrics, University of Milano-Bicocca, S. Gerardo Hospital, Monza, Italy.

Pter Smisek (P)

Department of Pediatric Hematology and Oncology, Carles University in Prague/Second Faculty of Medicine and University Hospital Motol, Prague, Czech Republic.

Ursula Creutzig (U)

Pediatric Hematology/Oncology, Hannover Medical School, Hannover, Germany.

Gertjan J L Kaspers (GJL)

Pediatric Oncology, Cancer Center Amsterdam, Emma Children's Hospital, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Clinical laboratory, Dutch Childhood Oncology Group, The Hague, The Netherlands.
Department of Pediatric Hematology, Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.

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