Auer rod-positive acute leukemia with predominantly lymphoid immunophenotype: Report on 11 cases and review of literature.

Auer rods biphenotypic acute leukemia early T‐cell precursor lymphoblastic leukemia

Journal

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

Informations de publication

Date de publication:
16 Oct 2024
Historique:
revised: 05 09 2024
received: 10 05 2024
accepted: 06 10 2024
medline: 17 10 2024
pubmed: 17 10 2024
entrez: 17 10 2024
Statut: aheadofprint

Résumé

Auer rods (AuRs) are prominent intracellular structures found almost exclusively in myeloid cell malignancies, such as acute myeloid leukemia (AML), chronic and juvenile myelomonocytic leukemia and myelodysplastic syndrome. Extremely rare AuRs have been reported in patients with acute lymphoblastic leukemia (ALL) or among ambiguous lineage leukemia patients with a dominantly lymphoblastic immunophenotype. We report diagnostic and follow-up data of an international cohort of 11 children suffering from leukemias with AuRs and with significant presence of T and myeloid markers, majority of whom categorized as early T-cell precursor (ETP, n = 7); or T-ALL (ETP status unknown, n = 2), ALAL (acute leukemia of ambiguous lineage, n = 1), and AML reclassified from ALAL (n = 1). We described other diagnostic details and treatment types and responses. Moreover, we summarize previously published data. Among the four patients who started and remained on ALL-type therapy, all were in the first complete remission, whereas both patients who started and remained on AML-type therapy relapsed and died. Of the patients who followed either a combined ALL/AML protocol (Interfant 06) or who switched from one of the two types of therapy to the other, one patient died, and the remaining four were in first complete remission at the most recent follow-up. We also searched for similar cases in the literature and found only three additional children with nonmyeloid leukemia and AuRs and 10 adults with this type of leukemia. Briefly, ALL- or combined ALL/AML-type therapy may be effective for treating AuR-positive leukemia patients with a lymphoid immunophenotype.

Sections du résumé

BACKGROUND BACKGROUND
Auer rods (AuRs) are prominent intracellular structures found almost exclusively in myeloid cell malignancies, such as acute myeloid leukemia (AML), chronic and juvenile myelomonocytic leukemia and myelodysplastic syndrome. Extremely rare AuRs have been reported in patients with acute lymphoblastic leukemia (ALL) or among ambiguous lineage leukemia patients with a dominantly lymphoblastic immunophenotype.
PROCEDURE METHODS
We report diagnostic and follow-up data of an international cohort of 11 children suffering from leukemias with AuRs and with significant presence of T and myeloid markers, majority of whom categorized as early T-cell precursor (ETP, n = 7); or T-ALL (ETP status unknown, n = 2), ALAL (acute leukemia of ambiguous lineage, n = 1), and AML reclassified from ALAL (n = 1). We described other diagnostic details and treatment types and responses. Moreover, we summarize previously published data.
RESULTS RESULTS
Among the four patients who started and remained on ALL-type therapy, all were in the first complete remission, whereas both patients who started and remained on AML-type therapy relapsed and died. Of the patients who followed either a combined ALL/AML protocol (Interfant 06) or who switched from one of the two types of therapy to the other, one patient died, and the remaining four were in first complete remission at the most recent follow-up. We also searched for similar cases in the literature and found only three additional children with nonmyeloid leukemia and AuRs and 10 adults with this type of leukemia.
CONCLUSIONS CONCLUSIONS
Briefly, ALL- or combined ALL/AML-type therapy may be effective for treating AuR-positive leukemia patients with a lymphoid immunophenotype.

Identifiants

pubmed: 39415351
doi: 10.1002/pbc.31394
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e31394

Subventions

Organisme : Univerzita Karlova v Praze
Organisme : European Union and state budget of Czechia
Organisme : Ministerstvo Zdravotnictví Ceské Republiky

Informations de copyright

© 2024 The Author(s). Pediatric Blood & Cancer published by Wiley Periodicals LLC.

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Auteurs

Ondrej Hrusak (O)

CLIP, Charles University, Prague, Czech Republic.
Department of Pediatric Hematology and Oncology, Motol Hospital, Prague, Czech Republic.

Jitka Stancikova (J)

CLIP, Charles University, Prague, Czech Republic.
Department of Pediatric Hematology and Oncology, Motol Hospital, Prague, Czech Republic.

Elena Vodickova (E)

Department of Clinical Hematology, Motol Hospital, Prague, Czech Republic.

Tereza Podolska (T)

CLIP, Charles University, Prague, Czech Republic.
Department of Cell Biology, Faculty of Science, Charles University, Prague, Czech Republic.

Anja Möricke (A)

Department of Paediatrics, University Medical Centre Schleswig-Holstein, Campus Kiel, Kiel, Germany.

Andishe Attarbaschi (A)

St. Anna Children's Cancer Research Institute (CCRI), Vienna, Austria.
Department of Pediatrics and Adolescent Medicine, St. Anna Children's Hospital, Medical University of Vienna, Vienna, Austria.

Michael Dworzak (M)

St. Anna Children's Cancer Research Institute (CCRI), Vienna, Austria.
Department of Pediatrics and Adolescent Medicine, St. Anna Children's Hospital, Medical University of Vienna, Vienna, Austria.

Zuzana Sestakova (Z)

Department of Laboratory Medicine, National Institute of Children's Diseases, Bratislava, Slovakia.

Peter Svec (P)

Department of Pediatric Hematology and Oncology, National Institute of Children's Diseases, Comenius University, Bratislava, Slovakia.

Marketa Kubricanova Zaliova (MK)

CLIP, Charles University, Prague, Czech Republic.

Iveta Janotova (I)

Department of Pediatric Hematology and Oncology, Motol Hospital, Prague, Czech Republic.

Ondrej Zapletal (O)

Department of Pediatric Hematology and Biochemistry, University Hospital and Masaryk University Brno, Brno, Czech Republic.

Ester Mejstrikova (E)

CLIP, Charles University, Prague, Czech Republic.
Department of Pediatric Hematology and Oncology, Motol Hospital, Prague, Czech Republic.

Jan Stary (J)

Department of Pediatric Hematology and Oncology, Motol Hospital, Prague, Czech Republic.

Classifications MeSH