Day-21 bone marrow findings incorrectly designate residual leukaemia in FLT3-mutated acute myeloid leukaemia treated with intensive induction plus midostaurin: a morphology-focused study.

7+3 induction Day-21 bone marrow FLT3 acute myeloid leukaemia false positive haematopathology midostaurin morphology

Journal

Pathology
ISSN: 1465-3931
Titre abrégé: Pathology
Pays: England
ID NLM: 0175411

Informations de publication

Date de publication:
13 Mar 2024
Historique:
received: 10 10 2023
revised: 28 12 2023
accepted: 08 01 2024
medline: 6 4 2024
pubmed: 6 4 2024
entrez: 5 4 2024
Statut: aheadofprint

Résumé

Early induction response assessment with day-21 bone marrow (D21-BM) is commonly performed in patients with FLT3-mutated acute myeloid leukaemia (AML), where detection of residual leukaemia (RL; blasts ≥5%) typically results in the administration of a second induction course. However, whether D21-BM results predict for RL at the end of first induction has not been systematically assessed. This study evaluates the predictive role of D21-BM morphology in detecting RL following first induction. Between August 2018 and March 2022, all patients with FLT3-AML receiving 7+3 plus midostaurin, with D21-BM performed, were identified. Correlation between D21-BM morphology vs D21-BM ancillary flow/molecular results, as well as vs D28-BM end of first induction response, were retrospectively reviewed. Subsequently, D21-BMs were subjected to anonymised morphological re-assessments by independent haematopathologists (total in triplicate per patient). Of nine patients included in this study, three (33%) were designated to have RL at D21-BM, all of whom entered complete remission at D28-BM. Furthermore, only low-level measurable residual disease was detected in all three cases by flow or molecular methods at D21-BM, hence none proceeded to a second induction. Independent re-evaluations of these cases failed to correctly reassign D21-BM responses, yielding a final false positive rate of 33%. In summary, based on morphology alone, D21-BM assessment following 7+3 intensive induction plus midostaurin for FLT3-AML incorrectly designates RL in some patients; thus correlating with associated flow and molecular results is essential before concluding RL following first induction. Where remission status is unclear, repeat D28-BMs should be performed.

Identifiants

pubmed: 38580614
pii: S0031-3025(24)00085-0
doi: 10.1016/j.pathol.2024.01.004
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 Royal College of Pathologists of Australasia. Published by Elsevier B.V. All rights reserved.

Auteurs

Aditya Tedjaseputra (A)

Monash Haematology, Clayton, Vic, Australia.

Sukanya Roy (S)

Monash Haematology, Clayton, Vic, Australia.

Kay Htun (K)

Monash Haematology, Clayton, Vic, Australia.

Danielle Oh (D)

Monash Haematology, Clayton, Vic, Australia.

Zoe McQuilten (Z)

Monash Haematology, Clayton, Vic, Australia; School of Public Health and Preventive Medicine, Monash University, Melbourne, Vic, Australia.

Paul Yeh (P)

Monash Haematology, Clayton, Vic, Australia; Department of Medicine, School of Clinical Sciences at Monash Health, Monash University, Clayton, Vic, Australia.

Ashwini Bennett (A)

Monash Haematology, Clayton, Vic, Australia; Department of Medicine, School of Clinical Sciences at Monash Health, Monash University, Clayton, Vic, Australia.

Michael Sze Yuan Low (MS)

Monash Haematology, Clayton, Vic, Australia; Department of Medicine, School of Clinical Sciences at Monash Health, Monash University, Clayton, Vic, Australia.

Sanjeev Chunilal (S)

Monash Haematology, Clayton, Vic, Australia; Department of Medicine, School of Clinical Sciences at Monash Health, Monash University, Clayton, Vic, Australia.

Erica M Wood (EM)

Monash Haematology, Clayton, Vic, Australia; School of Public Health and Preventive Medicine, Monash University, Melbourne, Vic, Australia.

Jake Shortt (J)

Monash Haematology, Clayton, Vic, Australia; Department of Medicine, School of Clinical Sciences at Monash Health, Monash University, Clayton, Vic, Australia. Electronic address: jake.shortt@monash.edu.

Classifications MeSH