Imatinib with intensive chemotherapy in AML with t(9;22)(q34.1;q11.2)/BCR::ABL1. A DATAML registry study

• Published in: Blood cancer journal (New York) Vol. 14; no. 1; pp. 91 - 10
• Main Authors: Gondran, Camille, Dumas, Pierre-Yves, Bérard, Emilie, Bidet, Audrey, Delabesse, Eric, Tavitian, Suzanne, Leguay, Thibaut, Huguet, Françoise, Borel, Cécile, Forcade, Edouard, Vergez, François, Vial, Jean-Philippe, Rieu, Jean Baptiste, Lechevalier, Nicolas, Luquet, Isabelle, Canali, Alban, Klein, Emilie, Sarry, Audrey, de Grande, Anne-Charlotte, Pigneux, Arnaud, Récher, Christian, Largeaud, Laetitia, Bertoli, Sarah
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 31.05.2024; Springer Nature B.V; Nature Publishing Group
• Subjects: 631/67/68; 692/699/1541/1990/283/1897; Adult; Aged; Antineoplastic Combined Chemotherapy Protocols - adverse effects; Antineoplastic Combined Chemotherapy Protocols - therapeutic use; Biomedical and Life Sciences; Biomedicine; Cancer Research; Chemotherapy; Chromosomes, Human, Pair 22 - genetics; Chromosomes, Human, Pair 9 - genetics; Female; Fusion Proteins, bcr-abl - genetics; Hematology; Humans; Imatinib Mesylate - administration & dosage; Imatinib Mesylate - therapeutic use; Kinases; Leukemia; Leukemia, Myeloid, Acute - drug therapy; Leukemia, Myeloid, Acute - genetics; Leukemia, Myeloid, Acute - mortality; Male; Middle Aged; Mutation; Nucleophosmin; Oncology; Registries; Remission (Medicine); Translocation, Genetic; Young Adult
• ISSN: 2044-5385; 2044-5385
• DOI: 10.1038/s41408-024-01069-9

Acute myeloid leukemia (AML) with t(9;22) (q34.1; q11.2)/ BCR::ABL1 , a distinct entity within the group of AML with defining genetic abnormalities, belong to the adverse-risk group of the 2022 ELN classification. However, there is little data on outcome since the era of tyrosine kinase inhibitors. Among 5819 AML cases included in the DATAML registry, 20 patients with de novo BCR::ABL1 + AML (0.3%) were identified. Eighteen patients treated with standard induction chemotherapy were analyzed in this study. Imatinib was added to chemotherapy in 16 patients. The female-to-male ratio was 1.25 and median age was 54 years. The t(9;22) translocation was the sole chromosomal abnormality in 12 patients. Main gene mutations detected by NGS were ASXL1 , RUNX1 and NPM1 . Compared with patients with myeloid blast phase of chronic myeloid leukemia (CML-BP), de novo BCR::ABL1 + AML had higher WBC, fewer additional chromosomal abnormalities, lower CD36 or CD7 expression and no ABL1 mutations. Seventeen patients (94.4%) achieved complete remission (CR) or CR with incomplete hematologic recovery. Twelve patients were allografted in first remission. With a median follow-up of 6.3 years, the median OS was not reached and 2-year OS was 77% (95% CI: 50–91). Four out of five patients who were not transplanted did not relapse. Comparison of BCR::ABL1 + AML, CML-BP, 2017 ELN intermediate ( n  = 643) and adverse-risk patients ( n  = 863) showed that patients with BCR::ABL1 + AML had a significant better outcome than intermediate and adverse-risk patients. BCR::ABL1 + AML patients treated with imatinib and intensive chemotherapy should not be included in the adverse-risk group of current AML classifications.