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Poor prognosis of SRSF2 gene mutations in patients treated with VEN-AZA for newly diagnosed acute myeloid leukemia.
Berton, Guillaume; Sedaki, Bochra; Collomb, Erwann; Benachour, Sami; Loschi, Michael; Mohty, Bilal; Saillard, Colombe; Hicheri, Yosr; Rouzaud, Camille; Maisano, Valerio; Villetard, Ferdinand; Corda, Evelyne D 'Incan; Charbonnier, Aude; Rey, Jerome; Hospital, Marie-Anne; Ittel, Antoine; Abbou, Norman; Fanciullino, Raphaelle; Dadone-Montaudié, Bérengère; Vey, Norbert; Venton, Geoffroy; Cluzeau, Thomas; Alary, Anne-Sophie; Garciaz, Sylvain.
Afiliação
  • Berton G; Department of Hematology, Institut Paoli-Calmettes, Marseille, France. Electronic address: bertong@ipc.unicancer.fr.
  • Sedaki B; Department of Hematology, University Hospital Centre L'Archet, Nice, France.
  • Collomb E; Department of Hematology and Cellular Therapy, La Conception Hospital, Marseille, France.
  • Benachour S; Department of Hematology, University Hospital Centre L'Archet, Nice, France.
  • Loschi M; Department of Hematology, University Hospital Centre L'Archet, Nice, France.
  • Mohty B; Department of Hematology, Institut Paoli-Calmettes, Marseille, France.
  • Saillard C; Department of Hematology, Institut Paoli-Calmettes, Marseille, France.
  • Hicheri Y; Department of Hematology, Institut Paoli-Calmettes, Marseille, France.
  • Rouzaud C; Department of Hematology, Institut Paoli-Calmettes, Marseille, France.
  • Maisano V; Department of Hematology, Institut Paoli-Calmettes, Marseille, France.
  • Villetard F; Department of Hematology, Institut Paoli-Calmettes, Marseille, France.
  • Corda ED'; Department of Hematology, Institut Paoli-Calmettes, Marseille, France.
  • Charbonnier A; Department of Hematology, Institut Paoli-Calmettes, Marseille, France.
  • Rey J; Department of Hematology, Institut Paoli-Calmettes, Marseille, France.
  • Hospital MA; Department of Hematology, Institut Paoli-Calmettes, Marseille, France; Aix-Marseille University, INSERM U1068, CNRS, Institut Paoli-Calmettes, CRCM, Marseille, France.
  • Ittel A; Department of Molecular Biology, Institut Paoli-Calmettes, Marseille, France.
  • Abbou N; Department of Molecular Biology, Hôpital Nord, Marseille, France.
  • Fanciullino R; SMARTc: Simulation and Modeling: Adaptative Response for Therapeutics in Cancer, Marseille, France; Faculté de Pharmacie de Marseille, CRCM Inserm UMR, Marseille 1068, France; Pharmacy, Hôpital de la Conception, Marseille, France.
  • Dadone-Montaudié B; Department of Pathology and Molecular Oncology, University Hospital Centre L'Archet, Nice, France.
  • Vey N; Department of Hematology, Institut Paoli-Calmettes, Marseille, France; Aix-Marseille University, INSERM U1068, CNRS, Institut Paoli-Calmettes, CRCM, Marseille, France.
  • Venton G; Department of Hematology and Cellular Therapy, La Conception Hospital, Marseille, France.
  • Cluzeau T; Department of Hematology, University Hospital Centre L'Archet, Nice, France; INSERMU1065, C3M / Cote d'Azur University; Nice, France.
  • Alary AS; Department of Molecular Biology, Institut Paoli-Calmettes, Marseille, France.
  • Garciaz S; Department of Hematology, Institut Paoli-Calmettes, Marseille, France; Aix-Marseille University, INSERM U1068, CNRS, Institut Paoli-Calmettes, CRCM, Marseille, France.
Leuk Res ; 141: 107500, 2024 Jun.
Article em En | MEDLINE | ID: mdl-38636413
ABSTRACT
Mutations in spliceosome genes (SRSF2, SF3B1, U2AF1, ZRSR2) correlate with inferior outcomes in patients treated with intensive chemotherapy for Acute Myeloid Leukemia. However, their prognostic impact in patients treated with less intensive protocols is not well known. This study aimed to evaluate the impact of Spliceosome mutations in patients treated with Venetoclax and Azacitidine for newly diagnosed AML. 117 patients treated in 3 different hospitals were included in the analysis. 34 harbored a mutation in at least one of the spliceosome genes (splice-mut cohort). K/NRAS mutations were more frequent in the splice-mut cohort (47% vs 19%, p=0.0022). Response rates did not differ between splice-mut and splice-wt cohorts. With a median follow-up of 15 months, splice mutations were associated with a lower 18-month LFS (p=0.0045). When analyzing splice mutations separately, we found SRSF2 mutations to be associated with poorer outcomes (p=0.034 and p=0.037 for OS and LFS respectively). This negative prognostic impact remained true in our multivariate analysis. We believe this finding should warrant further studies aimed at overcoming this negative impact.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Leucemia Mieloide Aguda / Protocolos de Quimioterapia Combinada Antineoplásica / Fatores de Processamento de Serina-Arginina / Mutação Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Leucemia Mieloide Aguda / Protocolos de Quimioterapia Combinada Antineoplásica / Fatores de Processamento de Serina-Arginina / Mutação Idioma: En Ano de publicação: 2024 Tipo de documento: Article