Clinical and Molecular Determinants of Clonal Evolution in Aplastic Anemia and Paroxysmal Nocturnal Hemoglobinuria. Issue 1 (1st January 2023)

• Record Type: Journal Article
• Authors: Gurnari, Carmelo; Pagliuca, Simona; Prata, Pedro Henrique; Galimard, Jacques-Emmanuel; Catto, Luiz Fernando B.; Larcher, Lise; Sebert, Marie; Allain, Vincent; Patel, Bhumika J.; Durmaz, Arda; Pinto, Andre L.; Inacio, Mariana C.B.; Hernandez, Lucie; Dhedin, Nathalie; Caillat-Zucman, Sophie; Clappier, Emmanuelle; Sicre de Fontbrune, Flore; Voso, Maria Teresa; Visconte, Valeria; Peffault de Latour, Régis; Soulier, Jean; Calado, Rodrigo T.; Socié, Gérard; Maciejewski, Jaroslaw P.
• Is Part Of: Journal of clinical oncology. Volume 41:Issue 1(2023)
• Page Start: 132
• Page End: 142
• Publication Date: 2023-01-01
• Subjects: Oncology -- Periodicals; Cancer -- Periodicals; Oncology; Medical Oncology; Cancérologie -- Périodiques; Cancer -- Périodiques; Cancérologie; Cancer; Oncology; Oncologia; Càncer; Periodicals; 616.994
• DOI: 10.1200/JCO.22.00710
• Languages: English
• ISSNs: 0732-183X

Abstract

Abstract : PURPOSE: Secondary myeloid neoplasms (sMNs) remain the most serious long-term complications in patients with aplastic anemia (AA) and paroxysmal nocturnal hemoglobinuria (PNH). However, sMNs lack specific predictors, dedicated surveillance measures, and early therapeutic interventions. PATIENTS AND METHODS: We studied a multicenter, retrospective cohort of 1, 008 patients (median follow-up 8.6 years) with AA and PNH to assess clinical and molecular determinants of clonal evolution. RESULTS: Although none of the patients transplanted upfront (n = 117) developed clonal complications (either sMN or secondary PNH), the 10-year cumulative incidence of sMN in nontransplanted cases was 11.6%. In severe AA, older age at presentation and lack of response to immunosuppressive therapy were independently associated with increased risk of sMN, whereas untreated patients had the highest risk among nonsevere cases. The elapsed time from AA to sMN was 4.5 years. sMN developed in 94 patients. The 5-year overall survival reached 40% and was independently associated with bone marrow blasts at sMN onset. Myelodysplastic syndrome with high-risk phenotypes, del7/7q, and ASXL1, SETBP1, RUNX1, and RAS pathway gene mutations were the most frequent characteristics. Cross-sectional studies of clonal dynamics from baseline to evolution revealed that PIGA/ human leukocyte antigen lesions decreased over time, being replaced by clones with myeloid hits. PIGA and BCOR/L1 mutation carriers had a lower risk of sMN progression, whereas myeloid driver lesions marked the group with a higher risk. CONCLUSION: The risk of sMN in AA is associated with disease severity, lack of response to treatment, and patients' age. sMNs display high-risk morphological, karyotypic, and molecular features. The landscape of acquired somatic mutations is complex and incompletely understood and should be considered with caution in medical management.