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Pastore, Friederike ORCID logoORCID: https://orcid.org/0000-0002-2220-2346; Gittinger, Hanna; Raab, Susanne; Tschuri, Sebastian; Ksienzyk, Bianka; Konstandin, Nikola P.; Schneider, Stephanie; Rothenberg‐Thurley, Maja; Horny, Hans‐Peter; Werner, Martin; Sauerland, Maria C. ORCID logoORCID: https://orcid.org/0000-0002-8748-8218; Amler, Susanne ORCID logoORCID: https://orcid.org/0000-0001-6903-2906; Görlich, Dennis ORCID logoORCID: https://orcid.org/0000-0002-2574-9419; Berdel, Wolfgang E. ORCID logoORCID: https://orcid.org/0000-0002-3030-6567; Wörmann, Bernhard ORCID logoORCID: https://orcid.org/0000-0003-2273-5502; Braess, Jan; Hiddemann, Wolfgang; Tischer, Johanna ORCID logoORCID: https://orcid.org/0000-0003-1821-1976; Herold, Tobias ORCID logoORCID: https://orcid.org/0000-0002-9615-9432; Metzeler, Klaus H. ORCID logoORCID: https://orcid.org/0000-0003-3920-7490 und Spiekermann, Karsten ORCID logoORCID: https://orcid.org/0000-0002-5139-4957 (2023): Acute megakaryoblastic leukaemia shows high frequency of chromosome 1q aberrations and dismal outcome. In: British Journal of Haematology, Bd. 202, Nr. 6: S. 1165-1177 [PDF, 1MB]

Abstract

Acute megakaryoblastic leukaemia (AMKL) is associated with poor prognosis. Limited information is available on its cytogenetics, molecular genetics and clinical outcome. We performed genetic analyses, evaluated prognostic factors and the value of allogeneic haematopoietic stem cell transplantation (allo-HSCT) in a homogenous adult AMKL patient cohort. We retrospectively analysed 38 adult patients with AMKL (median age: 58 years, range: 21–80). Most received intensive treatment in AML Cooperative Group (AMLCG) trials between 2001 and 2016. Cytogenetic data showed an accumulation of adverse risk markers according to ELN 2017 and an unexpected high frequency of structural aberrations on chromosome arm 1q (33%). Most frequently, mutations occurred in TET2 (23%), TP53 (23%), JAK2 (19%), PTPN11 (19%) and RUNX1 (15%). Complete remission rate in 33 patients receiving intensive chemotherapy was 33% and median overall survival (OS) was 33 weeks (95% CI: 21–45). Patients undergoing allo-HSCT (n = 14) had a superior median OS (68 weeks; 95% CI: 11–126) and relapse-free survival (RFS) of 27 weeks (95% CI: 4–50), although cumulative incidence of relapse after allo-HSCT was high (62%). The prognosis of AMKL is determined by adverse genetic risk factors and therapy resistance. So far allo-HSCT is the only potentially curative treatment option in this dismal AML subgroup.

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