2024
Mutations in myeloid transcription factors and activated signaling genes predict chronic myeloid leukemia outcomes
PERUSINI, Maria Agustina, Daniela ŽÁČKOVÁ, TaeHyung KIM, Katia B B PAGNANO, Carolina PAVLOVSKY et. al.Základní údaje
Originální název
Mutations in myeloid transcription factors and activated signaling genes predict chronic myeloid leukemia outcomes
Autoři
PERUSINI, Maria Agustina, Daniela ŽÁČKOVÁ (203 Česká republika, domácí), TaeHyung KIM, Katia B B PAGNANO, Carolina PAVLOVSKY, Ivana JEŽÍŠKOVÁ (203 Česká republika, domácí), Anežka KVETKOVÁ (703 Slovensko, domácí), Tomáš JURČEK (203 Česká republika, domácí), Jaeyoon John KIM, Young Seok YOO, Seongyoon YI, Hyewon LEE, Kyoung Ha KIM, Myunghee CHANG, Capo-Chichi JOSE-MARIO, Jessie MEDEIROS, Andrea ARRUDA, Mark D MINDEN, Zhaolei ZHANG, Sagi ABELSON, Jiří MAYER (203 Česká republika, domácí) a Dennis Dong Hwan KIM
Vydání
Blood advances, AMSTERDAM, ELSEVIER, 2024, 2473-9529
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30205 Hematology
Stát vydavatele
Nizozemské království
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 7.500 v roce 2022
Organizační jednotka
Lékařská fakulta
UT WoS
001293872300001
Klíčová slova anglicky
Myeloid Neoplasia
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 2. 9. 2024 15:00, Mgr. Tereza Miškechová
Anotace
V originále
Advancements in genomics are transforming the clinical management of chronic myeloid leukemia (CML) towards precision medicine. The impact of somatic mutations on treatment outcomes is still under debate. We studied the association of somatic mutations in epigenetic modifiers genes and activated signaling/myeloid transcription factor (AS/MTF), with disease progression and treatment failure in CML patients following tyrosine kinase inhibitor (TKI) therapy. A total of 394 CML samples were sequenced, including 254 samples collected at initial diagnosis, and 140 samples taken during follow-up. Single-molecule molecular inversion probe (smMIP)-based next-generation sequencing (NGS) was conducted targeting recurrently mutated loci in 40 genes with a limit of detection of 0.2%. A total of 70 mutations were detected in 57 (22.4%) diagnostic samples, while 64 mutations were detected in 39 (27.9%) of the follow-up samples. Carrying any mutation at initial diagnosis was associated with worse outcomes following TKI therapy, particularly in AS/MTF genes. Patients having these mutations at initial diagnosis and treated with Imatinib showed higher risks of treatment failure (HR 2.53, 95% CI [1.13-5.66], p=0.0239). The adverse prognostic impact of the mutations was not clear for patients treated with second-generation TKIs (2G-TKI). The multivariate analysis affirmed that mutations in AS/MTF genes independently serve as adverse prognostic factors for molecular response, failure-free survival (FFS), and progression risk. Additionally, there was an observable non-significant trend indicating a heightened risk of progression to advanced disease and worse overall survival (OS). Conclusion: Mutations in the AS/MTF genes using smMIP-based NGS can help identify patients with a potential risk of both treatment failure and progression, even from initial diagnosis, and may help upfront TKI selection.