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Outcome of 3q26.2/MECOM rearrangements in chronic myeloid leukemia.
Akiyama, Hiroki; Kantarjian, Hagop; Jabbour, Elias; Issa, Ghayas; Haddad, Fadi G; Short, Nicholas J; Hu, Shimin; Ishizawa, Jo; Andreeff, Michael; Sasaki, Koji.
Afiliação
  • Akiyama H; Department of Leukemia, The University of Texas, MD Anderson Cancer Center, 1515 Holcombe Blvd. Unit 428, Houston, TX, 77030, USA.
  • Kantarjian H; Department of Leukemia, The University of Texas, MD Anderson Cancer Center, 1515 Holcombe Blvd. Unit 428, Houston, TX, 77030, USA.
  • Jabbour E; Department of Leukemia, The University of Texas, MD Anderson Cancer Center, 1515 Holcombe Blvd. Unit 428, Houston, TX, 77030, USA.
  • Issa G; Department of Leukemia, The University of Texas, MD Anderson Cancer Center, 1515 Holcombe Blvd. Unit 428, Houston, TX, 77030, USA.
  • Haddad FG; Department of Leukemia, The University of Texas, MD Anderson Cancer Center, 1515 Holcombe Blvd. Unit 428, Houston, TX, 77030, USA.
  • Short NJ; Department of Leukemia, The University of Texas, MD Anderson Cancer Center, 1515 Holcombe Blvd. Unit 428, Houston, TX, 77030, USA.
  • Hu S; Department of Hematopathology, The University of Texas, MD Anderson Cancer Center, Houston, TX, 77030, USA.
  • Ishizawa J; Department of Leukemia, The University of Texas, MD Anderson Cancer Center, 1515 Holcombe Blvd. Unit 428, Houston, TX, 77030, USA.
  • Andreeff M; Department of Leukemia, The University of Texas, MD Anderson Cancer Center, 1515 Holcombe Blvd. Unit 428, Houston, TX, 77030, USA.
  • Sasaki K; Department of Leukemia, The University of Texas, MD Anderson Cancer Center, 1515 Holcombe Blvd. Unit 428, Houston, TX, 77030, USA. ksasaki1@mdanderson.org.
Int J Hematol ; 120(2): 203-211, 2024 Aug.
Article em En | MEDLINE | ID: mdl-38748089
ABSTRACT
STUDY

AIMS:

To evaluate the outcomes of patients with 3q26.2/MECOM-rearranged chronic myeloid leukemia (CML).

METHODS:

We reviewed consecutive adult patients with 3q26.2/MECOM-rearranged CML between January 1, 1998 and February 16, 2023. Rearrangements of 3q26.2/MECOM were confirmed by conventional cytogenetics, and fluorescence in situ hybridization starting in 2015.

RESULTS:

We identified 55 patients with MECOM-rearranged CML, including 23 in chronic phase (CP) or accelerated phase (AP) and 32 in blast phase (BP). Nine patients (16%) achieved a major cytogenetic response (MCyR) or deeper. At a median follow-up of 89 months, median survival was 14 months. The 5-year survival rate was 19% overall, 23% in CML-CP/AP, and 15% in CML-BP. In the 6-month landmark analysis, the 5-year survival rate was 41% for allogeneic stem cell transplantation (allo-SCT) recipients versus 17% for non-recipients (P = 0.050). Multivariate analysis showed that the percentage of marrow blasts and achievement of MCyR or deeper could predict survival.

CONCLUSION:

Outcomes of 3q26.2/MECOM-rearranged CML are poor despite the availability of multiple BCRABL1 tyrosine kinase inhibitors (TKIs). Third-generation TKIs in combination with novel agents and possible allo-SCT could be considered given the poor outcomes and resistance to second-generation TKIs.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 3 / Rearranjo Gênico / Leucemia Mielogênica Crônica BCR-ABL Positiva Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 3 / Rearranjo Gênico / Leucemia Mielogênica Crônica BCR-ABL Positiva Idioma: En Ano de publicação: 2024 Tipo de documento: Article