Drug resistance and BCR-ABL kinase domain mutations in philadelphia chromosome-positive acute lymphoblastic leukemia from the imatinib to the second-generation tyrosine kinase inhibitor era: The main changes are in the type of mutations, but not in the frequency of mutation involvement

  • Simona Soverini
  • , Caterina De Benedittis
  • , Cristina Papayannidis
  • , Stefania Paolini
  • , Claudia Venturi
  • , Ilaria Iacobucci
  • , Mario Luppi
  • , Paola Bresciani
  • , Marzia Salvucci
  • , Domenico Russo
  • , Simona Sica
  • , Ester Orlandi
  • , Tamara Intermesoli
  • , Antonella Gozzini
  • , Massimiliano Bonifacio
  • , Gian Matteo Rigolin
  • , Fabrizio Pane
  • , Michele Baccarani
  • , Michele Cavo
  • , Giovanni Martinelli

Risultato della ricerca: Contributo in rivistaArticolo

Abstract

Patients with Philadelphia chromosome-positive (Ph+) acute lymphoblastic leukemia (ALL) frequently relapse on imatinib with acquisition of BCR-ABL kinase domain (KD) mutations. To analyze the changes that second-generation tyrosine kinase inhibitors (TKIs) have brought in mutation frequency and type, a database review was undertaken of the results of all the BCR-ABL KD mutation analyses performed in the authors' laboratory from January 2004 to January 2013.
Lingua originaleInglese
pagine (da-a)1002-1009
Numero di pagine8
RivistaCancer
DOI
Stato di pubblicazionePubblicato - 2014

Keywords

  • BCR-ABL mutations
  • acute lymphoblastic leukemia
  • dasatinib
  • imatinib
  • resistance

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