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. Author manuscript; available in PMC: 2014 Sep 27.
Published in final edited form as: Cancer. 2009 Jul 1;115(13):2912–2921. doi: 10.1002/cncr.24325

Table 4.

Rates of Complete Cytogenetic Response (All Studies) and Major Molecular Response (CA180-013 Study Only) in Patients With Pre-existing BCR-ABL Mutations Treated With Dasatinib After Loss of Response to Prior Imatinib

Patients, n/N (%)
Variable Group 1: Loss of MCyR Group 2: Loss of MCyR and CHR Group 3: Loss of CHR
CCyR
No BCR-ABL mutation 51/75 (68) 5/10 (50) 8/26 (31)
Any BCR-ABL mutation 46/60 (77) 9/20 (45) 19/77 (25)
        T315I 0/2 (0) 0/1 (0) 0/1 (0)
        F317L 1/1 (100) 0/4 (0)
        F359C/I/V 8/8 (100) 1/6 (17)
        P-loop region* 13/19 (68) 2/7 (29) 7/30 (23)
                L248V 1/2 (50) 2/6 (33)
                G250E 5/6 (83) 1/4 (25) 1/12 (8)
                Q252H 0/1 (0) 1/2 (50)
                Y253F/H 6/8 (75) 1/1 (100) 2/8 (25)
                E255K/V 1/2 (50) 0/2 (0) 1/4 (25)
        Sample unavailable 11/16 (69) 0/3 (0) 1/6 (17)
MMR
        No BCR-ABL mutation 13/24 (54) 1/3 (33) 5/12 (42)
        Any BCR-ABL mutation 13/21 (62) 4/13 (31) 8/35 (23)
        Sample unavailable 2/2 (100) 0/1 (0) 0/3 (0)

MCyR indicates major cytogenetic response; CHR, complete hematologic response; CCyR, complete cytogenetic response; T315I, threonine-to-isoleucine mutation at codon 315; F317L, phenylalanine-to-leucine mutation at codon 317; F359C/I/V, phenylalanine-to-cysteine, valine, or isoleucine mutation at codon 359; P-loop, adenosine triphosphate phosphate-binding loop; L248V, leucine-to-valine mutation at codon 248; G250E, glycine-to-glutamic acid mutation at codon 250; Q252H, glutamine-to-histidine mutation at codon 252; Y253F/H, tyrosine-to-phenylalanine or histidine mutation at codon 253; E255K/V, glutamic acid-to-lysine or valine mutation at codon 255; MMR, major molecular response.

*

Residues 248 through 256.