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. 2014 Jan 16;110(5):1155–1162. doi: 10.1038/bjc.2013.826

Table 1. Patient characteristics.

Pat Dose level Age Sex # Pretreatments Type of pretreatment Gene, exon Primary mutation ECOG PET-response RECIST Days on study treatment
101
20
34
m
11
IM, SU, other
KIT exon 11, Exon 17
Del E554-V559; D820Y
0
mPD
PD
25
102
20
41
m
5
IM, SU, Nilo, Sora, other
PDGFR Exon 12
Del V559-P573; D820G
0
mPR
SD
116
103
30
60
m
4
IM, SU, Dasa, Nilo
PDGFR Exon 18
D842V
0
mSD
PD
12
104
30
38
w
5
IM, SU, Nilo, Sora, other
KIT exon 9
duplication A502 and Y503; Y823D
 
mPD
SD
26
106
20 Extension
75
w
4
IM, SU, Nilo, Sora

NA
1
mSD
SD
35
107
20 Extension
38
m
4
IM, SU, Nilo, other
KIT intron 10/exon 11
K550–558dela
0
mPD

18
108
20 Extension
55
m
5
IM, SU, other
KIT, Exon 11
K558-V559insP
0
mSD
SD
 
201
20
56
m
3
IM, SU, other
KIT, Exon 13
K642E
0
mSD
SD
74
202
30
54
w
4
IM, SU, other
c-KIT Exon 11
Del K558
1
mSD
SD
65
203
30
74
w
5
IM, SU, Sora, other

Exon 11 wt, other exons not analysed
1

PD
86
204
20
63
w
8
IM, SU,Nilo, Sora, other
KIT, Exon 9
Duplication A502 and Y503
1
mSD
SD
51
205 20 69 m 10 IM, SU, Nilo, Sora, other KIT, Exon 11 Y553-K558delinsW 1 mSD SD 72

Abbreviations: IM=imatinib; mPD=metabolic progressive disease; mPR=metabolic partial response; mSD=metabolic stable disease; NA=not applicable; Nilo=nilotinib; Sora=Sorafenib; SU=sunitinib.

a

Mutational analysis kindly provided by Professor Stephan Dirnhofer, Basel.