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. 2020 Jan 10;34(7):1775–1786. doi: 10.1038/s41375-019-0700-9

Table 2.

Baseline demographics and disease characteristics.

Baseline characteristic IM (n = 30) IM/HCQ (n = 32)
Median age, years (IQR) 49.5 (42.0–66.0) 50.0 (38.5–60.5)
Gender
   Female 33.3% 28.1%
   Male 66.7% 71.9%
Ethnicity
   White 93.1% 100.0%
   Afro/Caribbean 6.9% 0.0%
ECOG
   0 93.1% 87.5%
   1 6.9% 12.5%
IM dose at trial entry
   400 mg 90.0% 84.4%
   600 mg 6.7% 12.5%
   800 mg 3.3% 3.1%
Median time on IM pre-trial 52.2 (32.8–110.0) 49.7 (27.5–89.0)
Entry, months (IQR)
Response to imatinib at trial entry
   Complete haematological response 10.0% 0.0%
   Partial cytogenetic response 3.3% 0.0%
   Major cytogenetic response 3.3% 6.3%
   Complete cytogenetic response 30.0% 25.0%
   Major molecular response 50.0% 62.5%
   Deep molecular response 0.0% 0.0%
   Unknown 3.3% 6.3%
Additional chromosomal abnormalities 6.7%a 9.4%b

Data presented as percentage, or median (with IQR)

IM imatinib, HCQ hydroxychroroquine, IQR inter-quartile range (the 25th and 75th percentiles)

aOne patient on imatinib only had a variant Philadelphia chromosome translocation, and one had a deletion of chromosome 12

bOne patient on IM/HCQ had trisomy 21, one had a double Phliadelphia chromosome abnormality and one had a deletion of chromosome 9