Table 2.
. | WT Responders/All Carriers [n], (%) | Heterozygous Variant Responders/All Carriers [n], (%) | Homozygous Variant Responders/All Carriers [n], (%) | p |
---|---|---|---|---|
CYP3A4*2 (S222P) | 14/33 (42.42%) | — | — | N/A |
CYP3A4*1B (-289A->G) | 14/33 (42.42%) | — | — | N/A |
CYP3A4*3 (M445T) | 14/33 (42.42%) | — | — | N/A |
CYP2B6 (Q172H) | 12/27 (44.44%) | 2/5 (40%) | 0/1 (0%) | 0.62 |
CYP2B6 (K262R) | 4/14 (28.57%) | 9/16 (56.25%) | 1/3 (33%) | 0.12 |
GSTM1 (deletion) | 7/16 (43.75%) | N/A 1 | 7/17 (41.17%) | 0.88 |
GSTP1 (I105V) | 3/14 (21.42%) | 8/13 (61.53%) | 3/6 (50%) | 0.03* |
GSTT1 (deletion) | 9/24 (37.5%) | N/A 1 | 4/8 (50%) | 0.41 |
1 GSTM1 and GSTT1 deletion variants could only be detected in homozygous form. * The presented p value is from a post-hoc analysis assuming a dominant genetic model.