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. 2009 Oct 28;101(2):530–535. doi: 10.1111/j.1349-7006.2009.01418.x

Table 2.

 Response to FOLFOX‐4 treatment in patients with different genetic polymorphisms (n = 166)

Genotypes Responders (%) Non‐responders (%) P‐values
Overall 70 (42.2) 96 (57.8)
GSTP1‐105 status
 Ile/Ile (n = 125) 47 (37.6) 78 (62.4) 0.04
 Ile/Val or Val/Val (n = 41) 23 (56.1) 18 (43.9)
ERCC1‐118 genotype
 C/C (n = 78) 41 (52.6) 7 (47.4) 0.01
 C/T or T/T (n = 88) 29 (33.0) 59 (67.0)
XPD‐751 status
 Lys/Lys (n = 139) 64 (46.0) 75 (54.0) 0.02
 Lys/Gln (n = 27) 6 (22.2) 21 (77.8)
TSER 28‐bp polymorphism
 2R/2R or 2R/3R (n = 56) 26 (46.4) 30 (53.6) 0.43
 3R/3R (n = 110) 44 (40.0) 66 (60.0)
Any risk genotype
 Absence (n = 26) 18 (69.2) 8 (30.8) <0.01
 Presence (n = 140) 52 (37.1) 88 (62.9)

Risk genotypes: GSTP1‐105 Ile/Ile, ERCC1‐118 C/T or T/T, and XPD‐751 Lys/Gln. Non‐responders, patients with stable or progressive diseases; responders, patients with complete or partial remission after treatment with FOLFOX‐4.