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. 2014 Sep 6;4(5):528–536.

Table 6.

Univariate analysis of predictive factors for combined OTR and PFS in patients with mCRC treated with FOLFOX-based chemotherapy

Variables N gOTR/lPFS (%) Non-gOTR/lPFS (%)a P value
Primary tumor site
    Colon 55 20 (36) 35 (64) 0.11
    Rectum 24 4 (17) 20 (83)
Histological classification
    Well/moderate 75 22 (29) 53 (71) 0.58
    Poor/mucinous 4 2 (50) 2 (50)
Depth of invasion
    pT2/pT3 41 8 (20) 22 (80) 0.05
    pT4 38 16 (42) 33 (58)
Lymph node metastasis
    pN0/pN1 44 14 (32) 30 (68) 0.81
    pN2 35 10 (29) 25 (71)
Lymphatic invasion
    ly0/ly1 18 6 (33) 12 (67) 0.78
    ly2/ly3 61 18 (30) 43 (70)
Venous invasion
    v0/v1 21 6 (29) 15 (71) 1.00
    v2/v3 58 18 (31) 40 (69)
OAT2/OCT2
    High/high 18 11 (61) 7 (39) 0.003c
    Non-high/highb 61 13 (21) 48 (79)
a

Patients with unfavorable outcomes of at least one of OTR and PFS.

b

Tumors with low levels of at least one of OAT2 and OCT2.

c

Statistically significant.

This analysis was evaluable in 79 of the 90 patients. FOLFOX: 5-fluorouracil/leucovorin/oxaliplatin; gOTR/lPFS: good OTR/long PFS; mCRC: metastatic colorectal cancer; OAT2: organic anion transporter 2; OCT2: organic cation transporter 2; OTR: objective tumor response; PFS: progression-free survival.