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. 2012 Feb 13;3(5):755–762. doi: 10.3892/etm.2012.484

Table I.

Antitumor activity and body weight changes in mice implanted with human non-small cell lung cancer tumors from the cell lines, Lu-99 or PC-9, following treatment with S-1 and the EGFR kinase inhibitor, erlotinib.

Body weight changed
Tumor Drug (mg/kg) Treatment Tumor volumea (mm3, mean ± SD) TGIb (%) GDPc (days) (g, mean ± SD) (%)
Lu-99 Control - 1257±196 - 0.0 2.5±0.5 10.1
S-1 (8.3) days 1–14 728±94 42.1 3.3 1.5±1.4 6.0
Erlotinib (100) days 1–14 747±177 40.6 2.8 0.5±1.2 2.3
S-1 + erlotinib 563±60e 55.3 7.0 −3.0±2.5 NS −13.0
PC-9 Control - 661±95 - 0.0 0.9±0.5 3.0
S-1 (10.0) days 1–14 427±20 35.4 1.6 −0.09±0.8 −0.3
Erlotinib (12.5) days 1–14 289±55 56.4 8.8 0.4±0.9 1.6
S-1 + erlotinib 218±39e 67.0 10.9 −0.2±0.6 NS −0.5
a

Tumor volume on day 15;

b

tumor growth inhibition ratio on day 15;

c

GDP is the difference in time taken for the RTV to reach 2.0 between the treated and the control groups;

d

relative body weight change between days 0 and 15;

e

overall maximal P<0.05 by closed testing procedure using the Aspin-Welch t-test; NS, overall maximal P>0.05 by closed testing procedure using the Aspin-Welch t-test; EGFR, epidermal growth factor receptor; GDP, growth delay period; RTV, relative tumor volume; S-1, tegafur-gimeracil-oteracil.