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. 1998 Dec 22;95(26):15798–15802. doi: 10.1073/pnas.95.26.15798

Table 2.

Comparison of therapeutic effect and toxicity of dEpoB with different doses, solvents, schedules, and routes of administration in nude mice bearing MX-1 xenografts

Dose, mg/kg Schedule Solvent* Route Average tumor size (T/C) Tumor free mice/total mice Toxicity death/total mice
15 Q2D  ×  5 DMSO i.p. injection 0.41 0/5 0/5
20 Q2D  ×  8 DMSO i.p. injection 0.33 0/5 0/5
25 Q2D  ×  5 DMSO i.p. injection 0.04 0/6 0/6
35 Q2D  ×  5 DMSO i.p. injection 0.02 3/10 (6, 8, 10) 0/10
15 Q2D  ×  5 C/EtOH i.v. 30-min infusion ND ND 4/6 (15, 15, 15, 17)
20 Q2D  ×  2 C/EtOH i.v. 1-min injection ND ND 1/1 (4)
20 Q2D  ×  5 C/EtOH i.v. 30-min infusion ND ND 6/6 (10, 10, 11, 11, 11, 11)
20 Q2D  ×  1 C/EtOH i.p. injection ND ND 1/1 (3)
30 Q2D  ×  5 C/EtOH i.v. 2-hr infusion ND ND 2/3 (10, 10)
30 Q2D  ×  6 C/EtOH i.v. 6-hr infusion 0 5/5 (8, 12, 12, 12, 12) 0/5
30 Q1D  ×  4 C/EtOH i.v. 6-hr infusion ND ND 1/1 (6)
30 Q2D  ×  4 C/EtOH i.v. 24-hr infusion 0, ND 1/2 (10) 1/2 (12)
60 Q4D  ×  2 C/EtOH i.v. 24-hr infusion 0, ND 1/2 (12) 1/2 (16)
50 Q2D  ×  5 PEG§ oral 0.68 0/1 0/1

ND, not determined (mice died). MX-1, human mammary carcinoma, 50 mg per mouse implanted s.c. into mice on day 0. Treatments started on day 10. Q2D, every other day. 

*

DMSO: Dimethylsulfoxide 40 μl per mouse; C/EtOH: Cremophor/EtOH (1:1), 100 μl for i.p. injection; 100 μl + saline 0.2 ml for 1-min i.v. or 30-min injection; 100 μl + saline (3–5 ml) for 2–24 hr i.v. infusions. 

Average tumor size of treated group/average tumor size of the control group at 2 days after the last dose. 

B-16 melanoma tumor xenograph for this group; all other groups were for MX-1 xenografts. 

§

Polyethylene glycol-400/ethanol (10:1). 

The numbers in parenthesis refer to the number of days that mice, after the beginning of treatment, were tumor-free or the number of days before death due to toxicity after the beginning of treatment.