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. Author manuscript; available in PMC: 2024 Jan 29.
Published in final edited form as: Mol Cancer Ther. 2020 Feb 13;19(4):1059–1069. doi: 10.1158/1535-7163.MCT-19-0378

Figure 5.

Figure 5.

In vivo tumor responses, survival, and PSA in LuCaP 96CR PDX. Fox Chase CB17 SCID male mice were castrated and were implanted with LuCaP 96CR tumor fragments 2 weeks later. Once tumor volumes exceeded 101 mm3, animals were randomized to receive Natrosol vehicle control [p.o.; n = 15], ENZA (30 mg/kg p.o.; 5 days on, 2 days off, for 10 cycles; n = 15), or ENZA (dosing regimen as previously noted) plus XENT [200 mg/kg i.p., once weekly for 10 cycles; n = 14]. A) Change in tumor volume with time by treatment group; adjusted P values were calculated 7 weeks after start of treatment. B) Dot plot of tumor volumes in individual animals, by treatment group, 7 weeks after start of treatment. C) Survival by treatment group. D) Individual serum PSA levels, at 2 weeks of treatment, and at sacrifice. P values were calculated using one-sided decreasing Mann–Whitney tests (adjusted according to Bonferroni–Holm).