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. 2024 Dec 6;28(3):111536. doi: 10.1016/j.isci.2024.111536

Figure 5.

Figure 5

IN10018 enhances the antitumor efficacy of Enhertu in human PDX models

(A–B) The tumor growth curves and body weight changes for the efficacy study with NSCLC PDX model LU-01-1626. IN10018 was dosed to the model once daily by oral gavage. For day 0 to day 3, the dose was 25 mg/kg. Since day 4, the dose of IN10018 was adjusted to 12.5 mg/kg via oral gavage. Enhertu was dosed once weekly by tail vein injection. The dose was set as 10 mg/kg in week 1, 3 mg/kg in week 2, and adjusted to 6 mg/kg from week 3 till the end of the study. Scale bar: 100 μm.

(C) The representative images of the IHC staining with anti-FAP, anti-human IgG, anti-DXD, anti-Ki67, and TUNEL assay for the tumors from the LU-01-1626 model.

(D–F) The FAP-positive cells, anti-human immunoglobulin G (IgG)-positive cells, and anti-DXD-positive cells per unit area of the tumors from LU-01-1626 model.

(G–H) The Ki67 and TUNEL staining analysis of the tumors from LU-01-1626 model. The data from pathological assays were analyzed by ImageJ. Data represent mean ± SEM. The unpaired student’s t test was used for the statistical analysis. ∗p < 0.05, ∗∗p < 0.01. Scale bar: 50 μm.