Research Article

Personalized Treatment of Advanced Gastric Cancer Guided by the MiniPDX Model

Table 2

MiniPDX drug sensitivity results of the 4 patients.

NumberChemotherapy regimenInhibition rate (1-T/C%)Weight loss of mice >15%Source of cancer cells

Patient #15, Irinotecan68Gastroscopic biopsy of gastric cancer
6, Nab-paclitaxel47
7, Anlotinib46
8, Apatinib52
9, Pyrotinib55

Patient #25, Oxaliplatin + capecitabine20Gastroscopic biopsy of gastric cancer
6, Oxaliplatin + CF + 5-FU16
7, Docetaxel + S-16
8, S-123
9, Apatinib + irinotecan28
Patient #35, Irinotecan80Gastroscopic biopsy of gastric cancer
6, Nab-paclitaxel
7, Anlotinib
8, Apatinib81
5, Pyrotinib

Patient #45, Nab-paclitaxel + S-1Gastroscopic biopsy of gastric cancer
6, Docetaxel + S-1
7, Irinotecan + apatinib
8, Docetaxel + apatinib66
9, Fruquintinib + nab-paclitaxel71

1, Notes: Inhibition rate was calculated by 1-T/C% (T/C% = treatment group proliferation rate/control group proliferation rate%). Each regimen was used on MiniPDX models with the same doses. Detailed doses for the MiniPDX models—irinotecan: 50 mg/kg, IP, day 1 and day 5; nab-paclitaxel, 20 mg/kg, IV, day 1–day 5; anlotinib, 3 mg/kg, PO, day 1–day 7; apatinib: 100 mg/kg, PO, day 1–day 7; pyrotinib, 10 mg/kg, PO, day 1–day 7; (oxaliplatin + capecitabine): oxaliplatin (Oxa), 5 mg/kg, IP, day 1 + capecitabine (Cape), 400 mg/kg, PO, day 1–day 7; (oxaliplatin + CF+5-FU): oxaliplatin, 5 mg/kg, IP, day 1 + CF, 50 mg/kg, IP, day 1 + 5-FU, 25 mg/kg, IP, day 1–day 5; (docetaxel + S-1): docetaxel (Doc): 20 mg/kg, IP, day 1 and day 5 + S-1, 10 mg/kg, PO, day 1–day 5; S-1: S-1, 10 mg/kg, PO, day 1–day 5; (irinotecan + apatinib): 50 mg/kg, IP, day 1 and day 5+ 100 mg/kg, PO, day 1–day 7; (nab-paclitaxel + S-1): nab-paclitaxel 20 mg/kg, IV, day 1–day 5 + S-1, 10 mg/kg, PO, day 1–day 5; (docetaxel + apatinib): docetaxel: 20 mg/kg, IP, day 1 and day 5 + apatinib: 100 mg/kg, PO, day 1–day 7; (fruquintinib + nab-paclitaxel): fruquintinib (Fru): 20 mg/kg, PO, day 1–day 7 + 20 mg/kg, IV, day 1–day 5.