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. 2023 Jun 10;15(12):3137. doi: 10.3390/cancers15123137

Table 1.

Clinical outcomes of repeated IPC with systemic chemotherapy for gastric cancer with PM.

Author, Year IP Regimen Systemic Regimen Study n MST (mo) 1 y OS (%) Cytology Negative Conversion Rate (%)
Ishigami, 2010 [33] PTX (20 mg/m2) S-1 + PTX P2 40 22.5 78 86
Fujiwara, 2012 [34] DTX (40~60 mg/m2) S-1 R/S 18 24.6 76 78
Fushida, 2013 [35] DTX (45 mg/m2) S-1 P1/2 39 16.2 70.4 81
Yamaguchi, 2013 [36] PTX (20 mg/m2) S-1 + PTX P1 35 17.6 77.1 97
Ishigami, 2016 [37] PTX (20 mg/m2) S-1 + PTX P3 114 17.7 71.9 95
Fujiwara, 2016 [38] PTX (40 mg/m2) S-1 + L-OHP P2 60 NR 71.5 71
Fukushima, 2017 [39] DTX (10 mg/m2) Cap + CDDP P2 48 NR 75 76
Cho, 2017 [40] DTX (100 mg/m2) Cap + CDDP P1/2 39 15.1 - -
Shinkai, 2018 [41] PTX (60 mg/m2) S-1 + PTX + CDDP P2 17 23.9 82.4 -
Yonemura, 2020 [42] DTX (30 mg/m2) + CDDP (30 mg/m2) DTX + CDDP R/S 419 20.5 70 63.5
Saito, 2021 [43] PTX (40 mg/m2) S-1 + L-OHP R/S 44 25.8 79.5 86

Cap—capecitabine; CDDP—cisplatin; DTX—docetaxel; IPC—intraperitoneal chemotherapy; L-OHP—oxaliplatin; MST—median survival time; NR—not reached; OS—overall survival; PM—peritoneal metastases; PTX—paclitaxel; P1, 2, 3—phase I, II, III; R/S—retrospective study; -—not described.