Pressurized Intraperitoneal Aerosol Chemotherapy (PIPAC) with Low-Dose Cisplatin and Doxorubicin in Gastric Peritoneal Metastasis

被引:163
作者
Nadiradze, Giorgi [1 ]
Giger-Pabst, Urs [2 ]
Zieren, Juergen [2 ]
Strumberg, Dirk [3 ]
Solass, Wiebke [4 ]
Reymond, Marc-Andre [1 ,2 ,5 ]
机构
[1] Univ Magdeburg, Dept Surg, D-39106 Magdeburg, Germany
[2] Ruhr Univ Bochum, Dept Surg, Univ Str 150, Bochum, Germany
[3] Ruhr Univ Bochum, Dept Internal Med Oncol & Haematol, Univ Str 150, Bochum, Germany
[4] Med Sch Hanover, Inst Pathol, Hannover, Germany
[5] Ruhr Univ Bochum, Marienhosp Herne, Holkeskampring 40, D-44625 Herne, Germany
关键词
Gastric cancer; Peritoneal metastasis; Pressurized intraperitoneal aerosol chemotherapy; Intraperitoneal chemotherapy; Cisplatin; Doxorubicin; OVARIAN-CANCER; INTRAABDOMINAL PRESSURE; CYTOREDUCTIVE SURGERY; CARCINOMATOSIS; PENETRATION; RECURRENT; EFFICACY; THERAPY; PHASE-2; TUMORS;
D O I
10.1007/s11605-015-2995-9
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background Pressurized intraperitoneal aerosol chemotherapy (PIPAC) is a novel technique of intraperitoneal chemotherapy. First results obtained with PIPAC in patients with advanced peritoneal metastasis (PM) from gastric cancer (GC) are presented. Methods Retrospective analysis: Sixty PIPAC were applied in 24 consecutive patients with PM from GC. 67 % patients had previous surgery, and 79 % previous platinum-based systemic chemotherapy. Mean Peritoneal Carcinomatosis Index (PCI) of 16 +/- 10 and 18/24 patients had signet-ring GC. Cisplatin 7.5 mg/m(2) and doxorubicin 1.5 mg/m(2) were given for 30 min at 37 degrees C and 12 mmHg at 6 week intervals. Outcome criteria were survival, adverse events, and histological tumor response. Results Median follow-up was 248 days (range 105-748), and median survival time was 15.4 months. Seventeen patients had repeated PIPAC, and objective tumor response was observed in 12 (12/24=50 %): no vital tumor cells=6, major pathological response=6, minor response=3. Postoperative adverse events>CTCAE 2 were observed in 9 patients (9/24, 37.5 %). In 3/17 patients, a later PIPAC could not be performed due to non-access. Two patients (ECOG 3 and 4) died in the hospital due to disease progression. Conclusion PIPAC with low-dose cisplatin and doxorubicin was safe and induced objective tumor regression in selected patients with PM from recurrent, platinum-resistant GC. First survival data are encouraging and justify further clinical studies in this indication.
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收藏
页码:367 / 373
页数:7
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