Pressurized intraperitoneal aerosol chemotherapy (PIPAC) in association with systemic chemotherapy and bevacizumab, evaluation of safety and feasibility. A single center comparative study

被引:19
作者
Siebert, Matthieu [1 ,2 ]
Alyami, Mohammad [1 ,2 ,3 ]
Mercier, Frederic [1 ,4 ]
Gallice, Colin [1 ,2 ]
Villeneuve, Laurent [1 ,5 ]
Laplace, Nathalie [1 ,2 ]
Passot, Guillaume [1 ,2 ]
Bakrin, Naoual [1 ,2 ]
Glehen, Olivier [1 ,2 ]
Kepenekian, Vahan [1 ,2 ]
机构
[1] Hosp Civils Lyon, Ctr Hosp Lyon Sud, Dept Surg Oncol, Pierre Benite, France
[2] Lyon 1 Univ, EMR 3738, Lyon, France
[3] King Khalid Hosp, Dept Gen Surg & Surg Oncol, Najran, Saudi Arabia
[4] Ctr Hosp Univ Montreal, Dept Surg Oncol, Montreal, PQ, Canada
[5] Lyon Univ Hosp, Dept Publ Hlth Clin Res & Epidemiol, Lyon, France
来源
EJSO | 2021年 / 47卷 / 01期
关键词
Peritoneal metastasis; PIPAC; VEGF-A; Targeted therapies; METASTATIC COLORECTAL-CANCER; WOUND-HEALING COMPLICATIONS; CYTOREDUCTIVE SURGERY; PERITONEAL CARCINOMATOSIS; OXALIPLATIN; MANAGEMENT; PLACEMENT; MORBIDITY; HIPEC;
D O I
10.1016/j.ejso.2019.03.021
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: Pressurized intraperitoneal aerosol chemotherapy (PIPAC) is a promising technic for unresectable peritoneal metastasis (PM). Targeted therapies such as bevacizumab have demonstrated their efficacy in advanced colorectal and ovarian cancer. We aimed to evaluate the feasibility and safety of this bidimensional therapeutic association. Methods: A prospectively maintained PIPAC database was retrospectively analyzed from December 2015 to March 2018. All patients who underwent PIPAC for unresectable PM were selected. Patients with systemic chemotherapy including bevacizumab (BEVA group) were compared with patients with systemic chemotherapy without bevacizumab (NON-BEVA group). Major morbidity and mortality were analyzed. Results: 134 patients underwent 397 PIPAC in Lyon Sud University Hospital. 26 Patients had 88 PIPAC in the BEVA group were compared to 108 patients who had 309 PIPAC in the NON-BEVA group. Patients in the BEVA group demonstrated a higher Peritoneal Cancer Index (PCI 20 vs. 16, p <0.001). There was no statistical difference in overall 30-day morbidity (BEVA: 13 (14.8%) vs NON-BEVA: 29 (9.4%); p = 0.147). There was no statistical difference for grade III-IV complications (BEVA: 4 (4.5%) vs NON-BEVA 10 (3.2%); P = 0.521). Major complications from BEVA group were as follow, 2 bowel obstructions, one hematoma and one severe hypersensitivity reaction to platinum compound. There was no 30-day mortality in the BEVA group compared to 6 (5.5%) mortality in the NON-BEVA group. Conclusion: PIPAC associated with bevacizumab is feasible, safe and well tolerated. The potential oncologic benefit of the concomitant use of bevacizumab and PIPAC remains to be evaluated. (C) 2019 Published by Elsevier Ltd.
引用
收藏
页码:139 / 142
页数:4
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