Alyami Mohammad, Gagniere Johan, Sgarbura Olivia, Cabelguenne Delphine, Villeneuve Laurent, Pezet Denis, Quenet Francois, Glehen Olivier, Bakrin Naoual, Passot Guillaume
Department of Surgical Oncology, Centre Hospitalier Lyon-Sud, Hospices Civils de Lyon, Pierre-Bénite, France; EMR 3738, Lyon 1 University, Lyon, France; King Salman Scholarship Program, Saudi Arabian Cultural Bureau, Paris, France.
Department of Digestive and Hepatobiliary Surgery, Centre Hospitalier Univeristaire de Clermont Ferrand, Clermont-Ferrand, France; U1071 INSERM, Université Clermont Auvergne, Clermont-Ferrand, France.
Eur J Surg Oncol. 2017 Nov;43(11):2178-2183. doi: 10.1016/j.ejso.2017.09.010. Epub 2017 Sep 21.
PIPAC is a recent approach for intraperitoneal chemotherapy with promising results for patients with peritoneal carcinomatosis (PC). We aimed to evaluate the postoperative outcome of PIPAC in patients with non-resectable PC during our initial experience of the technique.
All patients who underwent PIPAC for non-resectable PC in three centers were analyzed regarding postoperative outcomes.
Seventy-three patients underwent 164 PIPAC. PC was from colorectal, gastric, ovarian, malignant mesothelioma, pseudomyxoma peritonei or other origins in 20, 26, 13, 8, 1 and 5 patients respectively. Forty-five (62%), 31 (42%), 8 (11%), 6 (8%), 1 (1%) patients underwent a second, third, fourth, fifth, and sixth PIPAC respectively. At the time of the first PIPAC, the median PCI was 17 (1-39), 57 patients presented with symptomatic PC (pain: 33; ascites: 35; transit disorder like diarrhea and constipation: 11). PCI improved in 64.5% of patients, 63.5% of patients presented with complete disappearance of symptoms. Major complications occurred as the outcome of 16 PIPAC (9.7%) and 5 (6.8%) patients died within 30 days of the PIPAC procedure. Rate of mortality and major complications 40% and 62% respectively occurred in first 20 treated patients. For 64 (88%) patients, systemic chemotherapy was associated with PIPAC and could be administered after PIPAC with a median delay of 14 days (2-28).
Implementing a PIPAC program in association with systemic chemotherapy is feasible and is associated with a risk of postoperative morbidity, even in teams highly experienced in PC management and requires a learning curve in patient selection.
腹腔内热灌注化疗(PIPAC)是一种近期开展的腹腔内化疗方法,对腹膜癌病(PC)患者有良好效果。我们旨在评估在初次应用该技术时,PIPAC治疗不可切除PC患者的术后结局。
分析三个中心所有接受PIPAC治疗不可切除PC的患者的术后结局。
73例患者接受了164次PIPAC治疗。PC分别起源于结直肠癌、胃癌、卵巢癌、恶性间皮瘤、腹膜假黏液瘤或其他部位,各有20、26、13、8、1和5例患者。分别有45例(62%)、31例(42%)、8例(11%)、6例(8%)、1例(1%)患者接受了第二次、第三次、第四次、第五次和第六次PIPAC治疗。首次PIPAC治疗时,腹膜癌指数(PCI)中位数为17(1 - 39),57例患者有症状性PC(疼痛:33例;腹水:35例;腹泻和便秘等肠道功能紊乱:11例)。64.5%的患者PCI改善,63.5%的患者症状完全消失。16次PIPAC治疗(9.7%)出现严重并发症,5例(6.8%)患者在PIPAC治疗后30天内死亡。在前20例接受治疗的患者中,死亡率和严重并发症发生率分别为40%和62%。64例(88%)患者在PIPAC治疗同时联合全身化疗,可在PIPAC治疗后进行,中位延迟时间为14天(2 - 28天)。
联合全身化疗实施PIPAC方案是可行的,但即使是在PC管理方面经验丰富的团队,也存在术后发病风险,且在患者选择方面需要一个学习曲线。