Indiana University School of Medicine, Department of Surgery, Indianapolis, Indiana, USA.
Dis Colon Rectum. 2012 Oct;55(10):1044-52. doi: 10.1097/DCR.0b013e318265ad42.
Delayed repeated intraperitoneal chemotherapy after cytoreductive surgery for carcinomatosis may be an alternative to intraoperative hyperthermic infusion.
The aim of this study was to evaluate the safety and feasibility of delayed repeated intraperitoneal chemotherapy after cytoreduction of colorectal and appendiceal carcinomatosis and pseudomyxoma peritonei.
This study constitutes a retrospective case series.
This study was conducted at a single institution.
A total of 31 patients with peritoneal carcinomatosis (23) and pseudomyxoma peritonei (8) were included.
Cytoreduction was followed by placement of an adhesion barrier and intraperitoneal catheters. Peritoneal scintigraphy preceded biweekly intraperitoneal 5-fluorouracil and systemic combination chemotherapy with leucovorin, fluorouracil, and oxaliplatin (FOLFOX).
The primary outcomes measured are safety, feasibility, and short-term survival.
Cytoreduction to a score of 0 to 1 was possible in 25 patients (80%). Complications occurred in 16 patients (51.6%) and were confined to grades I to III. There were no deaths, and no digestive fistulae occurred. Port malfunction or complication resulted in removal in 5 patients (16.1%). Intraperitoneal chemotherapy was possible in 83.8% of patients; 55% completed the full course. Peritoneal scintigraphy demonstrated free diffusion of tracer in 18 patients (58%), 4 (12.9%) had diffusion in each gutter with limited communication, 5 (16.1%) had limited diffusion around each catheter without communication, and 2 (6.5%) had no diffusion on scintigraphy. Overall survival for peritoneal carcinomatosis was 44.5% at 3 years (95% CI = 23%-65%).
The nonrandomized nature of this study and the early experience are limitations.
Delayed repeated intraperitoneal and systemic chemotherapy after cytoreduction is feasible and has acceptable morbidity rates. Delayed intraperitoneal chemotherapy is possible in 83% of patients.
细胞减灭术后延迟重复腹腔内化疗可能是腹腔内热灌注的替代方法。
本研究旨在评估结直肠和阑尾癌性腹膜转移和假性黏液瘤患者细胞减灭术后延迟重复腹腔内化疗的安全性和可行性。
本研究为回顾性病例系列研究。
本研究在一家机构进行。
共纳入 31 例腹膜转移患者(23 例)和假性黏液瘤患者(8 例)。
细胞减灭术后放置粘连屏障和腹腔内导管。在每周两次的腹腔内 5-氟尿嘧啶和全身联合化疗(亚叶酸钙、氟尿嘧啶和奥沙利铂)前进行腹腔闪烁扫描。
主要观察指标为安全性、可行性和短期生存率。
25 例患者(80%)可达到 0-1 分的细胞减灭评分。16 例患者(51.6%)出现并发症,且均为 I 至 III 级。无死亡,无消化道瘘。5 例患者(16.1%)因端口功能障碍或并发症而拔除。83.8%的患者可进行腹腔内化疗,55%的患者完成了全程化疗。18 例患者(58%)的示踪剂弥散良好,4 例(12.9%)各引流槽弥散良好但沟通有限,5 例(16.1%)各导管周围弥散有限但无沟通,2 例(6.5%)无弥散。腹膜转移患者的 3 年总生存率为 44.5%(95%CI=23%-65%)。
本研究的非随机性质和早期经验是其局限性。
细胞减灭术后延迟重复腹腔内和全身化疗是可行的,且发病率可接受。83%的患者可进行延迟性腹腔内化疗。