Li Wei-Wei, Ru Xiu-Mei, Xuan Hong-Yan, Fan Qi, Zhang Jing-Jing, Lu Jun
Department of Endocrinology, The Second Affiliated Hospital of Soochow University, Suzhou 215004, Jiangsu Province, China.
Department of Anus and Intestine Surgery, Xiangya Hospital of Central South University, Changsha 410008, Hunan Province, China.
World J Gastrointest Surg. 2024 Nov 27;16(11):3520-3530. doi: 10.4240/wjgs.v16.i11.3520.
Pseudomyxoma peritonei is a rare tumor that can produce a biological behavior similar to that of a malignant tumor. Surgical resection combined with chemotherapy is the traditional treatment method, but the effect is not good. Cell reduction (CRS) combined with intraperitoneal thermoperfusion chemotherapy (HIPEC) has become a new method for the treatment of peritoneal pseudomyxoma (PMP).
To find out if CRS and HIPEC can be used safely and effectively to treat PMP.
This is an observational study. Clinical data of PMP patients treated with CRS + HIPEC at our hospital from January 2013 to June 2023 was collated and analyzed. The main outcome measures were overall survival (OS), and the secondary outcome measures were the incidence of surgical complications and serious adverse events. Complications were graded according to common adverse event evaluation criteria. Peritoneal tumor staging was performed using the peritoneal tumor index (PCI) scoring system, and a cell reduction degree (CCR) score was performed after CRS. CCR-0 and CCR-1 were considered satisfactory CRS.
A total of 186 patients with PMP were included, with a median age of 56 (48-64) years, 65 (34.9%) years in males, and 121 (65.1%) years in females. The median PCI score was 28 (20-34) points. The median operative time was 300 (211-430) minutes, and no significant complications occurred. 91.4% (170/186) were from the appendix, 53.2% (99/186) were from the low grade, and 30.6% (57/186) were from the high grade. CCR scores showed that 55 patients (29.6%) achieved satisfactory CRS, and 113 patients (60.8%) did not achieve satisfactory CRS. The fatality rate at 30 days after surgery was 2.7% (5/186), 1.6% (3/186) needed a second operation, and the fatality rate at 90 days was 4.3% (8/186). The total incidence of III-IV complications was 43.0% (80/186), among which the higher incidence was mainly anemia (27.4%, 51/186), electrolyte disturbance (11.6%, 21/181), and albumin decrease (7.5%, 14/186). The main complications associated with abdominal surgery were gastrointestinal anastomotic leakage (2.2%, 4/186), abdominal hemorrhage (2.2%, 4/186), and abdominal infection (4.3%, 8/186). The median follow-up was 38.1 (95%CI: 31.2-45.1) months. The 5-year OS of PMP patients treated with CRS + HIPEC was 50.3% (95%CI: 40.7%-59.9%), and the median survival time was 66.1 (95%CI: 43.1-89.1) months. The results of the survival analysis showed that patients with a low pathological grade, a low PCI, and a satisfactory CCR score had a higher survival rate (all < 0.05). 5-year OS was 88.9% (95%CI: 68.3%-100.0%) in CCR-0 patients, 77.6% (95%CI: 62.7%-92.5%) in CCR-1 patients, and 42.0% (95%CI: 29.5%-54.5%) in CCR-2/3 patients.
The application of CRS + HIPEC in PMP is safe and feasible, and the survival benefit is high, especially in those who achieve satisfactory CRS, which can significantly extend the OS.
腹膜假黏液瘤是一种罕见肿瘤,可产生类似于恶性肿瘤的生物学行为。手术切除联合化疗是传统治疗方法,但效果不佳。细胞减灭术(CRS)联合腹腔热灌注化疗(HIPEC)已成为治疗腹膜假黏液瘤(PMP)的新方法。
探讨CRS和HIPEC用于治疗PMP是否安全有效。
本研究为观察性研究。整理并分析了2013年1月至2023年6月在我院接受CRS+HIPEC治疗的PMP患者的临床资料。主要观察指标为总生存期(OS),次要观察指标为手术并发症和严重不良事件的发生率。并发症根据常见不良事件评估标准进行分级。采用腹膜肿瘤指数(PCI)评分系统进行腹膜肿瘤分期,CRS后进行细胞减灭程度(CCR)评分。CCR-0和CCR-1被认为是满意的CRS。
共纳入186例PMP患者,中位年龄为56(48-64)岁,男性65例(34.9%),女性121例(65.1%)。中位PCI评分为28(20-34)分。中位手术时间为300(211-430)分钟,未发生明显并发症。91.4%(170/186)源于阑尾,53.2%(99/186)为低级别,30.6%(57/186)为高级别。CCR评分显示,55例患者(29.6%)达到满意的CRS,113例患者(60.8%)未达到满意的CRS。术后30天死亡率为2.7%(5/186),1.6%(3/186)需要二次手术,90天死亡率为4.3%(8/186)。Ⅲ-Ⅳ级并发症总发生率为43.0%(80/186),其中较高发生率主要为贫血(27.4%,51/186)、电解质紊乱(11.6%,21/181)和白蛋白降低(7.5%,14/186)。腹部手术相关的主要并发症为胃肠吻合口漏(2.2%,4/186)、腹腔出血(2.2%,4/186)和腹腔感染(4.3%,8/186)。中位随访时间为38.1(95%CI:31.2-45.1)个月。接受CRS+HIPEC治疗的PMP患者5年OS为50.3%(95%CI:40.7%-59.9%),中位生存时间为66.1(95%CI:43.1-89.1)个月。生存分析结果显示,病理分级低、PCI低且CCR评分满意的患者生存率较高(均P<0.05)。CCR-0患者5年OS为88.9%(95%CI:68.3%-100.0%),CCR-1患者为77.6%(95%CI:62.7%-92.5%),CCR-2/3患者为42.0%(95%CI:29.5%-54.5%)。
CRS+HIPEC应用于PMP安全可行,生存获益高,尤其是对于达到满意CRS的患者,可显著延长OS。