Analysis of therapeutic effect of cell reduction combined with intraperitoneal thermoperfusion chemotherapy in treatment of peritoneal pseudomyxoma.

IF 1.8 4区 医学 Q3 GASTROENTEROLOGY & HEPATOLOGY World Journal of Gastrointestinal Surgery Pub Date : 2024-11-27 DOI:10.4240/wjgs.v16.i11.3520
Wei-Wei Li, Xiu-Mei Ru, Hong-Yan Xuan, Qi Fan, Jing-Jing Zhang, Jun Lu
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Abstract

Background: 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).

Aim: To find out if CRS and HIPEC can be used safely and effectively to treat PMP.

Methods: 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.

Results: 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 P < 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.

Conclusion: 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.

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细胞减少联合腹腔热灌注化疗治疗腹膜假性黏液瘤的疗效分析。
背景:腹膜假性粘液瘤是一种罕见的肿瘤,其生物学行为与恶性肿瘤相似。手术切除联合化疗是传统的治疗方法,但效果不佳。细胞减少(CRS)联合腹腔热灌注化疗(HIPEC)已成为治疗腹膜假性黏液瘤(PMP)的新方法。目的:探讨CRS联合HIPEC治疗PMP是否安全有效。方法:观察性研究。整理分析我院2013年1月至2023年6月CRS + HIPEC治疗的PMP患者的临床资料。主要结局指标为总生存期(OS),次要结局指标为手术并发症和严重不良事件的发生率。根据常见不良事件评价标准对并发症进行分级。采用腹膜肿瘤指数(PCI)评分系统进行腹膜肿瘤分期,CRS后进行细胞减少度(CCR)评分。CCR-0和CCR-1为满意的CRS。结果:共纳入186例PMP患者,中位年龄56(48 ~ 64)岁,男性65(34.9%)岁,女性121(65.1%)岁。PCI评分中位数为28(20-34)分。中位手术时间为300(211 ~ 430)分钟,无明显并发症发生。91.4%(170/186)来自阑尾,53.2%(99/186)来自低分级,30.6%(57/186)来自高分级。CCR评分显示55例(29.6%)患者达到满意CRS, 113例(60.8%)患者未达到满意CRS。术后30 d病死率为2.7%(5/186),再次手术病死率为1.6% (3/186),90 d病死率为4.3%(8/186)。III-IV期并发症的总发生率为43.0%(80/186),其中较高的发生率主要为贫血(27.4%,51/186)、电解质紊乱(11.6%,21/181)和白蛋白降低(7.5%,14/186)。腹部手术并发症主要为胃肠道吻合口漏(2.2%,4/186)、腹部出血(2.2%,4/186)、腹部感染(4.3%,8/186)。中位随访时间为38.1个月(95%CI: 31.2 ~ 45.1)。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个月(95%CI: 43.1 ~ 89.1)。生存分析结果显示,病理分级低、PCI低、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%)。结论:CRS + HIPEC在PMP中的应用是安全可行的,生存获益高,特别是达到满意CRS的患者,可显著延长OS。
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