加压腹腔喷雾化疗(PIPAC)治疗终末期结直肠癌患者腹膜转移。

IF 1.4 Q4 ONCOLOGY Pleura and Peritoneum Pub Date : 2020-05-15 eCollection Date: 2020-06-01 DOI:10.1515/pp-2020-0109
Signe Bremholm Ellebæk, Martin Graversen, Sönke Detlefsen, Lars Lundell, Claus W Fristrup, Per Pfeiffer, Michael B Mortensen
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引用次数: 24

摘要

背景:加压腹腔内气溶胶化疗(PIPAC)是一种新的腹腔内化疗方法。在此,我们报告了PIPAC在结直肠癌(CRC)晚期腹膜转移(PM)患者中获得的结果。方法:报告前瞻性PIPAC-OPC1和PIPAC-OPC2试验中CRC患者(n = 24)的数据。奥沙利铂92 mg/m2,每隔4-6周给药。使用CE认证喷雾器雾化化疗药物。结果标准为客观肿瘤反应、生存和不良事件。结果:回顾性分析2015年10月至2019年2月连续24例结直肠癌PM患者的74例PIPAC手术。5例患者原发肿瘤仍在原位,22例患者接受了姑息性全身化疗。19例患者完成了两次以上的PIPAC手术,67%的患者根据组织学腹膜回归分级评分(PRGS)观察到客观肿瘤反应,21%的患者病情稳定。4例患者(21%)完全缓解(平均PRGS = 1,细胞学阴性)。我们记录了PM诊断后的中位生存期为37.6(7.3-48.9)个月,而首次PIPAC治疗后的中位生存期为20.5(0.13-34.7)个月。注意到轻微的术后并发症,很少被认为与PIPAC治疗有因果关系。然而,记录了2例严重的术后并发症(尿脓毒症和医源性肠穿孔)。结论:PIPAC联合低剂量奥沙利铂可诱导部分结直肠癌晚期PM患者客观肿瘤消退。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Pressurized IntraPeritoneal Aerosol Chemotherapy (PIPAC)-directed treatment of peritoneal metastasis in end-stage colo-rectal cancer patients.

Background: Pressurized IntraPeritoneal Aerosol Chemotherapy (PIPAC) represents a novel approach to intraperitoneal chemotherapy. Hereby results, obtained with PIPAC in patients with advanced peritoneal metastasis (PM) from colorectal cancer (CRC), are presented.

Methods: Data from CRC patients (n = 24) included in the prospective PIPAC-OPC1 and PIPAC-OPC2 trials are reported. Oxaliplatin 92 mg/m2 was administered at 4-6-week intervals. A CE certified nebulizer was used to aerosolize the chemotherapeutics. Outcome criteria were objective tumor response, survival and adverse events.

Results: Retrospective analysis of 74 PIPAC procedures carried out in 24 consecutive patients with PM from CRC included from October 2015 to February 2019. Five patients had still the primary tumor in situ, and 22 patients had received palliative systemic chemotherapy. Nineteen patients completed more than two PIPAC procedures, and objective tumor response according to the histological Peritoneal Regression Grading Score (PRGS) was observed in 67% of the patients, while 21% had stable disease. Four patients (21%) had complete response (mean PRGS = 1 and negative cytology). We recorded a median survival of 37.6 (range 7.3-48.9) months from the time of PM diagnosis, whereas it was 20.5 (range 0.13-34.7) months following the first PIPAC session. Minor postoperative complications were noted, and few were considered causally related to the PIPAC treatment. However, two cases of severe postoperative complications were recorded (urosepsis and iatrogenic bowel perforation).

Conclusions: PIPAC with low-dose oxaliplatin can induce objective tumor regression in selected patients with advanced PM from colorectal cancer.

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CiteScore
2.50
自引率
11.10%
发文量
23
审稿时长
9 weeks
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