Müller Catharina, Bergmann Michael, Stift Anton, Bachleitner-Hofmann Thomas, Riss Stefan
Department of Surgery, Division of General Surgery, Comprehensive Cancer Center Vienna, Medical University of Vienna, Spitalgasse 23, 1090, Vienna, Austria.
Wien Klin Wochenschr. 2025 Apr;137(7-8):237-243. doi: 10.1007/s00508-024-02460-z. Epub 2024 Oct 25.
Peritoneal mesothelioma (PM) is a rare disease with various histopathological subtypes. For malignant peritoneal mesothelioma and borderline subgroups locoregional therapy with cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC) has been implemented. The aim of our study was to retrospectively present the outcome after CRS and HIPEC for patients with different subtypes of peritoneal mesothelioma.
In total 15 patients received CRS and HIPEC due to peritoneal mesothelioma at our tertiary referral hospital between 2013 and 2022. Surgical and oncologic outcomes of 14 of those patients were retrospectively evaluated as one patient was lost to follow-up.
The cohort consisted of 9 patients with diffuse malignant peritoneal mesothelioma (64.3%), 3 patients with multicystic peritoneal mesothelioma (21.4%) and 2 patients with well-differentiated peritoneal mesothelioma (14.3%). Complete cytoreduction was possible in 85.7% (n = 12). The major complication rate was 28.6% (n = 4) and the reoperation rate was 14.3% (n = 2). Median follow-up was 55 months (standard error, SE 15.0%, 95% confidence interval, CI 25.6-84.4 months). Over this time period 64.3% (n = 9) had no evidence of disease, 21.4% (n = 3) were alive with disease and 14.3% (n = 2) died of peritoneal mesothelioma. The median recurrence-free survival of patients was 13 months (SE 13.0%, 95% CI 0.0-32.2 months). None of the patients with multicystic peritoneal mesothelioma had evidence of disease at the time of last follow-up.
Patients with peritoneal mesothelioma should receive locoregional treatment as good oncological results can be achieved with reasonable postoperative morbidity. Thus, awareness is necessary for this rare but potentially aggressive disease to offer the best medical care.
腹膜间皮瘤(PM)是一种罕见疾病,具有多种组织病理学亚型。对于恶性腹膜间皮瘤和交界性亚组,已实施了减瘤手术(CRS)和腹腔热灌注化疗(HIPEC)的局部区域治疗。我们研究的目的是回顾性呈现不同亚型腹膜间皮瘤患者接受CRS和HIPEC后的结果。
2013年至2022年期间,我们的三级转诊医院共有15例因腹膜间皮瘤接受CRS和HIPEC的患者。其中14例患者的手术和肿瘤学结果进行了回顾性评估,1例患者失访。
该队列包括9例弥漫性恶性腹膜间皮瘤患者(64.3%)、3例多囊性腹膜间皮瘤患者(21.4%)和2例高分化腹膜间皮瘤患者(14.3%)。85.7%(n = 12)的患者实现了完全减瘤。主要并发症发生率为28.6%(n = 4),再次手术率为14.3%(n = 2)。中位随访时间为55个月(标准误,SE 15.0%,95%置信区间,CI 25.6 - 84.4个月)。在此期间,64.3%(n = 9)的患者无疾病证据,21.4%(n = 3)的患者带瘤生存,14.3%(n = 2)的患者死于腹膜间皮瘤。患者的中位无复发生存期为13个月(SE 13.0%,95% CI 0.0 - 32.2个月)。多囊性腹膜间皮瘤患者在最后一次随访时均无疾病证据。
腹膜间皮瘤患者应接受局部区域治疗,因为可以在合理的术后发病率情况下取得良好的肿瘤学结果。因此,对于这种罕见但可能具有侵袭性的疾病,提高认识对于提供最佳医疗护理是必要的。