Muñoz-Casares Francisco Cristóbal, Martín-Broto Javier, Cascales-Campos Pedro, Torres-Melero Juan, López-Rojo Irene, Gómez-Barbadillo José, González-Bayón Luis, Sebio Ana, Serrano César, Carvalhal Sara, Abreu de Souza Joaquim, Souza Alexandre, Flores-Ayala Guillermo, Palacios Fuenmayor Luis José, Lopes-Bras Raquel, González-López José Antonio, Vasques Hugo, Asencio-Pascual José Manuel
Peritoneal Carcinomatosis and Retroperitoneal Sarcomas Unit, San Juan de Dios Hospital, 14012 Córdoba, Spain.
Medical Oncology Department, Jimenez Diaz Foundation University Hospital, 28040 Madrid, Spain.
Cancers (Basel). 2024 Jul 25;16(15):2646. doi: 10.3390/cancers16152646.
Peritoneal sarcomatosis is a rare malignant disease with a poor prognosis, secondary to peritoneal dissemination of abdominopelvic soft tissue sarcomas. Its rarity, together with the characteristic histological heterogeneity and the historically poor response to systemic treatments, has prevented the establishment of widely accepted treatment criteria with curative intent. In this sense, radical cytoreductive surgery (CRS) with peritonectomy procedures and hyperthermic intraperitoneal chemotherapy (HIPEC), widely used in peritoneal carcinomatosis with excellent results, have not had the same evolutionary development in patients with peritoneal sarcomatosis. A multidisciplinary working group of experts in sarcomas and peritoneal oncological surgery established a series of recommendations based on current scientific evidence for the management of peritoneal sarcomatosis, taking into account the different histological subgroups of abdominopelvic sarcomas that can cause it depending on their origin: retroperitoneal sarcomas, uterine sarcomas, and visceral/peritoneal sarcomas of GIST (gastrointestinal stromal tumor) and non-GIST origin. This article shows the results of sarcoma experts' voting on the recommendations presented during the I Ibero-American Consensus on the Management of Peritoneal Sarcomatosis, which took place during the recent celebration of the III Hispanic-Portuguese Meeting for Updates on the Treatment of Sarcomas.
腹膜肉瘤病是一种罕见的恶性疾病,预后较差,继发于腹盆腔软组织肉瘤的腹膜播散。其罕见性,加上组织学上的异质性以及历来对全身治疗反应不佳,阻碍了具有治愈意图的广泛接受的治疗标准的建立。从这个意义上说,广泛应用于腹膜癌病且效果极佳的根治性细胞减灭术(CRS)联合腹膜切除术及腹腔内热灌注化疗(HIPEC),在腹膜肉瘤病患者中并未有同样的发展。一个由肉瘤和腹膜肿瘤外科专家组成的多学科工作小组,基于当前科学证据,针对腹膜肉瘤病的管理制定了一系列建议,同时考虑到根据起源不同可导致该病的腹盆腔肉瘤的不同组织学亚组:腹膜后肉瘤、子宫肉瘤以及胃肠道间质瘤(GIST)和非GIST起源的内脏/腹膜肉瘤。本文展示了肉瘤专家对在最近举行的第三届西班牙裔 - 葡萄牙肉瘤治疗更新会议期间召开的第二届伊比利亚 - 美洲腹膜肉瘤病管理共识会议上提出的建议进行投票的结果。