Department of Surgery, The Ottawa Hospital, 501 Smyth Road, Ottawa, ON, K1H 8L6, Canada.
Department of Oncology, McMaster University & Program in Evidence-Based Care, Cancer Care Ontario, 1280 Main Street West, Hamilton, ON, L8S 4L8, Canada.
Eur J Cancer. 2020 Mar;127:76-95. doi: 10.1016/j.ejca.2019.10.034. Epub 2020 Jan 24.
The purpose of the present review was to describe evidence-based indications for hyperthermic intraperitoneal chemotherapy (HIPEC), with cytoreductive surgery (CRS), in patients with a diagnosis of mesothelioma, appendiceal (including appendiceal mucinous neoplasm), colorectal, gastric, ovarian or primary peritoneal carcinoma. Relevant studies were identified from a systematic MEDLINE and EMBASE search of studies published from 1985 to 2019. Studies were included if they were RCTs. If no RCTs were identified, prospective and retrospecctive comparative studies (where confounders are controlled for studies with greater than 30 patients) were included. Overall survival, progression-free survival, recurrence-free survival, adverse events and quality of life data were extracted. For patients with newly diagnosed, primary stage III epithelial ovarian, fallopian tube or primary peritoneal carcinoma, HIPEC with CRS should be considered for those with at least stable disease following neoadjuvant chemotherapy at the time of interval CRS if complete or optimal cytoreduction is achieved. There is insufficient evidence to recommend the addition of HIPEC when primary CRS is performed for patients with newly diagnosed, primary advanced epithelial ovarian, fallopian tube or primary peritoneal carcinoma or in those with recurrent ovarian cancer outside of a clinical trial. There is insufficient evidence to recommend HIPEC with CRS for the prevention of or for the treatment of peritoneal colorectal carcinomatosis outside of a clinical trial. There is insufficient evidence to recommend HIPEC with CRS for the prevention of or for the treatment of gastric peritoneal carcinomatosis outside of a clinical trial. There is insufficient evidence to recommend HIPEC with CRS in patients with malignant peritoneal mesothelioma or in those with disseminated mucinous neoplasm in the appendix as a standard of care; however, these patients should be referred to HIPEC specialty centres for assessment for treatment as part of an ongoing research protocol.
本综述的目的是描述基于证据的高热腹腔内化疗(HIPEC)联合细胞减灭术(CRS)用于间皮瘤、阑尾(包括阑尾黏液性肿瘤)、结直肠、胃、卵巢或原发性腹膜癌患者的适应证。从 1985 年至 2019 年发表的研究中,通过系统的 MEDLINE 和 EMBASE 搜索确定了相关研究。如果没有 RCT,则纳入前瞻性和回顾性比较研究(对混杂因素进行控制的研究中患者人数大于 30 人)。提取总生存、无进展生存、无复发生存、不良事件和生活质量数据。对于新诊断的原发性 III 期上皮性卵巢癌、输卵管癌或原发性腹膜癌患者,如果在间隔性 CRS 时新辅助化疗后至少达到稳定疾病(如果达到完全或最佳肿瘤细胞减灭术),应考虑行 HIPEC 联合 CRS。对于新诊断的原发性晚期上皮性卵巢癌、输卵管癌或原发性腹膜癌患者,或在临床试验之外发生复发性卵巢癌患者,没有足够的证据推荐在初次 CRS 时添加 HIPEC。没有足够的证据推荐 HIPEC 联合 CRS 用于预防或治疗临床试验之外的结直肠腹膜转移癌。没有足够的证据推荐 HIPEC 联合 CRS 用于预防或治疗临床试验之外的胃腹膜转移癌。没有足够的证据推荐 HIPEC 联合 CRS 用于恶性腹膜间皮瘤患者或阑尾广泛黏液性肿瘤患者作为标准治疗;然而,这些患者应被转诊到 HIPEC 专业中心,根据正在进行的研究方案评估是否进行治疗。