Affiliation:
1. University College London London UK
2. The Colorectal and Peritoneal Oncology Centre Christie NHS Foundation Trust London UK
3. Division of Cancer Studies University of Manchester London UK
Abstract
AbstractBackgroundThere is uncertainty in the relative benefits and harms of hyperthermic intraoperative peritoneal chemotherapy (HIPEC) when added to cytoreductive surgery (CRS) +/− systemic chemotherapy or systemic chemotherapy alone in people with peritoneal metastases from colorectal, gastric, or ovarian cancers.MethodsWe searched randomized controlled trials (RCTs) in the medical literature until April 14, 2022 and applied methods used for high‐quality systematic reviews.FindingsWe included a total of eight RCTs (seven RCTs included in quantitative analysis as one RCT did not provide data in an analyzable format). All comparisons other than ovarian cancer contained only one trial. For gastric cancer, there is high uncertainty about the effect of CRS + HIPEC + systemic chemotherapy. For stage III or greater epithelial ovarian cancer undergoing interval cytoreductive surgery, CRS + HIPEC + systemic chemotherapy probably decreases all‐cause mortality compared to CRS + systemic chemotherapy. For colorectal cancer, CRS + HIPEC + systemic chemotherapy probably results in little to no difference in all‐cause mortality and may increase the serious adverse events proportions compared to CRS +/− systemic chemotherapy, but probably decreases all‐cause mortality compared to fluorouracil‐based systemic chemotherapy alone.InterpretationThe role of CRS + HIPEC in gastric peritoneal metastases is uncertain. CRS + HIPEC should be standard of care in women with stage III or greater epithelial ovarian cancer undergoing interval CRS. CRS + systemic chemotherapy should be standard of care for people with colorectal peritoneal metastases, with HIPEC given only as part of a RCT focusing on subgroups and regimes.PROSPERO RegistrationCRD42019130504.
Reference56 articles.
1. International Agency for Research on Cancer (World Health Organization).2017. “Estimated Number of Incident Cases Both Sexes All Cancers Excluding Non‐melanoma Skin Cancer Worldwide in 2012.”.https://gco.iarc.fr/today/online‐analysis‐table?mode=cancer&mode_population=continents&population=900&sex=0&cancer=29&type=0&statistic=0&prevalence=0&color_palette=default. accessed on 3rd December 2017.
2. Predictors and survival of synchronous peritoneal carcinomatosis of colorectal origin: A population-based study
3. Patterns of metastasis in colon and rectal cancer
4. Incidence, prevalence and risk factors for peritoneal carcinomatosis from colorectal cancer
5. Metachronous peritoneal carcinomatosis after curative treatment of colorectal cancer
Cited by
1 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献