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. 2020 May 12;10(5):e039314.
doi: 10.1136/bmjopen-2020-039314.

Cytoreductive surgery (CRS) with hyperthermic intraoperative peritoneal chemotherapy (HIPEC) versus standard of care (SoC) in people with peritoneal metastases from colorectal, ovarian or gastric origin: protocol for a systematic review and individual participant data (IPD) meta-analyses of effectiveness and cost-effectiveness

Affiliations

Cytoreductive surgery (CRS) with hyperthermic intraoperative peritoneal chemotherapy (HIPEC) versus standard of care (SoC) in people with peritoneal metastases from colorectal, ovarian or gastric origin: protocol for a systematic review and individual participant data (IPD) meta-analyses of effectiveness and cost-effectiveness

Kurinchi Gurusamy et al. BMJ Open. .

Abstract

Introduction: There is uncertainty about whether cytoreductive surgery (CRS)+hyperthermic intraoperative peritoneal chemotherapy (HIPEC) improves survival and/or quality of life compared with standard of care (SoC) in people with peritoneal metastases who can withstand major surgery.

Primary objectives: To compare the relative benefits and harms of CRS+HIPEC versus SoC in people with peritoneal metastases from colorectal, ovarian or gastric cancers eligible to undergo CRS+HIPEC by a systematic review and individual participant data (IPD) meta-analysis.

Secondary objectives: To compare the cost-effectiveness of CRS+HIPEC versus SoC from a National Health Service (NHS) and personal social services perspective using a model-based cost-utility analysis.

Methods and analysis: We will perform a systematic review of literature by updating the searches from MEDLINE, Embase, Cochrane library, Science Citation Index as well as trial registers. Two members of our team will independently screen the search results and identify randomised controlled trials comparing CRS+HIPEC versus SoC for inclusion based on full texts for articles shortlisted during screening. We will assess the risk of bias in the trials and obtain data related to baseline prognostic characteristics, details of intervention and control, and outcome data related to overall survival, disease progression, health-related quality of life, treatment related complications and resource utilisation data. Using IPD, we will perform a two-step IPD, that is, calculate the adjusted effect estimate from each included study and then perform a random-effects model meta-analysis. We will perform various subgroup analyses, meta-regression and sensitivity analyses. We will also perform a model-based cost-utility analysis to assess whether CRS+HIPEC is cost-effective in the NHS setting.

Ethics and dissemination: This project was approved by the UCL Research Ethics Committee (Ethics number: 16023/001). We aim to present the findings at appropriate international meetings and publish the review, irrespective of the findings, in a peer-reviewed journal.

Prospero registration number: CRD42019130504.

Keywords: chemotherapy; health economics; oncology; qualitative research; surgery.

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Conflict of interest statement

Competing interests: The clinical practice of the clinicians in the project: TM, MM, MS, OA and SO may be altered by the findings of the review.

References

    1. International Agency for Research on Cancer (World Health Organization) Estimated number of incident cases, both sexes, all cancers excluding non-melanoma skin cancer, worldwide in 2012, 2017. Available: https://gco.iarc.fr/today/online-analysis-table?mode=cancer&mode_populat...
    1. Lemmens VE, Klaver YL, Verwaal VJ, et al. . Predictors and survival of synchronous peritoneal carcinomatosis of colorectal origin: a population-based study. Int J Cancer 2011;128:2717–25. 10.1002/ijc.25596 - DOI - PubMed
    1. Riihimäki M, Hemminki A, Sundquist J, et al. . Patterns of metastasis in colon and rectal cancer. Sci Rep 2016;6:29765. 10.1038/srep29765 - DOI - PMC - PubMed
    1. Segelman J, Granath F, Holm T, et al. . Incidence, prevalence and risk factors for peritoneal carcinomatosis from colorectal cancer. Br J Surg 2012;99:699–705. 10.1002/bjs.8679 - DOI - PubMed
    1. van Gestel YRBM, Thomassen I, Lemmens VEPP, et al. . Metachronous peritoneal carcinomatosis after curative treatment of colorectal cancer. Eur J Surg Oncol 2014;40:963–9. 10.1016/j.ejso.2013.10.001 - DOI - PubMed

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