Abstract
Cytoreductive surgery with heated intraperitoneal chemotherapy (CRS/HIPEC) involves resecting affected organs to remove macroscopic disease along with the administration of intraoperative chemotherapy to treat microscopic disease. Key principles include removing all macroscopic disease and then administering heated mitomycin C or a platinum-based chemotherapeutic agent intraperitoneal for 90–120 minutes intraoperatively. The addition of hyperthermia is synergistic, increasing cytotoxicity of the chemotherapeutic agent, and given the properties of peritoneal cavity, this treatment adds minimal toxicity. CRS/HIPEC has demonstrated utility in cancers that spread in the peritoneal cavity (peritoneal surface malignancies/peritoneal metastasis) and has demonstrated benefits in cancers arising from the ovarian, appendiceal, colon, as well as peritoneal mesothelioma.
Malignant peritoneal mesothelioma (MPM) is a rare but aggressive malignancy with a life expectancy of 4–12 months if left untreated. Efforts to treat and control MPM with intravenous chemotherapies alone have not dramatically improved outcomes for patients. These tumors spread and grow on the surface of abdominal organs often leading to symptoms for patients. Surgery, specifically cytoreductive surgery with heated intraperitoneal chemotherapy (CRS/HIPEC), has emerged as therapy that can resolve or prevent symptoms, extend survival, and yield long-term remission. Published data reports median survival following CRS/HIPEC of 40–100 months. This chapter briefly reviews the history CRS/HPEC and the utilization of CRS/HIPEC for MPM. Additionally the factors in patient selection and tools for preoperative assessment are reviewed. Similarly, how these factors influence not only patient selection for surgery but also the prognostic value in survival outcome are described.
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References
Alexander HR Jr, et al. Treatment factors associated with long-term survival after cytoreductive surgery and regional chemotherapy for patients with malignant peritoneal mesothelioma. Surgery. 2013;153(6):779–86.
Armstrong DK, et al. Intraperitoneal cisplatin and paclitaxel in ovarian cancer. N Engl J Med. 2006;354(1):34–43.
Chua TC, Yan TD, Morris DL. Outcomes of cytoreductive surgery and hyperthermic intraperitoneal chemotherapy for peritoneal mesothelioma: the Australian experience. J Surg Oncol. 2009;99(2):109–13.
Esquivel J, et al. Cytoreductive surgery and hyperthermic intraperitoneal chemotherapy in the management of peritoneal surface malignancies of colonic origin: a consensus statement. Society of Surgical Oncology. Ann Surg Oncol. 2007;14(1):128–33.
Foster JM, Gatalica Z, Lilleberg S, Haynatzki G, Loggie BW. Novel and existing mutations in the tyrosine kinase domain of the epidermal growth factor receptor are predictors of optimal resectability in malignant peritoneal mesothelioma. Ann Surg Oncol. 2009;16(1):152–8.
Foster JM, et al. Early identification of DPAM in at-risk low-grade appendiceal mucinous neoplasm patients: a new approach to surveillance for peritoneal metastasis. World J Surg Oncol. 2016;14(1):243.
Ghosh BC, Huvos AG, Whiteley HW. Pseudomyxoma peritonei. Dis Colon Rectum. 1972;15(6):420–5.
Glehen O, Gilly FN. Quantitative prognostic indicators of peritoneal surface malignancy: carcinomatosis, sarcomatosis, and peritoneal mesothelioma. Surg Oncol Clin N Am. 2003;12(3):649–71.
Griffiths CT. Surgical resection of tumor bulk in the primary treatment of ovarian carcinoma. Natl Cancer Inst Monogr. 1975;42:101–4.
Griffiths CT, Parker LM, Fuller AF Jr. Role of cytoreductive surgical treatment in the management of advanced ovarian cancer. Cancer Treat Rep. 1979;63(2):235–40.
Harmon RL, Sugarbaker PH. Prognostic indicators in peritoneal carcinomatosis from gastrointestinal cancer. Int Semin Surg Oncol. 2005;2(1):3.
Hassan R, et al. Current treatment options and biology of peritoneal mesothelioma: meeting summary of the first NIH peritoneal mesothelioma conference. Ann Oncol. 2006;17(11):1615–9.
Heller DR, et al. Recurrence of Optimally Treated Malignant Peritoneal Mesothelioma with Cytoreduction and Heated Intraperitoneal Chemotherapy. Ann Surg Oncol. 2017;24(13):3818–24.
Helm JH, et al. Cytoreductive surgery and hyperthermic intraperitoneal chemotherapy for malignant peritoneal mesothelioma: a systematic review and meta-analysis. Ann Surg Oncol. 2015;22(5):1686–93.
Jacquet P, Sugarbaker PH. Clinical research methodologies in diagnosis and staging of patients with peritoneal carcinomatosis. Cancer Treat Res. 1996;82:359–74. Review
Janne PA, et al. Open-label study of pemetrexed alone or in combination with cisplatin for the treatment of patients with peritoneal mesothelioma: outcomes of an expanded access program. Clin Lung Cancer. 2005;7(1):40–6.
Kepenekian V, et al. Diffuse malignant peritoneal mesothelioma: Evaluation of systemic chemotherapy with comprehensive treatment through the RENAPE Database: Multi-Institutional Retrospective Study. Eur J Cancer. 2016;65:69–79.
Meigs JV. Tumors of the female pelvic organs. New York: The Macmillan Company; 1934. p. xxxiv. p. 1 l., 533 p.
Munnell EW. The changing prognosis and treatment in cancer of the ovary. A report of 235 patients with primary ovarian carcinoma 1952-1961. Am J Obstet Gynecol. 1968;100(6):790–805.
Palta JR. Design and testing of a therapeutic infusion filtration system. M.S. thesis, University of Missouri, Columbia; 1977.
Sadeghi B, et al. Peritoneal carcinomatosis from non-gynecologic malignancies: results of the EVOCAPE 1 multicentric prospective study. Cancer. 2000;88(2):358–63.
Shingleton WW, Parker RT. Abdominal Perfusion for Cancer Chemotherapy Using Hypothermia and Hyperthermia. Acta Unio Int Contra Cancrum. 1964;20:465–8.
Spratt JS, Adcock RA, Muskovin M, Sherrill W, McKeown J. Clinical delivery system for intraperitoneal hyperthermic chemotherapy. Cancer Res. 1980;40(2):256–60.
Sugarbaker PH. Peritonectomy procedures. Ann Surg. 1995;221(1):29–42.
Sugarbaker PH, Chang D. Long-term regional chemotherapy for patients with epithelial malignant peritoneal mesothelioma results in improved survival. Eur J Surg Oncol. 2017;43(7):1228–35.
Sugarbaker PH, Turaga KK, Alexander HR Jr, Deraco M, Hesdorffer M. Management of malignant peritoneal mesothelioma using cytoreductive surgery and perioperative chemotherapy. J Oncol Pract. 2016;12(10):928–35.
Wittekind C, Compton CC, Greene FL, Sobin LH. TNM residual tumor classification revisited. Cancer. 2002;94(9):2511–6.
Yan TD, Welch L, Black D, Sugarbaker PH. A systematic review on the efficacy of cytoreductive surgery combined with perioperative intraperitoneal chemotherapy for diffuse malignancy peritoneal mesothelioma. Ann Oncol. 2007;18(5):827–34.
Yan TD, et al. Cytoreductive surgery and hyperthermic intraperitoneal chemotherapy for malignant peritoneal mesothelioma: multi-institutional experience. J Clin Oncol. 2009;27(36):6237–42.
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Malhortra, G., Patel, A., Foster, J.M. (2019). History Cytoreductive Surgery and Hyperthermic Intraperitoneal Chemotherapy for Peritoneal Metastasis and Evolution and Contemporary Application in Peritoneal Mesothelioma. In: Hesdorffer, M., Bates-Pappas, G. (eds) Caring for Patients with Mesothelioma: Principles and Guidelines. Springer, Cham. https://doi.org/10.1007/978-3-319-96244-3_2
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