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Taiwan Society of Colon and Rectal Surgeons (TSCRS) Consensus for Cytoreduction Selection in Metastatic Colorectal Cancer

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Abstract

Background

Taiwan has witnessed a surge in the incidence of colorectal cancer (CRC), of which 40–60% metastasize. Continuous updating of cytoreductive strategies in metastatic CRC (mCRC) has contributed to median overall survival reaching 40 months. In this changing scenario, to standardize the approaches across Taiwan, a group of experts from the Taiwan Society of Colon and Rectal Surgeons (TSCRS) convened to establish evidence- and opinion-based recommendations for defining the criteria of “resectability” in mCRC.

Methods

Over the course of one-on-one consultations, lasting 30–40 min each, with 30 medical specialists (19 colorectal surgeons, 4 general surgeons, and 7 medical oncologists) from 16 hospitals in Taiwan followed by a 2-h meeting with 8 physician experts (3 general surgeons, 4 colorectal surgeons, and 1 thoracic surgeon), 12 key questions on cytoreduction were addressed. This was further contextualized based on published literature.

Results

The final consensus includes eight recommendations regarding the criteria for metastasis resection, role of local control treatment in liver potentially resectable patients, management of synchronous liver metastases, approach for peritoneal metastasis, place for resection in multiple-organ metastasis, and general criteria for resectability.

Conclusions

mCRC patients undergoing R0 resection have the greatest survival advantage following surgery. Our role as a multidisciplinary team (MDT) should be to treat potentially resectable mCRC patients as rapidly and safely as possible, and achieve R0 resection as far as possible and for as long as possible (continuum of care). This TSCRS consensus statement aims to help build clinical capacity within the MDTs, while making better use of existing healthcare resources.

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References

  1. World Cancer Research Fund and American Institute for Cancer Research Food, Nutrition, Physical Activity, and the Prevention of Cancer: A Global Perspective. Washington, DC: American Institute for Cancer Research; 2007.

  2. Boyle P, Langman J S. ABC of colorectal cancer: epidemiology. BMJ. 2000;321(7264):805–8.

    CAS  PubMed  PubMed Central  Google Scholar 

  3. Yang L, Parkin DM, Li LD, Chen YD, Bray F. Estimation and projection of the national profile of cancer mortality in China: 1995 to 2005. Br J Cancer. 2004;90:2157–66.

    CAS  PubMed  PubMed Central  Google Scholar 

  4. Chiang CJ, Chen YC, Chen CJ, You SL, Lai MS. Taiwan Cancer Registry Task Force. Cancer trends in Taiwan. Jpn J Clin Oncol. 2010;40:897–904.

  5. Health Promotion Administration, Ministry of Health and Welfare, Taiwan. Health Promotion Administration Annual Report 2013. Available at: http://health99.hpa.gov.tw/EducZone/edu_detail.aspx?CatId=21759. Accessed on 1 Oct 17.

  6. Kumar R, Price TJ, Beeke C, Jain K, Patel G, Padbury R, et al. Colorectal cancer survival: an analysis of patients with metastatic disease synchronous and metachronous with the primary tumor. Clin Colorectal Cancer. 2014;13:87–93.

    PubMed  Google Scholar 

  7. Abdalla EK, Adam R, Bilchik AJ, Jaeck D, Vauthey JN, Mahvi D. Improving resectability of hepatic colorectal metastases: expert consensus statement. Ann Surg Oncol, 2006;13(10):1271–80.

    PubMed  Google Scholar 

  8. Dromain C, Caramella C, Dartigues P, Goere D, Ducreux M, Deschamps F. Métastases hépatiques, pulmonaires et péritonéales des cancers colorectaux. J Radiol Diagn Inter. 2004;95(5):514–24.

    Google Scholar 

  9. House MG, Ito H, Gönen M, et al. Survival after hepatic resection for metastatic colorectal cancer: trends in outcomes for 1,600 patients during two decades at a single institution. J Am Coll Surg. 2010;210:744-52, 752–5.

    Google Scholar 

  10. Gold JS, Are C, Kornprat P, et al. Increased use of parenchymal-sparing surgery for bilateral liver metastases from colorectal cancer is associated with improved mortality without change in oncologic outcome: trends in treatment over time in 440 patients. Ann Surg. 2008;247:109–17.

    PubMed  Google Scholar 

  11. Kingham TP, Correa-Gallego C, D’Angelica MI, et al. Hepatic parenchymal preservation surgery: decreasing morbidity and mortality rates in 4,152 resections for malignancy. J Am Coll Surg. 2015;220:471–9.

    PubMed  Google Scholar 

  12. Manfredi S, Lepage C, Hatem C, et al. Epidemiology and management of liver metastases from colorectal cancer. Ann Surg. 2006;244:254–9.

    PubMed  PubMed Central  Google Scholar 

  13. Misiakos EP, Karidis NP, Kouraklis G. Current treatment for colorectal liver metastases. World J Gastroenterol. 2011;17(36):4067–75. https://doi.org/10.3748/wjg.v17.i36.4067.

    Article  PubMed  PubMed Central  Google Scholar 

  14. TM Pawlik, RD Schulick, MA Choti. Expanding criteria for resectability of colorectal liver metastases. Oncologist. 2008;13:51–64.

    PubMed  Google Scholar 

  15. Karoui M, Penna C, Amin-Hashem M, et al. Influence of preoperative chemotherapy on the risk of major hepatectomy for colorectal liver metastases. Ann Surg. 2006;243:1–7.

    PubMed  PubMed Central  Google Scholar 

  16. Tomlinson JS, Jarnagin WR, DeMatteo RP, et al. Actual 10-year survival after resection of colorectal liver metastases defines cure. J Clin Oncol. 2007;25:4575–80.

    PubMed  Google Scholar 

  17. Mulier S, Ruers T, Jamart J. Radiorequency ablation versus resection for resectable colorectal liver metastases: time for a randomized trial? An update. Dig Surg. 2008;25:445–60. https://doi.org/10.1159/000184736.pmid:19212117.

    Article  PubMed  Google Scholar 

  18. Wong SL, Mangu PB, Choti MA. American Society of Clinical Oncology 2009 clinical evidence review on radiofrequency ablation of hepatic metastases from colorectal cancer. J Clin Oncol. 2010;28:493–508.

    PubMed  Google Scholar 

  19. Veltri A, Sacchetto P, Tosetti I. Radiofrequency ablation of colorectal liver metastases: small size favourably predicts technique effectiveness and survival. Cardiovasc Intervent Radiol. 2008;31:948–56. https://doi.org/10.1007/s00270-008-9362-0.pmid:18506519.

    Article  PubMed  Google Scholar 

  20. Oshowo A, Gillams A, Harisson E. Comparison of resection and radiofrequency ablation for treatment of solitary colorectal liver metastases. Br J Surg. 2003;90:1240–3.

    CAS  PubMed  Google Scholar 

  21. Ruers T, Joosten J, Wiering B. Comparison between local ablative therapy and chemotherapy for non-resectable colorectal liver metastases: a prospective study. Ann Surg Oncol. 2007;14:1161–9. https://doi.org/10.1245/s10434-006-9312-5.

    Article  PubMed  Google Scholar 

  22. Crocetti L, de Baere T, Lencioni R. Quality improvement guidelines for RFA of liver tumours. Cardiovasc Intervent Radiol. 2010;33:11–7. https://doi.org/10.1007/s00270-009-9736-y.pmid:19924474.

    Article  PubMed  Google Scholar 

  23. Guraya SY. Modern oncosurgical treatment strategies for synchronous liver metastases from colorectal cancer. JMAU 2013;1:1–7.

    Google Scholar 

  24. Gray B, van Hazel G, Hope M, et al. Randomised trial of SIR-Spheres® plus chemotherapy versus chemotherapy alone for treating patients with liver metastases from primary large bowel cancer. Ann Oncol. 2001;12:1711–20.

    CAS  PubMed  Google Scholar 

  25. Ruers T, Punt C, van Coevorden F, Pierie JP, Borel-Rinkes I, Ledermann JA, et al. Radiofrequency ablation combined with systemic treatment versus systemic treatment alone in patients with non-resectable colorectal liver metastases: a randomized EORTC Intergroup phase II study (EORTC 40004). Ann Oncol. 2012; 23: 2619–26.

    CAS  PubMed  PubMed Central  Google Scholar 

  26. LiverMetSurvey. International registry of patients operated for colorectal liver metastasis. http://www.livermetsurvey.org. Accessed on 23 Nov 11.

  27. Yin Z, Liu C, Chen Y, Bai Y, Shang C, Yin R, et al. Timing of hepatectomy in resectable synchronous colorectal liver metastases (SCRLM): simultaneous or delayed? Hepatology. 2013;57:2346–57.

    PubMed  Google Scholar 

  28. Adam R, et al. Managing synchronous liver metastases from colorectal cancer: A multidisciplinary international consensus. Cancer Treat Rev. 2015;41(9):729–41.

    PubMed  Google Scholar 

  29. Edge SB, Compton CC. The American Joint Committee on Cancer: the 7th edition of the AJCC cancer staging manual and the future of TNM. Ann Surg Oncol. 2010;17:1471–4.

  30. Mekenkamp LJ, Koopman M, Teerenstra S, van Krieken JH, Mol L, Nagtegaal ID, et al. Clinicopathological features and outcome in advanced colorectal cancer patients with synchronous vs metachronous metastases. Br J Cancer. 2010;103:159–64.

    CAS  PubMed  PubMed Central  Google Scholar 

  31. Reddy SK, Barbas AS, Turley RS, et al. A standard definition of major hepatectomy: resection of four or more liver segments. HPB. 2011;13(7):494–502. https://doi.org/10.1111/j.1477-2574.2011.00330.x.

    Article  PubMed  PubMed Central  Google Scholar 

  32. Lygidakis NJ, Vlachos L, Raptis S, et al. New frontiers in liver surgery: two-stage liver surgery for the management of advanced metastatic liver disease. Hepato-Gastroenterol. 1999; 46: 2216–28.

    CAS  Google Scholar 

  33. Narita M, Oussoultzoglou E, Jaeck D, Fuchschuber P, Rosso E, Pessaux P, et al. Two-stage hepatectomy for multiple bilobar colorectal liver metastases. Br J Surg. 2011;98(10):1463e75.

  34. Cunningham SC, Choti MA, Pawlik TM. Two-stage hepatectomy for colorectal cancer hepatic metastases. Curr Colorectal Cancer Rep, 2008; 4(2):93.

  35. Adam R, Laurent A, Azoulay D, Castaing D, Bismuth H. Two-stage hepatectomy: a planned strategy to treat irresectable liver tumors. Ann Surg. 2000;232(6):777–85.

    CAS  PubMed  PubMed Central  Google Scholar 

  36. Conférence de consensus. Prévention, dépistage et prise en charge des cancers du colon. Gastroenterol Clin Biol 1998; 22: S265–72.

    Google Scholar 

  37. Villeneuve PJ, Sundaresan RS. Surgical management of colorectal lung metastasis. Clin Colon Rectal Surg 2009;22:233–41.

    PubMed  PubMed Central  Google Scholar 

  38. Patel D, Townsend AR, Karapetis C, Beeke C, Padbury R, Roy A. Is survival for patients with resectable lung metastatic colorectal cancer comparable to those with resectable liver disease? Results from the South Australian metastatic colorectal registry. Ann Surg Oncol. 2016;23(11):3616–22. https://doi.org/10.1245/s10434-016-5290-4.

    Article  PubMed  Google Scholar 

  39. Salvatore L, Aprile G, Arnoldi E, et al. Management of metastatic colorectal cancer patients: guidelines of the Italian Medical Oncology Association (AIOM). ESMO Open. 2017;2(1):e000147. https://doi.org/10.1136/esmoopen-2016-000147.

    Article  PubMed  PubMed Central  Google Scholar 

  40. Brunelli A. Preoperative evaluation of lung resection candidates. Preface. Thorac Surg Clin. 2008;18:xi.

    PubMed  Google Scholar 

  41. McCormack PM, Burt ME, Bains MS, et al. Lung resection for colorectal metastases. 10-year results. Arch Surg 1992;127:1403–6.

  42. Rama N, Monteiro A, Bernardo JE, Eugénio L, Antunes MJ. Lung metastases from colorectal cancer: surgical resection and prognostic factors. Eur J Cardiothorac Surg 2009;35:444–9.

    PubMed  Google Scholar 

  43. Shiono S, Ishii G, Nagai K, et al. Histopathologic prognostic factors in resected colorectal lung metastases. Ann Thorac Surg. 2005;79:278–82; discussion 283.

  44. Kanzaki R, Higashiyama M, Oda K, et al. Outcome of surgical resection for recurrent pulmonary metastasis from colorectal carcinoma. Am J Surg. 2011;202:419–26.

    PubMed  Google Scholar 

  45. Gonzalez M, Poncet A, Combescure C, et al. Risk factors for survival after lung metastasectomy in colorectal cancer patients: a systematic review and meta-analysis. Ann Surg Oncol 2013;20:572–9.

    PubMed  Google Scholar 

  46. Jayne DG, Fook S, Loi C, Seow-Choen F. Peritoneal carcinomatosis from colorectal cancer. Br J Surg. 2002;89:1545–50.

    CAS  PubMed  Google Scholar 

  47. Franko J, Shi Q, Goldman CD, et al. Treatment of colorectal peritoneal carcinomatosis with systemic chemotherapy: a pooled analysis of North Central Cancer Treatment Group phase III trials N9741 and N9841. J Clin Oncol. 2012;30:263–7.

    PubMed  Google Scholar 

  48. Honoré C, Goéré D, Souadka A, Dumont F, Elias D. Definition of patients presenting a high risk of developing peritoneal carcinomatosis after curative surgery for colorectal cancer: a systematic review. Ann Surg Oncol. 2013;20(1):183–92. https://doi.org/10.1245/s10434-012-2473-5.

    Article  PubMed  Google Scholar 

  49. Elias D, Honoré C, Dumont F, Ducreux M, Boige V, Malka D. Results of systematic second-look surgery plus HIPEC in asymptomatic patients presenting a high risk of developing colorectal peritoneal carcinomatosis. Ann Surg. 2011;254(2):289–93. https://doi.org/10.1097/sla.0b013e31822638f6.

    Article  CAS  PubMed  Google Scholar 

  50. Elias D, Goéré D, Di Pietrantonio D, Boige V, Malka D, Kohneh-Shahri N. Results of systematic second-look surgery in patients at high risk of developing colorectal peritoneal carcinomatosis. Ann Surg. 2008;247(3):445–50. https://doi.org/10.1097/sla.0b013e31815f0113.

    Article  PubMed  Google Scholar 

  51. Gomes da Silva R, Sugarbaker PH. Analysis of 10 prognostic factors in 70 patients having complete cytoreduction plus perioperative intraperitoneal chemotherapy for carcinomatosis from colorectal cancer. J Am Coll Surg 2006;203:878–86.

  52. Elias D, Delperro JR, Sideris L, et al. Treatment of peritoneal carcinomatosis from colorectal cancer: impact of complete cytoreductive surgery and difficulties in conducting randomized trials. Ann Surg Oncol 2004;11:518–21.

    PubMed  Google Scholar 

  53. Elias D, Raynard B, Farkhondeh F, et al. Peritoneal carcinomatosis of colorectal origin: long-term results of intraperitoneal chemohyperthermia with oxaliplatin following complete cytoreductive surgery. Gastroenterol Clin Biol 2006;30:1200–4.

    CAS  PubMed  Google Scholar 

  54. Verwaal VJ, Van Ruth S, De Bree E, et al. Randomized trial of cytoreduction and hyperthermic intraperitoneal chemotherapy versus systemic chemotherapy and palliative surgery in patients with peritoneal carcinomatosis of colorectal cancer. J Clin Oncol 2003; 21:3737–43.

    PubMed  Google Scholar 

  55. Glehen O, Kwiatkowski F, Sugarbaker PH, et al. Cytoreductive surgery combined with perioperative intraperitoneal chemotherapy for the management of peritoneal carcinomatosis from colorectal cancer: a multiinstitutional study. J ClinOncol, 2004; 22:3284–92.

    CAS  Google Scholar 

  56. Yurttas C, Hoffmann G, Tolios A, et al. Systematic review of variations in hyperthermic intraperitoneal chemotherapy (HIPEC) for peritoneal metastasis from colorectal cancer. J Clin Med. 2018;7(12):567. https://doi.org/10.3390/jcm7120567.

  57. Van Cutsem E, on behalf of the ESMO Guidelines Working Group, Cervantes A, on behalf of the ESMO Guidelines Working Group, Nordlinger B, on behalf of the ESMO Guidelines Working Group, Arnold D, on behalf of the ESMO Guidelines Working Group; Metastatic colorectal cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann Oncol, 2014; 25(suppl_3)”iii1–9, https://doi.org/10.1093/annonc/mdu260.

  58. Brouquet A, Vauthey JN, Contreras CM, Walsh GL, Vaporciyan AA, Swisher SG, et al. Improved survival after resection of liver and lung colorectal metastases compared with liver-only metastases: a study of 112 patients with limited lung metastatic disease. J Am Coll Surg. 2011;213:62–9.

    PubMed  Google Scholar 

  59. Welter S, Jacobs J, Krbek T, et al. Long-term survival after repeated resection of pulmonary metastases from colorectal cancer. Ann Thorac Surg 2007;84:203–10.

    PubMed  Google Scholar 

  60. Lee SH, Kim SH, Lim JH, et al. Aggressive surgical resection for concomitant liver and lung metastasis in colorectal cancer. Korean J Hepatobiliary Pancreat Surg. 2016;20(3):110–5. https://doi.org/10.14701/kjhbps.2016.20.3.110.

    Article  PubMed  PubMed Central  Google Scholar 

  61. Sourrouille I, Mordant P, Maggiori L, Dokmak S, Lesèche G, Panis Y, et al. Long-term survival after hepatic and pulmonary resection of colorectal cancer metastases. J Surg Oncol. 2013;108:220–4.

    PubMed  Google Scholar 

  62. Ahmed S, Johnson K, Ahmed O, Iqbal N. Advances in the management of colorectal cancer: from biology to treatment. Int J Colorectal Dis. 2014;29:1031–42.

    PubMed  Google Scholar 

  63. Headrick JR, Miller DL, Nagorney DM, Allen MS, Deschamps C, Trastek VF, et al. Surgical treatment of hepatic and pulmonary metastases from colon cancer. Ann Thorac Surg. 2001;71:975–9.

    CAS  PubMed  Google Scholar 

  64. Reddy RH, Kumar B, Shah R, Mirsadraee S, Papagiannopoulos K, Lodge P. Staged pulmonary and hepatic metastasectomy in colorectal cancer—is it worth it? Eur J Cardiothorac Surg. 2004;25(2):151–4.

    PubMed  Google Scholar 

  65. Marín C, Robles R, López Conesa A, Torres J, Flores DP, Parrilla P. Outcome of strict patient selection for surgical treatment of hepatic and pulmonary metastases from colorectal cancer. Dis Colon Rectum. 2013;56(1):43–50. https://doi.org/10.1097/dcr.0b013e3182739f5e.

    Article  PubMed  Google Scholar 

  66. Kawano D, Takeo S, Tsukamoto S, et al. Prediction of the prognosis and surgical indications for pulmonary metastectomy from colorectal carcinoma in patients with combined hepatic metastases. Lung Cancer 2012;75:209–12.

    PubMed  Google Scholar 

  67. Zabaleta J, Aguinagalde B, Fuentes MG, et al. Survival after lung metastasectomy for colorectal cancer: importance of previous liver metastasis as a prognostic factor. Eur J Surg Oncol 2011;37:786–90.

    CAS  PubMed  Google Scholar 

  68. Lastoria S, Piccirillo MC, Caracò C, Nasti G, Aloj L, Arrichiello C, de Lutio di Castelguidone E, Tatangelo F, Ottaiano A, Iaffaioli RV, et al. Early PET/CT scan is more effective than RECIST in predicting outcome of patients with liver metastases from colorectal cancer treated with preoperative chemotherapy plus bevacizumab. J Nucl Med. 2013;54:2062–69.

  69. Celik B, Yalcin AD, Bisgin A, Dimitrakopoulou-Strauss A, Kargi A, Strauss LG. Level of TNF-related apoptosis-inducing-ligand and CXCL8 correlated with 2-[18F]Fluoro-2-deoxy-d-glucose uptake in anti-VEGF treated colon cancers. Med Sci Monit. 2013;19:875–82.

    PubMed  PubMed Central  Google Scholar 

  70. Imyanitov EN, Yanus GA. Neoadjuvant therapy: theoretical, biological and medical consideration. Chin Clin Oncol 2018;7(6):55.

    PubMed  Google Scholar 

  71. Hatano E, Okuno M, Nakamura K, et al. Conversion to complete resection with mFOLFOX6 with bevacizumab or cetuximab based on K-ras status for unresectable colorectal liver metastasis (BECK study). J Hepatobiliary Pancreat Sci. 2015;22:634–45.

    PubMed  Google Scholar 

  72. Kianmanesh R, Farges O, Abdalla EK, et al. Right portal vein ligation: a new planned two-step all-surgical approach for complete resection of primary gastrointestinal tumors with multiple bilateral liver metastases. J Am Coll Surg 2003, 197:164–70.

    PubMed  Google Scholar 

  73. Jaeck D, Bachellier P, Nakano H, et al. One or two-stage hepatectomy combined with portal vein embolization for initially nonresectable colorectal liver metastases. Am J Surg 2003, 185:221–9.

    PubMed  Google Scholar 

  74. Togo S, Nagano Y, Masui H, et al. Two-stage hepatectomy for multiple bilobular liver metastases from colorectal cancer. Hepatogastroenterology 2005, 52:913–9.

    PubMed  Google Scholar 

  75. Chun YS, Vauthey JN, Ribero D, et al. Systemic chemotherapy and two-stage hepatectomy for extensive bilateral colorectal liver metastases: perioperative safety and survival. J Gastrointest Surg 2007, 11:1498–04; discussion 1504–1505.

  76. Guerrera F, Mossetti C, Ceccarelli M, et al. Surgery of colorectal cancer lung metastases: analysis of survival, recurrence and re-surgery. J Thorac Dis. 2016;8(7):1764–71. https://doi.org/10.21037/jtd.2016.05.98.

    Article  PubMed  PubMed Central  Google Scholar 

  77. Riquet M, Foucault C, Cazes A, Mitry E, Dujon A, Le Pimpec Barthes F, Médioni J, Rougier P. Pulmonary resection for metastases of colorectal adenocarcinoma. Ann Thorac Surg. 2010;89:375–80.

    PubMed  Google Scholar 

  78. Pfannschmidt J, Muley T, Hoffmann H, Dienemann H. Prognostic factors and survival after complete resection of pulmonary metastases from colorectal carcinoma: experiences in 167 patients. J Thorac Cardiovasc Surg. 2003; 126: 732–9.

    PubMed  Google Scholar 

  79. Melloni G, Doglioni C, Bandiera A, et al. Prognostic factors and analysis of microsatellite instability in resected pulmonary metastases from colorectal carcinoma. Ann Thorac Surg. 2006;81:2008–13.

    PubMed  Google Scholar 

  80. Lee WS, Yun SH, Chun HK, et al. Pulmonary resection for metastases from colorectal cancer: prognostic factors and survival. Int J Colorectal Dis. 2006.

  81. P. J. Jaquet and P. H. Sugarbaker. Clinical research methodologies in diagnosis ans staging of patients with peritoneal carcinomatosis. in Peritoneal Carcinomatosis: Principles and Management, P. H. Sugarbaker, Ed., pp. 359–74, Kluwer Academic, Norwell, 1996.

    Google Scholar 

  82. Verwaal VJ, Van Ruth S, De Bree E, et al. Randomized trial of cytoreduction and hyperthermic intraperitoneal chemotherapy versus systemic chemotherapy and palliative surgery in patients with peritoneal carcinomatosis of colorectal cancer. J Clin Oncol 2003; 21(20):3737–43.

    PubMed  Google Scholar 

  83. Kelly ME, Spolverato G, Lê GN, Mavros MN, Doyle F, et al. Synchronous colorectal liver metastasis: A network meta-analysis review comparing classical, combined, and liver-first surgical strategies. J Surg Oncol 2015;111: 341–51.

    CAS  PubMed  Google Scholar 

  84. Valle M, Garofalo A. Laparoscopic staging of peritoneal surface malignancies. Eur J Surg Oncol 2006;32: 625–7.

    PubMed  Google Scholar 

  85. Nadler A, McCart JA, Govindarajan A. Peritoneal carcinomatosis from colon cancer: a systematic review of the data for cytoreduction and intraperitoneal chemotherapy. Clin Colon Rectal Surg. 2015;28(4):234–46. https://doi.org/10.1055/s-0035-1564431.

    Article  PubMed  PubMed Central  Google Scholar 

  86. Glehen O, Cotte E, Schreiber V, Sayag-Beaujard A C, Vignal J, Gilly F N. Intraperitoneal chemohyperthermia and attempted cytoreductive surgery in patients with peritoneal carcinomatosis of colorectal origin. Br J Surg. 2004;91(6):747–54.

    CAS  PubMed  Google Scholar 

  87. Elias D, Lefevre JH, Chevalier J, et al. Complete cytoreductive surgery plus intraperitoneal chemohyperthermia with oxaliplatin for peritoneal carcinomatosis of colorectal origin. J Clin Oncol. 2009;27(5):681–5.

    PubMed  Google Scholar 

  88. Passot G, Vaudoyer D, Cotte E, et al. Progression following neoadjuvant systemic chemotherapy may not be a contraindication to a curative approach for colorectal carcinomatosis. Ann Surg. 2012;256(1):125–9.

    PubMed  Google Scholar 

  89. da Silva RG, Sugarbaker PH. Analysis of prognostic factors in seventy patients having a complete cytoreduction plus perioperative intraperitoneal chemotherapy for carcinomatosis from colorectal cancer. J Am Coll Surg. 2006;203(6):878–86.

    PubMed  Google Scholar 

  90. Rajakannu M, Magdeleinat P, Vibert E, Ciacio O, Pittau G, Innominato P, et al. Is cure possible after sequential resection of hepatic and pulmonary metastases from colorectal cancer? Clin Colorectal Cancer. 2018;17(1):41–9. https://doi.org/10.1016/j.clcc.2017.06.006.

    Article  PubMed  Google Scholar 

  91. Al-Hajeili M, Marshall J L, Smaglo BG. Neoadjuvant treatment for surgically resectable metastatic colorectal cancer. Oncology. 30(1):10–16, 28.

  92. Ye LC, Liu TS, Ren L, et al. Randomized controlled trial of cetuximab plus chemotherapy for patients with KRAS wild-type unresectable colorectal liver-limited metastases. J Clin Oncol. 2013;31:1931–8.

    CAS  PubMed  Google Scholar 

  93. Falcone A, Ricci S, Brunetti I, et al. Phase III trial of infusional fluorouracil, leucovorin, oxaliplatin, and irinotecan (FOLFOXIRI) compared with infusional fluorouracil, leucovorin, and irinotecan (FOLFIRI) as first-line treatment for metastatic colorectal cancer: the Gruppo Oncologico Nord Ovest. J Clin Oncol. 2007;25:1670–6.

    CAS  PubMed  Google Scholar 

  94. Van Cutsem E, Kohne CH, Lang I, et al. Cetuximab plus irinotecan, fluorouracil, and leucovorin as first-line treatment for metastatic colorectal cancer: updated analysis of overall survival according to tumor KRAS and BRAF mutation status. J Clin Oncol. 2011;29:2011–9.

    PubMed  Google Scholar 

  95. Masi G, Loupakis F, Salvatore L, et al. Bevacizumab with FOLFOXIRI (irinotecan, oxaliplatin, fluorouracil, and folinate) as first-line treatment for metastatic colorectal cancer: a phase 2 trial. Lancet Oncol. 2010;11:845–52.

    CAS  PubMed  Google Scholar 

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Lin, CC., Chen, TH., Wu, YC. et al. Taiwan Society of Colon and Rectal Surgeons (TSCRS) Consensus for Cytoreduction Selection in Metastatic Colorectal Cancer. Ann Surg Oncol 28, 1762–1776 (2021). https://doi.org/10.1245/s10434-020-08914-8

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