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Treatment Failure After Percutaneous Radiofrequency Ablation for Nonsurgical Candidates With Pulmonary Metastases From Colorectal Carcinoma

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Abstract

Background

This study critically evaluated the local and overall treatment failure rates after percutaneous radiofrequency ablation (RFA) of pulmonary metastases from colorectal carcinoma.

Methods

Fifty-five nonsurgical candidates underwent RFA of colorectal pulmonary metastases. The primary end points of this study were local progression-free survival (PFS) and overall PFS. Univariate and multivariate analyses were performed to identify significant prognostic parameters for local and overall PFS.

Results

The local recurrence rate was 38%. For local PFS, univariate analysis demonstrated that the largest size of lung metastasis, the location of lung metastases, the post-RFA carcinoembryonic antigen level at 1 month, and the post-RFA carcinoembryonic antigen level at 3 months were significant prognostic indicators. In multivariate analysis, a largest size of lung metastasis of >3 cm and a post-RFA carcinoembryonic antigen level of >5 ng/mL at 1 month were independently associated with a reduced local PFS. The overall recurrence rate was 66%. For overall PFS, univariate analysis demonstrated that sex and the largest size of lung metastasis were significant prognostic indicators. In multivariate analysis, a largest size of lung metastasis of >3 cm was independently associated with a reduced overall PFS.

Conclusions

RFA of colorectal pulmonary metastases may have a useful role in local disease control for nonsurgical candidates, but its efficacy in patients with a lung metastasis of >3 cm is limited.

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References

  1. Pastorino U, Buyse M, Friedel G, et al. Long-term results of lung metastasectomy: prognostic analysis based on 5206 cases. J Thorac Cardiovasc Surg 1997; 113:37–49

    Article  Google Scholar 

  2. Okumura S, Kondo H, Tsuboi M, et al. Pulmonary resection for metastatic colorectal cancer: experiences with 159 patients. J Thorac Cardiovasc Surg 1996; 112:867–74

    Article  PubMed  CAS  Google Scholar 

  3. van Halteren HK, van Geel AN, Hart AA, et al. Pulmonary resection for metastases of colorectal origin. Chest 1995;107:1525–31

    Google Scholar 

  4. Brister SJ, de Varennes B, Gordon PH, et al. Contemporary operative management of pulmonary metastases of colorectal origin. Dis Colon Rectum 1998; 31:786–92

    Article  Google Scholar 

  5. Sakamoto T, Tsubota N, Iwanaga K, et al. Pulmonary resection for metastases from colorectal cancer. Chest 2001; 119:1069–72

    Article  PubMed  CAS  Google Scholar 

  6. Morrow CE, Vassilopoulos PP, Grage TB. Surgical resection for metastatic neoplasms of the lung: experience at the University of Minnesota Hospitals. Cancer 1980; 45:2981–5

    Article  PubMed  CAS  Google Scholar 

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

    PubMed  CAS  Google Scholar 

  8. Rusch VW. Pulmonary metastasectomy. Current indications. Chest 1995; 107:322S–331S

    PubMed  CAS  Google Scholar 

  9. Watanabe I, Arai T, Ono M, et al. Prognostic factors in resection of pulmonary metastasis from colorectal cancer. Br J Surg 2003; 90:1436–40

    Article  PubMed  CAS  Google Scholar 

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

    Article  PubMed  Google Scholar 

  11. Saito Y, Omiya H, Kohno K, et al. Pulmonary metastasectomy for 165 patients with colorectal carcinoma: a prognostic assessment. J Thorac Cardiovasc Surg 2002; 124:1007–13

    Article  PubMed  Google Scholar 

  12. Rena O, Casadio C, Viano F, et al. Pulmonary resection for metastases from colorectal cancer: factors influencing prognosis. Twenty-year experience. Eur J Cardiothorac Surg 2002; 21:906–12

    Article  PubMed  Google Scholar 

  13. Colucci G, Gebbin V, Paoletti G, et al. Phase III randomized trial of FOLFIRI versus FOLFOX4 in the treatment of advanced colorectal cancer: a multicenter study of the Gruppo Oncologico Dell’Italia Meridionale. J Clin Oncol 2005; 23:4866–75

    Article  PubMed  CAS  Google Scholar 

  14. Hurwitz H, Fehrenbacher L, Novotny W, et al. Bevacizumab plus irinotecan, fluorouracil, and leucovorin for metastatic colorectal cancer. N Engl J Med 2004; 350:2335–42

    Article  PubMed  CAS  Google Scholar 

  15. Rothenberg ML, Oza AM, Bigelow RH, et al. Superiority of oxaliplatin and fluorouracil-leucovorin compared with either therapy alone in patients with progressive colorectal cancer after irinotecan and fluorouracil-leucovorin: interim results of a phase III trial. J Clin Oncol 2003; 21:2059–69

    Article  PubMed  CAS  Google Scholar 

  16. de Gramont A, Figer A, Seymour M, et al. Leucovorin and fluorouracil with or without oxaliplatin as first-line treatment in advanced colorectal cancer. J Clin Oncol 2000; 18:2938–47

    PubMed  Google Scholar 

  17. Douillard J-Y, Cunningham D, Roth AD, et al. Irinotecan combined with fluorouracil compared with fluorouracil alone as first-line treatment for metastatic colorectal cancer: a multicenter randomized trial. Lancet 2000; 355:1041–7

    Article  PubMed  CAS  Google Scholar 

  18. Giacchetti S, Perpoint B, Zidani R, et al. Phase III multicenter randomized trial of oxaliplatin added to chronomodulated fluorouracil-leucovorin as first-line treatment of metastatic colorectal cancer. J Clin Oncol 2000; 18:136–47

    PubMed  CAS  Google Scholar 

  19. Steinke K, Glenn D, King J, et al. Percutaneous imaging-guided radiofrequency ablation in patients with colorectal pulmonary metastases: 1-year follow-up. Ann Surg Oncol 2004; 11:207–12

    Article  PubMed  Google Scholar 

  20. King J, Glenn D, Clark W, et al. Percutaneous radiofrequency ablation of pulmonary metastases in patients with colorectal cancer. Br J Surg 2004; 91:217–23

    Article  PubMed  CAS  Google Scholar 

  21. Steinke K, Sewell PE, Dupuy D, et al. Pulmonary radiofrequency ablation—an international study survey. Anticancer Res 2004; 24:339–43

    PubMed  Google Scholar 

  22. Dupuy DE, DiPetrillo T, Gandhi S, et al. Radiofrequency ablation followed by conventional radiotherapy for medically inoperable stage I non-small cell lung cancer. Chest 2006; 129:738–45

    Article  PubMed  Google Scholar 

  23. Lee J, Jin GY, Goldberg SN, et al. Percutaneous radiofrequency ablation for inoperable non-small cell lung cancer and metastases: preliminary report. Radiology 2004; 230:125–34

    Article  PubMed  Google Scholar 

  24. Fernando HC, De Hoyos A, Landreneau RJ, et al. Radiofrequency ablation for the treatment of non-small cell lung cancer in marginal surgical candidates. J Thorac Cardiovasc Surg 2005; 129:639–44

    Article  PubMed  Google Scholar 

  25. Herrera LJ, Fernando HC, Perry Y, et al. Radiofrequency ablation of pulmonary malignant tumors in nonsurgical candidates. J Thorac Cardiovasc Surg 2003; 125:929–37

    Article  PubMed  Google Scholar 

  26. Suh R, Reckamp K, Zeidler M, et al. Radiofrequency ablation in lung cancer: promising results in safety and efficacy. Oncology 2005; 19:12–21

    PubMed  Google Scholar 

  27. Steinke K, Glenn D, King J, et al. Percutaneous pulmonary radiofrequency ablation: difficulty achieving complete ablations in big lung lesions. Br J Radiol 2003; 76:742–5

    Article  PubMed  CAS  Google Scholar 

  28. Ambrogi MC, Lucchi M, Dini P, et al. Percutaneous radiofrequency ablation of lung tumours: results in the mid-term. Eur J Cardiothorac Surg 2006; 30:177–83

    Article  PubMed  Google Scholar 

  29. Akeboshi M, Yamakado K, Nakatsuka A, et al. Percutaneous radiofrequency ablation of lung neoplasms: initial therapeutic response. J Vasc Interv Radiol 2004; 15:463–70

    PubMed  Google Scholar 

  30. Goldberg SN, Gazelle GS, Compton CC, et al. Radiofrequency tissue ablation in the rabbit lung: efficacy and complications. Acad Radiol 1995; 2:776–84

    Article  PubMed  CAS  Google Scholar 

  31. Dupuy DE, Mayo-Smith WW, DiPettrillo T, et al. Clinical experience of pulmonary radiofrequency ablation in 27 patients (abstract 389). Radiological Society of North America Proceedings, Chicago, November 2001

  32. Vaughn C, Mychaskiw G II, Sewell P. Massive hemorrhage during radiofrequency ablation of a pulmonary neoplasm. Anesth Analg 2002; 94:1149–51

    Article  PubMed  Google Scholar 

  33. Avital I, DeMatteo R. Combined resection of liver and lung metastases for colorectal cancer. Thorac Surg Clin 2006; 16:145–55

    Article  PubMed  Google Scholar 

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Acknowledgments

The authors thank David Chang for his expertise in statistical analysis and Jing Zhao for maintaining the RFA database.

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Correspondence to David L. Morris MD, PhD.

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Yan, T.D., King, J., Sjarif, A. et al. Treatment Failure After Percutaneous Radiofrequency Ablation for Nonsurgical Candidates With Pulmonary Metastases From Colorectal Carcinoma. Ann Surg Oncol 14, 1718–1726 (2007). https://doi.org/10.1245/s10434-006-9271-x

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  • DOI: https://doi.org/10.1245/s10434-006-9271-x

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