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Hepatic Resection for Metastatic Melanoma: Distinct Patterns of Recurrence and Prognosis for Ocular Versus Cutaneous Disease

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Abstract

Background

Resection of melanoma metastatic to the liver remains controversial. We evaluated the efficacy of hepatic resection in patients with metastatic ocular and cutaneous melanoma and assessed factors that could affect survival after resection.

Methods

Forty patients with hepatic melanoma metastasis underwent resection at four major hepatobiliary centers. Clinicopathologic factors were evaluated with regard to recurrence and survival by using χ2 and log-rank tests.

Results

The primary tumor was ocular in 16 patients and cutaneous in 24. The median disease-free interval from the time of primary tumor treatment to hepatic metastasis was the same for both groups (ocular, 62.9 months; cutaneous, 63.1 months; P = .94). Most patients underwent either an extended hepatic resection (37.5%) or hemihepatectomy (22.5%). Twenty-six patients (65%) received perioperative systemic therapy. Thirty (75.0%) of 40 patients developed tumor recurrence. The median time to recurrence after hepatic resection was 8.3 months (ocular, 8.8 months; cutaneous, 4.7 months; P = .3). Patients with primary ocular melanoma were more likely to experience recurrence within the liver (53.3% vs. 17.4%; P = .015), whereas patients with a cutaneous primary tumor more often developed extrahepatic involvement. The 5-year survival rate for patients with a primary ocular melanoma was 20.5%, whereas there were no 5-year survivors for patients with cutaneous melanoma (P = .03).

Conclusions

Patterns of recurrence and prognosis after resection of hepatic melanoma metastasis differ depending on whether the primary melanoma is ocular or cutaneous. Resection should be performed as part of a multidisciplinary approach, because recurrence is common.

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References

  1. Jemal A, Tiwari RC, Murray T, et al. Cancer statistics, 2004. CA Cancer J Clin 2004; 54:8–29

    PubMed  Google Scholar 

  2. Singh AD, Topham A. Incidence of uveal melanoma in the United States: 1973-1997. Ophthalmology 2003; 110:956–61

    PubMed  Google Scholar 

  3. Reintgen DS, Cox C, Slingluff CL Jr, Seigler HF. Recurrent malignant melanoma: the identification of prognostic factors to predict survival. Ann Plast Surg 1992; 28:45–9

    CAS  PubMed  Google Scholar 

  4. Soong SJ, Harrison RA, McCarthy WH, Urist MM, Balch CM. Factors affecting survival following local, regional, or distant recurrence from localized melanoma. J Surg Oncol 1998; 67:228–33

    Article  CAS  PubMed  Google Scholar 

  5. Becker JC, Terheyden P, Kampgen E, et al. Treatment of disseminated ocular melanoma with sequential fotemustine, interferon alpha, and interleukin 2. Br J Cancer 2002; 87:840–5

    CAS  PubMed  Google Scholar 

  6. Leiter U, Meier F, Schittek B, Garbe C. The natural course of cutaneous melanoma. J Surg Oncol 2004; 86:172–8

    Article  PubMed  Google Scholar 

  7. Cohn-Cedermark G, Mansson-Brahme E, Rutqvist LE, Larsson O, Singnomklao T, Ringborg U. Metastatic patterns, clinical outcome, and malignant phenotype in malignant cutaneous melanoma. Acta Oncol 1999; 38:549–57

    CAS  PubMed  Google Scholar 

  8. Feldman ED, Pingpank JF, Alexander HR Jr. Regional treatment options for patients with ocular melanoma metastatic to the liver. Ann Surg Oncol 2004; 11:290–7

    Article  PubMed  Google Scholar 

  9. Soni S, Lee DS, DiVito J Jr, et al. Treatment of pediatric ocular melanoma with high-dose interleukin-2 and thalidomide. J Pediatr Hematol Oncol 2002; 24:488–91

    Article  PubMed  Google Scholar 

  10. Balch CM, Soong SJ, Gershenwald JE, et al. Prognostic factors analysis of 17,600 melanoma patients: validation of the American Joint Committee on Cancer melanoma staging system. J Clin Oncol 2001; 19:3622–34

    CAS  PubMed  Google Scholar 

  11. Barth A, Wanek LA, Morton DL. Prognostic factors in 1,521 melanoma patients with distant metastases. J Am Coll Surg 1995; 181:193–201

    CAS  PubMed  Google Scholar 

  12. Albert DM, Niffenegger AS, Willson JK. Treatment of metastatic uveal melanoma: review and recommendations. Surv Ophthalmol 1992; 36:429–38

    CAS  PubMed  Google Scholar 

  13. Pyrhonen S. The treatment of metastatic uveal melanoma. Eur J Cancer 1998;34(Suppl 3):S27–30

    PubMed  Google Scholar 

  14. Li Y, McClay EF. Systemic chemotherapy for the treatment of metastatic melanoma. Semin Oncol 2002; 29:413–26

    Article  CAS  PubMed  Google Scholar 

  15. Chapman PB, Einhorn LH, Meyers ML, et al. Phase III multicenter randomized trial of the Dartmouth regimen versus dacarbazine in patients with metastatic melanoma. J Clin Oncol 1999; 17:2745–51

    CAS  PubMed  Google Scholar 

  16. Duh EJ, Schachat AP, Albert DM, Patel SM. Long-term survival in a patient with uveal melanoma and liver metastasis. Arch Ophthalmol 2004; 122:285–7

    Article  PubMed  Google Scholar 

  17. Mondragon-Sanchez R, Barrera-Franco JL, Cordoba-Gutierrez H, Meneses-Garcia A. Repeat hepatic resection for recurrent metastatic melanoma. Hepatogastroenterology 1999; 46:459–61

    CAS  PubMed  Google Scholar 

  18. Gunduz K, Shields JA, Shields CL, Sato T, Mastrangelo MJ. Surgical removal of solitary hepatic metastasis from choroidal melanoma. Am J Ophthalmol 1998; 125:407–9

    Article  CAS  PubMed  Google Scholar 

  19. Vauthey JN, Winter MW, Blumgart LH. Solitary metastasis from cutaneous melanoma to the liver: resection by extended left hepatectomy (trisegmentectomy) with clearance of tumor from the portal vein. HPB Surg 1994; 8:53–6

    CAS  PubMed  Google Scholar 

  20. Papachristou DN, Fortner JJ. Surgical treatment of metastatic melanoma confined to the liver. Int Surg 1983; 68:145–8

    CAS  PubMed  Google Scholar 

  21. Stoelben E, Sturm J, Schmoll J, Keilholz U, Saeger HD. Resection of solitary liver metastases of malignant melanoma (in German). Chirurg 1995; 66:40–3; discussion 3–4

    CAS  PubMed  Google Scholar 

  22. Aoyama T, Mastrangelo MJ, Berd D, et al. Protracted survival after resection of metastatic uveal melanoma. Cancer 2000; 89:1561–8

    Article  CAS  PubMed  Google Scholar 

  23. Fournier GA, Albert DM, Arrigg CA, Cohen AM, Lamping KA, Seddon JM. Resection of solitary metastasis. Approach to palliative treatment of hepatic involvement with choroidal melanoma. Arch Ophthalmol 1984; 102:80–2

    CAS  PubMed  Google Scholar 

  24. Harrison LE, Brennan MF, Newman E, et al. Hepatic resection for noncolorectal, nonneuroendocrine metastases: a fifteen-year experience with ninety-six patients. Surgery 1997; 121:625–32

    Article  CAS  PubMed  Google Scholar 

  25. Khadra MH, Thompson JF, Milton GW, McCarthy WH. The justification for surgical treatment of metastatic melanoma of the gastrointestinal tract. Surg Gynecol Obstet 1990; 171:413–6

    CAS  PubMed  Google Scholar 

  26. Mosimann F, Fontolliet C, Genton A, Gertsch P, Pettavel J. Resection of metastases to the alimentary tract from malignant melanoma. Int Surg 1982; 67:257–60

    CAS  PubMed  Google Scholar 

  27. Lejeune FJ, Lienard D, Sales F, Badr-el-Din H. Surgical management of distant melanoma metastases. Semin Surg Oncol 1992; 8:381–91

    CAS  PubMed  Google Scholar 

  28. Haigh PI, Essner R, Wardlaw JC, Stern SL, Morton DL. Long-term survival after complete resection of melanoma metastatic to the adrenal gland. Ann Surg Oncol 1999; 6:633–9

    Article  CAS  PubMed  Google Scholar 

  29. Branum GD, Epstein RE, Leight GS, Seigler HF. The role of resection in the management of melanoma metastatic to the adrenal gland. Surgery 1991; 109:127–31

    CAS  PubMed  Google Scholar 

  30. Wong JH, Euhus DM, Morton DL. Surgical resection for metastatic melanoma to the lung. Arch Surg 1988; 123:1091–5

    CAS  PubMed  Google Scholar 

  31. Ollila DW, Morton DL. Surgical resection as the treatment of choice for melanoma metastatic to the lung. Chest Surg Clin North Am 1998; 8:183–96

    CAS  Google Scholar 

  32. Tafra L, Dale PS, Wanek LA, Ramming KP, Morton DL. Resection and adjuvant immunotherapy for melanoma metastatic to the lung and thorax. J Thorac Cardiovasc Surg 1995; 110:119–28; discussion 29

    CAS  PubMed  Google Scholar 

  33. Schwartz SI. Hepatic resection for noncolorectal nonneuroendocrine metastases. World J Surg 1995; 19:72–5

    Article  CAS  PubMed  Google Scholar 

  34. Foster JH, Lundy J. Liver metastases. Curr Probl Surg 1981; 18:160–202

    Google Scholar 

  35. Dousei T, Miyata M, Yamaguchi T, Nagaoka M, Takahashi E, Kawashima Y. Rupture of liver metastasis of malignant melanomaa case of hepatic resection. Jpn J Surg 1991; 21:480–4

    CAS  PubMed  Google Scholar 

  36. Rose DM, Essner R, Hughes TM, et al. Surgical resection for metastatic melanoma to the liver: the John Wayne Cancer Institute and Sydney Melanoma Unit experience. Arch Surg 2001; 136:950–5

    CAS  PubMed  Google Scholar 

  37. Albert DM, Ryan LM, Borden EC. Metastatic ocular and cutaneous melanoma: a comparison of patient characteristics and prognosis. Arch Ophthalmol 1996; 114:107–8

    CAS  PubMed  Google Scholar 

  38. Nathan FE, Sato T, Hart E, Berd D, Mastrangelo MJ. Response to combination chemotherapy of liver metastases from choroidal melanoma compared with cutaneous melanoma. Program Proceedings, Thirtieth Annual Meeting of the American Society of Clinical Oncology. 1994; 13:396.

    Google Scholar 

  39. Foster JH. Survival after liver resection for secondary tumors. Am J Surg 1978; 135:389–94

    Article  CAS  PubMed  Google Scholar 

  40. Elias D, Cavalcanti de Albuquerque A, Eggenspieler P, et al. Resection of liver metastases from a noncolorectal primary: indications and results based on 147 monocentric patients. J Am Coll Surg 1998; 187:487–93

    Article  CAS  PubMed  Google Scholar 

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Correspondence to Jean-Nicolas Vauthey MD.

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Pawlik, T.M., Zorzi, D., Abdalla, E.K. et al. Hepatic Resection for Metastatic Melanoma: Distinct Patterns of Recurrence and Prognosis for Ocular Versus Cutaneous Disease. Ann Surg Oncol 13, 712–720 (2006). https://doi.org/10.1245/ASO.2006.01.016

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  • DOI: https://doi.org/10.1245/ASO.2006.01.016

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