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Laparoscopic liver resection for metastatic melanoma

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Abstract

Background

Stage IV metastatic melanoma carries a poor prognosis. In the case of melanoma liver metastasis (MLM), surgical resection may improve survival and represents a therapeutic option, with varying levels of success. Laparoscopic liver resection (LLR) for metastatic melanoma is poorly studied. The aim of this study was to analyze the outcomes of LLR in patients with MLM.

Materials and methods

Between April 2000 and August 2013, 11 (1 cutaneous, 9 ocular and 1 unknown primary) patients underwent LLR for MLM at Oslo University Hospital—Rikshospitalet and 13 procedures in total were carried out. Perioperative and oncologic outcomes were analyzed. Postoperative morbidity was classified using the Accordion classification. Kaplan–Meier method was used for survival analysis.

Results

A total of 23 liver specimens were resected. The median operative time was 137 (65–470) min, while the median blood loss was less than 50 (<50–900) ml. No intraoperative unfavorable incidents and 30‐day mortality occurred. Median follow-up was 33 (9–92) months. Ten patients (91%) developed recurrence within a median of 5 months (2–18 months) and two patients underwent repeat LLR for recurrent liver metastases. One-, three-, and five-year overall survival rates were 82, 45 and 9%, respectively. The median overall survival was 30 (9–92) months.

Conclusion

Perioperative morbidity and long-term survival after LLR for MLM seems to be comparable to open liver resection. Thus, LLR may be preferred over open liver resection due to the well-known advantages of laparoscopy, such as reduced pain and improved possibility for repeated resections.

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References

  1. Patel JK et al (1978) Metastatic pattern of malignant melanoma. A study of 216 autopsy cases. Am J Surg 135(6):807–810

    Article  CAS  PubMed  Google Scholar 

  2. Cohn-Cedermark G et al (1999) Metastatic patterns, clinical outcome, and malignant phenotype in malignant cutaneous melanoma. Acta Oncol 38(5):549–557

    Article  CAS  PubMed  Google Scholar 

  3. Leiter U et al (2004) The natural course of cutaneous melanoma. J Surg Oncol 86(4):172–178

    Article  PubMed  Google Scholar 

  4. Albert DM, Ryan LM, Borden EC (1996) Metastatic ocular and cutaneous melanoma: a comparison of patient characteristics and prognosis. Arch Ophthalmol 114(1):107–108

    Article  CAS  PubMed  Google Scholar 

  5. Balch CM et al (2001) Prognostic factors analysis of 17,600 melanoma patients: validation of the American Joint Committee on Cancer melanoma staging system. J Clin Oncol 19(16):3622–3634

    Article  CAS  PubMed  Google Scholar 

  6. Aoyama T et al (2000) Protracted survival after resection of metastatic uveal melanoma. Cancer 89(7):1561–1568

    Article  CAS  PubMed  Google Scholar 

  7. Derek E et al (2013) Combined surgical resection and radiofrequency ablation as treatment for metastatic ocular melanoma. Surg Today 43(4):367–371

    Article  PubMed  Google Scholar 

  8. Mariani P et al (2009) Surgical management of liver metastases from uveal melanoma: 16 years’ experience at the Institut Curie. Eur J Surg Oncol 35(11):1192–1197

    Article  CAS  PubMed  Google Scholar 

  9. Salmon RJ et al (1998) Treatment of liver metastases from uveal melanoma by combined surgery-chemotherapy. Eur J Surg Oncol 24(2):127–130

    Article  CAS  PubMed  Google Scholar 

  10. Bedikian AY et al (1995) Treatment of uveal melanoma metastatic to the liver: a review of the M. D. Anderson Cancer Center experience and prognostic factors. Cancer 76(9):1665–1670

    Article  CAS  PubMed  Google Scholar 

  11. Pawlik TM et al (2006) Hepatic resection for metastatic melanoma: distinct patterns of recurrence and prognosis for ocular versus cutaneous disease. Ann Surg Oncol 13(5):712–720

    Article  PubMed  Google Scholar 

  12. Doussot A et al (2015) Liver resection and ablation for metastatic melanoma: a single center experience. J Surg Oncol 111(8):962–968

    Article  PubMed  PubMed Central  Google Scholar 

  13. Schelhorn J et al (2015) A single-center experience in radioembolization as salvage therapy of hepatic metastases of uveal melanoma. Acta Radiol Open 4(4):2047981615570417

    PubMed  PubMed Central  Google Scholar 

  14. Faries MB et al (2014) A 20-year experience of hepatic resection for melanoma: is there an expanding role? J Am Coll Surg 219(1):62–68

    Article  PubMed  PubMed Central  Google Scholar 

  15. Alvarez-Downing MM et al (2012) Minimally invasive liver resection to obtain tumor-infiltrating lymphocytes for adoptive cell therapy in patients with metastatic melanoma. World J Surg Oncol 10:113

    Article  PubMed  PubMed Central  Google Scholar 

  16. Olofsson R et al (2014) Isolated hepatic perfusion as a treatment for uveal melanoma liver metastases (the SCANDIUM trial): study protocol for a randomized controlled trial. Trials 15:317

    Article  PubMed  PubMed Central  Google Scholar 

  17. Hameed AM et al (2014) Hepatic resection for metastatic melanoma: a systematic review. Melanoma Res 24(1):1–10

    Article  CAS  PubMed  Google Scholar 

  18. Gomez D et al (2014) The Liverpool uveal melanoma liver metastases pathway: outcome following liver resection. J Surg Oncol 109(6):542–547

    Article  CAS  PubMed  Google Scholar 

  19. Ryu SW et al (2013) Liver resection for metastatic melanoma: equivalent survival for cutaneous and ocular primaries. J Surg Oncol 108(2):129–135

    Article  PubMed  Google Scholar 

  20. Ollila DW, Gleisner AL, Hsueh EC (2011) Rationale for complete metastasectomy in patients with stage IV metastatic melanoma. J Surg Oncol 104(4):420–424

    Article  PubMed  Google Scholar 

  21. Edwin B, Nordin A, Kazaryan AM (2011) Laparoscopic liver surgery: new frontiers. Scand J Surg 100(1):54–65

    Article  CAS  PubMed  Google Scholar 

  22. Kazaryan AM et al (2010) Laparoscopic resection of colorectal liver metastases: surgical and long-term oncologic outcome. Ann Surg 252(6):1005–1012

    Article  PubMed  Google Scholar 

  23. Kazaryan AM et al (2010) Laparoscopic liver resection for malignant and benign lesions: ten-year Norwegian single-center experience. Arch Surg 145(1):34–40

    Article  PubMed  Google Scholar 

  24. Wakabayashi G et al (2015) Recommendations for laparoscopic liver resection: a report from the second international consensus conference held in Morioka. Ann Surg 261(4):619–629

    PubMed  Google Scholar 

  25. Akyuz M et al (2016) Laparoscopic management of liver metastases from uveal melanoma. Surg Endosc 30(6):2567–2571

    Article  PubMed  Google Scholar 

  26. Edwin B et al (2001) Liver tumors and minimally invasive surgery: a feasibility study. J Laparoendosc Adv Surg Tech A 11(3):133–139

    Article  CAS  PubMed  Google Scholar 

  27. Mala T et al (2005) Laparoscopic liver resection: experience of 53 procedures at a single center. J Hepatobiliary Pancreat Surg 12(4):298–303

    Article  PubMed  Google Scholar 

  28. Strasberg SM, Linehan DC, Hawkins WG (2009) The accordion severity grading system of surgical complications. Ann Surg 250(2):177–186

    Article  PubMed  Google Scholar 

  29. Porembka MR et al (2010) Quantitative weighting of postoperative complications based on the accordion severity grading system: demonstration of potential impact using the american college of surgeons national surgical quality improvement program. J Am Coll Surg 210(3):286–298

    Article  PubMed  Google Scholar 

  30. Satava RM (2005) Identification and reduction of surgical error using simulation. Minim Invasive Ther Allied Technol 14(4):257–261

    Article  PubMed  Google Scholar 

  31. Kazaryan AM, Rosok BI, Edwin B (2013) Morbidity assessment in surgery: refinement proposal based on a concept of perioperative adverse events. ISRN Surg 2013:625093

    Article  PubMed  PubMed Central  Google Scholar 

  32. Reddy SK, Tsung A, Geller DA (2011) Laparoscopic liver resection. World J Surg 35(7):1478–1486

    Article  PubMed  Google Scholar 

  33. O’Rourke TR et al (2008) Long-term results of liver resection for non-colorectal, non-neuroendocrine metastases. Ann Surg Oncol 15(1):207–218

    Article  PubMed  Google Scholar 

  34. Takemura N et al (2013) Long-term results of hepatic resection for non-colorectal, non-neuroendocrine liver metastasis. Hepatogastroenterology 60(127):1705–1712

    PubMed  Google Scholar 

  35. Frenkel S et al (2009) Long-term survival of uveal melanoma patients after surgery for liver metastases. Br J Ophthalmol 93(8):1042–1046

    Article  CAS  PubMed  Google Scholar 

  36. Rose DM et al (2001) Surgical resection for metastatic melanoma to the liver: the John Wayne Cancer Institute and Sydney Melanoma Unit experience. Arch Surg 136(8):950–955

    Article  CAS  PubMed  Google Scholar 

  37. Kodjikian L, Grange JD, Rivoire M (2005) Prolonged survival after resection of liver metastases from uveal melanoma and intra-arterial chemotherapy. Graefes Arch Clin Exp Ophthalmol 243(6):622–624

    Article  PubMed  Google Scholar 

  38. Postriganova N et al (2014) Margin status after laparoscopic resection of colorectal liver metastases: does a narrow resection margin have an influence on survival and local recurrence? HPB (Oxford) 16(9):822–829

    Article  Google Scholar 

  39. Montalti R et al (2015) Impact of surgical margins on overall and recurrence-free survival in parenchymal-sparing laparoscopic liver resections of colorectal metastases. Surg Endosc 29(9):2736–2747

    Article  PubMed  Google Scholar 

  40. Kolandjian NA et al (2013) Delayed systemic recurrence of uveal melanoma. Am J Clin Oncol 36(5):443–449

    Article  PubMed  PubMed Central  Google Scholar 

  41. Li Y, McClay EF (2002) Systemic chemotherapy for the treatment of metastatic melanoma. Semin Oncol 29(5):413–426

    Article  CAS  PubMed  Google Scholar 

  42. Rivoire M et al (2005) Treatment of liver metastases from uveal melanoma. Ann Surg Oncol 12(6):422–428

    Article  PubMed  Google Scholar 

  43. Lui P et al (2007) Treatments for metastatic melanoma: synthesis of evidence from randomized trials. Cancer Treat Rev 33(8):665–680

    Article  PubMed  Google Scholar 

  44. Hamm C et al (2008) Biochemotherapy for the treatment of metastatic malignant melanoma: a systematic review. Cancer Treat Rev 34(2):145–156

    Article  CAS  PubMed  Google Scholar 

  45. Jilaveanu LB, Aziz SA, Kluger HM (2009) Chemotherapy and biologic therapies for melanoma: do they work? Clin Dermatol 27(6):614–625

    Article  PubMed  Google Scholar 

  46. Dillman RO et al (2012) Should high-dose interleukin-2 still be the preferred treatment for patients with metastatic melanoma? Cancer Biother Radiopharm 27(6):337–343

    Article  CAS  PubMed  Google Scholar 

  47. Coit DG et al (2013) Melanoma, version 2.2013: featured updates to the NCCN guidelines. J Natl Compr Canc Netw 11(4):395–407

    Article  CAS  PubMed  Google Scholar 

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Correspondence to Davit L. Aghayan.

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Disclosures

Davit L. Aghayan, Airazat M. Kazaryan, Åsmund Avdem Fretland, Mushegh A. Sahakyan, Bård I. Røsok, Bjørn Atle Bjørnbeth, and Bjørn Edwin have no conflicts of interest or financial ties to disclose.

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Aghayan, D.L., Kazaryan, A.M., Fretland, Å.A. et al. Laparoscopic liver resection for metastatic melanoma. Surg Endosc 32, 1470–1477 (2018). https://doi.org/10.1007/s00464-017-5834-0

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  • DOI: https://doi.org/10.1007/s00464-017-5834-0

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