Stephanie A Blankenstein1, Johannes J Bonenkamp2, Maureen J B Aarts3, Franchette W P J van den Berkmortel4, Christian U Blank5, Willeke A M Blokx6, Marye J Boers-Sonderen7, Alfons J M van den Eertwegh8, Margreet G Franken9, Jan Willem B de Groot10, John B A G Haanen5, Geke A P Hospers11, Ellen W Kapiteijn12, Olivier J van Not13,14, Djura Piersma15, Rozemarijn S van Rijn16, Karijn P M Suijkerbuijk13, Astrid A M van der Veldt17, Gerard Vreugdenhil18, Hans M Westgeest19, Michel W J M Wouters20,14,21, Alexander C J van Akkooi20. 1. Department of Surgical Oncology, Netherlands Cancer Institute-Antoni van Leeuwenhoek, Amsterdam, The Netherlands. s.blankenstein@nki.nl. 2. Department of Surgical Oncology, Radboud University Medical Centre, Nijmegen, The Netherlands. 3. Department of Medical Oncology, GROW School for Oncology and Developmental Biology, Maastricht University Medical Centre+, Maastricht, The Netherlands. 4. Department of Internal Medicine, Zuyderland Medical Centre Geleen-Heerlen, Sittard-Geleen, The Netherlands. 5. Department of Medical Oncology, Netherlands Cancer Institute-Antoni van Leeuwenhoek, Amsterdam, The Netherlands. 6. Department of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands. 7. Department of Medical Oncology, Radboud University Medical Centre, Nijmegen, The Netherlands. 8. Department of Medical Oncology, Cancer Center Amsterdam, Amsterdam UMC, Location VU University Medical Center (VUmc), Amsterdam, The Netherlands. 9. Institute for Medical Technology Assessment, Erasmus School of Health Policy & Management, Erasmus University, Rotterdam, The Netherlands. 10. Oncology Center Isala, Isala, Zwolle, The Netherlands. 11. Department of Medical Oncology, University Medical Centre Groningen, University of Groningen, Groningen, The Netherlands. 12. Department of Medical Oncology, Leiden University Medical Centre, Leiden, The Netherlands. 13. Department of Medical Oncology, University Medical Center Utrecht, Utrecht, The Netherlands. 14. Scientific Bureau, Dutch Institute for Clinical Auditing, Leiden, The Netherlands. 15. Department of Internal Medicine, Medisch Spectrum Twente, Enschede, The Netherlands. 16. Department of Internal Medicine, Medical Center Leeuwarden, Leeuwarden, The Netherlands. 17. Departments of Medical Oncology and Radiology and Nuclear Medicine, Erasmus Medical Center, Rotterdam, The Netherlands. 18. Department of Internal Medicine, Maxima Medical Center, Veldhoven, The Netherlands. 19. Department of Internal Medicine, Amphia Hospital, Breda, The Netherlands. 20. Department of Surgical Oncology, Netherlands Cancer Institute-Antoni van Leeuwenhoek, Amsterdam, The Netherlands. 21. Department of Biomedical Data Sciences, Leiden University Medical Center, Leiden, The Netherlands.
Abstract
INTRODUCTION: Sentinel lymph node biopsy (SLNB) is important for staging in patients with primary cutaneous melanoma. Did having previously undergone SLNB also affect outcomes in patients once they have progressed to metastatic melanoma in the era prior to adjuvant therapy? METHODS: Data were retrieved from the Dutch Melanoma Treatment Registry, a prospectively collected, nationwide database of patients with unresectable stage IIIC or IV (advanced) melanoma between 2012 and 2018. Melanoma-specific survival (MSS) was compared between patients with advanced cutaneous melanoma, previously treated with a wide local excision (WLE) or WLE combined with SLNB as initial treatment of their primary tumor. Cox regression analyses were used to analyze the influence of different variables on MSS. RESULTS: In total, 2581 patients were included, of whom 1412 were treated with a WLE of the primary tumor alone and 1169 in whom this was combined with SLNB. At a median follow-up of 44 months from diagnosis of advanced melanoma, MSS was significantly longer in patients who had previously undergone SLNB {median 23 months (95% confidence interval [CI] 19-29) vs. 18 months (95% CI 15-20) for patients treated with WLE alone; p = 0.002}. However, multivariate Cox regression did not identify SLNB as an independent favorable prognostic factor for MSS after diagnosis of advanced melanoma. CONCLUSION: Prior to the availability of adjuvant systemic therapy, once patients have unresectable stage IIIC or IV (advanced) melanoma, there was no difference in disease outcome for patients who were or were not previously staged with SLNB.
INTRODUCTION: Sentinel lymph node biopsy (SLNB) is important for staging in patients with primary cutaneous melanoma. Did having previously undergone SLNB also affect outcomes in patients once they have progressed to metastatic melanoma in the era prior to adjuvant therapy? METHODS: Data were retrieved from the Dutch Melanoma Treatment Registry, a prospectively collected, nationwide database of patients with unresectable stage IIIC or IV (advanced) melanoma between 2012 and 2018. Melanoma-specific survival (MSS) was compared between patients with advanced cutaneous melanoma, previously treated with a wide local excision (WLE) or WLE combined with SLNB as initial treatment of their primary tumor. Cox regression analyses were used to analyze the influence of different variables on MSS. RESULTS: In total, 2581 patients were included, of whom 1412 were treated with a WLE of the primary tumor alone and 1169 in whom this was combined with SLNB. At a median follow-up of 44 months from diagnosis of advanced melanoma, MSS was significantly longer in patients who had previously undergone SLNB {median 23 months (95% confidence interval [CI] 19-29) vs. 18 months (95% CI 15-20) for patients treated with WLE alone; p = 0.002}. However, multivariate Cox regression did not identify SLNB as an independent favorable prognostic factor for MSS after diagnosis of advanced melanoma. CONCLUSION: Prior to the availability of adjuvant systemic therapy, once patients have unresectable stage IIIC or IV (advanced) melanoma, there was no difference in disease outcome for patients who were or were not previously staged with SLNB.
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