Melanoma Cutáneo Etapa clínica IIIB-D: análisis retrospectivo de pacientes tratados en el Instituto Oncológico Nacional de Panamá
[Cutaneous Melanoma Clinical Stage IIIB-D: Retrospective analysis of patients treated at the National Oncology Institute of Panama.]David Espinosa1 , Marco Achurra1 , Patsy Moreno2
1. Departamento de Cirugía Oncológica, Instituto Oncológico Nacional, Panamá, Rep de Panamá; 2. Hospital Dr Gustavo Nelson Collado, Chitré, Rep de Panamá;
Descargas
Resumen
Antecedentes y objetivos: El melanoma cutáneo es una enfermedad agresiva. Aproximadamente el 10% de los casos son diagnosticados con enfermedad regional, siendo el manejo estándar, la resección del primario con linfadenectomía regional con inmunoterapia adyuvante o neoadyuvante. El objetivo de este estudio es reportar los resultados oncológicos en este grupo de pacientes y establecer factores asociados a mayor recurrencia y mortalidad. Materiales y métodos: Descriptivo, no experimental, transversal y retrospectivo. Se analizaron 44 pacientes con diagnóstico Melanoma cutáneo ECIIIB-D tratados en el Instituto Oncológico Nacional durante el período de enero 2017 a diciembre 2023. Resultados: 44 pacientes fueron tratados. El 49.5% con Breslow > 4 mm y 68.2% con ulceración, el 75% presentaban ≥2 ganglios positivos. La mediana de supervivencia global fue 30 meses y la mediana de supervivencia libre de recurrencia 12 meses. Los pacientes con recurrencia tuvieron peor mediana de supervivencia global (25 meses) que los que no tuvieron recurrencia (no alcanzada) (p 0.036). Los factores de riesgo asociados a mayor recurrencia fueron Breslow 2.1-4 mm (HR 4.88, IC 1.0-23.01, p 0.046) y ≥4 ganglios positivos (HR 4.2, IC 1.17-15.2, p 0.027). La ausencia de invasión linfovascular fue factor protector de muerte (HR 0.21, IC 0.06-0.67, p 0.008). Conclusiones: en el Instituto Oncológico Nacional, la supervivencia libre de recurrencia es ligeramente más baja que en la literatura mundial, los principales factores asociados a recurrencia fueron Breslow > 2 mm y ≥4 o más ganglios positivos. Esto crea la pregunta de si agregar inmunoterapia podría mejorar estos resultados.
Abstract
Background and Objectives: Cutaneous melanoma is an aggressive disease. Approximately 10% of cases are diagnosed with regional disease, with the standard management being primary resection with regional lymphadenectomy with adjuvant or neoadjuvant immunotherapy. The aim of this study is to report the oncological outcomes in this group of patients and establish factors associated with increased recurrence and mortality. Materials and Methods: Descriptive, non-experimental, cross-sectional, and retrospective. 44 patients with stage IIIB-D cutaneous melanoma diagnosed were analyzed at the National Oncology Institute during the period from January 2017 to December 2023. Results: 44 patients were treated. 49.5% had Breslow thickness > 4 mm and 68.2% had ulceration, 75% had ≥2 positive nodes. The median overall survival was 30 months and the median recurrence-free survival was 12 months. Patients with recurrence had worse median overall survival (25 months) than those without recurrence (not reached) (p 0.036). Risk factors associated with increased recurrence were Breslow 2.1-4 mm (HR 4.88, CI 1.0-23.01, p 0.046) and ≥4 positive nodes (HR 4.2, CI 1.17-15.2, p 0.027). Absence of lymphovascular invasion was a protective factor for death (HR 0.21, CI 0.06-0.67, p 0.008). Conclusions: At the National Oncology Institute, recurrence-free survival is slightly lower than in the global literature, the main factors associated with recurrence were Breslow > 2 mm and ≥4 or more positive nodes. This raises the question of whether adding immunotherapy could improve these results.
Citas
[1] International Agency for Research on Cancer, Global Cancer Observatory. Melanoma of Skin: IARC; 2022 [Available from: https://gco.iarc.who.int/media/globocan/factsheets/cancers/16-melanoma-of-skin-fact-sheet.pdf.
[2] National Cancer Institute S, Epidemiology and end Results Program. Cancer Stat Facts: Melanoma of the Skin: SEER
[3] [Available from: https://seer.cancer.gov/statfacts/html/melan.html.
[4] Knight A, Karapetyan L, Kirkwood JM. Immunotherapy in Melanoma: Recent Advances and Future Directions. Cancers (Basel). 2023;15(4).
[5] Swetter SM, Tsao H, Bichakjian CK, Curiel-Lewandrowski C, Elder DE, Gershenwald JE, et al. Guidelines of care for the management of primary cutaneous melanoma. J Am Acad Dermatol. 2019;80(1):208-50.
[6] Leiter U, Stadler R, Mauch C, Hohenberger W, Brockmeyer NH, Berking C, et al. Final Analysis of DeCOG-SLT Trial: No Survival Benefit for Complete Lymph Node Dissection in Patients With Melanoma With Positive Sentinel Node. J Clin Oncol. 2019;37(32):3000-8.
[7] Madu MF, Franke V, Van de Wiel BA, Klop WMC, Jó?wiak K, van Houdt WJ, et al. External validation of the American Joint Committee on Cancer 8th edition melanoma staging system: who needs adjuvant treatment? Melanoma Res. 2020;30(2):185-92.
[8] Long GV, Hauschild A, Santinami M, Atkinson V, Mandala M, Chiarion-Sileni V, et al. Adjuvant Dabrafenib plus Trametinib in Stage III BRAF-Mutated Melanoma. N Engl J Med. 2017;377(19):1813-23.
[9] Dummer R, Hauschild A, Santinami M, Atkinson V, Mandala M, Kirkwood JM, et al. Five-Year Analysis of Adjuvant Dabrafenib plus Trametinib in Stage III Melanoma. N Engl J Med. 2020;383(12):1139-48.
[10] Eggermont AM, Chiarion-Sileni V, Grob JJ, Dummer R, Wolchok JD, Schmidt H, et al. Adjuvant ipilimumab versus placebo after complete resection of high-risk stage III melanoma (EORTC 18071): a randomised, double-blind, phase 3 trial. Lancet Oncol. 2015;16(5):522-30.
[11] Ascierto PA, Del Vecchio M, Mandala M, Gogas H, Arance AM, Dalle S, et al. Adjuvant nivolumab versus ipilimumab in resected stage IIIB-C and stage IV melanoma (CheckMate 238): 4-year results from a multicentre, double-blind, randomised, controlled, phase 3 trial. Lancet Oncol. 2020;21(11):1465-77.
[12] Eggermont AMM, Blank CU, Mandala M, Long GV, Atkinson VG, Dalle S, et al. Longer Follow-Up Confirms Recurrence-Free Survival Benefit of Adjuvant Pembrolizumab in High-Risk Stage III Melanoma: Updated Results From the EORTC 1325-MG/KEYNOTE-054 Trial. J Clin Oncol. 2020;38(33):3925-36.
[13] Weber JS, Schadendorf D, Del Vecchio M, Larkin J, Atkinson V, Schenker M, et al. Adjuvant Therapy of Nivolumab Combined With Ipilimumab Versus Nivolumab Alone in Patients With Resected Stage IIIB-D or Stage IV Melanoma (CheckMate 915). J Clin Oncol. 2023;41(3):517-27.
[14] Menzies AM, Amaria RN, Rozeman EA, Huang AC, Tetzlaff MT, van de Wiel BA, et al. Pathological response and survival with neoadjuvant therapy in melanoma: a pooled analysis from the International Neoadjuvant Melanoma Consortium (INMC). Nat Med. 2021;27(2):301-9.
[15] Davis LE, Shalin SC, Tackett AJ. Current state of melanoma diagnosis and treatment. Cancer Biology & Therapy. 2019;20(11):1366-79.
[16] Koizumi S, Inozume T, Nakamura Y. Current surgical management for melanoma. J Dermatol. 2024;51(3):312-23.
[17] Seth R, Agarwala SS, Messersmith H, Alluri KC, Ascierto PA, Atkins MB, et al. Systemic Therapy for Melanoma: ASCO Guideline Update. Journal of Clinical Oncology. 2023;41(30):4794-820.
[18] Garbe C, Keim U, Suciu S, Amaral T, Eigentler TK, Gesierich A, et al. Prognosis of Patients With Stage III Melanoma According to American Joint Committee on Cancer Version 8: A Reassessment on the Basis of 3 Independent Stage III Melanoma Cohorts. J Clin Oncol. 2020;38(22):2543-51.
[19] Akiyama M, Matsuda Y, Arai T, Saeki H. Clinicopathological characteristics of malignant melanomas of the skin and gastrointestinal tract. Oncol Lett. 2018;16(2):2675-81.
[20] Weber J, Mandala M, Del Vecchio M, Gogas HJ, Arance AM, Cowey CL, et al. Adjuvant Nivolumab versus Ipilimumab in Resected Stage III or IV Melanoma. N Engl J Med. 2017;377(19):1824-35.
[21] Patel SP, Othus M, Chen Y, Wright GP, Yost KJ, Hyngstrom JR, et al. Neoadjuvant-Adjuvant or Adjuvant-Only Pembrolizumab in Advanced Melanoma. New England Journal of Medicine. 2023;388(9):813-23.
Licencia
Derechos de autor 2024 Infomedic Intl.Derechos autoriales y de reproducibilidad. La Revista Médica de Panama es un ente académico, sin fines de lucro, que forma parte de la Academia Panameña de Medicina y Cirugía. Sus publicaciones son de tipo acceso gratuito de su contenido para uso individual y académico, sin restricción. Los derechos autoriales de cada artículo son retenidos por sus autores. Al Publicar en la Revista, el autor otorga Licencia permanente, exclusiva, e irrevocable a la Sociedad para la edición del manuscrito, y otorga a la empresa editorial, Infomedic International Licencia de uso de distribución, indexación y comercial exclusiva, permanente e irrevocable de su contenido y para la generación de productos y servicios derivados del mismo. En caso que el autor obtenga la licencia CC BY, el artículo y sus derivados son de libre acceso y distribución.