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Clinicopathologic features and survival outcomes of ocular melanoma: a series of 31 cases from a tertiary university hospital

BACKGROUND: We aimed to determine the effect of clinicopathologic features on overall survival among Caucasian ocular melanoma patients in the Central Anatolia region of Turkey. METHODS: This single-center study included conjunctival (n = 12) and uveal (n = 19) melanoma patients diagnosed between Ja...

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Autores principales: Kestel, Selin, Göçün, Feriha Pınar Uyar, Öğüt, Betül, Erdem, Özlem
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Pathologists/The Korean Society for Cytopathology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9288897/
https://www.ncbi.nlm.nih.gov/pubmed/35501671
http://dx.doi.org/10.4132/jptm.2022.03.10
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author Kestel, Selin
Göçün, Feriha Pınar Uyar
Öğüt, Betül
Erdem, Özlem
author_facet Kestel, Selin
Göçün, Feriha Pınar Uyar
Öğüt, Betül
Erdem, Özlem
author_sort Kestel, Selin
collection PubMed
description BACKGROUND: We aimed to determine the effect of clinicopathologic features on overall survival among Caucasian ocular melanoma patients in the Central Anatolia region of Turkey. METHODS: This single-center study included conjunctival (n = 12) and uveal (n = 19) melanoma patients diagnosed between January 2008 and March 2020. Clinicopathologic features and outcomes were reviewed retrospectively. Five cases were tested for BRAF V600 mutations with real-time polymerase chain reaction, and one case was tested with next-generation sequencing. Survival was calculated using the Kaplan-Meier method. RESULTS: Thirty-one patients had a mean initial age of 58.32 years (median, 61 years; range 25 to 78 years). There were 13 male and 18 female patients. The median follow-up time was 43.5 months (range, 6 to 155 months) for conjunctival melanoma and 35 months (range, 8 to 151 months) for uveal melanoma. When this study ended, eight of the 12 conjunctival melanoma patients (66.7%) and nine of the 19 uveal melanoma patients (47.4%) had died. The presence of tumor-infiltrating lymphocytes was related to improved overall survival in conjunctival melanoma (p = .014), whereas the presence of ulceration (p = .030), lymphovascular invasion (p = .051), tumor in the left eye (p = .012), tumor thickness of > 2 mm (p = .012), and mitotic count of >1/mm(2) (p = .012) reduced the overall survival in conjunctival melanoma. Uveal melanoma tumors with the largest diameter of 9.1–15 mm led to the lowest overall survival among subgroups (p = .035). Involvement of the conjunctiva (p=.005) and lens (p = .003) diminished overall survival in uveal melanoma. BRAF V600 mutation was present in one case of conjunctival melanoma, GNAQ R183Q mutation was present in one case of uveal melanoma. Patients with uveal melanoma presented with an advanced pathological tumor stage compared to those with conjunctival melanoma (p = .019). CONCLUSIONS: This study confirmed the presence of tumor-infiltrating lymphocytes as a favorable factor in conjunctival melanoma and conjunctival and lens involvement as unfavorable prognostic factors in uveal melanoma for overall survival, respectively.
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spelling pubmed-92888972022-07-29 Clinicopathologic features and survival outcomes of ocular melanoma: a series of 31 cases from a tertiary university hospital Kestel, Selin Göçün, Feriha Pınar Uyar Öğüt, Betül Erdem, Özlem J Pathol Transl Med Original Article BACKGROUND: We aimed to determine the effect of clinicopathologic features on overall survival among Caucasian ocular melanoma patients in the Central Anatolia region of Turkey. METHODS: This single-center study included conjunctival (n = 12) and uveal (n = 19) melanoma patients diagnosed between January 2008 and March 2020. Clinicopathologic features and outcomes were reviewed retrospectively. Five cases were tested for BRAF V600 mutations with real-time polymerase chain reaction, and one case was tested with next-generation sequencing. Survival was calculated using the Kaplan-Meier method. RESULTS: Thirty-one patients had a mean initial age of 58.32 years (median, 61 years; range 25 to 78 years). There were 13 male and 18 female patients. The median follow-up time was 43.5 months (range, 6 to 155 months) for conjunctival melanoma and 35 months (range, 8 to 151 months) for uveal melanoma. When this study ended, eight of the 12 conjunctival melanoma patients (66.7%) and nine of the 19 uveal melanoma patients (47.4%) had died. The presence of tumor-infiltrating lymphocytes was related to improved overall survival in conjunctival melanoma (p = .014), whereas the presence of ulceration (p = .030), lymphovascular invasion (p = .051), tumor in the left eye (p = .012), tumor thickness of > 2 mm (p = .012), and mitotic count of >1/mm(2) (p = .012) reduced the overall survival in conjunctival melanoma. Uveal melanoma tumors with the largest diameter of 9.1–15 mm led to the lowest overall survival among subgroups (p = .035). Involvement of the conjunctiva (p=.005) and lens (p = .003) diminished overall survival in uveal melanoma. BRAF V600 mutation was present in one case of conjunctival melanoma, GNAQ R183Q mutation was present in one case of uveal melanoma. Patients with uveal melanoma presented with an advanced pathological tumor stage compared to those with conjunctival melanoma (p = .019). CONCLUSIONS: This study confirmed the presence of tumor-infiltrating lymphocytes as a favorable factor in conjunctival melanoma and conjunctival and lens involvement as unfavorable prognostic factors in uveal melanoma for overall survival, respectively. The Korean Society of Pathologists/The Korean Society for Cytopathology 2022-07 2022-05-03 /pmc/articles/PMC9288897/ /pubmed/35501671 http://dx.doi.org/10.4132/jptm.2022.03.10 Text en © 2022 The Korean Society of Pathologists/The Korean Society for Cytopathology https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited
spellingShingle Original Article
Kestel, Selin
Göçün, Feriha Pınar Uyar
Öğüt, Betül
Erdem, Özlem
Clinicopathologic features and survival outcomes of ocular melanoma: a series of 31 cases from a tertiary university hospital
title Clinicopathologic features and survival outcomes of ocular melanoma: a series of 31 cases from a tertiary university hospital
title_full Clinicopathologic features and survival outcomes of ocular melanoma: a series of 31 cases from a tertiary university hospital
title_fullStr Clinicopathologic features and survival outcomes of ocular melanoma: a series of 31 cases from a tertiary university hospital
title_full_unstemmed Clinicopathologic features and survival outcomes of ocular melanoma: a series of 31 cases from a tertiary university hospital
title_short Clinicopathologic features and survival outcomes of ocular melanoma: a series of 31 cases from a tertiary university hospital
title_sort clinicopathologic features and survival outcomes of ocular melanoma: a series of 31 cases from a tertiary university hospital
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9288897/
https://www.ncbi.nlm.nih.gov/pubmed/35501671
http://dx.doi.org/10.4132/jptm.2022.03.10
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