Francisco Javier Valentín-Bravo1; Álvaro Pérez-Rodríguez2; Ciro García-Álvarez1; Elena García-Lagarto3; María Antonia Saornil-Álvarez1
Purpose: Conjunctival melanoma is a rare and aggressive tumor with a propensity for regional and distant metastases. This study aimed to analyze BRAF/NRAS markers in conjunctival melanoma and their relationship with tumor recurrences and patient prognosis.
Methods: This retrospective, observational, single-center study included consecutive patients with an anatomopathological diagnosis of conjunctival melanoma, registered between January 1992 and December 2019. BRAF/NRAS mutations were analyzed using cobas®4800 kit (Roche®) in samples obtained by excisional or map biopsy. Additionally, the presence of other associated precancerous or tumor lesions was assessed.
Results: A total of 12 patients with positive histological samples for conjunctival melanoma were included (7 women, 5 men), with a mean age at diagnosis of 60 years and a mean evolution time of 6.38 ± 3.4 years. BRAF V600E mutation was observed in three biopsies (25%), similar to NRAS Q61X (25%). Recurrences occurred in all patients with positive BRAF or NRAS mutation, and five of these patients developed systemic dissemination (83.33%). Moreover, four of six patients with mutated BRAF or NRAS (66.66%) had histopathological findings of tumor or precancerous lesions.
Conclusions: BRAF and NRAS mutations may be risk factors for recurrence and shorter survival in conjunctival melanoma, which would make these patients candidates for targeted therapies and comprehensive and individualized follow-up. All these data warrant standardized prospective studies.
Keywords: Conjunctival neoplasms; Melanoma; Biomarkers; tumor; Proto-oncogene proteins B-raf; Genes ras.
Objetivo: O melanoma da conjuntiva é um tumor raro e agressivo, com propensão à disseminação metastática regional e distante. Este estudo tem como objetivo analisar os marcadores BRAF e NRAS no melanoma da conjuntiva e sua relação com recidivas tumorais e com o prognóstico do paciente.
Métodos: Este foi um estudo retrospectivo, observacional e unicêntrico de pacientes consecutivos com diagnóstico anatomopatológico de melanoma da conjuntiva feito entre janeiro de 1992 e dezembro de 2019. As mutações BRAF e NRAS foram analisadas com o kit cobas® 4800 (Roche®) em amostras obtidas através de biópsia excisional ou por mapa. Além disso, foi avaliada a presença de lesões pré-cancerosas ou tumorais associadas.
Resultados: Foram incluídos 12 pacientes com amostras histológicas positivas para melanoma da conjuntiva (7 mulheres e 5 homens), com idade média ao diagnóstico de 60 anos e tempo médio de evolução de 6,38 ± 3,4 anos. A mutação BRAF V600E foi encontrada em 3 biópsias (25%), bem como a NRAS Q61X (25%). Ocorreram recidivas em todos os pacientes positivos para mutações de BRAF ou NRAS e 5 desses pacientes desenvolveram disseminação sistêmica (83,33%). Além disso, 4 dos 6 pacientes com BRAF ou NRAS mutante (66,66%) apresentaram achados histopatológicos de lesões tumorais ou pré-cancerosas.
Conclusões: As mutações BRAF e NRAS podem ser fatores de risco para recorrência e menor sobrevida no melanoma da conjuntiva, o que tornaria esses pacientes candidatos a terapias direcionadas e a um acompanhamento mais abrangente e individualizado. Todos esses dados justificam mais estudos prospectivos padronizados.
Descritores: Neoplasias da túnica conjuntiva; Melanoma; Biomarcadores tumorais; Proteínas proto-oncogênicas B-raf; Genes ras.
Conjunctival melanoma (CM) is a rare and aggressive malignant neoplasm originating on the ocular surface of melanocytes. They represent 1%-2% of ocular malignancies and generally affect Caucasian adults without gender preference(1,2). Despite low CM incidence, estimated at 0.2-0.8 cases per million inhabitants/year in Caucasians, it is a potentially life-threatening cancer with a 10-year mortality of 23%-30%(2-4). Additionally, it typically presents as a raised mass of variable pigmentation, which, in up to 15%-19% of cases, may be amelanotic(5,6). Although it may originate de novo in 5%-10% of patients, the association between CM and two related conditions, such as primary acquired melanosis (PAM) in 75% and conjunctival nevus in 20%-30%, has been well established(2).
The main predictive factor for metastasis is the depth of tumor invasion, and metastasis is very unlikely if the thickness of the tumor is less than 0.8 mm(7). Other low prognostic factors described are tarsal or caruncle location, a high proliferation index (Ki67), pagetoid histological pattern, or recurrence(8). Local recurrence is frequent, and if the disease disseminates, the survival rate decreases markedly. However, there is no approved standard treatment for metastatic CM(6). Therefore, a better understanding of the genetic CM profile may help identify therapeutic targets for patients with advanced disease stages.
Although CMs have not been well-characterized genetically, cutaneous melanomas share specific chromosomal alterations with them and frequently harbor pathogenic variants in BRAF (50%), NRAS (20%), or NF1(9,10).
Pro-oncogenic BRAF mutations are present in 14%-50% of CM cases, with BRAF V600E being the most frequent (74%-82%), followed by V600K (12%-20%). Although other rare BRAF mutations can be found and account for 6%, the determination of those rare mutations is not cost effective in clinical practice(10). Additionally, NRAS mutations have been detected in up to 18% of the analyzed samples, and other mutations, such as telomerase reverse transcriptase promoter and c-KIT mutations, occur in 32%-41% of CM cases. These mutations were thought to be mutually exclusive in the past; however, studies have shown that there may be a coexistence between these mutations(11,12).
A better understanding of the genetics and molecular abnormalities involved in CM progression would allow the identification of the most locally and systemically aggressive lesions and improve these patients’ survival by amplifying existing therapies use and developing new therapeutic targets.
This study aimed to analyze BRAF/NRAS markers in CM and consider their relationship with tumor recurrences and patients’ prognosis.
This was a retrospective, observational, and single-center study, including consecutive patients registered in Ocular Tumor Unit Hospital database with a histopathological diagnosis of CM from January 1992 to December 2019. The selection process included patients with confirmed diagnoses in other hospital centers referred for treatment and initial pathology recurrences. Additionally, samples were collected from patients with melanoma who had undergone excisional or map biopsy.
Patients’ clinical history was reviewed, paying particular attention to information related to demographics, ophthalmologic examination (Figure 1), biopsy type, histopathological diagnosis, recurrences, and presence of regional or systemic metastasis.
The histological diagnoses based on hematoxylin-eosin and the immunohistochemical staining performed (S100, SOX10, MELAN A, and Ki67) were reviewed by Anatomic Pathology service, adding new sections when necessary and the amount of available tissue allowed it (Figure 2). BRAF/NRAS mutation analysis was performed using cobas®4800 kit (Roche®). BRAF V600 mutation test using cobas® 4800 detects BRAF V600 mutations in DNA extracted from formalin-fixed, paraffin-impregnated human melanoma tissue. It is a real-time polymerase chain reaction (PCR) assay designed to detect V600E mutation. Cobas® 4800 BRAF V600 mutation test is based on the following two processes: (1) manual sample preparation to obtain genomic DNA from formalin-fixed, paraffin-embedded tissue and (2) target DNA PCR amplification and detection using a pair of complementary primers and two oligonucleotide probes labeled with different fluorescent dyes. One search is aimed to detect wild-type BRAF V600, and another is aimed to detect V600E mutation sequence. Two external run controls were provided, and the wild-type allele served as internal complete process control. For this, a 5-μm deparaffinized section of a paraffin-fixed sample was lysed by incubation at elevated temperature with a protease and lysis/chaotropic binding buffer that releases nucleic acids and protects the released genomic DNA from DNAases. Subsequently, isopropanol was added to the lysis mixture and centrifuged through a column containing a glass fiber filter. During centrifugation, genomic DNA binds to the glass fiber filter surface. Unbound substances, such as salts, proteins, and other cellular impurities, are removed by centrifugation. Genomic DNA amount was determined spectrophotometrically and adjusted to a fixed concentration and the amplification and detection mixture. The target DNA was then amplified and detected using the amplification and detection reagents included in the cobas® 4800 BRAF V600 Mutation Test Kit.
The Clinical Research Ethics Committee approved the present study protocol of Valladolid Eastern Health Area, Hospital Clínico Universitário de Valladolid (CEIC-VA-ESTE-HCUV). This study was conducted in accordance with the guidelines of the Helsinki declaration.
A total of 24 histological samples with CM anatomopathological diagnosis was included. However, to detect BRAF or NRAS mutations, PCR was only performed in 12 biopsies. This study could not be performed in the remaining 12 samples due to insufficient material for DNA extraction or because they were not available in our center.
The details of the 12 included patients are shown in table 1. Sex distribution was almost similar, with seven females (58.33%) and five males (41.67%). The mean subjects’ age at diagnosis was 60 years (median 58; range 35-88 years), with a slightly lower age at presentation in patients without the mutation, 57.16 vs. 62.83 years with positive mutation. The right eye (RE) was predominantly affected (10 occasions; 83.33%). A total of 10 tumors presented multicentrically (83.33%), and the remaining 2 had a circumscribed presentation (16.67%). Considering melanomas origin, nine developed from PAM (75%) and one developed from melanocytic nevus malignization (8.33%). The remaining two CMs developed de novo (16.67%) without a previous predisposing lesion. The mean follow-up was 6.38 ± 3.4 years.
BRAF V600E mutation was observed in three patients with CM, accounting for 25% of cases. Additionally, three other biopsies were positive for Q61X mutation in NRAS.
Recurrence was observed in all patients with positive BRAF or NRAS mutation, whereas only two of the six patients without the mutations developed recurrence. Likewise, metastases were identified in 5 BRAF- or NRAS-positive samples, of which three died. However, only one of the six mutation-negative patients had locoregional or systemic involvement (16.67%).
More aggressive treatment with enucleation or exenteration was performed in three patients, all of whom had a previous recurrence and two of whom possessed NRAS mutations.
Of the 12 patients, 5 had been diagnosed with precancerous or cancerous lesions in other locations. Specifically, four of the six patients with mutated BRAF or NRAS (66.66%) had histopathological findings of such lesions as cutaneous melanoma, pulmonary hamartoma, uterine myoma, or intestinal and gastric polyps. On the contrary, such a lesion was only found in one patient out of the total without mutation.
CM is an uncommon pathology with high mortality due to potential metastasis and recurrence(13). Despite the absence of strict clinical practice guidelines for disease management, every patient suspected of this neoplasm should be directed to a referral center(6). On the one hand, local adjuvant treatment has failed to improve survival in CM patients, especially in those with metastatic disease; thus, the search for targets and new therapeutic options is necessary(14). Recent publications have proposed targeted therapy against CM with BRAF/NRAS mutations, possibly improving patient prognosis(15).
The present study results support the hypothesis of the relationship between recurrence and worse prognosis in CM patients with mutated BRAF and NRAS(16). This fact makes these patients subsidiary to the abovementioned therapies.
Despite the small sample size included in the study (n=12), few studies have related the described mutations with disease prognosis and their association with other tumors.
These findings should be evaluated with caution due to certain limitations, such as its retrospective design and the referral bias inherent in an ocular ophthalmology referral unit. Similarly, a small patients’ number due to low disease prevalence and the limited sample size for the histological study constitute a barrier to the statistical research. Another limitation comprises the absent analysis of different BRAF variations, such as V600K, or alterations in NF1, present in up to 14% of tumors(17), resulting in underestimation of the mutations in the sample.
In this study, we present the clinical and genetic data of 12 patients with a histopathological diagnosis of CM. No differences were found in terms of sex or age at presentation. However, CM with alterations in these markers has been occurring more frequently in young males(18,19), although without statistical significance.
The study showed positivity for BRAF V600E and Q61X NRAS mutations in 25% of the cases each, which is similar to the data described by Griewank et al.(20) (29% and 20%). However, other publications, such as Kenawy et al.(18) and Larsen et al.(19), identified BRAF V600E mutations in primary tumors with much higher numbers, 40.4% and 50%, respectively. Recently, Gkiala et al.(17) have shown that in a literature review with 563 CMs, 29.7% (n=167) harbored BRAF mutations and only 6.4% (n=36) harbored NRAS mutations. In our study, these differences may be explained by the insufficient material amount in the samples, the detection method, or the absence of searching for other infrequent mutations in BRAF, such as V600K or T1799A(16,21).
Although recent studies have correlated BRAF/NRAS mutations with advanced CM(16), the influence of these biomarkers on disease prognosis is still uncertain(22). However, their identification provides a possibility of a targeted systemic chemotherapeutic treatment that could increase patients’ survival with disseminated disease(3). Some authors reported that mutated CMs show a higher metastatic tendency and lower survival(16,23,24), whereas others did not confirm this correlation(25). In our study, disease recurrence was documented in all patients with BRAF or NRAS mutations, and 83.3% of them had disseminated disease during the follow-up. Additionally, 50% of patients died from the primary tumor. This suggests that mutation implies a higher risk of recurrences and metastases, worsening the prognosis for life.
Since 2002, BRAF and NRAS mutations have been described in a wide range of benign neoplasms and up to 8% of malignancies(26). These include cutaneous melanoma, colon adenocarcinoma (10%-15%), gastrointestinal polyps(27), thyroid carcinoma (45% papillary), and metanephric adenoma(28). Despite the high prevalence of gastrointestinal polyps in the general population, these precancerous lesions were observed on biopsy in three of the six patients with mutations. In addition, cutaneous melanoma was found in a BRAF-positive patient. This would support studies, such as Rabbie et al. 2019, which concluded that BRAF gene mutation acts as a driver mutation in the early stage of tumorigenesis(29).
Finally, recent publications, such as Zeng et al.(30), have recommended the routine detection of BRAF mutations in patients with advanced CM to individualize their treatment and follow-up.
In conclusion, BRAF and NRAS mutations may be risk factors for disease recurrence and shorter survival in CM, warranting targeted therapies and a more detailed and individualized follow-up. However, future prospective multicenter studies that include a larger sample size are needed to confirm the predictive value of these mutations and evaluate the efficacy and safety of drugs aimed at these therapeutic targets.
1. Lee YJ, Lee C, Kim MK, Khwarg SI, Oh JY. Conjunctival pigmented lesion: Clinicopathological analysis of 85 cases in Korean population. Sci Rep [Internet]. 2019 [cited 2020 Nov 28];9(1):18204. Available from: Conjunctival pigmented lesion: Clinicopathological analysis of 85 cases in Korean population (nih.gov)
2. Saornil MA, Becerra E, Méndez MC, Blanco G. [Conjunctival tumors]. Arch Soc Esp Oftalmol. 2009;84(1):7-22. Spanish.
3. Kaštelan S, Gverović Antunica A, Beketić Orešković L, Salopek Rabatić J, Kasun B, Bakija I. Conjunctival melanoma - epidemiological trends and features. Pathol Oncol Res [Internet]. 2018 [cited 2020 Nov 28];24(4):787-96. Available from: Conjunctival Melanoma - Epidemiological Trends and Features (por.hu)
4. Pacheco GE, Garcia-Onrubia L, Garcia-Alvarez C, Muñoz MF, Garcia-Lagarto E, Perez DM, et al. A retrospective review of conjunctival melanoma: presentation, treatment and evolution. Arch Soc Esp Oftalmol. 2019;94(5):218-24.
5. Lai JC, Stinnett SS, McCuen BW. A comparison of silicone oil versus gas tamponade in the treatment of idiopathic full-thickness macular hole. Ophthalmology. 2003;110(6):1170-4.
6. Wong JR, Nanji AA, Galor A, Karp CL. Management of conjunctival malignant melanoma: a review and update. Expert Rev Ophthalmol [Internet]. 2014[cited 2020 Nov 28].;9(3):185-204. Available from: Management of conjunctival malignant melanoma: a review and update (nih.gov)
7. Shields CL, Shields JA, Gündüz K, Cater J, Mercado G V, Gross N, et al. Conjunctival melanoma: risk factors for recurrence, exenteration, metastasis, and death in 150 consecutive patients. Arch Ophthalmol. 2000;118(11):1497-507. Comment on: Arch Ophthalmol. 2000;118(11):1525-33.
8. Paridaens AD, Minassian DC, McCartney AC, Hungerford JL. Prognostic factors in primary malignant melanoma of the conjunctiva: a clinicopathological study of 256 cases. Br J Ophthalmol [Internet]. 1994 [cited 2020 Nov 28];78(4):252-9. Available from: Prognostic factors in primary malignant melanoma of the conjunctiva: a clinicopathological study of 256 cases. (nih.gov)
9. Scholz SL, Cosgarea I, Süßkind D, Murali R, Möller I, Reis H, et al. NF1 mutations in conjunctival melanoma. Br J Cancer [Internet]. 2018 [cited 2020 Nov 29];118(9):1243-7. Available from: NF1 mutations in conjunctival melanoma (nih.gov)
10. Rossi E, Schinzari G, Maiorano BA, Pagliara MM, Di Stefani A, Bria E, et al. Conjunctival melanoma: genetic and epigenetic insights of a distinct type of melanoma. Int J Mol Sci [Internet]. 2019 [cited 2020 Nov 29];20(21):5447. Available from: Conjunctival Melanoma: Genetic and Epigenetic Insights of a Distinct Type of Melanoma (nih.gov)
11. Larki P, Gharib E, Yaghoob Taleghani M, Khorshidi F, Nazemalhosseini-Mojarad E, Asadzadeh Aghdaei H. Coexistence of kras and braf mutations in colorectal cancer: a case report supporting the concept of tumoral heterogeneity. Cell J [Internet]. 2017 [cited 2020 Nov 28];19(Suppl 1):113-7. Available from: Coexistence of KRAS and BRAF Mutations in Colorectal Cancer: A Case Report Supporting The Concept of Tumoral Heterogeneity (nih.gov)
12. Rossi E, Maiorano BA, Pagliara MM, Sammarco MG, Dosa T, Martini M, et al. Dabrafenib and trametinib in BRAF mutant metastatic conjunctival melanoma. Front Oncol [Internet]. 2019 [cited 2020 Nov 28];9:232. Available from: Dabrafenib and Trametinib in BRAF Mutant Metastatic Conjunctival Melanoma (nih.gov)
13. Larki P, Gharib E, Yaghoob Taleghani M, Khorshidi F, Nazemalhosseini-Mojarad E, Asadzadeh Aghdaei H. Coexistence of KRAS and BRAF mutations in colorectal cancer: a case report supporting the concept of tumoral heterogeneity. Cell J [Internet]. 2017 [cited 2020 Nov 28];19(Suppl 1):113-7. Available from: Coexistence of KRAS and BRAF Mutations in Colorectal Cancer: A Case Report Supporting The Concept of Tumoral Heterogeneity (nih.gov)
14. Milman T, Zhang Q, Ang SM, Elder D, Ida CM, Salomao DR, et al. Conjunctival nevi and melanoma: multiparametric immunohistochemical analysis, including p16, SOX10, HMB45, and Ki-67. Hum Pathol. 2020;103:107-19.
15. Esmaeli B. Disseminated conjunctival melanoma. Ophthalmology. 2004;111(12):2317; author reply 2317-8. Comment on: Ophthalmology. 2004;j111(4):816-21.
16. Kim JM, Weiss S, Sinard JH, Pointdujour-Lim R. Dabrafenib and trametinib for BRAF-Mutated conjunctival melanoma. Ocul Oncol Pathol [Internet]. 2020 [cited 2020 Nov 28];6(1):35-8. Available from: Dabrafenib and Trametinib for BRAF-Mutated Conjunctival Melanoma (nih.gov)
17. Larsen AC, Dahmcke CM, Dahl C, Siersma VD, Toft PB, Coupland SE, et al. A retrospective review of conjunctival melanoma presentation, treatment, and outcome and an investigation of features associated with BRAF mutations. JAMA Ophthalmol. 2015;133(11):1295-303.
18. Gkiala A, Palioura S. Conjunctival melanoma: update on genetics, epigenetics and targeted molecular and immune-based therapies. Clin Ophthalmol [Internet]. 2020 [cited 2020 Nov 28];14:3137-52. Available from: Conjunctival Melanoma: Update on Genetics, Epigenetics and Targeted Molecular and Immune-Based Therapies (nih.gov)
19. Kenawy N, Lake SL, Coupland SE, Damato BE. Conjunctival melanoma and melanocytic intra-epithelial neoplasia. Eye (Lond) [Internet]. 2013 [cited 2020 Nov 28]. 27(2):142-52. Available from: Conjunctival melanoma and melanocytic intra-epithelial neoplasia (nih.gov)
20. Larsen AC, Dahl C, Dahmcke CM, Lade-Keller J, Siersma VD, Toft PB, et al. BRAF mutations in conjunctival melanoma: investigation of incidence, clinicopathological features, prognosis and paired premalignant lesions. Acta Ophthalmol [Internet]. 2016 [cited 2020 Nov 28];94(5):463-70. Available from: BRAF mutations in conjunctival melanoma: investigation of incidence, clinicopathological features, prognosis and paired premalignant lesions - Larsen - 2016 - Acta Ophthalmologica - Wiley Online Library.
21. Griewank KG, Westekemper H, Murali R, Mach M, Schilling B, Wiesner T, et al. Conjunctival melanomas harbor BRAF and NRAS mutations and copy number changes similar to cutaneous and mucosal melanomas. Clin Cancer Res [Internet]. 2013 [cited 2020 Nov 28];19(12):3143-52. Available from: Conjunctival Melanomas Harbor BRAF and NRAS Mutations and Copy Number Changes Similar to Cutaneous and Mucosal Melanomas | Clinical Cancer Research (aacrjournals.org)
22. Goldenberg-Cohen N, Cohen Y, Rosenbaum E, Herscovici Z, Chowers I, Weinberger D, et al. T1799A BRAF mutations in conjunctival melanocytic lesions. Investig Ophthalmol Vis Sci [Internet]. 2005 [cited 2020 Nov 28];46(9):3027-30. Available from: T1799A BRAF Mutations in Conjunctival Melanocytic Lesions | IOVS | ARVO Journals
23. Bol KF, Donia M, Heegaard S, Kiilgaard JF, Svane IM. Genetic biomarkers in melanoma of the ocular region: what the medical oncologist should know. Int J Molecular Sci [Internet]. 2020 [cited 2020 Nov 28];21(15):5231. Available from: Genetic Biomarkers in Melanoma of the Ocular Region: What the Medical Oncologist Should Know (nih.gov)
24. Jakob JA, Bassett RL Jr, Ng CS, Curry JL, Joseph RW, Alvarado GC, et al. NRAS mutation status is an independent prognostic factor in metastatic melanoma. Cancer [Internet]. 2012 [cited 2020 Nov 29];118(16):4014-23. Available from: NRAS Mutation Status is an Independent Prognostic Factor in Metastatic Melanoma (nih.gov)
25. Thomas NE, Edmiston SN, Alexander A, Groben PA, Parrish E, Kricker A, Armstrong BK, Anton-Culver H, Gruber SB, From L, Busam KJ, Hao H, Orlow I, Kanetsky PA, Luo L, Reiner AS, Paine S, Frank JS, Bramson JI, Marrett LD, Gallagher RP, Zanetti R, Rosso S, Dwyer T, Cust AE, Ollila DW, Begg CB, Berwick M, Conway K; GEM Study Group. Association Between NRAS and BRAF mutational status and melanoma-specific survival among patients with higher-risk primary melanoma. JAMA Oncol [nternet]. 2015 [cited 2020 Nov 24];1(3):359-68. Available from: Association Between NRAS and BRAF Mutational Status and Melanoma-Specific Survival Among Patients With Higher Risk Primary Melanoma (nih.gov)
26. Sheng X, Li S, Chi Z, Si L, Cui C, Mao L, et al. Prognostic factors for conjunctival melanoma: a study in ethnic Chinese patients. Br J Ophthalmol. 2015;99(7):990-6.
27. Davies H, Bignell GR, Cox C, Stephens P, Edkins S, Clegg S, et al. Mutations of the BRAF gene in human cancer. Nature. 2002; 417(6892):949-54. Comment in: Nature. 2002;417(6892):906-7. Clin Exp Dermatol. 2013;38(2):222-3.
28. Murakami T, Sakamoto N, Nagahara A. Endoscopic diagnosis of sessile serrated adenoma/polyp with and without dysplasia/carcinoma World J Gastroenterol [Internet]. 2018 [cited 2020 Nov 28];24(29):3250-9. Available from: Endoscopic diagnosis of sessile serrated adenoma/polyp with and without dysplasia/carcinoma (nih.gov)
29. Ritterhouse LL, Barletta JA. BRAF V600E mutation-specific antibody: a review. Semin Diagn Pathol. 2015;32(5):400-8.
30. Rabbie R, Ferguson P, Molina-Aguilar C, Adams DJ, Robles-Espinoza CD. Melanoma subtypes: genomic profiles, prognostic molecular markers and therapeutic possibilities. J Pathol [Internet].2019 [cited 2020 Nov 28];247(5):539-51. Available from: Melanoma subtypes: genomic profiles, prognostic molecular markers and therapeutic possibilities (nih.gov)
31. Zeng Y, Hu C, Shu L, Pan Y, Zhao L, Pu X, et al. Clinical treatment options of early stage and advanced conjunctival melanoma. Surv Ophthalmol. 2021;66(3):461-70.
Submitted for publication:
June 1, 2021.
Accepted for publication: December 13, 2021.
Approved by the following research ethics committee: Hospital Clinico Universitario de Valladolid (PI 21-2149).
Funding: This study received no specific financial support.
Disclosure of potential conflicts of interest: None of the authors have any potential conflicts of interest to disclose.