Genetic and clinico-pathologic analysis of metastatic uveal melanoma Journal Article

Authors: Griewank, K. G.; van de Nes, J.; Schilling, B.; Moll, I.; Sucker, A.; Kakavand, H.; Haydu, L. E.; Asher, M.; Zimmer, L.; Hillen, U.; Thompson, J. F.; Scolyer, R. A.; Schadendorf, D.; Murali, R.
Article Title: Genetic and clinico-pathologic analysis of metastatic uveal melanoma
Abstract: Uveal melanoma is the most common malignant tumor of the adult eye. Fifty percent of tumors will eventually metastasize, and there are no effective treatments for them. Recent studies of uveal melanoma have identified activating mutations in GNAQ and GNA11, loss-of-function mutations in the tumor suppressor gene BAP1, and recurrent mutations in codon 625 of SF3B1. Previous studies have reported the existence of a higher frequency of GNA11 than GNAQ mutations, frequent BAP1 loss, and rare SF3B1 mutations in metastatic uveal melanoma. We analyzed a cohort of 30 uveal melanoma metastases for the occurrence of GNAQ, GNA11, and SF3B1 mutations, as well as BAP1 loss, and correlated these parameters with clinical and histopathologic features. Most (92%) tumors were composed of cells with an epithelioid or mixed (<100% spindle cells) morphology. Tumor samples composed exclusively of spindle cells were rare (n=2, 8%). Most tumors showed a moderate to marked degree of nuclear pleomorphism (n=24, 96%), and contained hyperchromatic, vesicular nuclei with variably conspicuous nucleoli. GNA11 mutations were considerably more frequent than GNAQ mutations (GNA11, GNAQ, and wild-type in 18 (60%), 6 (20%), and 6 (20%) cases, respectively). SF3B1 mutation was found in 1 of 26 tumors (4%), whereas loss of BAP1 expression was present in 13 of 16 tumors (81%). Patients with GNA11-mutant tumors had poorer disease-specific survival (60.0 vs 121.4 months, P=0.03) and overall survival (50.6 vs 121.4 months, P=0.03) than those with tumors lacking GNA11 mutations. The survival data, combined with the predominance of GNA11 mutations in metastases, raises the possibility that GNA11-mutant tumors may be associated with a higher risk of metastasis and poorer prognosis than GNAQ-mutant tumors. Further studies of uveal melanoma are required to investigate the functional and prognostic relevance of oncogenic mutations in GNA11 and GNAQ.
Journal Title: Modern Pathology
Volume: 27
Issue: 2
ISSN: 0893-3952
Publisher: Nature Publishing Group  
Date Published: 2014-01-01
Start Page: 175
End Page: 183
Language: English
DOI: 10.1038/modpathol.2013.138
PROVIDER: scopus
PUBMED: 23887304
Notes: Export Date: 3 March 2014 -- CODEN: MODPE -- Source: Scopus
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MSK Authors
  1. Rajmohan Murali
    153 Murali
  2. Marina Asher
    19 Asher