| Literature DB >> 28753783 |
Andrea Necchi1, Bernhard J Eigl2, Eddy Shih-Hsin Yang3, Sejong Bae4, Darshan Chandrashekar5, Dongquan Chen4, Gurudatta Naik6, Amitkumar Mehta6, Patrizia Giannatempo1, Maurizio Colecchia1, Jennifer Gordetsky5, Shi Wei5, Tiffiny Cooper3, Sooryanarayana Varambally5, Guru Sonpavde7.
Abstract
In men with advanced penile squamous cell carcinoma receiving first-line chemotherapy, visceral metastases (VM) and Eastern Cooperative Oncology Group performance status ≥1 are poor prognostic factors for overall survival (OS). We hypothesized that tumor gene expression profiling may enhance prognostic stratification and identify potential therapeutic targets. In this retrospective study, RNA extracted from macrodissected tumors underwent profiling for the expression of 738 genes using NanoString. Univariate and multivariate analyses assessed the association of genes, VM, and performance status with OS. Tumors were available from 25 men who received first-line cisplatin-based chemotherapy. In univariate analysis, upregulated MAML2 (p=0.004), KITLG (p≤0.0001), and JAK1 (p=0.029) genes were associated with poor OS, and upregulated FANCA was associated with better OS (p=0.024). In stepwise multivariate analyses, VM (hazard ratio=12.75, p=0.0001) and MAML2 (hazard ratio=10.411, p=0.003) were associated with poor OS. The presence of none, one, and both of these poor risk factors was associated with significantly different median OS of 18.4 mo, 7.2 mo, and 2.1 mo, respectively. Unsupervised clustering demonstrated two major molecular subtypes with trend for different survivals (p=0.052). Validation of results is necessary. PATIENTEntities:
Keywords: Advanced; Cisplatin; Gene expression; Penile squamous cell carcinoma; Prognosis
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Year: 2016 PMID: 28753783 PMCID: PMC5537039 DOI: 10.1016/j.euf.2016.08.001
Source DB: PubMed Journal: Eur Urol Focus ISSN: 2405-4569