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Gene-Expression Profiling of Mucinous Ovarian Tumors and Comparison with Upper and Lower Gastrointestinal Tumors Identifies Markers Associated with Adverse Outcomes

基因表达谱 卵巢癌 肿瘤科 基因表达 癌症研究 生物 病理 医学 内科学 基因 癌症 遗传学
作者
Nicola S. Meagher,Kylie L. Gorringe,Matthew J. Wakefield,Adelyn Bolithon,Chi Nam Ignatius Pang,Derek S. Chiu,Michael S. Anglesio,Kylie‐Ann Mallitt,Jennifer A. Doherty,Holly Ruth Harris,Joellen M. Schildkraut,Andrew Berchuck,Kara L. Cushing‐Haugen,Ksenia Chezar,Angela S. Y. Chou,Adeline L. Y. Tan,Jennifer Alsop,Ellen L. Barlow,Matthias W. Beckmann,Jessica Boros
出处
期刊:Clinical Cancer Research [American Association for Cancer Research]
卷期号:28 (24): 5383-5395 被引量:23
标识
DOI:10.1158/1078-0432.ccr-22-1206
摘要

PURPOSE: Advanced-stage mucinous ovarian carcinoma (MOC) has poor chemotherapy response and prognosis and lacks biomarkers to aid stage I adjuvant treatment. Differentiating primary MOC from gastrointestinal (GI) metastases to the ovary is also challenging due to phenotypic similarities. Clinicopathologic and gene-expression data were analyzed to identify prognostic and diagnostic features. EXPERIMENTAL DESIGN: Discovery analyses selected 19 genes with prognostic/diagnostic potential. Validation was performed through the Ovarian Tumor Tissue Analysis consortium and GI cancer biobanks comprising 604 patients with MOC (n = 333), mucinous borderline ovarian tumors (MBOT, n = 151), and upper GI (n = 65) and lower GI tumors (n = 55). RESULTS: Infiltrative pattern of invasion was associated with decreased overall survival (OS) within 2 years from diagnosis, compared with expansile pattern in stage I MOC [hazard ratio (HR), 2.77; 95% confidence interval (CI), 1.04-7.41, P = 0.042]. Increased expression of THBS2 and TAGLN was associated with shorter OS in MOC patients (HR, 1.25; 95% CI, 1.04-1.51, P = 0.016) and (HR, 1.21; 95% CI, 1.01-1.45, P = 0.043), respectively. ERBB2 (HER2) amplification or high mRNA expression was evident in 64 of 243 (26%) of MOCs, but only 8 of 243 (3%) were also infiltrative (4/39, 10%) or stage III/IV (4/31, 13%). CONCLUSIONS: An infiltrative growth pattern infers poor prognosis within 2 years from diagnosis and may help select stage I patients for adjuvant therapy. High expression of THBS2 and TAGLN in MOC confers an adverse prognosis and is upregulated in the infiltrative subtype, which warrants further investigation. Anti-HER2 therapy should be investigated in a subset of patients. MOC samples clustered with upper GI, yet markers to differentiate these entities remain elusive, suggesting similar underlying biology and shared treatment strategies.
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