Discovery of candidate tumor biomarkers for treatment with intraperitoneal chemotherapy for ovarian cancer

Tumor mRNA expression was used to discover genes associated with worse survival or no survival benefit after intraperitoneal (IP) chemotherapy. Data for high grade serous ovarian cancer patients treated with IP (n = 90) or IV-only (n = 398) chemotherapy was obtained from The Cancer Genome Atlas. Pro...

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Veröffentlicht in:Scientific reports 2016-02, Vol.6 (1), p.21591-21591, Article 21591
Hauptverfasser: Seagle, Brandon-Luke L., Eng, Kevin H., Yeh, Judy Y., Dandapani, Monica, Schiller, Emily, Samuelson, Robert, Odunsi, Kunle, Shahabi, Shohreh
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Sprache:eng
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Zusammenfassung:Tumor mRNA expression was used to discover genes associated with worse survival or no survival benefit after intraperitoneal (IP) chemotherapy. Data for high grade serous ovarian cancer patients treated with IP (n = 90) or IV-only (n = 398) chemotherapy was obtained from The Cancer Genome Atlas. Progression free survival (PFS) and overall survival (OS) were compared between IP and IV groups using Kaplan-Meier analysis and Cox regression. Validations were performed by analyses of microarray and RNA-Seq mRNA expression data. PFS and OS were compared between IP and IV groups by permutation testing stratified by gene expression. P-values are two-tailed. IP chemotherapy increased PFS (26.7 vs 16.0 months, HR 0.43 (0.28–0.66), p = 0.0001) and OS (49.6 vs 38.2 months, HR 0.46 (0.25–0.83), p = 0.01). Increased expression of NCAM2 and TSHR and decreased expression of GCNT1 was associated with decreased PFS and OS after IV chemotherapy (p 
ISSN:2045-2322
2045-2322
DOI:10.1038/srep21591