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Gene expression profiles predict early relapse in ovarian cancer after platinum-paclitaxel chemotherapy

  • Lynn C. Hartmann
  • , Karen H. Lu
  • , Gerald P. Linette
  • , William A. Cliby
  • , Kimberly R. Kalli
  • , David Gershenson
  • , Robert C. Bast
  • , James Stec
  • , Natalia Iartcliouk
  • , David I. Smith
  • , Jeffrey S. Ross
  • , Sebastian Hoersch
  • , Viji Shridhar
  • , James Lillie
  • , Scott H. Kaufmann
  • , Edwin A. Clark
  • , Andrew I. Damokosli

Research output: Contribution to journal › Article › peer-review

Abstract

Purpose: Women with advanced epithelial ovarian cancer are routinely treated with platinum-paclitaxel chemotherapy following cytoreductive surgery, yet only ∼20% achieve long-term disease-free survival. We hypothesized that differences in gene expression before treatment could distinguish patients with short versus long time to recurrence after administration of platinum-paclitaxel combination chemotherapy. Experimental Design: To test this hypothesis, gene expression profiling of 79 primary surgically resected tumors from women with advanced-stage, high-grade epithelial ovarian cancer was done using cDNA microarrays containing 30,721 genes. Supervised learning algorithms were applied in an effort to develop a binary classifier that could discriminate women at risk for early (≤21 months) versus late (>21 months) relapse after initial chemotherapy. Results: A 14-gene predictive model was developed using a set of training samples (n = 51) and subsequently tested using an independent set of test samples (n = 28). This model correctly predicted the outcome of 24 of the 28 test samples (86% accuracy) with 95% positive predictive value for early relapse. Conclusions: Predictive markers for early recurrence can be identified for platinum-paclitaxel combination chemotherapy in primary ovarian carcinoma. The proposed 14-gene model requires further validation.

Original languageEnglish (US)
Pages (from-to)2149-2155
Number of pages7
JournalClinical Cancer Research
Volume11
Issue number6
DOIs
StatePublished - Mar 15 2005

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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