BMC Cancer (Nov 2008)

Risk estimation of distant metastasis in node-negative, estrogen receptor-positive breast cancer patients using an RT-PCR based prognostic expression signature

  • Gray Joe,
  • Buerger Horst,
  • Anderson Steve,
  • Kam-Morgan Lauren,
  • McCallie Blair,
  • Cane Paul,
  • Springall Robert,
  • Shu Henry,
  • Ryder Kenneth,
  • Kwok Shirley,
  • Dai Hongyue,
  • Chew Karen,
  • Lau Kit,
  • Gillett Cheryl,
  • Rowland Charles,
  • Wang Alice,
  • Tutt Andrew,
  • Bennington James,
  • Esserman Laura,
  • Hastie Trevor,
  • Broder Samuel,
  • Sninsky John,
  • Brandt Burkhard,
  • Waldman Fred

DOI
https://doi.org/10.1186/1471-2407-8-339
Journal volume & issue
Vol. 8, no. 1
p. 339

Abstract

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Abstract Background Given the large number of genes purported to be prognostic for breast cancer, it would be optimal if the genes identified are not confounded by the continuously changing systemic therapies. The aim of this study was to discover and validate a breast cancer prognostic expression signature for distant metastasis in untreated, early stage, lymph node-negative (N-) estrogen receptor-positive (ER+) patients with extensive follow-up times. Methods 197 genes previously associated with metastasis and ER status were profiled from 142 untreated breast cancer subjects. A "metastasis score" (MS) representing fourteen differentially expressed genes was developed and evaluated for its association with distant-metastasis-free survival (DMFS). Categorical risk classification was established from the continuous MS and further evaluated on an independent set of 279 untreated subjects. A third set of 45 subjects was tested to determine the prognostic performance of the MS in tamoxifen-treated women. Results A 14-gene signature was found to be significantly associated (p Conclusion The 14-gene signature is significantly associated with risk of distant metastasis. The signature has a predominance of proliferation genes which have prognostic significance above that of Ki-67 LI and may aid in prioritizing future mechanistic studies and therapeutic interventions.