Prognostic significance of occult tumor cells in the apheresis products of patients with advanced breast cancer receiving high-dose chemotherapy and autologous hematopoietic progenitor cell support

Yago Nieto, Wilbur A. Franklin, Roy B. Jones, Scott I. Berman, Julie Pellom, Anna E. Barón, Elizabeth J. Shpall

Research output: Contribution to journalArticlepeer-review

23 Scopus citations

Abstract

We prospectively evaluated the prognostic significance of occult tumor cells (OTCs) contaminating the peripheral blood progenitor cell apheresis products of patients with advanced breast cancer receiving high-dose chemotherapy. Immunocytochemistry of peripheral blood progenitor cells was performed in 242 patients with high-risk primary breast cancer (HRPBC) and in 111 patients with metastatic breast cancer (MBC). OTCs were detected in 6.6% of HRPBC patients and in 16.2% of MBC patients (P = .005). In HRPBC, OTCs correlated with worse prognostic scores and larger tumor sizes, but not with axillary nodal status, hormone receptors, or HER2. In the MBC group, OTCs correlated with bone marrow involvement and with disease status at transplantation. The number of apheresis procedures was not associated with the risk of contamination. In HRPBC patients, at a median follow-up of 7 years (range, 1.5-11 years), the presence of OTCs correlated with worse event-free survival (P = .007) and overall survival (P = .002). In the MBC group, OTCs correlated with worse event-free survival (P = .04), but not overall survival (P = .2). In multivariate analyses, the presence of OTCs had an independent adverse effect on outcome in HRPBC, but not MBC. Our observations imply a direct role of OTCs in posttransplantation relapse in HRPBC.

Original languageEnglish (US)
Pages (from-to)415-425
Number of pages11
JournalBiology of Blood and Marrow Transplantation
Volume10
Issue number6
DOIs
StatePublished - Jun 2004

Keywords

  • Advanced breast cancer
  • Apheresis products
  • High-dose chemotherapy
  • Tumor contamination

ASJC Scopus subject areas

  • Hematology
  • Transplantation

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