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Gene expression profiles in circulating tumor cells to predict prognosis in metastatic breast cancer patients.
Mostert, B; Sieuwerts, A M; Kraan, J; Bolt-de Vries, J; van der Spoel, P; van Galen, A; Peeters, D J; Dirix, L Y; Seynaeve, C M; Jager, A; de Jongh, F E; Hamberg, P; Stouthard, J M L; Kehrer, D F S; Look, M P; Smid, M; Gratama, J W; Foekens, J A; Martens, J W M; Sleijfer, S.
Affiliation
  • Mostert B; Department of Medical Oncology.
  • Sieuwerts AM; Department of Medical Oncology Department of Medical Oncology and Cancer Genomics Netherlands, Erasmus MC Cancer Institute, Erasmus University Medical Center, Rotterdam, The Netherlands.
  • Kraan J; Department of Medical Oncology.
  • Bolt-de Vries J; Department of Medical Oncology.
  • van der Spoel P; Department of Medical Oncology.
  • van Galen A; Department of Medical Oncology.
  • Peeters DJ; Translational Cancer Research Unit, Center for Oncological Research, GZA Hospitals Sint-Augustinus and University of Antwerp, Antwerp, Belgium.
  • Dirix LY; Translational Cancer Research Unit, Center for Oncological Research, GZA Hospitals Sint-Augustinus and University of Antwerp, Antwerp, Belgium.
  • Seynaeve CM; Department of Medical Oncology.
  • Jager A; Department of Medical Oncology.
  • de Jongh FE; Ikazia Hospital, Rotterdam.
  • Hamberg P; Sint Franciscus Gasthuis, Rotterdam.
  • Stouthard JM; Maasstad Hospital, Rotterdam.
  • Kehrer DF; Department of Internal Medicine, IJsselland Hospital, Capelle aan den IJssel, The Netherlands.
  • Look MP; Department of Medical Oncology.
  • Smid M; Department of Medical Oncology.
  • Gratama JW; Department of Medical Oncology.
  • Foekens JA; Department of Medical Oncology.
  • Martens JW; Department of Medical Oncology Department of Medical Oncology and Cancer Genomics Netherlands, Erasmus MC Cancer Institute, Erasmus University Medical Center, Rotterdam, The Netherlands.
  • Sleijfer S; Department of Medical Oncology Department of Medical Oncology and Cancer Genomics Netherlands, Erasmus MC Cancer Institute, Erasmus University Medical Center, Rotterdam, The Netherlands s.sleijfer@erasmusmc.nl.
Ann Oncol ; 26(3): 510-6, 2015 Mar.
Article in En | MEDLINE | ID: mdl-25471333
ABSTRACT

BACKGROUND:

A circulating tumor cell (CTC) count is an established prognostic factor in metastatic breast cancer (MBC). Besides enumeration, CTC characterization promises to improve outcome prediction and treatment guidance. Having shown the feasibility of quantifying clinically relevant mRNA transcripts in CTCs, we determined the prognostic value of CTC gene expression in MBC. PATIENTS AND

METHODS:

CTCs were isolated and enumerated from blood of 197 MBC patients who were about to start first-line systemic therapy. Of these, 180 were assessable for quantification of mRNA expression by RT-qPCR in relation to time-to-treatment failure (TTF). A prognostic CTC gene profile was generated by leave-one-out cross validation in a 103 patient discovery set and validated in 77 patients. Additionally, all 180 patients were randomly divided into two equal sets to discover and validate a second prognostic profile.

RESULTS:

CTC count predicted for TTF at baseline {≥5 versus <5 CTCs/7.5 ml blood, hazard ratio (HR) 2.92 [95% confidence interval (CI) 1.71-4.95] P < 0.0001}. A 16-gene CTC profile was generated in the first discovery set, which identified patients with death or TTF <9 months versus those with a better outcome. In multivariate analysis, the 16-gene profile was the only factor associated with TTF [HR 3.15 (95% CI 1.35-7.33) P 0.008]. Validation of this profile in the independent patient set pointed into the same direction, but was not statistically significant. A newly generated 8-gene profile showed similarly favorable test characteristics as the 16-gene profile, but did not significantly pass validation either.

CONCLUSION:

A 16-gene CTC profile was identified, which provided prognostic value on top of CTC count in MBC patients. However, validation of this profile in an independent cohort, nor of a second profile, reached statistical significance, underscoring the need to further fine-tune the still promising approach of CTC characterization.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Breast Neoplasms / Biomarkers, Tumor / Gene Expression Profiling / Neoplastic Cells, Circulating Type of study: Clinical_trials / Etiology_studies / Guideline / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Female / Humans / Middle aged Country/Region as subject: Europa Language: En Journal: Ann Oncol Journal subject: NEOPLASIAS Year: 2015 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Breast Neoplasms / Biomarkers, Tumor / Gene Expression Profiling / Neoplastic Cells, Circulating Type of study: Clinical_trials / Etiology_studies / Guideline / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Female / Humans / Middle aged Country/Region as subject: Europa Language: En Journal: Ann Oncol Journal subject: NEOPLASIAS Year: 2015 Document type: Article