Clinical validity of circulating tumour cells in patients with metastatic breast cancer: a pooled analysis of individual patient data

Summary Background We aimed to assess the clinical validity of circulating tumour cell (CTC) quantification for prognostication of patients with metastatic breast cancer by undertaking a pooled analysis of individual patient data. Methods We contacted 51 European centres and asked them to provide re...

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Veröffentlicht in:The lancet oncology 2014-04, Vol.15 (4), p.406-414
Hauptverfasser: Bidard, François-Clément, MD, Peeters, Dieter J, MD, Fehm, Tanja, Prof, Nolé, Franco, MD, Gisbert-Criado, Rafael, MD, Mavroudis, Dimitrios, Prof, Grisanti, Salvatore, MD, Generali, Daniele, MD, Garcia-Saenz, Jose A, MD, Stebbing, Justin, Prof, Caldas, Carlos, Prof, Gazzaniga, Paola, MD, Manso, Luis, MD, Zamarchi, Rita, MD, de Lascoiti, Angela Fernandez, MD, De Mattos-Arruda, Leticia, MD, Ignatiadis, Michail, MD, Lebofsky, Ronald, PhD, van Laere, Steven J, Prof, Meier-Stiegen, Franziska, PhD, Sandri, Maria-Teresa, MD, Vidal-Martinez, Jose, MD, Politaki, Eleni, MSc, Consoli, Francesca, MD, Bottini, Alberto, MD, Diaz-Rubio, Eduardo, Prof, Krell, Jonathan, MD, Dawson, Sarah-Jane, MD, Raimondi, Cristina, MD, Rutten, Annemie, MD, Janni, Wolfgang, Prof, Munzone, Elisabetta, MD, Carañana, Vicente, MD, Agelaki, Sofia, MD, Almici, Camillo, MD, Dirix, Luc, MD, Solomayer, Erich-Franz, Prof, Zorzino, Laura, MSc, Johannes, Helene, MSc, Reis-Filho, Jorge S, Prof, Pantel, Klaus, Prof, Pierga, Jean-Yves, Prof, Michiels, Stefan, PhD
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Zusammenfassung:Summary Background We aimed to assess the clinical validity of circulating tumour cell (CTC) quantification for prognostication of patients with metastatic breast cancer by undertaking a pooled analysis of individual patient data. Methods We contacted 51 European centres and asked them to provide reported and unreported anonymised data for individual patients with metastatic breast cancer who participated in studies between January, 2003, and July, 2012. Eligible studies had participants starting a new line of therapy, data for progression-free survival or overall survival, or both, and CTC quantification by the CellSearch method at baseline (before start of new treatment). We used Cox regression models, stratified by study, to establish the association between CTC count and progression-free survival and overall survival. We used the landmark method to assess the prognostic value of CTC and serum marker changes during treatment. We assessed the added value of CTCs or serum markers to prognostic clinicopathological models in a resampling procedure using likelihood ratio (LR) χ2 statistics. Findings 17 centres provided data for 1944 eligible patients from 20 studies. 911 patients (46·9%) had a CTC count of 5 per 7·5 mL or higher at baseline, which was associated with decreased progression-free survival (hazard ratio [HR] 1·92, 95% CI 1·73–2·14, p
ISSN:1470-2045
1474-5488
DOI:10.1016/S1470-2045(14)70069-5