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The clinical use of circulating tumor cells (CTCs) enumeration for staging of metastatic breast cancer (MBC): International expert consensus paper.
Cristofanilli, Massimo; Pierga, Jean-Yves; Reuben, James; Rademaker, Alfred; Davis, Andrew A; Peeters, Dieter J; Fehm, Tanja; Nolé, Franco; Gisbert-Criado, Rafael; Mavroudis, Dimitrios; Grisanti, Salvatore; Giuliano, Mario; Garcia-Saenz, Jose A; Stebbing, Justin; Caldas, Carlos; Gazzaniga, Paola; Manso, Luis; Zamarchi, Rita; de Lascoiti, Angela Fernandez; De Mattos-Arruda, Leticia; Ignatiadis, Michail; Cabel, Luc; van Laere, Steven J; Meier-Stiegen, Franziska; Sandri, Maria-Teresa; Vidal-Martinez, Jose; Politaki, Eleni; Consoli, Francesca; Generali, Daniele; Cappelletti, Maria Rosa; Diaz-Rubio, Eduardo; Krell, Jonathan; Dawson, Sarah-Jane; Raimondi, Cristina; Rutten, Annemie; Janni, Wolfgang; Munzone, Elisabetta; Carañana, Vicente; Agelaki, Sofia; Almici, Camillo; Dirix, Luc; Solomayer, Erich-Franz; Zorzino, Laura; Darrigues, Lauren; Reis-Filho, Jorge S; Gerratana, Lorenzo; Michiels, Stefan; Bidard, François-Clément; Pantel, Klaus.
Afiliação
  • Cristofanilli M; Department of Medicine, Division of Hematology and Oncology, Robert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA. Electronic address: Massimo.Cristofanilli@nm.org.
  • Pierga JY; Department of Medical Oncology, Institut Curie, PSL Research University, Paris, France.
  • Reuben J; Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
  • Rademaker A; Department of Medicine, Division of Hematology and Oncology, Robert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
  • Davis AA; Department of Medicine, Division of Hematology and Oncology, Robert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
  • Peeters DJ; Translational Cancer Research Unit, GZA Hospitals Sint-Augustinus, Antwerp, Belgium; University of Antwerp, Antwerp, Belgium.
  • Fehm T; Department of Gynecology and Obstetrics, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
  • Nolé F; Division of Medical Senology, European Institute of Oncology, Milan, Italy.
  • Gisbert-Criado R; Clinical Laboratory, Hospital Arnau de Vilanova, Valencia, Spain.
  • Mavroudis D; Laboratory of Translational Oncology, School of Medicine, University of Crete, Heraklion, Greece; Department of Medical Oncology, University Hospital of Heraklion, Greece.
  • Grisanti S; Department of Transfusion Medicine, Laboratory for Stem Cells Manipulation and Cryopreservation, AO Spedali Civili di Brescia, Brescia, Italy.
  • Giuliano M; Department of Clinical Medicine and Surgery, University Federico II, Naples, Italy.
  • Garcia-Saenz JA; DCIBERONC, IdISCC Madrid, Spain.
  • Stebbing J; Division of Cancer, Department of Surgery and Cancer, Imperial College London, London, UK.
  • Caldas C; Cancer Research UK Cambridge Institute and Department of Oncology Li Ka Shing Centre, University of Cambridge, Cambridge, UK.
  • Gazzaniga P; Department of Molecular Medicine, Sapienza University of Rome, Rome, Italy.
  • Manso L; Hospital 12 de Octubre, Madrid, Spain.
  • Zamarchi R; Veneto Institute of Oncology IOV-IRCCS, Padua, Italy.
  • de Lascoiti AF; Hospital de Navarra, Pamplona, Spain.
  • De Mattos-Arruda L; Val d'Hebron Institute of Oncology, Val d'Hebron University Hospital, and Universitat Autònoma de Barcelona, Barcelona, Spain.
  • Ignatiadis M; Department of Medical Oncology and Breast Cancer Translational Research Laboratory, Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium.
  • Cabel L; Department of Medical Oncology, Institut Curie, PSL Research University, Paris, France.
  • van Laere SJ; Translational Cancer Research Unit, GZA Hospitals Sint-Augustinus, Antwerp, Belgium; University of Antwerp, Antwerp, Belgium.
  • Meier-Stiegen F; Department of Gynecology and Obstetrics, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
  • Sandri MT; Division of Laboratory Medicine, Humanitas Reseach Hospital, Rozzano, Milan, Italy.
  • Vidal-Martinez J; Clinical Laboratory, Hospital Arnau de Vilanova, Valencia, Spain.
  • Politaki E; Laboratory of Translational Oncology, School of Medicine, University of Crete, Heraklion, Greece; Department of Medical Oncology, University Hospital of Heraklion, Greece.
  • Consoli F; Department of Transfusion Medicine, Laboratory for Stem Cells Manipulation and Cryopreservation, AO Spedali Civili di Brescia, Brescia, Italy.
  • Generali D; Women Cancer Center, Azienda Socio Sanitaria Territoriale di Cremona, University of Trieste, Italy.
  • Cappelletti MR; Women Cancer Center, Azienda Socio Sanitaria Territoriale di Cremona, University of Trieste, Italy.
  • Diaz-Rubio E; DCIBERONC, IdISCC Madrid, Spain.
  • Krell J; Division of Cancer, Department of Surgery and Cancer, Imperial College London, London, UK.
  • Dawson SJ; Peter MacCallum Cancer Centre, East Melbourne, Victoria, Australia; Sir Peter MacCallum Department of Oncology, The University of Melbourne, Victoria, Australia.
  • Raimondi C; Department of Molecular Medicine, Sapienza University of Rome, Rome, Italy.
  • Rutten A; Translational Cancer Research Unit, GZA Hospitals Sint-Augustinus, Antwerp, Belgium; University of Antwerp, Antwerp, Belgium.
  • Janni W; Frauenklinik, University of Ulm, Ulm, Germany.
  • Munzone E; Division of Medical Senology, European Institute of Oncology, Milan, Italy.
  • Carañana V; Clinical Oncology, Hospital Arnau de Vilanova, Valencia, Spain.
  • Agelaki S; Laboratory of Translational Oncology, School of Medicine, University of Crete, Heraklion, Greece; Department of Medical Oncology, University Hospital of Heraklion, Greece.
  • Almici C; Department of Transfusion Medicine, Laboratory for Stem Cells Manipulation and Cryopreservation, AO Spedali Civili di Brescia, Brescia, Italy.
  • Dirix L; Translational Cancer Research Unit, GZA Hospitals Sint-Augustinus, Antwerp, Belgium; University of Antwerp, Antwerp, Belgium.
  • Solomayer EF; Saarland University, Homburg, Germany.
  • Zorzino L; Division of Laboratory Medicine, Humanitas Reseach Hospital, Rozzano, Milan, Italy.
  • Darrigues L; Department of Medical Oncology, Institut Curie, PSL Research University, Paris, France.
  • Reis-Filho JS; Department of Pathology, Memorial Sloan-Kettering Cancer Center, New York, NY, USA.
  • Gerratana L; Department of Medicine, Division of Hematology and Oncology, Robert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA; Department of Medicine, University of Udine, Udine, UD, Italy.
  • Michiels S; Service de Biostatistique et d'Epidémiologie, Gustave Roussy, CESP, INSERM U1018, University Paris-Saclay, University Paris-Sud, Villejuif, France.
  • Bidard FC; Department of Medical Oncology, Institut Curie, PSL Research University, Paris, France.
  • Pantel K; Department of Tumor Biology, Center of Experimental Medicine, University Cancer Center Hamburg, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Crit Rev Oncol Hematol ; 134: 39-45, 2019 Feb.
Article em En | MEDLINE | ID: mdl-30771872
BACKGROUND: The heterogeneity of metastatic breast cancer (MBC) necessitates novel biomarkers allowing stratification of patients for treatment selection and drug development. We propose to use the prognostic utility of circulating tumor cells (CTCs) for stratification of patients with stage IV disease. METHODS: In a retrospective, pooled analysis of individual patient data from 18 cohorts, including 2436 MBC patients, a CTC threshold of 5 cells per 7.5 ml was used for stratification based on molecular subtypes, disease location, and prior treatments. Patients with ≥ 5 CTCs were classified as Stage IVaggressive, those with < 5 CTCs as Stage IVindolent. Survival was analyzed using Kaplan-Meier curves and the log rank test. RESULTS: For all patients, Stage IVindolent patients had longer median overall survival than those with Stage IVaggressive (36.3 months vs. 16.0 months, P < 0.0001) and similarly for de novo MBC patients (41.4 months Stage IVindolent vs. 18.7 months Stage IVaggressive, p < 0.0001). Moreover, patients with Stage IVindolent disease had significantly longer overall survival across all disease subtypes compared to the aggressive cohort: hormone receptor-positive (44 months vs. 17.3 months, P < 0.0001), HER2-positive (36.7 months vs. 20.4 months, P < 0.0001), and triple negative (23.8 months vs. 9.0 months, P < 0.0001). Similar results were obtained regardless of prior treatment or disease location. CONCLUSIONS: We confirm the identification of two subgroups of MBC, Stage IVindolent and Stage IVaggressive, independent of clinical and molecular variables. Thus, CTC count should be considered an important tool for staging of advanced disease and for disease stratification in prospective clinical trials.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Biomarcadores Tumorais / Seleção de Pacientes / Células Neoplásicas Circulantes / Estadiamento de Neoplasias Tipo de estudo: Guideline / Prognostic_studies Limite: Female / Humans Idioma: En Revista: Crit Rev Oncol Hematol Assunto da revista: HEMATOLOGIA / NEOPLASIAS Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Biomarcadores Tumorais / Seleção de Pacientes / Células Neoplásicas Circulantes / Estadiamento de Neoplasias Tipo de estudo: Guideline / Prognostic_studies Limite: Female / Humans Idioma: En Revista: Crit Rev Oncol Hematol Assunto da revista: HEMATOLOGIA / NEOPLASIAS Ano de publicação: 2019 Tipo de documento: Article