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Circulating Tumor Cells in Breast Cancer Patients Treated by Neoadjuvant Chemotherapy: A Meta-analysis.
Bidard, François-Clément; Michiels, Stefan; Riethdorf, Sabine; Mueller, Volkmar; Esserman, Laura J; Lucci, Anthony; Naume, Bjørn; Horiguchi, Jun; Gisbert-Criado, Rafael; Sleijfer, Stefan; Toi, Masakazu; Garcia-Saenz, Jose A; Hartkopf, Andreas; Generali, Daniele; Rothé, Françoise; Smerage, Jeffrey; Muinelo-Romay, Laura; Stebbing, Justin; Viens, Patrice; Magbanua, Mark Jesus M; Hall, Carolyn S; Engebraaten, Olav; Takata, Daisuke; Vidal-Martínez, José; Onstenk, Wendy; Fujisawa, Noriyoshi; Diaz-Rubio, Eduardo; Taran, Florin-Andrei; Cappelletti, Maria Rosa; Ignatiadis, Michail; Proudhon, Charlotte; Wolf, Denise M; Bauldry, Jessica B; Borgen, Elin; Nagaoka, Rin; Carañana, Vicente; Kraan, Jaco; Maestro, Marisa; Brucker, Sara Yvonne; Weber, Karsten; Reyal, Fabien; Amara, Dominic; Karhade, Mandar G; Mathiesen, Randi R; Tokiniwa, Hideaki; Llombart-Cussac, Antonio; Meddis, Alessandra; Blanche, Paul; d'Hollander, Koenraad; Cottu, Paul.
Afiliação
  • Bidard FC; Institut Curie, UVSQ and Paris Saclay University, Saint Cloud, France.
  • Michiels S; Gustave Roussy, Villejuif, France.
  • Riethdorf S; Universitätsklinikum Hamburg-Eppendorf, Hamburg, Germany.
  • Mueller V; Universitätsklinikum Hamburg-Eppendorf, Hamburg, Germany.
  • Esserman LJ; University of California at San Francisco, San Francisco, CA.
  • Lucci A; MD Anderson Cancer Center, Houston, TX.
  • Naume B; Oslo University Hospital, Oslo, Norway.
  • Horiguchi J; Institute for Clinical Medicine, University of Oslo, Oslo, Norway.
  • Gisbert-Criado R; Gunma University Hospital, Gunma, Japan.
  • Sleijfer S; Hospital Arnau de Vilanova, Valencia, Spain.
  • Toi M; Erasmus MC Cancer Institute, Rotterdam, the Netherlands.
  • Garcia-Saenz JA; Kyoto University Hospital, Kyoto, Japan.
  • Hartkopf A; Hospital Clinico San Carlos, Universidad Complutense, Madrid, Spain.
  • Generali D; Women's Health Center, University of Tuebingen, Tuebingen, Germany.
  • Rothé F; Women Cancer Centre, University of Trieste, ASST of Cremona, Cremona, Italy.
  • Smerage J; Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium.
  • Muinelo-Romay L; University of Michigan Comprehensive Cancer Center, Ann Arbor, MI.
  • Stebbing J; Complejo Hospitalario Universitario, Santiago de Compostela, Spain.
  • Viens P; Imperial College, London, UK.
  • Magbanua MJM; Institut Paoli Calmettes, Aix Marseille University, CNRS, Inserm, Marseilles, France.
  • Hall CS; University of California at San Francisco, San Francisco, CA.
  • Engebraaten O; MD Anderson Cancer Center, Houston, TX.
  • Takata D; Institute for Clinical Medicine, University of Oslo, Oslo, Norway.
  • Vidal-Martínez J; Gunma University Hospital, Gunma, Japan.
  • Onstenk W; Hospital Arnau de Vilanova, Valencia, Spain.
  • Fujisawa N; Erasmus MC Cancer Institute, Rotterdam, the Netherlands.
  • Diaz-Rubio E; Kyoto University Hospital, Kyoto, Japan.
  • Taran FA; Hospital Clinico San Carlos, Universidad Complutense, Madrid, Spain.
  • Cappelletti MR; Women's Health Center, University of Tuebingen, Tuebingen, Germany.
  • Ignatiadis M; Women Cancer Centre, University of Trieste, ASST of Cremona, Cremona, Italy.
  • Proudhon C; Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium.
  • Wolf DM; Institut Curie, PSL Research University, Paris, France.
  • Bauldry JB; University of California at San Francisco, San Francisco, CA.
  • Borgen E; MD Anderson Cancer Center, Houston, TX.
  • Nagaoka R; Oslo University Hospital, Oslo, Norway.
  • Carañana V; Gunma University Hospital, Gunma, Japan.
  • Kraan J; Hospital Arnau de Vilanova, Valencia, Spain.
  • Maestro M; Erasmus MC Cancer Institute, Rotterdam, the Netherlands.
  • Brucker SY; Hospital Clinico San Carlos, Universidad Complutense, Madrid, Spain.
  • Weber K; Women's Health Center, University of Tuebingen, Tuebingen, Germany.
  • Reyal F; German Breast Group, Neu-Isenburg, Germany.
  • Amara D; Institut Curie, PSL Research University, Paris, France.
  • Karhade MG; University of California at San Francisco, San Francisco, CA.
  • Mathiesen RR; MD Anderson Cancer Center, Houston, TX.
  • Tokiniwa H; Oslo University Hospital, Oslo, Norway.
  • Llombart-Cussac A; Gunma University Hospital, Gunma, Japan.
  • Meddis A; Hospital Arnau de Vilanova, Valencia, Spain.
  • Blanche P; Institut Curie, Inserm U900, Saint Cloud, France.
  • d'Hollander K; LMBA, Université de Bretagne Sud, Vannes, France.
  • Cottu P; International Drug Development Institute, Louvain La Neuve, Belgium.
J Natl Cancer Inst ; 110(6): 560-567, 2018 06 01.
Article em En | MEDLINE | ID: mdl-29659933
ABSTRACT

Background:

We conducted a meta-analysis in nonmetastatic breast cancer patients treated by neoadjuvant chemotherapy (NCT) to assess the clinical validity of circulating tumor cell (CTC) detection as a prognostic marker.

Methods:

We collected individual patient data from 21 studies in which CTC detection by CellSearch was performed in early breast cancer patients treated with NCT. The primary end point was overall survival, analyzed according to CTC detection, using Cox regression models stratified by study. Secondary end points included distant disease-free survival, locoregional relapse-free interval, and pathological complete response. All statistical tests were two-sided.

Results:

Data from patients were collected before NCT (n = 1574) and before surgery (n = 1200). CTC detection revealed one or more CTCs in 25.2% of patients before NCT; this was associated with tumor size (P < .001). The number of CTCs detected had a detrimental and decremental impact on overall survival (P < .001), distant disease-free survival (P < .001), and locoregional relapse-free interval (P < .001), but not on pathological complete response. Patients with one, two, three to four, and five or more CTCs before NCT displayed hazard ratios of death of 1.09 (95% confidence interval [CI] = 0.65 to 1.69), 2.63 (95% CI = 1.42 to 4.54), 3.83 (95% CI = 2.08 to 6.66), and 6.25 (95% CI = 4.34 to 9.09), respectively. In 861 patients with full data available, adding CTC detection before NCT increased the prognostic ability of multivariable prognostic models for overall survival (P < .001), distant disease-free survival (P < .001), and locoregional relapse-free interval (P = .008).

Conclusions:

CTC count is an independent and quantitative prognostic factor in early breast cancer patients treated by NCT. It complements current prognostic models based on tumor characteristics and response to therapy.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Células Neoplásicas Circulantes / Antineoplásicos Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Células Neoplásicas Circulantes / Antineoplásicos Idioma: En Ano de publicação: 2018 Tipo de documento: Article