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Selection of an early biomarker for vascular normalization using dynamic contrast-enhanced ultrasonography to predict outcomes of metastatic patients treated with bevacizumab.
Lassau, N; Coiffier, B; Kind, M; Vilgrain, V; Lacroix, J; Cuinet, M; Taieb, S; Aziza, R; Sarran, A; Labbe-Devilliers, C; Gallix, B; Lucidarme, O; Ptak, Y; Rocher, L; Caquot, L M; Chagnon, S; Marion, D; Luciani, A; Feutray, S; Uzan-Augui, J; Benatsou, B; Bonastre, J; Koscielny, S.
Affiliation
  • Lassau N; Gustave Roussy, Université Paris-Saclay, Imaging Department, Villejuif, and IR4M, Centre National de la Recherche Scientifique, Université Paris-Sud, Université Paris-Saclay, Villejuif nathalie.lassau@gustaveroussy.fr.
  • Coiffier B; Gustave Roussy, Université Paris-Saclay, Imaging Department, Villejuif, and IR4M, Centre National de la Recherche Scientifique, Université Paris-Sud, Université Paris-Saclay, Villejuif.
  • Kind M; Imaging Department, Institut Bergonié, Bordeaux.
  • Vilgrain V; Radiology Department, Assistance Publique-Hôpitaux de Paris, Hôpital Beaujon, Clichy.
  • Lacroix J; Radiology Department, Centre François Baclesse, Caen.
  • Cuinet M; Radiology Department, Centre Léon Bérard, Lyon.
  • Taieb S; Radiology Department, Centre Oscar Lambret, Lille.
  • Aziza R; Radiodiagnostics Department, Centre Claudius Regaud, Toulouse.
  • Sarran A; Imaging Department, Institut Paoli Calmettes, Marseille.
  • Labbe-Devilliers C; Radiodiagnostics Department, Centre René Gauducheau, ICO Nantes.
  • Gallix B; Department of Abdominal and Digestive Imaging, Hôpital Saint-Eloi, Montpellier and Department of Radiology, McGill University Health Center, Montreal, Canada.
  • Lucidarme O; Radiology Department, CHU La Pitié-Salpêtrière, Paris.
  • Ptak Y; Radiodiagnostics Department, Centre Jean Perrin, Clermont-Ferrand.
  • Rocher L; Radiology Department, CHU Bicêtre, Le Kremlin-Bicêtre.
  • Caquot LM; Radiodiagnostics and Imaging Department, Institut Jean Godinot, Reims.
  • Chagnon S; Radiology Department, Hôpital Ambroise Paré, Boulogne-Billancourt.
  • Marion D; Radiology Department, CHU Hôtel-Dieu, Lyon.
  • Luciani A; Radiology Department, CHU Henri Mondor, Créteil.
  • Feutray S; Radiology Department, Centre Georges-François Leclerc, Dijon.
  • Uzan-Augui J; Radiology Department, Hôpital Cochin, Paris.
  • Benatsou B; Gustave Roussy, Université Paris-Saclay, Imaging Department, Villejuif, and IR4M, Centre National de la Recherche Scientifique, Université Paris-Sud, Université Paris-Saclay, Villejuif.
  • Bonastre J; Service biostatistique et épidémiologie, Gustave Roussy and CESP Centre for Research in Epidemiology and Population Health, INSERM U1018, Paris-Sud Univ., Villejuif, France.
  • Koscielny S; Service biostatistique et épidémiologie, Gustave Roussy and CESP Centre for Research in Epidemiology and Population Health, INSERM U1018, Paris-Sud Univ., Villejuif, France.
Ann Oncol ; 27(10): 1922-8, 2016 10.
Article in En | MEDLINE | ID: mdl-27502701
ABSTRACT

BACKGROUND:

Dynamic contrast-enhanced ultrasonography (DCE-US) has been used for evaluation of tumor response to antiangiogenic treatments. The objective of this study was to assess the link between DCE-US data obtained during the first week of treatment and subsequent tumor progression. PATIENTS AND

METHODS:

Patients treated with antiangiogenic therapies were included in a multicentric prospective study from 2007 to 2010. DCE-US examinations were available at baseline and at day 7. For each examination, a 3 min perfusion curve was recorded just after injection of a contrast agent. Each perfusion curve was modeled with seven parameters. We analyzed the correlation between criteria measured up to day 7 on freedom from progression (FFP). The impact was assessed globally, according to tumor localization and to type of treatment.

RESULTS:

The median follow-up was 20 months. The mean transit time (MTT) evaluated at day 7 was the only criterion significantly associated with FFP (P = 0.002). The cut-off point maximizing the difference between FFP curves was 12 s. Patients with at least a 12 s MTT had a better FFP. The results according to tumor type were significantly heterogeneous the impact of MTT on FFP was more marked for breast cancer (P = 0.004) and for colon cancer (P = 0.025) than for other tumor types. Similarly, the differences in FFP according to MTT at day 7 were marked (P = 0.004) in patients receiving bevacizumab.

CONCLUSION:

The MTT evaluated with DCE-US at day 7 is significantly correlated to FFP of patients treated with bevacizumab. This criterion might be linked to vascular normalization. AFSSAPS NO 2007-A00399-44.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ultrasonography / Bevacizumab / Neoplasms Type of study: Clinical_trials / Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: En Journal: Ann Oncol Journal subject: NEOPLASIAS Year: 2016 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ultrasonography / Bevacizumab / Neoplasms Type of study: Clinical_trials / Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: En Journal: Ann Oncol Journal subject: NEOPLASIAS Year: 2016 Type: Article