Selection of an early biomarker for vascular normalization using dynamic contrast-enhanced ultrasonography to predict outcomes of metastatic patients treated with bevacizumab

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TitreSelection of an early biomarker for vascular normalization using dynamic contrast-enhanced ultrasonography to predict outcomes of metastatic patients treated with bevacizumab
Type de publicationJournal Article
Year of Publication2016
AuteursLassau 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.
JournalANNALS OF ONCOLOGY
Volume27
Pagination1922-1928
Date PublishedOCT
Type of ArticleArticle
ISSN0923-7534
Mots-clésBevacizumab, Breast cancer, colon cancer, dynamic contrast-enhanced ultrasonography (DCE-US), early evaluation, imaging biomarker
Résumé

Dynamic contrast-enhanced ultrasonography is a functional technique enabling quantitative assessment of solid tumor perfusion in metastatic patients treated with antiangiogenic therapies. In this study, we show that the mean transit time evaluated by DCE-US at day 7 may be used as a vascular normalization biomarker to predict the outcome of metastatic patients treated with bevacizumab.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 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. 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. 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. 2007-A00399-44.

DOI10.1093/annonc/mdw280