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Volume 42, Issue 15, Pages 2472-2479 (October 2006)


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To predict progression-free survival and overall survival in metastatic renal cancer treated with sorafenib: Pilot study using dynamic contrast-enhanced Doppler ultrasound

Michele Lamuragliaac, Bernard Escudierb, Linda Chamia, Brian Schwartzd, Jérome Leclèrea, Alain Rochea, Nathalie LassauaCorresponding Author Informationemail address

Received 15 February 2006; received in revised form 18 April 2006; accepted 20 April 2006.

Refers to erratum:
Erratum to “To predict progression-free survival and overall survival in metastatic renal cancer treated with sorafenib: Pilot study using dynamic contrast-enhanced Doppler ultrasound” [European Journal of Cancer, 42 (2006) 2472–2479]
Michele Lamuraglia, Bernard Escudier, Linda Chami, Brian Schwartz, Jérome Leclère, Alain Roche, Nathalie Lassau
European Journal of Cancer
May 2007 (Vol. 43, Issue 8, Page 1336)
Full Text | Full-Text PDF (91 KB)

Abstract 

Introduction

The objective of this study was to evaluate dynamic contrast-enhanced Doppler ultrasound (DCE-US) with perfusion software (Vascular Recognition Imaging) and contrast agent injection as a predictor of tumour response, progression-free survival (PFS) and overall survival (OS).

Patients and methods

Thirty patients with a metastatic renal cell carcinoma (RCC) already enrolled in a double-blind randomised study were evaluated. Examinations were performed at baseline, and after 3 and 6weeks on sorafenib or a placebo in patients with tumour targets that were accessible to DCE-US.

Results

A total of 85 examinations were performed, 30 at baseline, 28 at 3weeks and 27 at 6weeks. The combination of a decrease in contrast uptake exceeding 10% and stability or a decrease in tumour volume allowed us to discriminate seven good responders and 20 poor responders at 3weeks. There was a statistically significant difference in PFS (p=10−4) and OS (p=10−4) between good and poor responders.

Conclusion

DCE-US is a new noninvasive imaging technique which might be an effective tool for evaluating antiangiogenic drugs in renal cancer.

a Department of Medical Imaging, Institut Gustave Roussy, 39 rue Camille Desmoulins, 94805 Villejuif, France

b Department of Medicine, Institut Gustave Roussy, 39 rue Camille Desmoulins, 94805 Villejuif, France

c Section of Internal Medicine, Department of Internal Medicine and Public Medicine, University of Bari, Piazza Giulio Cesare 11, 70124 Bari, Italy

d Bayer Pharmaceuticals Corporation, West Haven CT 06516, USA

Corresponding Author InformationCorresponding author: Tel.: +33 1 42 11 60 14; fax: +33 1 42 11 60 29.

 This work was presented at the ASCO and ECCO meetings in 2005.

PII: S0959-8049(06)00607-1

doi:10.1016/j.ejca.2006.04.023


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