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Radiofrequency ablation combined with systemic treatment versus systemic treatment alone in patients with non-resectable colorectal liver metastases: a randomized EORTC Intergroup phase II study (EORTC 40004).

T Ruers ,
C Punt ,
F Van Coevorden ,
J P E N Pierie ,
I Borel-Rinkes ,
J A Ledermann ,
G Poston ,
W Bechstein ,
M A Lentz ,
M Mauer ,
E Van Cutsem ,
M P Lutz ,
B Nordlinger ,
,

Abstract

METHODS

This phase II study, originally started as a phase III design, randomly assigned 119 patients with non-resectable colorectal liver metastases between systemic treatment (n = 59) or systemic treatment plus RFA ( ± resection) (n = 60). Primary objective was a 30-month overall survival (OS) rate >38% for the combined treatment group.

CONCLUSIONS

This is the first randomized study on the efficacy of RFA. The study met the primary end point on 30-month OS; however, the results in the control arm were in the same range. RFA plus systemic treatment resulted in significant longer PFS. At present, the ultimate effect of RFA on OS remains uncertain.

RESULTS

The primary end point was met, 30-month OS rate was 61.7% [95% confidence interval (CI) 48.2-73.9] for combined treatment. However, 30-month OS for systemic treatment was 57.6% (95% CI 44.1-70.4), higher than anticipated. Median OS was 45.3 for combined treatment and 40.5 months for systemic treatment (P = 0.22). PFS rate at 3 years for combined treatment was 27.6% compared with 10.6% for systemic treatment only (hazard ratio = 0.63, 95% CI 0.42-0.95, P = 0.025). Median progression-free survival (PFS) was 16.8 months (95% CI 11.7-22.1) and 9.9 months (95% CI 9.3-13.7), respectively.

BACKGROUND

This study investigates the possible benefits of radiofrequency ablation (RFA) in patients with non-resectable colorectal liver metastases.

More about this publication

Annals of oncology : official journal of the European Society for Medical Oncology

Volume 23
Issue nr. 10
Pages 2619-2626
Publication date 01-10-2012

Full text links

Publisher website (DOI) 10.1093/annonc/mds053
Europe PubMed Central 22431703
Pubmed 22431703

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