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Intra-arterial hepatic beads loaded with irinotecan (DEBIRI) with mFOLFOX6 in unresectable liver metastases from colorectal cancer: a Phase 2 study.

Authors :
Pernot, Simon
Pellerin, Olivier
Artru, Pascal
Montérymard, Carole
Smith, Denis
Raoul, Jean-Luc
De La Fouchardière, Christelle
Dahan, Laetitia
Guimbaud, Rosine
Sefrioui, David
Jouve, Jean-Louis
Lepage, Côme
Tougeron, David
Taieb, Julien
for FFCD1201-DEBIRI investigators/Collaborators
Source :
British Journal of Cancer. Aug2020, Vol. 123 Issue 4, p518-524. 7p.
Publication Year :
2020

Abstract

<bold>Background: </bold>Chemo-embolisation with drug-eluting beads loaded with irinotecan (DEBIRI) increased survival as compared with intravenous irinotecan in chemorefractory patients with liver-dominant metastases from colorectal cancer (LMCRC). First-line DEBIRI with systemic chemotherapy may increase survival and secondary resection.<bold>Methods: </bold>In the FFCD-1201 single-arm Phase 2 study, patients with untreated, non-resectable LMCRC received DEBIRI plus mFOLFOX6. Four courses of DEBIRI were performed alternating right and left lobe or two sessions with both lobes treated during the same session.<bold>Results: </bold>Fifty-seven patients were enrolled. Grade 3-5 toxicities were more frequent when both lobes were treated during the same session (90.5% versus 52.8%). Nine-month PFS rate was 53.6% (95% CI, 41.8-65.1%). The objective response rate (RECIST 1.1) was 73.2%, and the secondary R0 surgery was 33%. With a median follow-up of 38.3 months, median OS was 37.4 months (95% CI, 25.7-45.8), and median PFS 10.8 months (95% CI, 8.2-12.3).<bold>Conclusions: </bold>Front-line DEBIRI + mFOLFOX6 should not be recommended as the hypothesised 9-month PFS was not met. However, high response rate, deep responses, and prolonged OS encourage further evaluation in strategies integrating biologic agent, in particular in patients with secondary surgery as the main goal.<bold>Clinical Trial Registration: </bold>NCT01839877. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00070920
Volume :
123
Issue :
4
Database :
Academic Search Index
Journal :
British Journal of Cancer
Publication Type :
Academic Journal
Accession number :
145257553
Full Text :
https://doi.org/10.1038/s41416-020-0917-4