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Patterns of progression, treatment of progressive disease and post-progression survival in the New EPOC study.

Authors :
Pugh SA
Bowers M
Ball A
Falk S
Finch-Jones M
Valle JW
O'Reilly DA
Siriwardena AK
Hornbuckle J
Rees M
Rees C
Iveson T
Hickish T
Maishman T
Stanton L
Dixon E
Corkhill A
Radford M
Garden OJ
Cunningham D
Maughan TS
Bridgewater JA
Primrose JN
Source :
British journal of cancer [Br J Cancer] 2016 Aug 09; Vol. 115 (4), pp. 420-4. Date of Electronic Publication: 2016 Jul 19.
Publication Year :
2016

Abstract

Background: The addition of cetuximab (CTX) to perioperative chemotherapy (CT) for operable colorectal liver metastases resulted in a shorter progression-free survival. Details of disease progression are described to further inform the primary study outcome.<br />Methods: A total of 257 KRAS wild-type patients were randomised to CT alone or CT with CTX. Data regarding sites and treatment of progressive disease were obtained for the 109 (CT n=48, CT and CTX n=61) patients with progressive disease at the cut-off date for analysis of November 2012.<br />Results: The liver was the most frequent site of progression (CT 67% (32/48); CT and CTX 66% (40/61)). A higher proportion of patients in the CT and group had multiple sites of progressive disease (CT 8%, 4/48; CT and CTX 23%, 14/61 P=0.04). Further treatment for progressive disease is known for 84 patients of whom 69 received further CT, most frequently irinotecan based. Twenty-two patients, 11 in each arm, received CTX as a further line agent.<br />Conclusions: Both the distribution of progressive disease and further treatment are as expected for such a cohort. The pattern of disease progression seen is consistent with failure of systemic micrometastatic disease control rather than failure of local disease control following liver surgery.

Details

Language :
English
ISSN :
1532-1827
Volume :
115
Issue :
4
Database :
MEDLINE
Journal :
British journal of cancer
Publication Type :
Academic Journal
Accession number :
27434036
Full Text :
https://doi.org/10.1038/bjc.2016.208