TY - JOUR
T1 - Patterns of progression, treatment of progressive disease and post-progression survival in the New EPOC study
AU - Pugh, Siân A.
AU - Bowers, Megan
AU - Ball, Alexandre
AU - Falk, Stephen J
AU - Finch-Jones, Margaret
AU - Valle, Juan W.
AU - O'Reilly, Derek A.
AU - Siriwardena, Ajith K.
AU - Hornbuckle, Joanne
AU - Rees, Myrddin
AU - Rees, Charlotte
AU - Iveson, Tim
AU - Hickish, Tamas
AU - Maishman, Tom
AU - Stanton, Louise
AU - Dixon, Elizabeth
AU - Corkhill, Andrea
AU - Radford, Mike
AU - Garden, O. James
AU - Cunningham, David
AU - Maughan, Tim S.
AU - Bridgewater, John A.
AU - Primrose, John N.
PY - 2016/8/9
Y1 - 2016/8/9
N2 - 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.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.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.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.
AB - 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.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.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.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.
UR - https://www.scopus.com/pages/publications/84978737363
U2 - 10.1038/bjc.2016.208
DO - 10.1038/bjc.2016.208
M3 - Article (Academic Journal)
C2 - 27434036
AN - SCOPUS:84978737363
SN - 0007-0920
VL - 115
SP - 420
EP - 424
JO - British Journal of Cancer
JF - British Journal of Cancer
IS - 4
ER -