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

  • Siân A. Pugh*
  • , Megan Bowers
  • , Alexandre Ball
  • , Stephen J Falk
  • , Margaret Finch-Jones
  • , Juan W. Valle
  • , Derek A. O'Reilly
  • , Ajith K. Siriwardena
  • , Joanne Hornbuckle
  • , Myrddin Rees
  • , Charlotte Rees
  • , Tim Iveson
  • , Tamas Hickish
  • , Tom Maishman
  • , Louise Stanton
  • , Elizabeth Dixon
  • , Andrea Corkhill
  • , Mike Radford
  • , O. James Garden
  • , David Cunningham
  • Tim S. Maughan, John A. Bridgewater, John N. Primrose
*Corresponding author for this work

Research output: Contribution to journalArticle (Academic Journal)peer-review

10 Citations (Scopus)

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.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.

Original languageEnglish
Pages (from-to)420-424
Number of pages5
JournalBritish Journal of Cancer
Volume115
Issue number4
DOIs
Publication statusPublished - 9 Aug 2016

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