Literature DB >> 18222689

Quantification of risk of a positive (R1) resection margin following hepatic resection for metastatic colorectal cancer: an aid to clinical decision-making.

Fenella K S Welsh1, Paris P Tekkis, Tom O'Rourke, Timothy G John, Myrddin Rees.   

Abstract

BACKGROUND AND AIMS: Margin involvement following liver resection for colorectal cancer is associated with early disease recurrence and shorter long-term survival. This study aimed to develop a predictive index for quantifying the likelihood of a positive resection margin (R1) for patients undergoing hepatic resection for metastatic colorectal cancer.
METHODS: Clinical, pathological and complete follow-up data were prospectively collected from 1005 consecutive liver resections performed in 929 patients for colorectal liver metastases with curative intent at a single centre between 1987 and 2005. Ninety-four resections in 81 patients with extra-hepatic disease were excluded, leaving 911 resections (844 primary and 67 repeat) in 848 patients for analysis. Multivariate logistic regression was used to identify independent predictors of margin involvement and from the beta-coefficients generated, develop a predictive model that was validated using measures of discrimination and calibration.
RESULTS: There were 80 (8.8%) R1 resections, with a 5-year cancer-specific survival for R0 and R1 hepatic resections of 39.7% and 17.8%, respectively; p<0.001. On multivariate analysis, five risk factors were found to be independent predictors of an R1 resection: non-anatomical resection vs. anatomical resection (odds ratio (OR)=4.3, p=0.001), >3 hepatic metastases involving >50% of the liver vs. <3 metastases (OR=4.0, p<0.001); bilobar vs. unilobar disease (OR=2.9, p<0.001); repeat vs. primary hepatic resection (OR=3.1, p=0.006); abnormal vs. normal pre-operative liver function tests (OR=1.6, p=0.044). These five factors were used to develop a predictive model, which when tested, fitted the data well, with an area under the receiver operating characteristic curve of 78.1% (S.E.=2.7%).
CONCLUSIONS: This study describes an accurate model for quantifying the risk of a positive margin following hepatic resection for liver metastases. It may be used pre-operatively by multi-disciplinary teams to identify patients who may benefit from neoadjuvant therapy prior to liver surgery, thus minimizing the risk of a positive resection margin.

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Year:  2008        PMID: 18222689     DOI: 10.1016/j.suronc.2007.12.003

Source DB:  PubMed          Journal:  Surg Oncol        ISSN: 0960-7404            Impact factor:   3.279


  18 in total

Review 1.  [Interventional procedures for hepatic metastases].

Authors:  T Helmberger
Journal:  Chirurg       Date:  2010-06       Impact factor: 0.955

2.  What defines 'cure' after liver resection for colorectal metastases? Results after 10 years of follow-up.

Authors:  Carlo Pulitanò; Federico Castillo; Luca Aldrighetti; Martin Bodingbauer; Rowan W Parks; Gianfranco Ferla; Stephen J Wigmore; O James Garden
Journal:  HPB (Oxford)       Date:  2010-05       Impact factor: 3.647

3.  Open liver resection for colorectal metastases: better short- and long-term outcomes in patients potentially suitable for laparoscopic liver resection.

Authors:  Fenella K S Welsh; Paris P Tekkis; Timothy G John; Myrddin Rees
Journal:  HPB (Oxford)       Date:  2010-04       Impact factor: 3.647

Review 4.  New paradigms in post-hepatectomy liver failure.

Authors:  Nicolas Golse; Petru O Bucur; René Adam; Denis Castaing; Antonio Sa Cunha; Eric Vibert
Journal:  J Gastrointest Surg       Date:  2012-11-18       Impact factor: 3.452

5.  Margin Status is Still an Important Prognostic Factor in Hepatectomies for Colorectal Liver Metastases: A Propensity Score Matching Analysis.

Authors:  Riccardo Memeo; Vito de Blasi; Rene Adam; Diane Goéré; Tullio Piardi; Emilie Lermite; Olivier Turrini; Francis Navarro; Nicola de'Angelis; Antonio Sa Cunha; Patrick Pessaux
Journal:  World J Surg       Date:  2018-03       Impact factor: 3.352

6.  Histopathological growth patterns and positive margins after resection of colorectal liver metastases.

Authors:  Pieter M H Nierop; Diederik J Höppener; Eric P van der Stok; Boris Galjart; Florian E Buisman; Vinod P Balachandran; William R Jarnagin; T Peter Kingham; Peter J Allen; Jinru Shia; Peter B Vermeulen; Bas Groot Koerkamp; Dirk J Grünhagen; Cornelis Verhoef; Michael I D'Angelica
Journal:  HPB (Oxford)       Date:  2019-11-15       Impact factor: 3.647

7.  Current state of surgical treatment of liver metastases from colorectal cancer.

Authors:  Reinhart T Grundmann
Journal:  World J Gastrointest Surg       Date:  2011-12-27

8.  Liver resection for colorectal liver metastases with peri-operative chemotherapy: oncological results of R1 resections.

Authors:  Clarisse Eveno; Mehdi Karoui; Etienne Gayat; Alain Luciani; Marie-Luce Auriault; Michael D Kluger; Isabelle Baumgaertner; Laurence Baranes; Alexis Laurent; Claude Tayar; Daniel Azoulay; Daniel Cherqui
Journal:  HPB (Oxford)       Date:  2012-10-22       Impact factor: 3.647

9.  Patient tailored resection planning in patients undergoing liver surgery for colorectal liver metastases; how and why should you do it?

Authors:  C S van Kessel; M S van Leeuwen; R van Hillegersberg; I H M Borel Rinkes; M A A J van den Bosch; I Q Molenaar
Journal:  J Gastrointest Surg       Date:  2013-04-25       Impact factor: 3.452

10.  Repeat liver resection after a hepatic or extended hepatic trisectionectomy for colorectal liver metastasis.

Authors:  Oliver Ziff; Ibrahim Rajput; Robert Adair; Giles J Toogood; K Rajendra Prasad; J Peter A Lodge
Journal:  HPB (Oxford)       Date:  2013-07-22       Impact factor: 3.647

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