KRAS mutational status impacts pathologic response to pre-hepatectomy chemotherapy: a study from the International Genetic Consortium for Liver Metastases

Georgios A. Margonis, Neda Amini, Nikolaos Andreatos, Kazunari Sasaki, Jack McVey, Muhammad B. Mirza, Samuel Warner, Stefan Buettner, Carlotta Barbon, Jane Wang, Alessandra Pulvirenti, Anastasios Angelou, Carsten Kamphues, Efstathios Antoniou, Emmanouil Pikoulis, Timothy M. Pawlik, Klaus Kaczirek, George Poultsides, Doris Wagner, Itaru EndoKatsunori Imai, Federico Aucejo, Martin E. Kreis, Christopher L. Wolfgang, Matthew J Weiss

Research output: Contribution to journalArticlepeer-review

3 Scopus citations

Abstract

Background: A major response to pre-hepatectomy chemotherapy has been associated with improved survival in patients who undergo resection of colorectal liver metastases (CRLM). However, the role of tumor biology, as exemplified by overall and codon-specific KRAS mutational status, in predicting response to chemotherapy is not well defined. Methods: Pathologic response was characterized as minor or major depending on the percentage of remnant viable cells (>50% vs <50%, respectively). Multivariable logistic regression was used to identify factors associated with major response. Results: 319 patients met inclusion criteria. 229 patients had a KRAS wild-type (wtKRAS) tumor and 90 harbored KRAS mutations (mutKRAS). A major pathologic response was more commonly noted in patients with wtKRAS compared to mutKRAS (48.5% vs 33.3%, P = 0.01) and wtKRAS status remained independently associated with a major response (P = 0.04). On a codon-specific level, major pathologic response occurred less frequently in those with codon 13 mutations (17.7%) compared to those with codon 12 (35.4%), and other KRAS mutations (33.3%). Importantly, codon 13 mutations were independently associated with minor pathologic response (P = 0.023). Conclusions: Patients with wtKRAS tumors appear to have the highest likelihood of experiencing a major response after preoperative chemotherapy. Future studies in “all-comer” cohorts are needed to confirm these findings and further investigate the response of codon 13 mutations.

Original languageEnglish (US)
Pages (from-to)1527-1534
Number of pages8
JournalHPB
Volume21
Issue number11
DOIs
StatePublished - Nov 2019

ASJC Scopus subject areas

  • Hepatology
  • Gastroenterology

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