Abstract

BackgroundThe relationship between KRAS mutational status and timing of colorectal liver metastasis (CRLM) remains unclear. This study evaluated the relationship between KRAS mutational status and long-term survival in patients with synchronous CRLM.MethodsOf the 255 patients who underwent initial hepatic resection for CRLM between January 2001 and December 2018, the KRAS mutational status was examined in 101 patients. Medical records of these patients were reviewed to evaluate recurrence and survival outcomes.ResultsKRAS mutant status was identified in 38 patients (37.6%). The overall survival (OS) was significantly better in patients with wild-type KRAS than in those with mutant KRAS status. In patients with synchronous metastases, the OS of patients with wild-type KRAS was significantly better than those with mutant KRAS. Multivariate analyses indicated shorter OS to be independently associated with positive primary lymph node, and large tumor size and R1 resection in patients with metachronous metastasis, whereas to be independently associated with mutant KRAS status in patients with synchronous metastasis. Furthermore, in the subgroup of patients with synchronous metastases, the repeat resection rate for hepatic recurrence was significantly high in those with wild type KRAS than in those with mutant KRAS.ConclusionKRAS mutation is an independent prognostic factor in patients with synchronous CRLM, but not in patients with metachronous CRLM.

Highlights

  • Colorectal cancer (CRC) is one of the common causes of cancer-related mortality worldwide

  • We aimed to delineate the relationship between KRAS mutational status and long-term survival in patients with colorectal liver metastasis (CRLM), and assess whether there were any differences in the effect of KRAS mutational status on the disease outcome based on the timing of metastasis

  • The present study clearly demonstrated that the effect of the mutation status of KRAS varied according to the timing of liver metastasis

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Summary

Introduction

Colorectal cancer (CRC) is one of the common causes of cancer-related mortality worldwide. During the course of CRC, colorectal liver metastases (CRLM) occur in approximately half of the patients [1]. Recent data have shown that a 1 cm margin is not a requisite for curative resection, and that margin width does not affect long-term survival [10, 11]. One reason for these changes might be attributable to the use of perioperative chemotherapy with molecular targeted agents [12]. The relationship between KRAS mutational status and timing of colorectal liver metastasis (CRLM) remains unclear.

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