Abstract

BackgroundIn patients receiving preoperative chemotherapy, colorectal liver metastases (CLM) are expected to demonstrate a similar behaviour because of similar organ microenvironment and tumour cell chemosensitivity. We focused on the occurrence of pathological and genetic heterogeneity within CLM.MethodsPatients resected for multiple CLM between 2004 and 2011 after > three cycles of chemotherapy were included. Pathological heterogeneity was arbitrarily defined as a > 50% difference in the percentage of remaining tumour cells between individual CLM. In patients with pathological heterogeneity, the mutational genotyping (KRAS, NRAS, BRAF and PIK3CA) was determined from the most heterogeneous CLM.ResultsPathological heterogeneity was observed in 31 of 157 patients with multiple CLM (median = 4, range, 2–32) (19.7%). In 72.4% of them, we found a concordance of the mutation status between the paired CLM: both wild-type in 55%, and both mutated in 17.2%. We observed a discordance of the mutation status of 27.6% between CLM: one mutated and the other wild-type. The mutated CLM was the less florid one in 75% of patients with genetic heterogeneity.ConclusionsPathological heterogeneity is present in 19.7% of patients with multiple CLM. Genetic heterogeneity is present in 27.6% of patients with pathological heterogeneity. Heterogeneity could refine guide management for tissue sampling.

Highlights

  • Preoperative chemotherapy is an important part of the management of patients with colorectal liver metastases (CLM)

  • The pathological response (PR) is assessed by four methods based on the presence of viable cancer cells, which differed in patients with multiple CLM [3,4,5,6]

  • Our result demonstrated that a greater heterogeneity in PR was associated with a number of CLM > 3 and the use of preoperative portal vein embolization (PVE)

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Summary

Introduction

Preoperative chemotherapy is an important part of the management of patients with colorectal liver metastases (CLM). Response evaluation is usually assessed on a radiological basis using the RECIST criteria [1]. The RECIST criteria do not take account individual lesion response. The PR is assessed by four methods based on the presence of viable cancer cells, which differed in patients with multiple CLM [3,4,5,6]. CLM are expected to demonstrate a similar behaviour since the organ microenvironment and tumour cell chemosensitivity were thought similar. In patients receiving preoperative chemotherapy, colorectal liver metastases (CLM) are expected to demonstrate a similar behaviour because of similar organ microenvironment and tumour cell chemosensitivity. We focused on the occurrence of pathological and genetic heterogeneity within CLM

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