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Immunohistochemical evaluation of microsatellite instability in resected colorectal liver metastases: a preliminary experience. | LitMetric

AI Article Synopsis

  • The study analyzed the impact of mismatch repair (MMR) protein expression on intra-hepatic recurrence rates in patients with colorectal liver metastasis (CRLM) who underwent liver resection, involving 93 patients after excluding 15.
  • Among the patients, 30% showed no loss of MMR expression, 63% had a hybrid loss, and 7% exhibited complete loss, with those showing complete or hybrid loss experiencing significantly higher recurrence rates (54% vs. 21%).
  • Despite the higher recurrence rates in patients with MMR loss, the study found no significant differences in disease-free survival or overall survival outcomes.

Article Abstract

In this retrospective study, we evaluated the predictive role of different immunohistochemical expression (IHC) of the mismatch repair proteins (MMR) in patients with colorectal liver metastasis (CRLM) submitted to liver resection. A total of 108 patients were retrieved, and 15 patients were excluded from the study because of the impossibility to obtain adequate formalin-fixed tissue blocks. The final analysis included 93 patients. Twenty-eight cases (30%) presented a no loss of expression or microsatellite stability (MSS) status, 59 cases (63%) showed a hybrid loss of expression, while 6 cases (7%) presented a complete loss of expression or microsatellite instability status (MSI). Patients with complete or hybrid loss of expression of MMR developed a high intra-hepatic recurrence rate compared to other ones (54% vs 21% OR of 4.278, 95% CI 1.53-11.93) (p = 0.004). The same difference in terms of liver recurrence has been found among patients with R0 resection (50% vs 17% OR of 0.2, 95% CI 0.06-0.65) (p = 0.005). However, there was no difference in terms of disease-free survival and overall survival. Complete or hybrid loss of expression of MMR could be considered a risk factor for intra-hepatic recurrences after liver resections for CRLM.

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Source
http://dx.doi.org/10.1007/s12032-020-01388-4DOI Listing

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