Abstract
Although elevated neutrophil-to-lymphocyte ratio (NLR) has been associated with survival in some liver cancers, its prognostic relevance has not been studied in the context of combined hepatocellular cholangiocarcinoma CHCC-CC, a rare primary liver cancer. We investigated whether elevated NLR and a predominance of cholangiocarcinoma might predict poor prognosis in patients with resectable CHCC-CC. We retrospectively reviewed the clinicopathologic data of forty-two patients with CHCC-CC receiving hepatectomies at our hospital. We used Kaplan-Meier and Cox regression to analyze survival. Two-year disease-free survival and five-year overall survival rates were 43.2% and 32.9%, respectively. Univariate analyses showed that patients with NLR ≥3 had significantly worse 2-year DFS and 5-year OS rates. Univariant Kaplan-Meier survival analysis also associated these rates with a predominance in intrahepatic cholangiocarcinoma, AJCC tumor stage, pathological T stage and lymph-vascular invasion. However, our multivariate analysis found NLR ≥3 to be the only independent predictor of disease recurrence and poorer survival. Neutrophil-to-lymphocyte ratio was the most important independent predictor of poorer survival in patients with resectable CHCC-CC. Predominance of intrahepatic cholangiocarcinoma, advanced AJCC tumor stage and pathological T stage, and lymph-vascular invasion also may affect poor prognosis in patients receiving complete tumor resections.
Highlights
Combined hepatocellular cholangiocarcinoma (CHCC-CC) is an uncommon primary liver malignancy
We investigated whether elevated neutrophil-to-lymphocyte ratio (NLR) and a predominance of cholangiocarcinoma might predict poor prognosis in patients with resectable combined hepatocellular cholangiocarcinoma (CHCC-CC)
While some of them have reported that CHCC-CC has a worse median survival than hepatocellular carcinoma (HCC) and intrahepatic cholangiocarcinoma (IHC) [3, 9, 11], others report its survival rate to fall between the survival rates of HCC and IHC [12,13,14] or be equal to IHC but worse than HCC [15]
Summary
Combined hepatocellular cholangiocarcinoma (CHCC-CC) is an uncommon primary liver malignancy. It is unique in that it shares pathological characteristics of hepatocellular carcinoma (HCC) and intrahepatic cholangiocarcinoma (IHC) coexisting within the same tumor. It makes up between 1% to 14.3% of all primary liver tumors depending on the study [1,2,3,4,5,6,7,8,9]. One study found IHC-dominant patients with recurrent tumors to have significantly shorter mean survival rates than those with HCC-dominance [16]. It remains unclear how a predominance of HCC cells vs. IHC cells might affect surgical outcomes in patients with CHCC-CC
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