AI Article Synopsis

  • TARE (Trans-arterial radioembolization) shows promise as a safe treatment for patients with unresectable intrahepatic cholangiocarcinoma (ICC), with no major complications reported in the study of 73 patients.
  • Patients with higher baseline cholinesterase levels (≥ 4.62 kU/L) and lower tumor burden (≤ 25%) experience significantly longer overall survival (OS) rates, suggesting these factors can predict treatment outcomes.
  • Receiving multiple TARE cycles is associated with improved progression-free survival (PFS), indicating potential benefits from more frequent treatments, although further research is needed to confirm these findings.

Article Abstract

Trans-arterial radioembolization (TARE) is increasingly evaluated for unresectable intrahepatic cholangiocarcinoma (ICC). Not all ICC patients benefit equally well from TARE. Therefore, we sought to evaluate variables predicting progression-free survival (PFS) and overall survival (OS). Patients with non-resectable ICC underwent TARE and were treated with 90Y resin microspheres. Baseline characteristics, biochemical/clinical toxicities, and response were examined for impact on PFS and OS. A total of 103 treatments were administered to 73 patients without major complications or toxicity. Mean OS was 18.9 months (95% confidence intervals (CI); 13.9-23.9 months). Mean and median PFS were 10.1 months (95% CI; 7.9-12.2) and 6.4 months (95% CI; 5.20-7.61), respectively. Median OS and PFS were significantly prolonged in patients with baseline cholinesterase (CHE) ≥ 4.62 kU/L (OS: 14.0 vs. 5.5 months; PFS: 6.9 vs. 3.2 months; < 0.001). Patients with a tumor burden ≤ 25% had a significantly longer OS (15.2 vs. 6.6 months; = 0.036). Median PFS was significantly longer for patients with multiple TARE cycles (24.4 vs. 5.8 months; = 0.04). TARE is a considerable and safe option for unresectable ICC. CA-19-9, CHE, and tumor burden have predictive value for survival in patients treated with TARE. Multiple TARE treatments might further improve survival; this has to be confirmed by further studies.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8582544PMC
http://dx.doi.org/10.3390/cancers13215399DOI Listing

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