AI Article Synopsis
- The study investigated improvements in hepatocellular carcinoma (HCC) management, focusing on patients diagnosed through surveillance.
- The cohort included 1,074 patients divided into three groups based on the method of HCC detection, with variations in outcomes observed between those diagnosed in different time periods.
- Results showed that later diagnosis (2001-2006) associated with better patient conditions and increased treatment rates, leading to improved cumulative survival rates compared to earlier years (1995-2000).
Article Abstract
Aim: This study explored recent improvements in the management of hepatocellular carcinoma (HCC) diagnosed during surveillance.
Methods: The subjects were 1074 patients with HCC, subdivided into three groups. Group A comprised 211 patients for whom HCC was detected during periodic follow-up examinations at Kurume University School of Medicine, Group B comprised 544 patients diagnosed with HCC during periodic follow-up examinations at other institutions, and, Group C comprised 319 patients with HCC detected incidentally or because of symptoms.
Results: In 1995-2000 and 2001-2006, 91% and 91% of group A, 68% and 70% of group B, and 27% and 26% of group C patients with HCC, respectively, met the Milan criteria. For groups A and B, the proportions of patients with Child-Pugh class A and use of promising treatment increased in the later periods compared to those diagnosed during the earlier periods (group A, Child-Pugh class A, 72% vs 58% [P = 0.040], receiving treatment, 90% vs 70% [P < 0.0001]; group B, Child-Pugh class A, 71% vs 62% [P = 0.031]; receiving treatment, 72% vs 52% [P < 0.0001], respectively). The cumulative survival rates of the 405 patients with HCC detected in the latter 6 years tended to be better than those for patients diagnosed in the former 6 years (350 patients) (4 years, 58% vs 50% [P = 0.0349]).
Conclusion: The use of promising treatment and prognosis have improved in the last 6 years for patients with HCC diagnosed through surveillance relative to those identified in 1995-2000.
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| http://dx.doi.org/10.1111/j.1872-034X.2010.00706.x | DOI Listing |
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