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Prognostic Evaluation and Survival Prediction for Combined Hepatocellular-Cholangiocarcinoma Following Hepatectomyopen access

Authors
Chun, Seok-JooJung, Yu JungChoi, YoungrokYi, Nam-JoonLee, Kwang-WoongSuh, Kyung-SukLee, Kyoung BunKang, Hyun-CheolChie, Eui KyuKim, Kyung Su
Issue Date
Jan-2025
Publisher
대한암학회
Keywords
Combined hepatocellular-cholangiocarcinoma; Hepatectomy; Nomograms
Citation
Cancer Research and Treatment, v.57, no.1, pp 229 - 239
Pages
11
Indexed
SCIE
SCOPUS
KCICANDI
Journal Title
Cancer Research and Treatment
Volume
57
Number
1
Start Page
229
End Page
239
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/57540
DOI
10.4143/crt.2024.176
ISSN
1598-2998
2005-9256
Abstract
Purpose This study aimed to assess prognostic factors associated with combined hepatocellular-cholangiocarcinoma (cHCC-CCA) and to predict 5-year survival based on these factors. Materials and Methods Patients who underwent definitive hepatectomy from 2006 to 2022 at a single institution was retrospectively analyzed. Inclusion criteria involved a pathologically confirmed diagnosis of cHCC-CCA. Results A total of 80 patients with diagnosed cHCC-CCA were included in the analysis. The median progression-free survival was 15.6 months, while distant metastasis-free survival (DMFS), hepatic progression-free survival, and overall survival (OS) were 50.8, 21.5, and 85.1 months, respectively. In 52 cases of recurrence, intrahepatic recurrence was the most common initial recurrence (34/52), with distant metastasis in 17 cases. Factors associated with poor DMFS included tumor necrosis, lymphovascular invasion (LVI), perineural invasion, and histologic compact type. Postoperative carbohydrate antigen 19-9, tumor necrosis, LVI, and close/positive margin were associated with poor OS. LVI emerged as a key factor affecting both DMFS and OS, with a 5-year OS of 93.3% for patients without LVI compared to 35.8% with LVI. Based on these factors, a nomogram predicting 3-year and 5-year DMFS and OS was developed, demonstrating high concordance with actual survival in the cohort (Harrell C-index 0.809 for OS, 0.801 for DMFS, respectively). Conclusion The prognosis of cHCC-CCA is notably poor when combined with LVI. Given the significant impact of adverse features, accurate outcome prediction is crucial. Moreover, consideration of adjuvant therapy may be warranted for patients exhibiting poor survival and increased risk of local recurrence or distant metastasis.
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