TY - JOUR
T1 - Insights into synchronous peritoneal metastases from hepatobiliary origin
T2 - Incidence, risk factors, treatment, and survival from a nationwide database
AU - Rijken, Anouk
AU - Bakkers, Checca
AU - Klümpen, Heinz-Josef
AU - van der Geest, Lydia G.
AU - de Vos-Geelen, Judith
AU - van Erning, Felice N.
AU - de Hingh, Ignace H. J. T.
N1 - Funding Information: This study is endorsed by the Dutch Hepatocellular & Cholangiocarcinoma Group (DHCG). Publisher Copyright: © 2023 Elsevier Ltd, BASO ~ The Association for Cancer Surgery, and the European Society of Surgical Oncology
PY - 2023/8
Y1 - 2023/8
N2 - Introduction: – This population-based study aimed to investigate incidence, risk factors, treatment, and survival of synchronous peritoneal metastases (PM) of hepatobiliary origin. Methods: – All Dutch patients diagnosed with hepatobiliary cancer between 2009 and 2018 were selected. Factors associated with PM were identified with logistic regression analyses. Treatments for patients with PM were categorized into local therapy, systemic therapy, and best supportive care (BSC). Overall survival (OS) was investigated using log-rank test. Results: – In total, 12 649 patients were diagnosed with hepatobiliary cancer of whom 8% (n = 1066) were diagnosed with synchronous PM (12% [n = 882/6519] in biliary tract cancer [BTC] vs. 4% [n = 184/5248] in hepatocellular carcinoma [HCC]). Factors that were positively associated with PM were the female sex (OR 1.18, 95% CI 1.03–1.35), BTC (OR 2.93, 95% CI 2.46–3.50), diagnosis in more recent years (2013–2015: OR 1.42, 95% CI 1.20–1.68; 2016–2018: OR 1.48, 95% CI 1.26–1.75), T3/T4 stage (OR 1.84, 95% CI 1.55–2.18), N1/N2 stage (OR 1.31, 95% CI 1.12–1.53) and other synchronous systemic metastases (OR 1.85, 95% CI 1.62–2.12). Of all PM patients, 723 (68%) received BSC only. Median OS was 2.7 months (IQR 0.9–8.2) in PM patients. Conclusion: – Synchronous PM were found in 8% of all hepatobiliary cancer patients and occurred more often in BTC than in HCC. Most patients with PM received BSC only. Given the high incidence and dismal prognosis of PM patients, extended research in hepatobiliary PM is needed to achieve better outcome in these patients.
AB - Introduction: – This population-based study aimed to investigate incidence, risk factors, treatment, and survival of synchronous peritoneal metastases (PM) of hepatobiliary origin. Methods: – All Dutch patients diagnosed with hepatobiliary cancer between 2009 and 2018 were selected. Factors associated with PM were identified with logistic regression analyses. Treatments for patients with PM were categorized into local therapy, systemic therapy, and best supportive care (BSC). Overall survival (OS) was investigated using log-rank test. Results: – In total, 12 649 patients were diagnosed with hepatobiliary cancer of whom 8% (n = 1066) were diagnosed with synchronous PM (12% [n = 882/6519] in biliary tract cancer [BTC] vs. 4% [n = 184/5248] in hepatocellular carcinoma [HCC]). Factors that were positively associated with PM were the female sex (OR 1.18, 95% CI 1.03–1.35), BTC (OR 2.93, 95% CI 2.46–3.50), diagnosis in more recent years (2013–2015: OR 1.42, 95% CI 1.20–1.68; 2016–2018: OR 1.48, 95% CI 1.26–1.75), T3/T4 stage (OR 1.84, 95% CI 1.55–2.18), N1/N2 stage (OR 1.31, 95% CI 1.12–1.53) and other synchronous systemic metastases (OR 1.85, 95% CI 1.62–2.12). Of all PM patients, 723 (68%) received BSC only. Median OS was 2.7 months (IQR 0.9–8.2) in PM patients. Conclusion: – Synchronous PM were found in 8% of all hepatobiliary cancer patients and occurred more often in BTC than in HCC. Most patients with PM received BSC only. Given the high incidence and dismal prognosis of PM patients, extended research in hepatobiliary PM is needed to achieve better outcome in these patients.
KW - Biliary tract cancer
KW - Hepatocellular carcinoma
KW - Incidence
KW - Peritoneal metastases
KW - Risk factors
KW - Survival
KW - Treatment
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85149797610&origin=inward
UR - https://www.ncbi.nlm.nih.gov/pubmed/36898900
UR - http://www.scopus.com/inward/record.url?scp=85149797610&partnerID=8YFLogxK
U2 - https://doi.org/10.1016/j.ejso.2023.03.004
DO - https://doi.org/10.1016/j.ejso.2023.03.004
M3 - Article
C2 - 36898900
SN - 0748-7983
VL - 49
SP - 1436
EP - 1443
JO - European Journal of Surgical Oncology
JF - European Journal of Surgical Oncology
IS - 8
ER -