Abstract
Objective
The aim of this study was to examine the impact of anatomical resection (AR) versus non-anatomical resection (NAR) on the survival outcomes in patients with intrahepatic cholangiocarcinoma (ICC).
Patients and Methods
Data on 702 consecutive patients who underwent either AR (n = 319) or NAR (n = 383) for ICC were reviewed. Disease-free survival (DFS) and overall survival (OS) following AR versus NAR was compared using propensity score matching (PSM). Subgroups of patients who benefited from AR versus NAR were examined after being stratified by the 8th TNM staging of ICC.
Results
AR and NAR had similar complication rates (26.6% vs. 25.1%, p = 0.634). AR was associated with better 1-, 3-, and 5-year DFS and OS rates compared with NAR after PSM (58.1%, 35.7% and 28.1% vs. 44.1%, 23.9% and 18.0%; 72.9%, 45.7% and 36.0% vs. 62.0%, 30.8% and 25.3%; both p = 0.002). On multivariate analysis, NAR was associated with worse DFS and OS than AR [hazard ratio (HR) 1.461 and 1.488; 95% confidence interval (CI) 1.184–1.804 and 1.189–1.863, respectively]. Stratified analysis demonstrated similar outcomes following AR versus NAR for ICC at stages IA, II with vascular invasion, and III with visceral peritoneum perforation, local extrahepatic invasion and nodal metastasis, while NAR was associated with worse DFS and OS versus AR for stages IB (HR 1.897 and 2.321; 95% CI 1.179–3.052 and 1.376–3.914, respectively) or II ICC without vascular invasion (2.071 and 2.077; 95% CI 1.239–3.462 and 1.205–3.579, respectively).
Conclusions
AR was associated with better survival outcomes compared with NAR in ICC patients with stage IB or II tumors without vascular invasion.
Similar content being viewed by others
References
Amin MB, Edge S, Greene F et al. AJCC cancer staging manual, 8th edition. New York: Springer International Publishing. 2017; pp. 295–302.
Bridgewater J, Galle PR, Khan SA et al. Guidelines for the diagnosis and management of intrahepatic cholangiocarcinoma. J Hepatol. 2014; 60:1268–89.
Makuuchi M, Hasegawa H, Yamazaki S. Ultrasonically guided subsegmentectomy. Surg Gynecol Obstet. 1985; 161:346–50.
Imamura H, Matsuyama Y, Tanaka E, et al. Risk factors contributing to early and late phase intrahepatic recurrence of hepatocellular carcinoma after hepatectomy. J Hepatol. 2003; 38:200–7.
European Association for the Study of the Liver; European Organisation for Research and Treatment of Cancer. EASL-EORTC clinical practice guidelines: management of hepatocellular carcinoma. J Hepatol. 2012; 56:908–43.
Haga H, Patel T. Molecular diagnosis of intrahepatic cholangiocarcinoma. J Hepatobiliary Pancreat Sci. 2015; 22:114–23.
Hwang S, Lee YJ, Song GW, et al. Prognostic impact of tumor growth type on 7th AJCC staging system for intrahepatic cholangiocarcinoma: a single-center experience of 659 cases. J Gastrointest Surg. 2015; 19: 1291–304.
Spolverato G, Yakoob MY, Kim Y et al. The impact of surgical margin status on long-term outcome after resection for intrahepatic cholangiocarcinoma. Ann Surg Oncol. 2015; 22:4020–8.
Wang Y, Li J, Xia Y et al. Prognostic nomogram for intrahepatic cholangiocarcinoma after partial hepatectomy. J Clin Oncol. 2013; 31:1188–95.
Cucchetti A, Cescon M, Ercolani G, et al. A comprehensive meta-regression analysis on outcome of anatomic resection versus nonanatomic resection for hepatocellular carcinoma. Ann Surg Oncol. 2012; 19:3697–705.
Bosman FT, Bosman FT, Carneiro F et al. WHO classification of tumours of the digestive system. 4th ed. Lyon: International Agency for Research on Cancer; 2010. pp. 205–27.
Liver Cancer Study Group of Japan. Classification of primary liver cancer (1st ed). Kanehara: Tokyo; 2011.
Roayaie S, Blume IN, Thung SN et al. A system of classifying microvascular invasion to predict outcome after resection in patients with hepatocellular carcinoma. Gastroenterology. 2009; 137:850–5.
Dindo D, Demartines N, Clavien PA. Classification of surgical complications. Ann Surg. 2004; 240:205–13.
D’Agostino RB Jr. Propensity score methods for bias reduction in the comparison of a treatment to a non-randomized control group. Stat Med. 1998; 17: 2265–81.
Honda M, Yamamoto K, Furukawa TA. Retrospective propensity score matching and the selection of surgical procedures: how precise can a propensity estimate be? J Clin Oncol. 2014; 32:3200–1.
Austin PC. Some methods of propensity-score matching had superior performance to others: results of an empirical investigation and Monte Carlo simulations. Biom J. 2009; 51:171–84.
De Jong MC, Nathan H, Sotiropoulos GC et al. Intrahepatic cholangiocarcinoma: an international multi-institutional analysis of prognostic factors and lymph node assessment. J Clin Oncol. 2011; 29:3140–5.
Lei Z, Li J, Wu D, et al. Nomogram for preoperative estimation of microvascular invasion risk in hepatitis B virus-related hepatocellular carcinoma within the Milan criteria. JAMA Surg. 2016; 151:356–63.
Acknowledgment
The authors would like to thank Drs. Lehua Shi and Zheng Li for their assistance with the data collection.
Funding
This study was supported by the State Key Project on Infectious Diseases of China (2012ZX10002-016), and the Creative Research Groups of the National Natural Science Foundation of China (30921006, 81521091).
Author information
Authors and Affiliations
Contributions
FS had full access to all the data in the study and is responsible for the integrity of the data and accuracy of the data analyses. FS, AS, JL, ZY: study concept and design, and drafting of the manuscript. AS, JL, ZY, YX, TY, ZL: Collection and assembly of the data. FS, AS, JL, TY, ZC: data collection, analysis and interpretation. FS, TMP, WYL: critical revision of the manuscript for important intellectual content and administrative support. All authors read and approved the final version of the manuscript.
Corresponding author
Ethics declarations
Disclosures
No potential conflicts of interest were disclosed.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Electronic supplementary material
Below is the link to the electronic supplementary material.
10434_2019_7260_MOESM7_ESM.pdf
DFS and OS rates after AR versus NAR for stage III ICC patients. (a) DFS rates in all stage III patients; (b) OS rates in all stage III patients; (c) DFS rates in stage IIIA patients without nodal metastasis; (d) OS rates in stage IIIA patients without nodal metastasis; (e) DFS rates in stage IIIB patients with nodal metastasis; (f) OS rates in stage IIIB patients with nodal metastasis. DFS disease-free survival, OS overall survival, AR anatomical resection, NAR non-anatomical resection, ICC intrahepatic cholangiocarcinoma (PDF 518 kb)
Rights and permissions
About this article
Cite this article
Si, A., Li, J., Yang, Z. et al. Impact of Anatomical Versus Non-anatomical Liver Resection on Short- and Long-Term Outcomes for Patients with Intrahepatic Cholangiocarcinoma. Ann Surg Oncol 26, 1841–1850 (2019). https://doi.org/10.1245/s10434-019-07260-8
Received:
Published:
Issue Date:
DOI: https://doi.org/10.1245/s10434-019-07260-8