Anatomic Resection for Hepatocellular Carcinoma: Prognostic Impact Assessed from Recurrence Treatment View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2021-09-21

AUTHORS

Masaaki Minagawa, Yoshihiro Mise, Kiyohiko Omichi, Hirofumi Ichida, Tomoya Mizuno, Ryuji Yoshioka, Hiroshi Imamura, Naotake Yanagisawa, Yosuke Inoue, Yu Takahashi, Akio Saiura

ABSTRACT

BackgroundThe oncologic advantage of anatomic resection (AR) for primary hepatocellular carcinoma (HCC) remains controversial. This study aimed to evaluate the clinical advantages of AR for primary HCC by using propensity score-matching and by assessing treatment strategies for recurrence after surgery.MethodsThe study reviewed data of patients who underwent AR or non-anatomic resection (NAR) for solitary HCC (≤ 5 cm) in two institutions between 2004 and 2017. Surgical outcomes were compared between the two groups in a propensity score-adjusted cohort. The time-to-interventional failure (TIF), defined as the elapsed time from resection to unresectable/unablatable recurrence, also was evaluated.ResultsThe inclusion criteria were met by 250 patients: 77 patients (31%) with AR and 173 patients (69%) with NAR. In the propensity score-matched populations (AR, 67; NAR, 67), the 5-year recurrence-free survival (RFS) for AR was better than for NAR (62% vs 35%; P = 0.005). No differences, however, were found in the 5-year overall survival between the two groups (72% vs 78%; P = 0.666). The 5-year TIF rates for the NAR group (60%) also were similar to those for the AR group (66%) (P = 0.413). In the cohort of 67 patients, curative repeat resection or ablation therapy was performed more frequently for the NAR patients (42%) than for the AR patients (10%) (P < 0.001).ConclusionFor solitary HCC, AR decreases recurrence after the initial hepatectomy. However, aggressive curative-intent interventions for recurrence compensate for the impaired RFS, even for patients undergoing NAR. More... »

PAGES

913-921

Identifiers

URI

http://scigraph.springernature.com/pub.10.1245/s10434-021-10380-9

DOI

http://dx.doi.org/10.1245/s10434-021-10380-9

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1141284559

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/34549363


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