2015
DOI: 10.1159/000343877
|View full text |Cite
|
Sign up to set email alerts
|

Insufficient Ablative Margin Determined by Early Computed Tomography May Predict the Recurrence of Hepatocellular Carcinoma after Radiofrequency Ablation

Abstract: Tumor recurrence in hepatocellular carcinoma (HCC) patients after radiofrequency ablation (RFA) remains common; some studies have reported that insufficient ablative margin after RFA might contribute to HCC recurrence. The aim of this study was to investigate whether insufficient ablative safety margins determined by early computed tomography (CT) predicts HCC recurrence after RFA. This retrospective study recruited patients with a single HCC lesion after RFA in our department between May 2013 and March 2014. … Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1

Citation Types

1
65
0

Year Published

2015
2015
2022
2022

Publication Types

Select...
10

Relationship

1
9

Authors

Journals

citations
Cited by 87 publications
(66 citation statements)
references
References 27 publications
1
65
0
Order By: Relevance
“…However, in previous combination studies with TACE, the median OS ranged from 18 months (shortest) to 32 months (longest) ( Table 1 ), suggesting that the duration of the study needs to be extremely long when evaluating OS as a primary endpoint. In clinical studies that are terminated early because of tumor progression or adverse effects, patients often receive various post-trial treatments, such as hepatic artery infusion chemotherapy [20][21][22] , ablation [23][24][25] , or systemic therapy [26][27][28][29] . In such cases, post-trial treatment likely affects OS, making it difficult to evaluate treatment outcomes using OS, especially in studies of TACE in patients with intermediate-stage HCC.…”
Section: Proposal Of a New Primary Endpoint In Tace Combination Trialsmentioning
confidence: 99%
“…However, in previous combination studies with TACE, the median OS ranged from 18 months (shortest) to 32 months (longest) ( Table 1 ), suggesting that the duration of the study needs to be extremely long when evaluating OS as a primary endpoint. In clinical studies that are terminated early because of tumor progression or adverse effects, patients often receive various post-trial treatments, such as hepatic artery infusion chemotherapy [20][21][22] , ablation [23][24][25] , or systemic therapy [26][27][28][29] . In such cases, post-trial treatment likely affects OS, making it difficult to evaluate treatment outcomes using OS, especially in studies of TACE in patients with intermediate-stage HCC.…”
Section: Proposal Of a New Primary Endpoint In Tace Combination Trialsmentioning
confidence: 99%
“…Because most patients are diagnosed with advanced disease stages, only 30% of patients receive potentially curative therapies, such as surgical resection [2,3,4], transplantation [5,6,7,8] or percutaneous ablation [9,10,11,12,13]. A majority of patients with unresectable HCC usually undergo palliative treatments, such as transarterial chemoembolization (TACE) [14,15,16], hepatic arterial infusion chemotherapy (HAIC) [17] and systemic chemotherapy, including therapy using molecular targeted agents [17,18,19,20].…”
Section: Introductionmentioning
confidence: 99%
“…This huge database is an extremely important asset that is not available in any other country. Because HCC was treated only by surgical resection [15,16,17] in the 1970s before locoregional therapy [18,19,20,21,22] was developed in the 1980s, the general rules describe surgery-related items and the macroscopic and histopathological findings of surgical specimens in immense detail. In contrast, descriptions of locoregional therapies, such as ablation [21] and transcatheter arterial chemoembolization (TACE) [13,23,24], were relatively scarce up until the fourth edition, which was published in 2001.…”
Section: General Rules For the Clinical And Pathological Study Of Primentioning
confidence: 99%