论文已发表
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Authors Ye X, Li G, Han C, Han Q, Shang L, Su H, Han B, Gong Y, Lu GD, Peng T
Received 27 May 2018
Accepted for publication 6 August 2018
Published 15 November 2018 Volume 2018:10 Pages 5639—5647
DOI https://doi.org/10.2147/CMAR.S175489
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Colin Mak
Peer reviewer comments 3
Editor who approved publication: Professor Raphael Catane
Background: This
study aimed to determine if the number of circulating tumor cells (CTCs) and
changes in their numbers affected tumor recurrence and metastasis after
surgical resection in patients with hepatitis B virus (HBV)-related hepatocellular
carcinoma (HCC).
Methods: The
primary endpoints were overall survival (OS) and progression-free survival
(PFS). A total of 42 patients with HCC were selected from the First Affiliated
Hospital of Guangxi Medical College from 2014 to 2017. CTCs were counted 1 day
prior to and 30 days after surgical excision of HCC using the CanPatrol™
system.
Results: Numbers
of CTCs (> 2 CTCs and > 5 CTCs per 5 ml peripheral blood) were
significantly associated with Edmondson stage in HBV-related HCC prior to
surgery (P =
0.004 and 0.014, respectively). However there were no significant associations
between other tested clinicopathological factors and CTC counts. Postoperative
CTC counts (> 2 and > 5) and pre/postoperative change in CTC counts were
significantly associated with PFS (P = 0.02, 0.009, and 0.001, respectively), but
not with OS. Receiver operating characteristic curve analysis showed that
pre/postoperative changes in the CTC count were a better predictor of
performance than absolute count. The postoperative CTC count was also
significantly associated with positive TP53 expression (P <
0.05).
Conclusion: These
results demonstrate that postoperative CTC counts (> 2 and > 5) and
changes in CTC counts may be independent prognostic indicators for PFS in
patients with HBV-related HCC, with the change in number of CTCs showing better
predictive performance.
Keywords: circulating
tumor cell, hepatocellular carcinoma, progression-free survival, overall
survival
