Evidence map›Paper›PMID 26544731›Full record

ArticleOncotarget2016

pERK/pAkt phenotyping in circulating tumor cells as a biomarker for sorafenib efficacy in patients with advanced hepatocellular carcinoma.

Jun Li, Lehua Shi, Xiaofeng Zhang, Bin Sun, Yefa Yang, Naijian Ge, Huiying Liu, Xia Yang, Lei Chen, Haihua Qian and 2 more

Abstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 2 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

37 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Utility of Liquid Biopsy Analysis in Detection of Hepatocellular Carcinoma, Determination of Prognosis, and Disease Monitoring: A Systematic Review.Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association · 2020
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Jun LiEastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai, China.
Lehua ShiEastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai, China.
Xiaofeng ZhangEastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai, China.
Bin SunEastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai, China.
Yefa YangEastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai, China.
Naijian GeEastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai, China.
Huiying LiuEastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai, China.
Xia YangEastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai, China.
Lei ChenEastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai, China.
Haihua QianEastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai, China.
Mengchao WuEastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai, China.
Zhengfeng YinEastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sorafenib is a multikinase inhibitor approved for the treatment of advanced hepatocellular carcinoma (HCC). However, therapeutic response to sorafenib was not equal among HCC patients. Here we present a novel system to provide quantitative information concerning sorafenib-related targets by simultaneous detection of phosphorylated ERK (pERK) and pAkt expressions in circulating tumor cells (CTCs) isolated from HCC patients. Our results showed that 90.0% of patients had a molecular classification of tissues concordant with that of CTCs. CTC counts showed a shaper decline in patients with pERK+/pAkt- CTCs after two weeks of sorafenib treatment (P < 0.01). Disease control rates were significantly different between patients with pERK+/pAkt- CTCs (11/15; 73.3%) and those without (13/44; 29.5%) (P < 0.05). Univariate and multivariate analysis indicated pERK+/pAkt- CTCs as an independent predictive factor of progression-free survival (PFS) (hazard ratio = 9.389; P < 0.01). PFS correlated with the proportion of pERK+/pAkt- CTCs (r = 0.968, P < 0.01), and was higher in patients with ≥ 40% pERK+/pAkt- CTCs compared to those with < 40% (8.4 vs. 1.3 mo; P < 0.05). In a validation set of twenty HCC patients, CTCs from patients with ≥ 40% pERK+/pAkt- CTCs had significantly higher inhibition rates of spheroid formation compared to those with < 40% (61.2 vs. 19.8%; P < 0.01). Our findings demonstrated that CTCs can be used in place of tumor tissue for characterization of pERK/pAkt expression. pERK+/pAkt- CTCs are most sensitive to sorafenib and an independent predictive factor of PFS in HCC patients treated with sorafenib.

Indexed as

Antineoplastic AgentsApoptosisBiomarkers, TumorBlotting, WesternCarcinoma, HepatocellularCell ProliferationExtracellular Signal-Regulated MAP KinasesFemaleFluorescent Antibody TechniqueFollow-Up StudiesHumansImmunoenzyme TechniquesLiver NeoplasmsMaleMiddle AgedNeoplasm StagingAntineoplastic AgentsBiomarkers, TumorExtracellular Signal-Regulated MAP KinasesNiacinamidePhenylurea CompoundsProto-Oncogene Proteins c-aktSorafenibcirculating tumor cellsERK/Akthepatocellular carcinomasorafenib

Identifiers

PMID26544731
PMCPMC4823061

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.