Literature DB >> 35035699

The longitudinal change of circulating tumor cell during chemotherapy and its correlation with disease features, treatment response and survival profile of advanced gallbladder carcinoma.

Yinping Wang1,2, Zhiqing Yuan1,2, Sibo Zhu3, Xunxia Bao3, Zhiliang Fu3, Timing Zhen3, Kaichen Xing3, Yijue Zhang4, Xinxing Li5,6, Jianhua Sun1,2, Qiwei Li1,2, Linshi Wu1,2.   

Abstract

The current study aimed to investigate the relation of circulating tumor cell (CTC) with clinicopathological features. In addition, its longitudinal change during chemotherapy and its correlation with prognosis in advanced gallbladder carcinoma (GBC) patients were explored. Totally 45 unresectable, locally advanced or metastatic GBC patients who underwent chemotherapy were enrolled in this prospective study. The CTC in 7.5 ml blood was detected at pre-treatment and 3 months post-treatment. CTC was almost detectable in all advanced GBC patients before treatment, whose count was positively correlated with metastatic disease (vs. local advanced disease) (P=0.002), number of organs with metastases (P=0.006), and CA199 level (P=0.002). After treatment, CTC count declined from 4.0 (range: 0.0-83.0) at pre-treatment to 2.0 (range: 0.0-36.0) at post-treatment (P=0.003). Interestingly, pre-treatment CTC count (P=0.270) was of no difference, while post-treatment CTC count was lower (P=0.038) in objective-response patients compared to that in non-objective-response patients; meanwhile, both pre-treatment CTC count (P=0.017) and post-treatment CTC count (P<0.001) were lower in disease-control patients compared with those in non-disease-control patients. Importantly, pre-treatment CTC count ≥2 (versus <2) was only correlated with worse progression-free survival (PFS) (P=0.014) but not overall survival (OS) (P=0.057); while pre-treatment CTC count ≥5 (versus <5), post-treatment CTC count ≥2 (versus <2), post-treatment CTC count ≥5 (versus <5), CTC count up (versus equal/down) were all correlated with poor PFS and OS (all P<0.050). In conclusion, higher CTC count during chemotherapy correlates with worse treatment response, PFS and OS in advanced GBC patients, which implies that CTC measurement may optimize the prognostication and individualized treatment in these patients. AJTR
Copyright © 2021.

Entities:  

Keywords:  Advanced gallbladder carcinoma; chemotherapy; circulating tumor cell; clinicopathological features; prognosis

Year:  2021        PMID: 35035699      PMCID: PMC8748159     

Source DB:  PubMed          Journal:  Am J Transl Res        ISSN: 1943-8141            Impact factor:   4.060


  19 in total

Review 1.  Clinical indications for, and the future of, circulating tumor cells.

Authors:  Dominic H Moon; Daniel P Lindsay; Seungpyo Hong; Andrew Z Wang
Journal:  Adv Drug Deliv Rev       Date:  2018-04-05       Impact factor: 15.470

Review 2.  Staging, Treatment, and Future Approaches of Gallbladder Carcinoma.

Authors:  Sanjeev Kumar Shukla; Govind Singh; K S Shahi; Prabhat Pant
Journal:  J Gastrointest Cancer       Date:  2018-03

Review 3.  Current management of gallbladder carcinoma.

Authors:  Andrew X Zhu; Theodore S Hong; Aram F Hezel; David A Kooby
Journal:  Oncologist       Date:  2010-02-10

Review 4.  Circulating Tumor Cells: Diagnostic and Therapeutic Applications.

Authors:  Eric Lin; Thong Cao; Sunitha Nagrath; Michael R King
Journal:  Annu Rev Biomed Eng       Date:  2018-03-14       Impact factor: 9.590

Review 5.  Clinical Applications of Circulating Tumor Cells and Circulating Tumor DNA as Liquid Biopsy.

Authors:  Catherine Alix-Panabières; Klaus Pantel
Journal:  Cancer Discov       Date:  2016-03-11       Impact factor: 39.397

6.  Circulating Tumor Cells for Predicting the Prognostic of Patients with Hepatocellular Carcinoma: A Meta Analysis.

Authors:  Jun-Li Fan; Yi-Fei Yang; Chun-Hui Yuan; Hao Chen; Fu-Bing Wang
Journal:  Cell Physiol Biochem       Date:  2015

Review 7.  Detection of Circulating Tumor Cells and Their Implications as a Biomarker for Diagnosis, Prognostication, and Therapeutic Monitoring in Hepatocellular Carcinoma.

Authors:  Joseph C Ahn; Pai-Chi Teng; Pin-Jung Chen; Edwin Posadas; Hsian-Rong Tseng; Shelly C Lu; Ju Dong Yang
Journal:  Hepatology       Date:  2021-01-18       Impact factor: 17.425

8.  Circulating tumor cells as a potential biomarker for postoperative clinical outcome in HBV-related hepatocellular carcinoma.

Authors:  Xinping Ye; Guanghui Li; Chuangye Han; Quanfa Han; Liming Shang; Hao Su; Bowen Han; Yizhen Gong; Guodong Lu; Tao Peng
Journal:  Cancer Manag Res       Date:  2018-11-15       Impact factor: 3.989

Review 9.  A conduit to metastasis: circulating tumor cell biology.

Authors:  Douglas S Micalizzi; Shyamala Maheswaran; Daniel A Haber
Journal:  Genes Dev       Date:  2017-09-15       Impact factor: 11.361

10.  Clinical value of circulating tumor cells for the diagnosis and prognosis of hepatocellular carcinoma (HCC): A systematic review and meta-analysis.

Authors:  Kai Cui; Yang Ou; Yangyang Shen; Sheng Li; Ziqiang Sun
Journal:  Medicine (Baltimore)       Date:  2020-10-02       Impact factor: 1.817

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