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The longitudinal change of circulating tumor cell during chemotherapy and its correlation with disease features, treatment response and survival profile of advanced gallbladder carcinoma.
Wang, Yinping; Yuan, Zhiqing; Zhu, Sibo; Bao, Xunxia; Fu, Zhiliang; Zhen, Timing; Xing, Kaichen; Zhang, Yijue; Li, Xinxing; Sun, Jianhua; Li, Qiwei; Wu, Linshi.
Affiliation
  • Wang Y; Department of General Surgery, Renji Hospital, School of Medicine, Shanghai Jiaotong University Shanghai 201112, China.
  • Yuan Z; Department of Biliary-Pancreatic Surgery, Renji Hospital, School of Medicine, Shanghai Jiaotong University Shanghai 200127, China.
  • Zhu S; Department of General Surgery, Renji Hospital, School of Medicine, Shanghai Jiaotong University Shanghai 201112, China.
  • Bao X; Department of Biliary-Pancreatic Surgery, Renji Hospital, School of Medicine, Shanghai Jiaotong University Shanghai 200127, China.
  • Fu Z; Cinoasia Institute Shanghai 200438, China.
  • Zhen T; Cinoasia Institute Shanghai 200438, China.
  • Xing K; Cinoasia Institute Shanghai 200438, China.
  • Zhang Y; Cinoasia Institute Shanghai 200438, China.
  • Li X; Cinoasia Institute Shanghai 200438, China.
  • Sun J; Department of Anesthesiology, South Campus, Renji Hospital, School of Medicine, Shanghai Jiaotong University Shanghai 200127, China.
  • Li Q; Department of General Surgery, Changzheng Hospital, The Second Military Medical University Shanghai 200003, China.
  • Wu L; Department of Gastroenterological Surgery, Tongji Hospital, School of Medicine, Tongji University Shanghai 200065, China.
Am J Transl Res ; 13(12): 13590-13598, 2021.
Article in En | MEDLINE | ID: mdl-35035699
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.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Observational_studies Language: En Journal: Am J Transl Res Year: 2021 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Observational_studies Language: En Journal: Am J Transl Res Year: 2021 Document type: Article Affiliation country: China
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