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The Prognostic Value of Circulating Tumor Cells in Asian Neuroendocrine Tumors
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The Prognostic Value of Circulating Tumor Cells in Asian Neuroendocrine Tumors

Jason Chia-Hsun Hsieh, Guan-Yu Chen, David Da-Wei Jhou, Wen-Chi Chou, Chun-Nan Yeh, Tsann-Long Hwang, Hung-Chi Lin, Hui-Chun Chu, Hung-Ming Wang, Tzu-Chen Yen, …
Scientific reports, 卷.9(1), 頁碼.19917-10
27/12/2019
PMID: 31882775
Web of Science ID: WOS:000509284000004

摘要

Adult Aged Aged, 80 and over Biomarkers, Tumor - metabolism Disease-Free Survival Female Humans Kaplan-Meier Estimate Male Middle Aged Multivariate Analysis Neoplastic Cells, Circulating - pathology Neuroendocrine Tumors - pathology Prognosis Proportional Hazards Models Young Adult
Circulating tumor cells (CTC) play important roles in various cancers; however, few studies have assessed their clinical utility in neuroendocrine tumors. This study aimed to prospectively evaluate the prognostic value of CTC counts in Asian patients with neuroendocrine tumors before and during anti-cancer therapy. Patients who were diagnosed with unresectable histological neuroendocrine tumors between September 2011 and September 2017 were enrolled. CTC testing was performed before and during anti-cancer therapy using a negative selection protocol. Chromogranin A levels were also assessed. Univariate and multivariate Cox's proportional hazard model with forward LR model was performed to investigate the impact of independent factors on overall survival and progression-free survival. Kaplan-Meier method with log-rank tests were used to determine the difference among different clinicopathological signatures and CTC cutoff. The baseline CTC detection rate was 94.3% (33/35). CTC counts were associated with cancer stages (I-III vs. IV, P = 0.015), liver metastasis (P = 0.026), and neuroendocrine tumor grading (P = 0.03). The median progression-free survival and overall survivals were 12.3 and 30.4 months, respectively. In multivariate Cox regression model, neuroendocrine tumors grading and baseline CTC counts were both independent prognostic factors for progression-free survival (PFS, P = 0.005 and 0.015, respectively) and overall survival (OS, P = 0.018 and 0.023, respectively). In Kaplan-Meier analysis, lower baseline chromogranin A levels were associated with longer PFS (P = 0.024). Baseline CTC counts are associated with the clinicopathologic features of neuroendocrine tumors and are an independent prognostic factor for this malignancy.

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https://doi.org/10.1038/s41598-019-56539-z檢視
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