Development and validation of circulating tumour cell enumeration (Epic Sciences) as a prognostic biomarker in men with metastatic castration-resistant prostate cancer

被引:27
|
作者
Scher, H. I. [1 ,2 ]
Armstrong, A. J. [3 ]
Schonhoft, J. D. [4 ]
Gill, A. [4 ]
Zhao, J. L. [1 ]
Barnett, E. [1 ]
Carbone, E. [1 ]
Lu, J. [4 ]
Antonarakis, E. S. [5 ]
Luo, J. [5 ]
Tagawa, S. [2 ]
dos Anjos, C. H. [1 ]
Yang, Q. [6 ]
George, D. [3 ]
Szmulewitz, R. [6 ]
Danila, D. C. [1 ,2 ]
Wenstrup, R. [4 ,7 ]
Gonen, M. [1 ]
Halabi, S. [3 ,6 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Med, Genitourinary Oncol Serv, 1275 York Ave, New York, NY 10021 USA
[2] Weill Cornell Med Coll, Dept Med, New York, NY USA
[3] Duke Univ, Duke Canc Inst Ctr Prostate & Urol Canc, Durham, NC USA
[4] Epic Sci, San Diego, CA USA
[5] Johns Hopkins Univ, Baltimore, MD USA
[6] Duke Univ, Dept Biostat & Bioinformat, Durham, NC USA
[7] Univ Chicago, Chicago, IL 60637 USA
关键词
CTC; Prognosis; Biomarker; Prostate cancer; FREE SURVIVAL; PROGRESSION; MARKERS; DISEASE; MODEL;
D O I
10.1016/j.ejca.2021.02.042
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To evaluate the prognostic significance of circulating tumour cell (CTC) number determined on the Epic Sciences platform in men with metastatic castration-resistant prostate cancer (mCRPC) treated with an androgen receptor signalling inhibitor (ARSI). Patients and methods: A pre-treatment blood sample was collected from men with progressing mCRPC starting either abiraterone or enzalutamide as a first-, second- or third-line systemic therapy at Memorial Sloan Kettering Cancer Center (Discovery cohort, N=171) or as a first- or second-line therapy as part of the multicenter PROPHECY trial (NCT02269982) (Validation cohort, N = 107). The measured CTC number was then associated with overall survival (OS) in the Discovery cohort, and progression-free survival (PFS) and OS in the Validation cohort. CTC enumeration was also performed on a concurrently obtained blood sample using the CellSearch (R) Circulating Tumor Cell Kit. Results: In the MSKCC Discovery cohort, CTC count was a statistically significant prognostic factor of OS as a dichotomous (<3 CTCs/ mL versus > 3 CTCs/ mL; hazard ratio [HR] = 1.8 [95% confidence interval {CI} 1.3-3.0]) and a continuous variable when adjusting for line of therapy, presence of visceral metastases, prostate-specific antigen, lactate dehydrogenase and alkaline phosphatase. The findings were validated in an independent datas et from PROPHECY (HR [95% CI] = 1.8 [1.1-3.0] for OS and 1.7 [1.1-2.9] for PFS). A strong correlation was also observed between CTC counts determined in matched samples on the CellSearch (R) and Epic platforms (r = 0.84). Conclusion: The findings validate the prognostic significance of pretreatment CTC number determined on the Epic Sciences platform for predicting OS in men with progressing mCRPC starting an ARSI. (C) 2021 Published by Elsevier Ltd.
引用
收藏
页码:83 / 94
页数:12
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