Circulating Tumor Cells in Biochemical Recurrence of Prostate Cancer

被引:14
作者
Aragon-Ching, Jeanny B. [1 ]
Siegel, Robert S. [1 ]
Frazier, Harold, II [2 ]
Andrawis, Ramez [2 ]
Hendricks, Frederick [2 ]
Phillips, Michael [2 ]
Jarrett, Thomas [2 ]
Guebre-Xabiher, Hiwot [1 ]
Patierno, Steven [3 ]
Simmens, Samuel J. [4 ]
机构
[1] George Washington Univ, Dept Med, Div Hematol & Oncol, Washington, DC 20037 USA
[2] George Washington Univ, Med Ctr, Dept Urol, Washington, DC 20037 USA
[3] Duke Canc Inst, Dept Med, Durham, NC USA
[4] George Washington Univ, Dept Epidemiol & Biostat, Washington, DC 20037 USA
关键词
Biochemical recurrence; Circulating tumor cells; Prostate cancer; Prostate specific antigen; PSA doubling times; PRACTICE GUIDELINE; PERIPHERAL-BLOOD; AMERICAN-SOCIETY; BREAST-CANCER; TRIAL; RADIOTHERAPY; SURVIVAL; SORAFENIB; BIOMARKER; ANTIGEN;
D O I
10.1016/j.clgc.2015.04.003
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Circulating tumor cells (CTCs) have shown prognostic importance in men with metastatic castration-resistant prostate cancer. Little information exists as to the yield of CTCs in men presenting with biochemical recurrence. This study sought to determine whether CTCs are detectable in such men and whether it correlates with known clinicopathologic parameters. Although the overall yield was low (8%), finding a detectable CTC raises a suspicion for metastatic disease in our series. Objective: Circulating tumor cells (CTCs) have known prognostic implications in metastatic castration-resistant prostate cancer, but little is known regarding its utility in biochemical recurrence (BR) of prostate cancer. The primary objectives were to determine whether CTCs are measurable in patients with BR and whether it can reliably predict prostate-specific antigen (PSA) increase and PSA doubling times (PSADTs). Methods: BR was identified in patients after prostatectomy or radiation or both, with a PSA increase of >= 0.2 for prior prostatectomy or >2 mg/dL increase for post-nadir in prior radiotherapy. CTCs were enumerated at baseline at the time of study entry using the CellSearch (Janssen Diagnostics, Raritan, NJ) test. Results: The median age for all 36 patients accrued was 69.5 years (range, 5191) with a median PSA of 1.65 ng/mL (range, 0.2-65.8). Gleason scores ranged from 5 to 9 (median, 7). The majority had prostatectomy (n = 25), external beam radiotherapy (n = 9), (Accuray, Sunnyvale, CA) (n = 1), and combined radiohormonal therapy (n = 1). PSADT ranged from 0.35 to 55 months, with a median of 7.43 months. The incidence of positive CTCs was 8.3% (3 patients), of whom 2 had biopsy-proven bony lesions on presenting with equivocal scans and PSADTs of 2.27 and 3.08 months, respectively. The third CTC-positive patient had a PSADT of 4.99 months. Conclusions: Obtaining CTCs in unselected patients presenting with BR has a relatively low yield. However, obtaining a positive CTC raises the suspicion of the presence of metastatic disease and may have utility for longitudinal follow-ups of patients with BR. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:E341 / E345
页数:5
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