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Analytic and Clinical Validation of a Prostate Cancer-enhanced Messenger RNA Detection Assay in Whole Blood As a Prognostic Biomarker for Survival

Overview
Journal Eur Urol
Specialty Urology
Date 2013 Aug 20
PMID 23954088
Citations 39
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Abstract

Background: Biomarkers based on detecting prostate cancer (PCa)-specific transcripts in blood are associated with inferior outcomes, but their validation in a clinical context is lacking.

Objective: To determine whether detecting enhanced transcripts for PCa in whole blood using an analytically valid assay has prognostic significance relative to circulating tumor cell (CTC) enumeration.

Design, Setting, And Participants: The detection of KLK3, KLK2, HOXB13, GRHL2, and FOXA1 in whole blood by reverse transcription polymerase chain reaction (RT-PCR) was studied in 97 men with metastatic castration-resistant PCa (mCRPC) as a prognostic factor for overall survival.

Intervention: The 2.5 ml of blood was collected in PAXgene tubes for total RNA extraction and 7.5 ml for CTC enumeration from patients with progressive mCRPC.

Outcome Measurements And Statistical Analysis: PCa-enriched genes were detected using a sensitive RT-PCR assay in whole blood from patients with mCRPC. Analytical validity of the assay was established in a clinical laboratory environment. The frequency of detecting transcripts was compared to CTC enumeration using CellSearch in an independent data set and survival associations were explored by concordance probability estimate (CPE).

Results And Limitations: Two or more genes were detected by PCR in 53% of patients (51 of 97; 95% confidence interval [CI], 43-63%), and unfavorable CTC counts (five of more cells) were seen in 46% (45 of 97; 95% CI, 36-56%). Importantly, transcripts were detectable in 11 of 52 patients with favorable CTC counts (21%; 95% CI, 8-35%). Transcript detection predicted overall survival in a proportional hazards model. Significantly, the predictive accuracy of RT-PCR detection in combination with CTC enumeration had a CPE of 0.752 (standard error: 0.038), although this was limited by the number of patients evaluated.

Conclusions: This validated RT-PCR assay detecting prostate-specific RNA in whole blood is prognostic for survival and may assess patient risk in tandem with CellSearch CTC enumeration. Its clinical utility is being prospectively explored.

Citing Articles

Liquid biopsy-based targeted gene screening highlights tumor cell subtypes in patients with advanced prostate cancer.

Derderian S, Vesval Q, Wissing M, Hamel L, Cote N, Vanhuyse M Clin Transl Sci. 2022; 15(11):2597-2612.

PMID: 36172886 PMC: 9652435. DOI: 10.1111/cts.13372.


Whole blood expression as a prognostic biomarker in metastatic hormone-sensitive and castration-resistant prostate cancer.

Kwan E, Fettke H, Crumbaker M, Docanto M, To S, Bukczynska P Transl Androl Urol. 2021; 10(4):1688-1699.

PMID: 33968657 PMC: 8100842. DOI: 10.21037/tau-20-1444.


Liquid biopsy reveals KLK3 mRNA as a prognostic marker for progression free survival in patients with metastatic castration-resistant prostate cancer undergoing first-line abiraterone acetate and prednisone treatment.

Boerrigter E, Benoist G, van Oort I, Verhaegh G, van Hooij O, Groen L Mol Oncol. 2021; 15(9):2453-2465.

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Spotlight on the Granules (Grainyhead-Like Proteins) - From an Evolutionary Conserved Controller of Epithelial Trait to Pioneering the Chromatin Landscape.

Sundararajan V, Pang Q, Choolani M, Huang R Front Mol Biosci. 2020; 7:213.

PMID: 32974388 PMC: 7471608. DOI: 10.3389/fmolb.2020.00213.


Analysis of AR-FL and AR-V1 in Whole Blood of Patients with Castration Resistant Prostate Cancer as a Tool for Predicting Response to Abiraterone Acetate.

Stuopelyte K, Sabaliauskaite R, Bakavicius A, Haflidadottir B, Visakorpi T, Vaananen R J Urol. 2020; 204(1):71-78.

PMID: 32068491 PMC: 7301408. DOI: 10.1097/JU.0000000000000803.


References
1.
Danila D, Fleisher M, Scher H . Circulating tumor cells as biomarkers in prostate cancer. Clin Cancer Res. 2011; 17(12):3903-12. PMC: 3743247. DOI: 10.1158/1078-0432.CCR-10-2650. View

2.
Kang X, Chen W, Kim R, Kang M, Park N . Regulation of the hTERT promoter activity by MSH2, the hnRNPs K and D, and GRHL2 in human oral squamous cell carcinoma cells. Oncogene. 2008; 28(4):565-74. PMC: 2919678. DOI: 10.1038/onc.2008.404. View

3.
Allard W, Matera J, Miller M, Repollet M, Connelly M, Rao C . Tumor cells circulate in the peripheral blood of all major carcinomas but not in healthy subjects or patients with nonmalignant diseases. Clin Cancer Res. 2004; 10(20):6897-904. DOI: 10.1158/1078-0432.CCR-04-0378. View

4.
Danila D, Pantel K, Fleisher M, Scher H . Circulating tumors cells as biomarkers: progress toward biomarker qualification. Cancer J. 2011; 17(6):438-50. PMC: 3985131. DOI: 10.1097/PPO.0b013e31823e69ac. View

5.
Ghossein R, Scher H, Gerald W, Kelly W, Curley T, Amsterdam A . Detection of circulating tumor cells in patients with localized and metastatic prostatic carcinoma: clinical implications. J Clin Oncol. 1995; 13(5):1195-200. DOI: 10.1200/JCO.1995.13.5.1195. View