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Eur Urol. 2017 Feb;71(2):183-192. doi: 10.1016/j.eururo.2016.07.008. Epub 2016 Jul 21.

Intratumoral and Intertumoral Genomic Heterogeneity of Multifocal Localized Prostate Cancer Impacts Molecular Classifications and Genomic Prognosticators.

Author information

1
Department of Biostatistics and Bioinformatics, Roswell Park Cancer Institute, Buffalo, NY, USA.
2
Department of Cancer Biology, Cleveland Clinic, Cleveland, OH, USA.
3
Department of Cancer Genetics, Roswell Park Cancer Institute, Buffalo, NY, USA.
4
Center for Personalized Medicine, Roswell Park Cancer Institute, Buffalo, NY, USA.
5
Department of Pathology, Roswell Park Cancer Institute, Buffalo, NY, USA.
6
Department of Urology, Roswell Park Cancer Institute, Buffalo, NY, USA.
7
Department of Cancer Biology, Cleveland Clinic, Cleveland, OH, USA; Department of Urology, Cleveland Clinic, Cleveland, OH, USA; Department of Hematology/Medical Oncology, Cleveland Clinic, Cleveland, OH, USA. Electronic address: heemerh@ccf.org.

Abstract

BACKGROUND:

Next-generation sequencing is revealing genomic heterogeneity in localized prostate cancer (CaP). Incomplete sampling of CaP multiclonality has limited the implications for molecular subtyping, stratification, and systemic treatment.

OBJECTIVE:

To determine the impact of genomic and transcriptomic diversity within and among intraprostatic CaP foci on CaP molecular taxonomy, predictors of progression, and actionable therapeutic targets.

DESIGN, SETTING, AND PARTICIPANTS:

Four consecutive patients with clinically localized National Comprehensive Cancer Network intermediate- or high-risk CaP who did not receive neoadjuvant therapy underwent radical prostatectomy at Roswell Park Cancer Institute in June-July 2014. Presurgical information on CaP content and a customized tissue procurement procedure were used to isolate nonmicroscopic and noncontiguous CaP foci in radical prostatectomy specimens. Three cores were obtained from the index lesion and one core from smaller lesions. RNA and DNA were extracted simultaneously from 26 cores with ≥90% CaP content and analyzed using whole-exome sequencing, single-nucleotide polymorphism arrays, and RNA sequencing.

OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS:

Somatic mutations, copy number alternations, gene expression, gene fusions, and phylogeny were defined. The impact of genomic alterations on CaP molecular classification, gene sets measured in Oncotype DX, Prolaris, and Decipher assays, and androgen receptor activity among CaP cores was determined.

RESULTS AND LIMITATIONS:

There was considerable variability in genomic alterations among CaP cores, and between RNA- and DNA-based platforms. Heterogeneity was found in molecular grouping of individual CaP foci and the activity of gene sets underlying the assays for risk stratification and androgen receptor activity, and was validated in independent genomic data sets. Determination of the implications for clinical decision-making requires follow-up studies.

CONCLUSIONS:

Genomic make-up varies widely among CaP foci, so care should be taken when making treatment decisions based on a single biopsy or index lesions.

PATIENT SUMMARY:

We examined the molecular composition of individual cancers in a patient's prostate. We found a lot of genetic diversity among these cancers, and concluded that information from a single cancer biopsy is not sufficient to guide treatment decisions.

KEYWORDS:

Actionable target; Active surveillance; Androgen deprivation therapy; Castration; Indolent; Personalized medicine; Prostatic adenocarcinoma; Radiation therapy; Somatic alterations

PMID:
27451135
PMCID:
PMC5906059
DOI:
10.1016/j.eururo.2016.07.008
[Indexed for MEDLINE]
Free PMC Article

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