Literature DB >> 27273062

A Novel System for Estimating Residual Disease and Pathologic Response to Neoadjuvant Treatment of Prostate Cancer.

Claire Murphy1, Lawrence True1, Funda Vakar-Lopez1, Jing Xia2, Roman Gulati2, Bruce Montgomery3, Maria Tretiakova1.   

Abstract

BACKGROUND: Pathologic variables that characterize response of prostate carcinoma to current neoadjuvant therapy have not been characterized in detail. This study reports (i) the histological features of prostate cancer treated with abiraterone and enzalutamide and inter-pathologist variance in identifying these features, and (ii) the effect of the novel androgen deprivation agents on residual cancer volume.
METHODS: We reviewed sections of prostatectomies from 37 patients treated with neoadjuvant agents and 22 untreated patients, tabulated the frequency of nine features of cancer (intact cancer glands, isolated cancer cells, poorly formed glands, cribriform architecture, clear spaces, intraductal carcinoma, solid sheets of cancer cells, prominent nucleoli, and previously described ABC grouping) and two features of benign glands (prominent basal cells and coalescent corpora amylacea). We used several methods, including a novel metric (visual grid system), to estimate residual tumor volume.
RESULTS: The most highly reproducible features were ABC grouping (κ = 0.56-0.7), presence of intraductal carcinoma (κ = 0.34-0.72), cribriform architecture (κ = 0.42-0.68), solid sheets of tumor cells (κ = 0.44-0.56), and coalescent corpora amylacea (κ = 0.4-0.54). Among poorly reproducible features were prominent nucleoli (κ = 0.03-0.11), clear spaces (κ = 0.05-0.07), and poorly formed cancer glands (κ = 0.02-0.1). Determination of tumor mass was excellent regardless of the method used-maximum tumor size (κ = 0.9-0.94), tumor area (κ = 0.94-0.96), and grid-based tumor cellularity (κ = 0.9).
CONCLUSIONS: We propose using a set of parameters including maximum tumor size, tumor area/volume, cellularity, volume, and ABC grouping for evaluating radical prostatectomies post-neoadjuvant therapy. Prostate 76:1285-1292, 2016.
© 2016 Wiley Periodicals, Inc. © 2016 Wiley Periodicals, Inc.

Entities:  

Keywords:  cellularity; interobserver variability; neoadjuvant; prostate cancer; reproducibility; residual disease

Mesh:

Year:  2016        PMID: 27273062      PMCID: PMC4988926          DOI: 10.1002/pros.23215

Source DB:  PubMed          Journal:  Prostate        ISSN: 0270-4137            Impact factor:   4.104


  34 in total

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3.  Percentage carcinoma as a measure of prostatic tumor size in radical prostatectomy tissues.

Authors:  P A Humphrey; R T Vollmer
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4.  Randomized prospective study comparing radical prostatectomy alone versus radical prostatectomy preceded by androgen blockade in clinical stage B2 (T2bNxM0) prostate cancer. The Lupron Depot Neoadjuvant Prostate Cancer Study Group.

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5.  Pathology of androgen deprivation therapy in prostate carcinoma. A comparative study of 173 patients.

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6.  A streamlined three-dimensional volume estimation method accurately classifies prostate tumors by volume.

Authors:  Michael E Chen; Dennis Johnston; Adriana O Reyes; Cindy P Soto; R Joseph Babaian; Patricia Troncoso
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Authors:  Peter A Humphrey
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2.  Targeting backdoor androgen synthesis through AKR1C3 inhibition: A presurgical hormonal ablative neoadjuvant trial in high-risk localized prostate cancer.

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Review 3.  Neoadjuvant hormonal therapy before radical prostatectomy in high-risk prostate cancer.

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