Abstract

Prostate cancer is the second most common and fifth most aggressive neoplasm among men worldwide. It is particularly incident in high human development index (HDI) nations, with an estimated one in seven men in the US receiving a prostate cancer diagnosis in their lifetime. A rapid rise and then fall in prostate cancer incidence in the US and Europe corresponded to the implementation of widespread prostate specific antigen (PSA) testing in 1986 and then subsequent fall from favor due to high rates of false positives, overdiagnosis, and overtreatment (as many as 20–50% of men diagnosed could have remained asymptomatic in their lifetimes). Though few risk factors have been characterized, the best known include race (men of African descent are at higher risk), genetics (e.g., BRCA1/2 mutations), and obesity. The Gleason scoring system is used for histopathological staging and is combined with clinical staging for prognosis and treatment. National guidelines have grown more conservative over the past decades in management, recommending watchful waiting and observation in older men with low to intermediate risk disease. Among higher risk patients, prostatectomy (robotic is preferred) and/or external beam radiotherapy is the most common interventions, followed by ADT maintenance. Following progression on androgen deprivation therapy (ADT) (known as castration-resistance), next generation endocrine therapies like enzalutamide, often in combination with cytotoxic agent docetaxel, are standard of care. Other promising treatments include Radium-223 for bone metastases, pembrolizumab for programmed death ligand-1 (PDL1) and microsatellite instability (MSI) high disease, and poly ADP ribose polymerase (PARP) inhibitors for those with mutations in homologous recombination (most commonly BRCA2).

Highlights

  • One in seven men in the US [1] and one in 25 worldwide [2] is likely to receive a prostate cancer diagnosis within his lifetime

  • BRCA2 carriers are recommended for prostate cancer screening beginning at age 40 [7]

  • If the biopsy is positive, the cancer is graded by Gleason Score. Approved molecular biomarkers such as Decipher, Oncotype DX Prostate, Prolaris, or ProMark are recommended by the NCCN guidelines for low-risk disease but not by the American Society of Clinical Oncology (ASCO) or the American Urological Association (AUA)

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Summary

Introduction

One in seven men in the US [1] and one in 25 worldwide [2] is likely to receive a prostate cancer diagnosis within his lifetime. The alkalinity of prostatic fluid helps to protect the sperm in the acidic environment of the (BPH), causing symptoms (e.g., urinary frequency due to bladder compression) in one-third of men vagina [3]. BPH has been characterized by some as a stepping stone to prostate causing symptoms (e.g., urinary frequency due to bladder compression) in one-third of men over 60 cancer tumorigenesis due to common histopathology and molecular drivers, but their precise and about half over 80 [4]. Recent developments in though many point to the ready accessibility of PSA testing as a chief driver of rising incidence, the ever-evolving landscape of prostate cancer epidemiology, staging and management guidelines over-diagnosis, and over-treatment of prostate cancer [7,8]. Landscape of prostate cancer epidemiology, staging and management guidelines are summarized below

Incidence
16 African
Mortality
Survival
Risk Factors
[16]. (Figures
Genetics
Obesity
Other Risk Factors
Diagnosis
Grading and Staging
Treatment and Management
Findings
Conclusions
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