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Introduction
Prostate cancer is the second most common cancer in men and one of the most common cancers in men >50 years of age.
Epidemiology
In Asia, prostate cancer is one of the most diagnosed cancers, leading to as many as 120,485 deaths in 2022, the highest among the different continents. Prostate cancer has the third highest incidence in the Philippines, accounting for 9,764 new cases in 2022 (lung cancer and colorectal cancer being more common). In that same year, prostate cancer caused as many as 3,850 deaths in the Philippines.
Pathophysiology
The prostate is a male sex glandular structure located in the pelvis at the base of the penis. Prostate cancer arises from the epithelium, normally in the peripheral glandular portion of the prostate. Key to the pathogenesis of prostate cancer is its heavy reliance on androgenic reliance, that is why hormonal therapy has been so effective. However, castrate-resistant tumors are thought to have mutations that improve the functional activity of the androgen receptor, sometimes even generating intracellular androgens. Malignant transformation involves what is called prostatic intraepithelial neoplasia (PIN) as precursor in the peripheral basal cells. Progressive accumulation of genetic alterations (eg androgen receptor bypass, tumor suppressor gene inactivation, etc.) is postulated to facilitate cellular transformation from normal epithelium to PIN, invasive neoplasia, and then castration resistance.
Risk Factors
The risk of developing
prostate cancer increases with age, particularly among men >50 years old. A
positive family history, either first- or second-degree relatives diagnosed with
metastatic prostate, ovarian, breast (female ≤45 years old), colorectal,
endometrial (≤50 years old) or pancreatic cancer, and those with ≥2 first- or
second-degree relatives diagnosed with prostate, breast, colorectal, or
endometrial cancer at any age are also at risk.
Genetic mutations such
as breast cancer gene 1 (BRCA1), breast cancer gene 2 (BRCA2)
mutations, ataxia telangiectasia mutated (ATM), checkpoint kinase 2 (CHEK2),
homeobox B13 (HOXB13), epithelial cellular adhesion molecule (EPCAM),
nibrin (NBN), tumor protein 53 (TP53), partner and localizer of BRCA2
(PALB2), deoxyribonucleic acid (DNA) mismatch repair genes (mutS
homolog 2 [MSH2], mutL homolog 1 [MLH1], Lynch syndrome, mutS
homolog 6 [MSH6], post-meiotic segregation increased 2 [PMS2]),
and insulin-like growth factor-1 (IGF-1) are all implicated in the development
of prostate cancer.
Ethnicity, especially
those of African ancestry and Ashkenazi Jewish descent, and chemical exposures
(eg toxic combustion products) are also risk factors for the development of the
disease. Other risk factors under research include a positive medical history
of inflammation of the prostate gland (eg prostatitis, sexually transmitted
diseases [STDs], proliferative inflammatory atrophy [PIN]) and vasectomy.