The Navigation Model of Therapy: Why Awareness Changes Everything
November 16, 2025
Background
The disease is defined as the malignant transformation of cells in the prostate gland, a small, walnut-shaped organ that synthesizes seminal fluid. It is one of the prominent male cancers, most experienced by men who have reached old age.Â
Epidemiology
Global Incidence: It is statistically clinically documented that prostate carcinoma is the third most prevalent cancer in man. Research indicates that it accounts for around half of all cancer cases that develop and causes most cancer-related problems.Â
Prevalence: The rate of occurrence is not constant throughout the world and is affected by factors such as hereditary disposition, lifestyle parameters and other available programs.Â
Anatomy
Pathophysiology
Genetic Factors
Hereditary Prostate Cancer: About 5-10% of breast cancers could be attributed to hereditary factors and other genes including BRCA1 and BRCA2 and HOXB13.
Somatic Mutations: Somatic mutations which occur in prostate cells include those affecting the TP53 gene, PTEN, and ETS gene fusions such as TMPRSS2-ERG.
Molecular Pathways
Androgen Receptor (AR) Signaling: Testosterone and DHT are needed for prostate cancer development and progression; AR signaling is sustained in patients with minimal androgen levels (CRPC).Â
PI3K/AKT/mTOR Pathway: Dysregulation translates to proliferation; common alterations include PTEN loss.Â
Â
Cellular Changes
Hyperplasia and Dysplasia: Starts with PIN (prostatic intraepithelial neoplasia); HGPS is defined as high-grade PIN and is associated with invasive prostate cancer.
Invasive Carcinoma: Transitions from limited to invasive type located in lungs and spreads to legs and lymph nodes.
Hormonal Influence
Androgens: Playing a vital role in prostate growth; treatments aim at lowering androgen levels or inhibiting the AR pathways.
Estrogens and Other Hormones: Estrogen receptor signaling can affect the prostate cancer and hormonal homeostasis affects tumour progression.
Microenvironment and Inflammation
Tumor Microenvironment: Comprises cancer cells, characters of stroma, host leucocytes, and matrix ground substance, which supports cancer growth and promotes metastasis.Â
Chronic Inflammation: Among effects of obesity, it raises inflammatory cytokines which contribute to cancer development including prostate cancer.Â
Etiology
Age: Prostate cancer risk rises with age. Men over 50 are diagnosed with most instances.Â
Genetics: Prostate cancer risk has been associated with certain genes.Â
Race and ethnicity: Nevertheless, African American men were found to be at the highest risk for the disease than Hispanic and white men. Asian American males have the utmost protection against the disease.
Family history: A family history of the disease can also predispose a man. The risk is especially high if the relative was diagnosed when he was still young.Â
Genetics
Prognostic Factors
Stage: Prostate cancer stage also affects prognosis.Â
PSA level: Prostate specific antigen (PSA) is a marker or a protein that is released by the prostate gland. PSA is known to be a marker and might be found at high levels in men diagnosed with the prostate cancer.
Age and overall health: It was further observed that the men who are comparatively younger developed prostate cancer, the prognosis of which is generally much higher than that of men of relatively higher age.Â
Clinical History
Age Group:Â
Age 65 and Older: Men 65 years of age and older receive most prostate cancer diagnoses. This age group is affected by prostate cancer in about 60% of instances.Â
Ages 55 to 64: This age category is vulnerable to prostate cancer in high proportions as observed among men. More than a quarter of the patients are men over fifty-five; specifically, 25% of men are affected when they are between fifty-five and sixty-four years old.Â
Physical Examination
Prostate-Specific Antigen (PSA) TestÂ
Ultrasound and BiopsyÂ
Age group
Associated comorbidity
Associated activity
Acuity of presentation
Asymptomatic Presentation
Screening Detection: Most of the prostate cancer diagnosed after employing simple screening techniques like PSA or DRE. In these cases, the man does not manifest signs and symptoms and the cancer is invariably detected during other tests.
Early-Stage Disease: Prostate cases are often localized and have a better prognosis as they are easier to treat.
Symptomatic Presentation
Lower Urinary Tract Symptoms (LUTS):Â
Urinary Frequency: Persists, frequent or urgent to urinate specially at night known as nocturia.Â
Urgency: A compelling need to pee; a feeling of pressure that one must release urine.
Hesitancy: Difficulty starting urination.
Weak Stream: A reduction in the urine stream’s strength.
Incomplete emptying: Feeling that the bladder hasn’t been emptied.Â
Differential Diagnoses
Laboratory Studies
Imaging Studies
Procedures
Histologic Findings
Staging
Treatment Paradigm
Active Surveillance: This strategy is applied concerning low-grade malignancies or slowly progressive androgen-sensitive disease localized to the prostate with less than stage T2 tumor, small volume, clinically localized and not indicated for immediate treatment because of a low likelihood of symptoms or consequences in the coming years. It is controlled by going for routine tests such as PSA tests, digital rectal exams and infrequent biopsies just in case the cancer starts progressing.
Surgery (Prostatectomy): Radical prostatectomy is a surgical procedure that involves the removal of the entire prostate gland and is recommended for the early stage of prostate cancer, which has limited its spread to the prostate gland only. This can involve a direct approach, making an incision in the affected area, or it can involve endoscopic procedures like laparoscopic or robotic surgery.
Radiation Therapy: This can be employed as first-line therapy for prostate cancer that has not spread beyond the gland.Â
Types of radiation therapy include:
External Beam Radiation Therapy (EBRT): With the help of a particle accelerator located outside the body, rays with high energy are aimed at the prostate gland.
Brachytherapy: Iodine-125 in the form of radioactive seeds or pellets that are placed near the tumor within the prostate gland.
Proton Therapy: Sites protons instead of photons and this may reduce the chances of certain side effects especially those affecting the tissues surrounding the tumor.
Hormone Therapy (Androgen Deprivation Therapy ADT): Malignant prostate cells possess the potential for growth and survival with the help of male sex hormones or androgens such as testosterone. Hormone therapy works to decrease the levels of these hormones or prevent their action by using drugs or by carrying out the surgical removal of the testicles.
Chemotherapy: When the prostate cancer has affected other parts of the body in addition to the prostate gland and is PSA resistant. Chemotherapy medications are known to remove this abnormal cell tissues and decrease the slow of cancerous growth.Â
by Stage
by Modality
Chemotherapy
Radiation Therapy
Surgical Interventions
Hormone Therapy
Immunotherapy
Hyperthermia
Photodynamic Therapy
Stem Cell Transplant
Targeted Therapy
Palliative Care
nonpharmacological-approach-for-treating-prostate-cancer
Use of Antineoplastics, GNRH Agonist in treating prostate cancer
Role of Antineoplastics, Antiandrogen in treating prostate cancer
Chemotherapy modulating agents in treating prostate cancer
Sipuleucel-TÂ
Sipuleucel-T (Provenge) is considered as immunotherapy which is effective for individuals who have advanced prostate cancer. They operate through the enhancement of the patient’s immunity to fight the prostate cancerous cells.Â
Bisphosphonate derivatives in treating prostate cancer
Zolendronic acid (Zometa)Â
This is a bisphosphonate drug under the trade name Zometa, and it is approved for use in the treatment of prostate cancer especially in patients whose disease has advanced or has spread to the other parts of the body. It acts through prevention of bone resorption that is a process catalysed by osteoclasts, because the drug aids in maintaining a low incidence of skeletal related events (SREs) such as fractures, spinal cord compression, bone radiation or surgery.Â
role-of-surgery-in-treating-prostate-cancer
role-of-management-in-treating-prostate-cancer-specialty-urology-diagnosis-and-staging
Medication
Initial dose:
300
mg
Tablet
Orally 
once a day
30
days
Maintenance dose:
150
mg
Tablet
Orally 
once a day
continue until disease progression or severe health side effects
Dose Adjustments
• Mild or moderate impairment: no significant dose adjustment provided • Serious hepatic impairment: Avoid the use of nilutamide • Hepatotoxic during treatment (ALT > 2 x ULN or jaundice): permanently terminate the treatment
Metastatic cancer:
1000
mg
Orally 
once a day
in combination with prednisone 5 mg twice a day.
Or
500 mg orally once a day in combination with methyl prednisone 4 mg twice a day.
Dose Adjustments
Moderate hepatotoxicity: 125 mg once a day
Severe hepatotoxicity: discontinue the treatment
3.75
mg
Intramuscular (IM)
4
weeks
or 11.25 mg shown IM for every 12 weeks, or 22.5 mg given IM for every 24 weeks
Dose Adjustments
Renal Dose Adjustments:
There is no adjustment recommended
Liver Dose Adjustments:
There is no adjustment recommended
200 - 300
mg
Orally 
given in 2 to 3 divided doses in a day.
Or
300 mg IM once a week, reduce the dose to 300 mg once every 2 weeks depending on clinical symptoms.
Dose Adjustments
Meningioma: Terminate the cyproterone administration permanently.
Thrombophlebitis/thromboembolism: Discontinue treatment.
Prostate-specific antigen progression: discontinue cyproterone treatment and monitor for withdrawal symptoms.
Metastatic cancer:
20
mg/m^2
Intravenous (IV)
every 3 weeks
in combination with prednisone 10 mg orally throughout the treatment.
Dose Adjustments
Grade ≥3 diarrhea despite appropriate medication, fluid, and electrolyte replacement: Delay treatment until improvement or resolution, then reduce dose by 1 level.
Grade 2 peripheral neuropathy, delay treatment and reduce dose by 1 level.
Grade >3 peripheral neuropathy Discontinue.
Metastatic/non-metastatic:
250
mg
Orally 
3 times a day
in combination with a luteinizing hormone-releasing agonist
Dose Adjustments
Use of flutamide in severe hepatic impairment is contraindicated.
The use of flutamide is prohibited for patients under dialysis.
Metastatic:
160
mg
orally
once a day
Dose Adjustments
Metastatic/non-metastatic:
240
mg
Tablet
Orally 
once a day
in combination with continuous androgen deprivation therapy
Dose Adjustments
Grade 3 or higher toxicity: Hold the dosing temporarily until symptoms improve to grade 1 or lower and resume the dose with 120 to 180 mg. Cerebrovascular events, grade 3 or 4: discontinue the dosing Dermatologic toxicity: if not managed by oral antihistamines and topical corticosteroids, interrupt or reduce apalutamide dose until symptoms improve Fracture: manage with the use of bone-modifying agents Seizure: discontinue apalutamide dosing permanently Thyroid dysfunction: adjust/ reduce the dose initially, initiate thyroid replacement therapy if indicated
When bicalutamide is combined with an LHRH analog:
50
mg
Orally
once a day
Dose Adjustments
Renal Dose Adjustments
No adjustment required
Liver Dose Adjustments
Caution recommended.
The initial dose was 240 mg as two subcutaneous injections of 120 mg each at a concentration of 40 mg per ml.
80 mg is given as the Maintenance Dose for one subcutaneous injection at a concentration of 20 mg per ml every 28 days
the first maintenance dose should be administered 28 days only after the initial dose
Dose Adjustments
Renal Dose Adjustments:
No adjustment is recommended for mild renal impairment (CrCl 50-80 ml per min)
Use with caution for moderate to severe renal impairment (CrCl <50 ml per min)
Liver Dose Adjustments:
No adjustment is recommended for mild to moderate Hepatic Impairment (Child-Pugh A and B)
Data not available and used with caution for Severe Hepatic Impairment (Child-Pugh C)
Monthly implant: 3.6 mg subcutaneously placed in the upper abdominal wall for every 28days
3-month implant: 10.8 mg subcutaneously placed in the upper abdominal wall for every 12week
Long term treatment intended for unless clinically inappropriate
50 mg implant given SC for every 12 months
The maximum duration of treatment includes removing the implant after 12 months
Dose Adjustments
Renal Impairment:
Dose adjustment not required
Liver impairment:
No data available
55kBq/kg intravenous infusion for 1 minute. Repeat every four weeks for total of 6 weeks
Dose Adjustments
The volume of radium-223 to be administered to a patient should be calculated using the patient's body weight in kilograms, the dosage level of 55 kBq/kg or 1.49 microcurie/kg, the radioactivity concentration of the product at the reference date (1,100 kBq/mL or 30 microcurie/mL), and a decay correction factor to account for the physical decay of the radium-223
The formula for this calculation is (body weight in kg x dosage level) Ă· (decay factor x radioactivity concentration)
The decay correction factor can be found in the prescribing information based on the vial's reference date
Indicated for Metastatic Castration-Resistant Prostate Cancer
300 mg orally twice daily. Continue for a year or until unacceptable toxicity, disease recurrence, or whichever occurs first
rucaparib is a therapeutic agent for the treatment of prostate cancer in men who have been treated with taxane-based chemotherapy and androgen receptor-directed therapy before
A dose of 600 mg is administered orally twice daily
The medication is continued until the disease is reduced to acceptable toxicity
Dose Modifications
In case of adverse reactions, the dose is modified or reduced
The pattern of dose reduction goes like this
First dose reduction: 500 mg daily (two tablets of 250 mg per day)
Second dose reduction: 400 mg daily (two tablets of 200 mg per day)
Third dose reduction: 300 mg daily (one tablet of 300 mg per day)
Hepatic impairment
In case of mild to moderate impairment (total bilirubin <3 x upper limit of normal or AST > upper limit of normal): No dosage modification is recommended
In case of severe impairment (total bilirubin > 3 x upper normal limit and any AST), no studies performed
Renal impairment
In case of mild-to-moderate impairment (when CrCl is 30-89), no dose adjustment is required
In case of severe impairment (when CrCl <30 mL/min) or patients are on dialysis, no studies are performed
12-14 mg/m2 intravenous every 21 days for three weeks when combined with corticosteroids
The drug is indicated for non-operable prostate cancer
1.25-2.5 mg orally every 8 hours
500mg orally twice a day
lutetium lu 177 vipivotide tetraxetanÂ
Indicated in the treatment of Castration-Resistant Prostate Cancer in people who are treated with taxane chemotherapy and androgen receptor pathway inhibition
7.4 GBq intravenously every 6 weeks up to 6 doses or until the disease is progressed
lutetium lu 177 vipivotide tetraxetanÂ
Indicated in the treatment of Castration-Resistant Prostate Cancer in people who are treated with taxane chemotherapy and androgen receptor pathway inhibition
7.4 GBq intravenously every 6 weeks up to 6 doses or until the disease is progressed
Dose Modifications
If the treatment gets delayed for more than 4 weeks, discontinue the treatment
Reduce the dose by 20% (up to 5.9GBq) once
In the case of 2nd to 3rd-grade myelosuppression, reduce the dose by 20%
For 3rd-grade myelosuppression, discontinue permanently
In the case of renal and hepatic impairment, no dose adjustment is required
Indicated for Localized Prostate Cancer
The suggested dose is 3.66 mg/kg intravenously one time given by using the vascular-targeted photodynamic treatment process
1 mg administered intravenously by subcutaneous injection. The Intramuscular or subcutaneous route may administer depot formulations; the dosage and route may vary between brands and countries. For the UK: 3.75 mg as a single Intramuscular or subcutaneous injection every month or 11.25 mg as a Subcutaneous injection every three months are the depot preparations. As part of the US depot's preparations: 7.5 mg per month, 22.5 mg every three months, 30 mg every four months, or 45 mg every six months through Intramuscular or subcutaneous, depending on the preparation
250
mg
Tablets
Orally 
twice a day
The dose can be increased to 250mg orally every 6 hours after 14 days
The dose range may be 250mg to 1g per day
Advanced prostate carcinoma can be treated with this medication via SC administration with the recommended dose of 500 mcg for one week with 8-hour time intervals. After one week of SC administration, treatment can be shifted to the intranasal route from the 8th day
From the 8th day after SC administration, intranasal spray is given with the recommended dose of 400 mcg with 200 mcg sprayed into each nostril three times a day
Take a dose of 0.15 to 1.5 mg orally one time daily
synthetic conjugated estrogens, bÂ
synthetic conjugated estrogens, bÂ
1.25 - 2.5
mg
Tablets
Orally 
3 times a day
synthetic conjugated estrogens, bÂ
1.25 - 2.5
mg
Tablets
Orally 
3 times a day
These days, it is hardly ever used to treat prostate cancer due to its adverse consequences
It is sometimes administered to postmenopausal women who have breast cancer
Oral administration of 1-3 mg per day is the usual dosage for the treatment of prostate cancer
Dose Adjustments
Limited data is available
This drug, a synthetic estrogen, is prescribed to treat prostate cancer, menopausal symptoms, and deficiencies in ovarian function
The recommended dose is 12 to 25 mg via oral administration per day
Dose Adjustments
Limited data is available
100 mg intramuscularly, which is administered to the buttock on the day 1, 15, 29 (week 4) and after that every four weeks
Indicated for Metastatic prostate cancer
1000 mg orally once a day in combination with prednisone 5 mg twice a day
or
500 mg orally once a day in combination with methylprednisolone 4 mg twice a day
Dose adjustments for toxicity:
Moderate hepatotoxicity: 125 mg once a day
Severe hepatotoxicity: discontinue the treatment
Future Trends
The disease is defined as the malignant transformation of cells in the prostate gland, a small, walnut-shaped organ that synthesizes seminal fluid. It is one of the prominent male cancers, most experienced by men who have reached old age.Â
Global Incidence: It is statistically clinically documented that prostate carcinoma is the third most prevalent cancer in man. Research indicates that it accounts for around half of all cancer cases that develop and causes most cancer-related problems.Â
Prevalence: The rate of occurrence is not constant throughout the world and is affected by factors such as hereditary disposition, lifestyle parameters and other available programs.Â
Genetic Factors
Hereditary Prostate Cancer: About 5-10% of breast cancers could be attributed to hereditary factors and other genes including BRCA1 and BRCA2 and HOXB13.
Somatic Mutations: Somatic mutations which occur in prostate cells include those affecting the TP53 gene, PTEN, and ETS gene fusions such as TMPRSS2-ERG.
Molecular Pathways
Androgen Receptor (AR) Signaling: Testosterone and DHT are needed for prostate cancer development and progression; AR signaling is sustained in patients with minimal androgen levels (CRPC).Â
PI3K/AKT/mTOR Pathway: Dysregulation translates to proliferation; common alterations include PTEN loss.Â
Â
Cellular Changes
Hyperplasia and Dysplasia: Starts with PIN (prostatic intraepithelial neoplasia); HGPS is defined as high-grade PIN and is associated with invasive prostate cancer.
Invasive Carcinoma: Transitions from limited to invasive type located in lungs and spreads to legs and lymph nodes.
Hormonal Influence
Androgens: Playing a vital role in prostate growth; treatments aim at lowering androgen levels or inhibiting the AR pathways.
Estrogens and Other Hormones: Estrogen receptor signaling can affect the prostate cancer and hormonal homeostasis affects tumour progression.
Microenvironment and Inflammation
Tumor Microenvironment: Comprises cancer cells, characters of stroma, host leucocytes, and matrix ground substance, which supports cancer growth and promotes metastasis.Â
Chronic Inflammation: Among effects of obesity, it raises inflammatory cytokines which contribute to cancer development including prostate cancer.Â
Age: Prostate cancer risk rises with age. Men over 50 are diagnosed with most instances.Â
Genetics: Prostate cancer risk has been associated with certain genes.Â
Race and ethnicity: Nevertheless, African American men were found to be at the highest risk for the disease than Hispanic and white men. Asian American males have the utmost protection against the disease.
Family history: A family history of the disease can also predispose a man. The risk is especially high if the relative was diagnosed when he was still young.Â
Stage: Prostate cancer stage also affects prognosis.Â
PSA level: Prostate specific antigen (PSA) is a marker or a protein that is released by the prostate gland. PSA is known to be a marker and might be found at high levels in men diagnosed with the prostate cancer.
Age and overall health: It was further observed that the men who are comparatively younger developed prostate cancer, the prognosis of which is generally much higher than that of men of relatively higher age.Â
Age Group:Â
Age 65 and Older: Men 65 years of age and older receive most prostate cancer diagnoses. This age group is affected by prostate cancer in about 60% of instances.Â
Ages 55 to 64: This age category is vulnerable to prostate cancer in high proportions as observed among men. More than a quarter of the patients are men over fifty-five; specifically, 25% of men are affected when they are between fifty-five and sixty-four years old.Â
Prostate-Specific Antigen (PSA) TestÂ
Ultrasound and BiopsyÂ
Asymptomatic Presentation
Screening Detection: Most of the prostate cancer diagnosed after employing simple screening techniques like PSA or DRE. In these cases, the man does not manifest signs and symptoms and the cancer is invariably detected during other tests.
Early-Stage Disease: Prostate cases are often localized and have a better prognosis as they are easier to treat.
Symptomatic Presentation
Lower Urinary Tract Symptoms (LUTS):Â
Urinary Frequency: Persists, frequent or urgent to urinate specially at night known as nocturia.Â
Urgency: A compelling need to pee; a feeling of pressure that one must release urine.
Hesitancy: Difficulty starting urination.
Weak Stream: A reduction in the urine stream’s strength.
Incomplete emptying: Feeling that the bladder hasn’t been emptied.Â
Active Surveillance: This strategy is applied concerning low-grade malignancies or slowly progressive androgen-sensitive disease localized to the prostate with less than stage T2 tumor, small volume, clinically localized and not indicated for immediate treatment because of a low likelihood of symptoms or consequences in the coming years. It is controlled by going for routine tests such as PSA tests, digital rectal exams and infrequent biopsies just in case the cancer starts progressing.
Surgery (Prostatectomy): Radical prostatectomy is a surgical procedure that involves the removal of the entire prostate gland and is recommended for the early stage of prostate cancer, which has limited its spread to the prostate gland only. This can involve a direct approach, making an incision in the affected area, or it can involve endoscopic procedures like laparoscopic or robotic surgery.
Radiation Therapy: This can be employed as first-line therapy for prostate cancer that has not spread beyond the gland.Â
Types of radiation therapy include:
External Beam Radiation Therapy (EBRT): With the help of a particle accelerator located outside the body, rays with high energy are aimed at the prostate gland.
Brachytherapy: Iodine-125 in the form of radioactive seeds or pellets that are placed near the tumor within the prostate gland.
Proton Therapy: Sites protons instead of photons and this may reduce the chances of certain side effects especially those affecting the tissues surrounding the tumor.
Hormone Therapy (Androgen Deprivation Therapy ADT): Malignant prostate cells possess the potential for growth and survival with the help of male sex hormones or androgens such as testosterone. Hormone therapy works to decrease the levels of these hormones or prevent their action by using drugs or by carrying out the surgical removal of the testicles.
Chemotherapy: When the prostate cancer has affected other parts of the body in addition to the prostate gland and is PSA resistant. Chemotherapy medications are known to remove this abnormal cell tissues and decrease the slow of cancerous growth.Â
Urology
Urology
Urology
Urology
Sipuleucel-TÂ
Sipuleucel-T (Provenge) is considered as immunotherapy which is effective for individuals who have advanced prostate cancer. They operate through the enhancement of the patient’s immunity to fight the prostate cancerous cells.Â
Urology
Zolendronic acid (Zometa)Â
This is a bisphosphonate drug under the trade name Zometa, and it is approved for use in the treatment of prostate cancer especially in patients whose disease has advanced or has spread to the other parts of the body. It acts through prevention of bone resorption that is a process catalysed by osteoclasts, because the drug aids in maintaining a low incidence of skeletal related events (SREs) such as fractures, spinal cord compression, bone radiation or surgery.Â
Urology
Urology
The disease is defined as the malignant transformation of cells in the prostate gland, a small, walnut-shaped organ that synthesizes seminal fluid. It is one of the prominent male cancers, most experienced by men who have reached old age.Â
Global Incidence: It is statistically clinically documented that prostate carcinoma is the third most prevalent cancer in man. Research indicates that it accounts for around half of all cancer cases that develop and causes most cancer-related problems.Â
Prevalence: The rate of occurrence is not constant throughout the world and is affected by factors such as hereditary disposition, lifestyle parameters and other available programs.Â
Genetic Factors
Hereditary Prostate Cancer: About 5-10% of breast cancers could be attributed to hereditary factors and other genes including BRCA1 and BRCA2 and HOXB13.
Somatic Mutations: Somatic mutations which occur in prostate cells include those affecting the TP53 gene, PTEN, and ETS gene fusions such as TMPRSS2-ERG.
Molecular Pathways
Androgen Receptor (AR) Signaling: Testosterone and DHT are needed for prostate cancer development and progression; AR signaling is sustained in patients with minimal androgen levels (CRPC).Â
PI3K/AKT/mTOR Pathway: Dysregulation translates to proliferation; common alterations include PTEN loss.Â
Â
Cellular Changes
Hyperplasia and Dysplasia: Starts with PIN (prostatic intraepithelial neoplasia); HGPS is defined as high-grade PIN and is associated with invasive prostate cancer.
Invasive Carcinoma: Transitions from limited to invasive type located in lungs and spreads to legs and lymph nodes.
Hormonal Influence
Androgens: Playing a vital role in prostate growth; treatments aim at lowering androgen levels or inhibiting the AR pathways.
Estrogens and Other Hormones: Estrogen receptor signaling can affect the prostate cancer and hormonal homeostasis affects tumour progression.
Microenvironment and Inflammation
Tumor Microenvironment: Comprises cancer cells, characters of stroma, host leucocytes, and matrix ground substance, which supports cancer growth and promotes metastasis.Â
Chronic Inflammation: Among effects of obesity, it raises inflammatory cytokines which contribute to cancer development including prostate cancer.Â
Age: Prostate cancer risk rises with age. Men over 50 are diagnosed with most instances.Â
Genetics: Prostate cancer risk has been associated with certain genes.Â
Race and ethnicity: Nevertheless, African American men were found to be at the highest risk for the disease than Hispanic and white men. Asian American males have the utmost protection against the disease.
Family history: A family history of the disease can also predispose a man. The risk is especially high if the relative was diagnosed when he was still young.Â
Stage: Prostate cancer stage also affects prognosis.Â
PSA level: Prostate specific antigen (PSA) is a marker or a protein that is released by the prostate gland. PSA is known to be a marker and might be found at high levels in men diagnosed with the prostate cancer.
Age and overall health: It was further observed that the men who are comparatively younger developed prostate cancer, the prognosis of which is generally much higher than that of men of relatively higher age.Â
Age Group:Â
Age 65 and Older: Men 65 years of age and older receive most prostate cancer diagnoses. This age group is affected by prostate cancer in about 60% of instances.Â
Ages 55 to 64: This age category is vulnerable to prostate cancer in high proportions as observed among men. More than a quarter of the patients are men over fifty-five; specifically, 25% of men are affected when they are between fifty-five and sixty-four years old.Â
Prostate-Specific Antigen (PSA) TestÂ
Ultrasound and BiopsyÂ
Asymptomatic Presentation
Screening Detection: Most of the prostate cancer diagnosed after employing simple screening techniques like PSA or DRE. In these cases, the man does not manifest signs and symptoms and the cancer is invariably detected during other tests.
Early-Stage Disease: Prostate cases are often localized and have a better prognosis as they are easier to treat.
Symptomatic Presentation
Lower Urinary Tract Symptoms (LUTS):Â
Urinary Frequency: Persists, frequent or urgent to urinate specially at night known as nocturia.Â
Urgency: A compelling need to pee; a feeling of pressure that one must release urine.
Hesitancy: Difficulty starting urination.
Weak Stream: A reduction in the urine stream’s strength.
Incomplete emptying: Feeling that the bladder hasn’t been emptied.Â
Active Surveillance: This strategy is applied concerning low-grade malignancies or slowly progressive androgen-sensitive disease localized to the prostate with less than stage T2 tumor, small volume, clinically localized and not indicated for immediate treatment because of a low likelihood of symptoms or consequences in the coming years. It is controlled by going for routine tests such as PSA tests, digital rectal exams and infrequent biopsies just in case the cancer starts progressing.
Surgery (Prostatectomy): Radical prostatectomy is a surgical procedure that involves the removal of the entire prostate gland and is recommended for the early stage of prostate cancer, which has limited its spread to the prostate gland only. This can involve a direct approach, making an incision in the affected area, or it can involve endoscopic procedures like laparoscopic or robotic surgery.
Radiation Therapy: This can be employed as first-line therapy for prostate cancer that has not spread beyond the gland.Â
Types of radiation therapy include:
External Beam Radiation Therapy (EBRT): With the help of a particle accelerator located outside the body, rays with high energy are aimed at the prostate gland.
Brachytherapy: Iodine-125 in the form of radioactive seeds or pellets that are placed near the tumor within the prostate gland.
Proton Therapy: Sites protons instead of photons and this may reduce the chances of certain side effects especially those affecting the tissues surrounding the tumor.
Hormone Therapy (Androgen Deprivation Therapy ADT): Malignant prostate cells possess the potential for growth and survival with the help of male sex hormones or androgens such as testosterone. Hormone therapy works to decrease the levels of these hormones or prevent their action by using drugs or by carrying out the surgical removal of the testicles.
Chemotherapy: When the prostate cancer has affected other parts of the body in addition to the prostate gland and is PSA resistant. Chemotherapy medications are known to remove this abnormal cell tissues and decrease the slow of cancerous growth.Â
Urology
Urology
Urology
Urology
Sipuleucel-TÂ
Sipuleucel-T (Provenge) is considered as immunotherapy which is effective for individuals who have advanced prostate cancer. They operate through the enhancement of the patient’s immunity to fight the prostate cancerous cells.Â
Urology
Zolendronic acid (Zometa)Â
This is a bisphosphonate drug under the trade name Zometa, and it is approved for use in the treatment of prostate cancer especially in patients whose disease has advanced or has spread to the other parts of the body. It acts through prevention of bone resorption that is a process catalysed by osteoclasts, because the drug aids in maintaining a low incidence of skeletal related events (SREs) such as fractures, spinal cord compression, bone radiation or surgery.Â
Urology
Urology

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