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Lines of ttt of p ca
Prostate cancer: Risk stratification
and choice of initial treatment
Lines of ttt of p ca
• RISK STRATIFICATION
• Or
• cancer risk prediction models
• Weigh therapeutic options on
comparative benefits and risks in
domains, such as life expectancy, disease
control, health-related quality-of life and
treatment complications.
• Reduction of inconsistent management
due to physician bias, or differences in
experience and knowledge
Cancer risk prediction models
• Planning intervention trials
• Assisting in creating benefit–risk indices
• Estimating the cost of the population burden
of disease
• Identifying individuals at high risk
• Designing population prevention strategies
• Improving clinical decision-making (genetic
counseling)
Pre-treatment
PSA
clinical T
category
Gleason score
overall survival
disease-free survival
metastasis-free
survival
extracapsular disease
seminal vesicle
involvement
positive margins
lymph node positivity
PSA biochemical-free
failure
Lines of ttt of p ca
Lines of ttt of p ca
Prediction tables and algorithms
Prediction tables and algorithms
• Partin et al, 1997, 2001;
• Makarov et al, 2007;
• Eifler et al, 2013
• However, such statistical aids are more useful in
groups of patients than in individual patients
• wide confidence intervals surrounding estimates
of outcomes may limit the usefulness of risk
assessment for an individual patient.
• Accordingly, it has been claimed that the
simultaneous assessment of multiple variables in
nomograms provides more accurate predictions
than do tables for individual patients (Kattan,
2003).
Lines of ttt of p ca
Lines of ttt of p ca
Prostate Imaging-Data and Reporting System
[PI-RADS]
• Characterization of the Primary Tumor
• Evaluation of the Patient
Characterization of the Primary
Tumor
• DRE
• prostate ultrasound
• serum PSA data
including the total PSA level, the rate of change of PSA
(PSA velocity and doubling time), the PSA density
(serum PSA divided by prostate volume), the
percentage of PSA in the free or complexed isoforms
• Prostate Health Index are significantly associated with
prostate cancer aggressiveness
• (Benson et al, 1992; Carter, 1997; Catalona et al, 1998;
D’Amico et al, 2004; Thompson et al, 2004; Kundu et al,
2007; Catalona et al, 2011).
Characterization of the Primary
Tumor
The biopsy findings
• Gleason score
• number of cores containing cancer
• distribution and volume of cancer in the biopsy cores
• presence of perineural space invasion, lymphovascular
invasion,
• ductal, signet ring, or neuroendocrine differentiation)
also correlate
• with cancer aggressiveness and the likelihood of the
cancer’s being organ confined (Loeb et al, 2010a).
Lines of ttt of p ca
Lines of ttt of p ca
Lines of ttt of p ca
• Evaluation of the Patient
Lines of ttt of p ca
Evaluating the patients
Evaluation of life expectancy
Health status
• Comorbidity
• dependence in daily activities
• malnutrition
• Cognitive impairment
Lines of ttt of p ca
PRINCIPLES OF LIFE EXPECTANCY
ESTIMATION
• critical to informed decision-making in
prostate cancer early detection and
treatment.
• Life expectancy can be estimated using the
• Social Security Administration tables
(www.ssa.gov/OACT/STATS/table4c6.html)
• the WHO’s Life Tables by country
(http://apps.who.int/gho/data/view.main.60
000?lang=en).
• Life expectancy can then be adjusted using
the clinician’s assessment of overall health as
follows:
• Best quartile of health - add 50%
• Worst quartile of health - subtract 50%
• Middle two quartiles of health - no
adjustment
Lines of ttt of p ca
Comorbidity
• Comorbidity is a major predictor of non-
cancer-specific death in localised Pca
• Cumulative Illness Score Rating-Geriatrics
(CISR-G] is the best tool for assessing mortality
risk unrelated to Pca
Lines of ttt of p ca
Lines of ttt of p ca
Lines of ttt of p ca
Lines of ttt of p ca
Lines of ttt of p ca
Dependence in daily activities
• The level of dependence in daily activities
influences survival in senior adults.
• The Activities of Daily Living (ADL) scale rates
accomplishment of basic activities of daily
living, while the Instrumental Activities of
Daily Living (IADL) scale rates activities
requiring higher cognition and judgment.
Lines of ttt of p ca
Malnutrition
• Malnutrition is associated with increased
mortality in senior patients
• Nutritional status can be estimated from body
weight during the previous three months:
• • Good nutritional status < 5% weight loss;
• • Risk of malnutrition: 5-10% weight loss;
• • Severe malnutrition: > 10% weight loss.
Cognitive impairment
• Cognitive impairment is associated with
increased mortality risk in senior adults
• In patients undergoing major elective surgery,
there is an association between baseline
cognitive impairment and long-term
postoperative complications and mortality
[598].
• Intervention is unlikely to reverse cognitive
impairment, except in depression
• The mini-COG is the best available tool to
evaluate cognitive function in order to assess
the patient’s ability to make an informed
decision
Lines of ttt of p ca
Lines of ttt of p ca
• Baseline screening using the G8 screening tool
The International Society of Geriatric
Oncology (SIOG) PCa Working Group (PCWG)
recommends that btreatment for senior adults
should be based on a systematic evaluation of
health status
• The G8 (Geriatric 8) health status screening
tool is described, the Karnofsky and ECOG
Scores .
Lines of ttt of p ca
Lines of ttt of p ca
Lines of ttt of p ca
Lines of ttt of p ca
Lines of ttt of p ca
Definitive
DISEASE MANAGEMENT
• Deferred treatment (active surveillance/watchful
waiting
• Radical prostatectomy
• Definitive radiotherapy
• Options other than surgery and radiotherapy
for the primary treatment of localised prostate
cancer
• Hormonal therapy
Active surveillance
• achieve correct timing for curative treatment
in patients with clinically localised PCa, rather
than delay palliative treatment .
• Patients remain under close surveillance, and
treatment is prompted by predefined
thresholds indicative of potentially life-
threatening disease, still potentially curable,
while considering individual life expectancy.
Watchful waiting
• known as deferred or symptom-guided
treatment.
• conservative management, until the
development of local or systemic progression
with (imminent) disease-related complaints.
• Patients are then treated according to their
symptoms, in order to maintain QoL.
Lines of ttt of p ca
Lines of ttt of p ca
Lines of ttt of p ca
Low-risk PCa
Active surveillance
Low-risk PCa
• Radical prostatectomy
Low-risk PCa
• Radiotherapy
Low-risk PCa
Intermediate-risk PCa
Intermediate-risk PCa
• Radical prostatectomy
Intermediate-risk PCa
• Radiotherapy
Intermediate-risk PCa
High-risk PCa
• Watchful waiting
High-risk PCa
• Active surveillance
High-risk PCa
• Radical prostatectomy
Lines of ttt of p ca
• Radiotherapy
• Androgen suppression monotherapy
N1 patients
• cN1
• pN1 after extended lymph node dissection
(eLND)
Metastatic PCa
Metastatic PCa
• Androgen suppression
Metastatic PCa
Metastatic PCa
Metastatic PCa
Lines of ttt of p ca
Lines of ttt of p ca
Lines of ttt of p ca
Lines of ttt of p ca
Lines of ttt of p ca
Lines of ttt of p ca
Lines of ttt of p ca
Lines of ttt of p ca
Communicate with your patients
External beam radiation therapy Radical prostatectomy
•Effective long-term cancer control with high-
dose treatments
•Very low risk of urinary incontinence
•Wide range of ages and in those with
significant comorbidity
•Combined with hormone therapy treatment,
•eradicate extensions of tumor beyond the
margins of the prostate
•Effective long-term cancer control
•pathologic features in specimen
•Pelvic lymph node dissection is
possible through the same incision
•PSA failure is easy to detect
Brachytherapy Active Observation
•Cancer control rates appear equal to surgery
and EBRT for organ-confined tumors
•Quicker than EBRT (single treatment)
•Risk of incontinence is low in patients
without a previous TURP
•Available for cure of patients over a wide
range of ages and in those with some
comorbidity
•Reduces overtreatment
•Avoids or postpones treatment-
associated complications
•Has no effect on work or social activities
External beam radiation therapy Radical prostatectomy
•Significant risk of impotence
•Best outcomes require 3-D conformal
treatments with doses above 72 Gy
•Low risk of later rectal symptoms
•Knowledge of possible metastasis to lymph
nodes is not available
•Up to half of patients have some temporary
bladder or bowel symptoms during treatment
•Significant risk of impotence
•Risk of operative morbidity
•The risk of complications is operator
dependent, to some extent
•Low risk of long-term incontinence
Brachytherapy Active Observation
•Significant risk of impotence
•Successful cancer control is operator dependent,
to some extent
•Low risk of later rectal symptoms
•Knowledge of possible metastasis to lymph
nodes is not available
•Treatment not appropriate for tumor outside
the prostate capsule
•Up to half of patients have some temporary
bladder or bowel symptoms with treatment
•Tumor may progress beyond the
possibility for cure
•Later treatment may result in more
side effects
•Living with untreated cancer may
cause anxiety
External beam radiation therapy Radical prostatectomy
•Previous pelvic irradiation
•Active inflammatory disease of the rectum
•Very low bladder capacity
•Chronic moderate or severe diarrhea from
any cause
•Higher medical operative risk,
•Neurogenic bladder
Brachytherapy Active Observation
•Previous pelvic irradiation
•Prior TURP
•Large-volume gland
•Marked voiding symptoms
•Large or high-grade tumor burdens
•Chronic moderate or severe diarrhea
•Active inflammatory disease of the rectum
•High-grade tumors
•Expected survival of more than 10
years
Lines of ttt of p ca
Lines of ttt of p ca
Lines of ttt of p ca
• REFERENCES
• Humphrey PA. Cancers of the male reproductive organs. In:
World Cancer Report, Stewart BW, Wild CP (Eds), World He
alth Organization, Lyon 2014.
• Barry MJ, Nelson JB. Patients Present with More Advanced
Prostate Cancer since the USPSTF Screening
Recommendations. J Urol 2015; 194:1534.
• Kasivisvanathan V, Rannikko AS, Borghi M, et al. MRI-
Targeted or Standard Biopsy for Prostate-Cancer Diagnosis.
N Engl J Med 2018; 378:1767.
• Epstein JI, Zelefsky MJ, Sjoberg DD, et al. A Contemporary
Prostate Cancer Grading System: A Validated Alternative to
the Gleason Score. Eur Urol 2016; 69:428.
• D'Amico AV, Whittington R, Malkowicz SB, et al. Clinical
utility of the percentage of positive prostate biopsies in
defining biochemical outcome after radical prostatectomy
for patients with clinically localized prostate cancer. J Clin
Oncol 2000; 18:1164.
• Lee AK, Schultz D, Renshaw AA, et al. Optimizing patient
selection for prostate monotherapy. Int J Radiat Oncol Biol
Phys 2001; 49:673.
• D'Amico AV, Schultz D, Silver B, et al. The clinical utility of
the percent of positive prostate biopsies in predicting
biochemical outcome following external-beam radiation
therapy for patients with clinically localized prostate cancer.
Int J Radiat Oncol Biol Phys 2001; 49:679.
• Grossfeld GD, Latini DM, Lubeck DP, et al.
Predicting disease recurrence in intermediate and
high-risk patients undergoing radical
prostatectomy using percent positive biopsies:
results from CaPSURE. Urology 2002; 59:560.
• D'Amico AV, Keshaviah A, Manola J, et al. Clinical
utility of the percentage of positive prostate
biopsies in predicting prostate cancer-specific and
overall survival after radiotherapy for patients
with localized prostate cancer. Int J Radiat Oncol
Biol Phys 2002; 53:581.
• Freedland SJ, Aronson WJ, Csathy GS, et al. Comparison of
percentage of total prostate needle biopsy tissue with cancer to
percentage of cores with cancer for predicting PSA recurrence after
radical prostatectomy: results from the SEARCH database. Urology
2003; 61:742.
• Greene KL, Elkin EP, Karapetian A, et al. Prostate biopsy tumor
extent but not location predicts recurrence after radical
prostatectomy: results from CaPSURE. J Urol 2006; 175:125.
• National Comprehensive Cancer Network (NCCN). NCCN Clinical pra
ctice guidelines in oncology. https://www.nccn.org/professionals/p
hysician_gls/pdf/neuroendocrine.pdf (Accessed on February 20, 20
18).
• ps://www.nccn.org/professionals/physician_gls/default.aspx (Acces
sed on March 28, 2018).
• Caster JM, Falchook AD, Hendrix LH, Chen RC. Risk of
Pathologic Upgrading or Locally Advanced Disease in Early
Prostate Cancer Patients Based on Biopsy Gleason Score and
PSA: A Population-Based Study of Modern Patients. Int J
Radiat Oncol Biol Phys 2015; 92:244.
• Winters BR, Wright JL, Holt SK, et al. Extreme Gleason
Upgrading From Biopsy to Radical Prostatectomy: A
Population-based Analysis. Urology 2016; 96:148.
• Klein EA, Santiago-Jiménez M, Yousefi K, et al. Molecular
Analysis of Low Grade Prostate Cancer Using a Genomic
Classifier of Metastatic Potential. J Urol 2017; 197:122.
• Mahal BA, Yang DD, Wang NQ, et al. Clinical and Genomic
Characterization of Low-Prostate-specific Antigen, High-grade
Prostate Cancer. Eur Urol 2018.
• Aggarwal R, Zhang T, Small EJ, Armstrong AJ. Neuroendocrine prostate
cancer: subtypes, biology, and clinical outcomes. J Natl Compr Canc Netw
2014; 12:719.
• Epstein JI, Amin MB, Beltran H, et al. Proposed morphologic classification
of prostate cancer with neuroendocrine differentiation. Am J Surg Pathol
2014; 38:756.
• Deorah S, Rao MB, Raman R, et al. Survival of patients with small cell
carcinoma of the prostate during 1973-2003: a population-based study.
BJU Int 2012; 109:824.
• Sanda MG, Cadeddu JA, Kirkby E, et al. Clinically Localized Prostate Cancer:
AUA/ASTRO/SUO Guideline. Part I: Risk Stratification, Shared Decision
Making, and Care Options. J Urol 2017.
• Sanda MG, Cadeddu JA, Kirkby E, et al. Clinically Localized Prostate Cancer:
AUA/ASTRO/SUO Guideline. Part II: Recommended Approaches and
Details of Specific Care Options. J Urol 2018; 199:990.
• Spratt DE, Zhang J, Santiago-Jiménez M, et al. Development and
Validation of a Novel Integrated Clinical-Genomic Risk Group
Classification for Localized Prostate Cancer. J Clin Oncol 2018;
36:581.
• Hamdy FC, Donovan JL, Lane JA, et al. 10-Year Outcomes after
Monitoring, Surgery, or Radiotherapy for Localized Prostate Cancer.
N Engl J Med 2016; 375:1415.
• Donovan JL, Hamdy FC, Lane JA, et al. Patient-Reported Outcomes
after Monitoring, Surgery, or Radiotherapy for Prostate Cancer. N
Engl J Med 2016; 375:1425.
• Ellis CL, Partin AW, Han M, Epstein JI. Adenocarcinoma of the
prostate with Gleason score 9-10 on core biopsy: correlation with
findings at radical prostatectomy and prognosis. J Urol 2013;
190:2068.
• Tsao CK, Gray KP, Nakabayashi M, et al. Patients with Biopsy
Gleason 9 and 10 Prostate Cancer Have Significantly Worse
Outcomes Compared to Patients with Gleason 8 Disease. J Urol
2015; 194:91.
• http://uroweb.org/wp-content/uploads/EAU-Guidelines-Prostate-C
ancer-2016.pdf.
• Kishan AU, Cook RR, Ciezki JP, et al. Radical Prostatectomy, External
Beam Radiotherapy, or External Beam Radiotherapy With
Brachytherapy Boost and Disease Progression and Mortality in
Patients With Gleason Score 9-10 Prostate Cancer. JAMA 2018;
319:896.
• O'Shaughnessy MJ, McBride SM, Vargas HA, et al. A Pilot Study of a
Multimodal Treatment Paradigm to Accelerate Drug Evaluations in
Early-stage Metastatic Prostate Cancer. Urology 2017; 102:164.
• D'Amico AV, Wu Y, Chen MH, et al. Perineural invasion as a
predictor of biochemical outcome following radical
prostatectomy for select men with clinically localized
prostate cancer. J Urol 2001; 165:126.
• Anderson PR, Hanlon AL, Patchefsky A, et al. Perineural
invasion and Gleason 7-10 tumors predict increased failure
in prostate cancer patients with pretreatment PSA <10
ng/ml treated with conformal external beam radiation
therapy. Int J Radiat Oncol Biol Phys 1998; 41:1087.
• O'Malley KJ, Pound CR, Walsh PC, et al. Influence of biopsy
perineural invasion on long-term biochemical disease-free
survival after radical prostatectomy. Urology 2002; 59:85.
• Ng JC, Koch MO, Daggy JK, Cheng L. Perineural invasion in radical prostatectomy
specimens: lack of prognostic significance. J Urol 2004; 172:2249.
• Donovan MJ, Hamann S, Clayton M, et al. Systems pathology approach for the
prediction of prostate cancer progression after radical prostatectomy. J Clin Oncol
2008; 26:3923.
• Cheville JC, Karnes RJ, Therneau TM, et al. Gene panel model predictive of
outcome in men at high-risk of systemic progression and death from prostate
cancer after radical retropubic prostatectomy. J Clin Oncol 2008; 26:3930.
• Klein EA, Stephenson AJ, Raghavan D, Dreicer R. Systems pathology and predicting
outcome after radical prostatectomy. J Clin Oncol 2008; 26:3916.
• Shariat SF, Karakiewicz PI, Suardi N, Kattan MW. Comparison of nomograms with
other methods for predicting outcomes in prostate cancer: a critical analysis of the
literature. Clin Cancer Res 2008; 14:4400.
• Shariat SF, Karakiewicz PI, Roehrborn CG, Kattan MW. An updated catalog of
prostate cancer predictive tools. Cancer 2008; 113:3075.

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Lines of ttt of p ca

  • 2. Prostate cancer: Risk stratification and choice of initial treatment
  • 4. • RISK STRATIFICATION • Or • cancer risk prediction models
  • 5. • Weigh therapeutic options on comparative benefits and risks in domains, such as life expectancy, disease control, health-related quality-of life and treatment complications. • Reduction of inconsistent management due to physician bias, or differences in experience and knowledge
  • 6. Cancer risk prediction models • Planning intervention trials • Assisting in creating benefit–risk indices • Estimating the cost of the population burden of disease • Identifying individuals at high risk • Designing population prevention strategies • Improving clinical decision-making (genetic counseling)
  • 7. Pre-treatment PSA clinical T category Gleason score overall survival disease-free survival metastasis-free survival extracapsular disease seminal vesicle involvement positive margins lymph node positivity PSA biochemical-free failure
  • 10. Prediction tables and algorithms Prediction tables and algorithms • Partin et al, 1997, 2001; • Makarov et al, 2007; • Eifler et al, 2013
  • 11. • However, such statistical aids are more useful in groups of patients than in individual patients • wide confidence intervals surrounding estimates of outcomes may limit the usefulness of risk assessment for an individual patient. • Accordingly, it has been claimed that the simultaneous assessment of multiple variables in nomograms provides more accurate predictions than do tables for individual patients (Kattan, 2003).
  • 14. Prostate Imaging-Data and Reporting System [PI-RADS]
  • 15. • Characterization of the Primary Tumor • Evaluation of the Patient
  • 16. Characterization of the Primary Tumor • DRE • prostate ultrasound • serum PSA data including the total PSA level, the rate of change of PSA (PSA velocity and doubling time), the PSA density (serum PSA divided by prostate volume), the percentage of PSA in the free or complexed isoforms • Prostate Health Index are significantly associated with prostate cancer aggressiveness • (Benson et al, 1992; Carter, 1997; Catalona et al, 1998; D’Amico et al, 2004; Thompson et al, 2004; Kundu et al, 2007; Catalona et al, 2011).
  • 17. Characterization of the Primary Tumor The biopsy findings • Gleason score • number of cores containing cancer • distribution and volume of cancer in the biopsy cores • presence of perineural space invasion, lymphovascular invasion, • ductal, signet ring, or neuroendocrine differentiation) also correlate • with cancer aggressiveness and the likelihood of the cancer’s being organ confined (Loeb et al, 2010a).
  • 21. • Evaluation of the Patient
  • 23. Evaluating the patients Evaluation of life expectancy Health status • Comorbidity • dependence in daily activities • malnutrition • Cognitive impairment
  • 25. PRINCIPLES OF LIFE EXPECTANCY ESTIMATION • critical to informed decision-making in prostate cancer early detection and treatment. • Life expectancy can be estimated using the • Social Security Administration tables (www.ssa.gov/OACT/STATS/table4c6.html) • the WHO’s Life Tables by country (http://apps.who.int/gho/data/view.main.60 000?lang=en).
  • 26. • Life expectancy can then be adjusted using the clinician’s assessment of overall health as follows: • Best quartile of health - add 50% • Worst quartile of health - subtract 50% • Middle two quartiles of health - no adjustment
  • 28. Comorbidity • Comorbidity is a major predictor of non- cancer-specific death in localised Pca • Cumulative Illness Score Rating-Geriatrics (CISR-G] is the best tool for assessing mortality risk unrelated to Pca
  • 34. Dependence in daily activities • The level of dependence in daily activities influences survival in senior adults. • The Activities of Daily Living (ADL) scale rates accomplishment of basic activities of daily living, while the Instrumental Activities of Daily Living (IADL) scale rates activities requiring higher cognition and judgment.
  • 36. Malnutrition • Malnutrition is associated with increased mortality in senior patients • Nutritional status can be estimated from body weight during the previous three months: • • Good nutritional status < 5% weight loss; • • Risk of malnutrition: 5-10% weight loss; • • Severe malnutrition: > 10% weight loss.
  • 37. Cognitive impairment • Cognitive impairment is associated with increased mortality risk in senior adults • In patients undergoing major elective surgery, there is an association between baseline cognitive impairment and long-term postoperative complications and mortality [598]. • Intervention is unlikely to reverse cognitive impairment, except in depression
  • 38. • The mini-COG is the best available tool to evaluate cognitive function in order to assess the patient’s ability to make an informed decision
  • 41. • Baseline screening using the G8 screening tool The International Society of Geriatric Oncology (SIOG) PCa Working Group (PCWG) recommends that btreatment for senior adults should be based on a systematic evaluation of health status
  • 42. • The G8 (Geriatric 8) health status screening tool is described, the Karnofsky and ECOG Scores .
  • 48. Definitive DISEASE MANAGEMENT • Deferred treatment (active surveillance/watchful waiting • Radical prostatectomy • Definitive radiotherapy • Options other than surgery and radiotherapy for the primary treatment of localised prostate cancer • Hormonal therapy
  • 49. Active surveillance • achieve correct timing for curative treatment in patients with clinically localised PCa, rather than delay palliative treatment . • Patients remain under close surveillance, and treatment is prompted by predefined thresholds indicative of potentially life- threatening disease, still potentially curable, while considering individual life expectancy.
  • 50. Watchful waiting • known as deferred or symptom-guided treatment. • conservative management, until the development of local or systemic progression with (imminent) disease-related complaints. • Patients are then treated according to their symptoms, in order to maintain QoL.
  • 55. Low-risk PCa • Radical prostatectomy
  • 63. High-risk PCa • Active surveillance
  • 64. High-risk PCa • Radical prostatectomy
  • 69. • pN1 after extended lymph node dissection (eLND)
  • 84. External beam radiation therapy Radical prostatectomy •Effective long-term cancer control with high- dose treatments •Very low risk of urinary incontinence •Wide range of ages and in those with significant comorbidity •Combined with hormone therapy treatment, •eradicate extensions of tumor beyond the margins of the prostate •Effective long-term cancer control •pathologic features in specimen •Pelvic lymph node dissection is possible through the same incision •PSA failure is easy to detect Brachytherapy Active Observation •Cancer control rates appear equal to surgery and EBRT for organ-confined tumors •Quicker than EBRT (single treatment) •Risk of incontinence is low in patients without a previous TURP •Available for cure of patients over a wide range of ages and in those with some comorbidity •Reduces overtreatment •Avoids or postpones treatment- associated complications •Has no effect on work or social activities
  • 85. External beam radiation therapy Radical prostatectomy •Significant risk of impotence •Best outcomes require 3-D conformal treatments with doses above 72 Gy •Low risk of later rectal symptoms •Knowledge of possible metastasis to lymph nodes is not available •Up to half of patients have some temporary bladder or bowel symptoms during treatment •Significant risk of impotence •Risk of operative morbidity •The risk of complications is operator dependent, to some extent •Low risk of long-term incontinence Brachytherapy Active Observation •Significant risk of impotence •Successful cancer control is operator dependent, to some extent •Low risk of later rectal symptoms •Knowledge of possible metastasis to lymph nodes is not available •Treatment not appropriate for tumor outside the prostate capsule •Up to half of patients have some temporary bladder or bowel symptoms with treatment •Tumor may progress beyond the possibility for cure •Later treatment may result in more side effects •Living with untreated cancer may cause anxiety
  • 86. External beam radiation therapy Radical prostatectomy •Previous pelvic irradiation •Active inflammatory disease of the rectum •Very low bladder capacity •Chronic moderate or severe diarrhea from any cause •Higher medical operative risk, •Neurogenic bladder Brachytherapy Active Observation •Previous pelvic irradiation •Prior TURP •Large-volume gland •Marked voiding symptoms •Large or high-grade tumor burdens •Chronic moderate or severe diarrhea •Active inflammatory disease of the rectum •High-grade tumors •Expected survival of more than 10 years
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