NCCN Prostate Cancer Early Detection Guideline



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NCCN Prostate Cancer Early Detection Guideline Joan McClure Senior Vice President National Comprehensive Cancer Network African American Prostate Cancer Disparity Summit September 22, 2006 Washington, DC

What is NCCN? Alliance of 20 academic cancer centers in the United States Goal: Improve patient care Develop programs to support missions in education, research patient care, and health information National Outcomes Research Network

NCCN Clinical Practice Guidelines-- Goals Improve the quality of care for patients with cancer Reflect evolving data and treatment patterns by updating continuously Reinforce multidisciplinary interactions in oncology care Provide standard for evaluating cancer care in the United States

NCCN Guidelines Program Clinical practice guidelines for cancer Risk reduction Early detection Treatment Supportive care 48 panels consist of over 750 multidisciplinary cancer specialists

Guidelines Principles Ensure multidisciplinary input Evaluate available evidence Manage bias Develop consensus on appropriate recommendations Update continuously to reflect evolving data Measure adherence to guidelines

Prostate Cancer Early Detection Panel Composition Urologists Internists Epidemiologists Radiation oncologist Medical oncologist Biostatistician Pathologist Patient Advocate

Guidelines Development Evidence based Consensus derived

Evidence There is inadequate evidence to base decisions on in many areas of oncology New studies WILL change the standard of care over time Continuous review of evidence and guideline updates are required

NCCN Consensus Process Review Iteration

NCCN Categories of Consensus Category Level of Evidence Degree of Consensus 1 High Uniform 2 A Lower Uniform 2 B Lower Non-uniform 3 Any Major disagreement

NCCN Prostate Early Detection Guideline Does not make recommendation on whether or not to screen If screening is elected, the guideline recommends how to do it

The Controversy Screening identifies both clinically insignificant and clinically significant prostate cancers Not all prostate cancers require treatment; however, it is difficult to differentiate prospectively between those that do and those that don t Treatment of clinically insignificant prostate cancers can result in significant morbidity Not treating clinically significant prostate cancers can result in advanced disease and death

Guidelines Comparison Guideline Developer Recommend Screening? Age to Begin Screening NCCN Silent If screening elected baseline at 40 AUA YES 50 normal risk 40 high risk ACS YES 50 normal risk 45 high risk USPSTF NO NA ACP NO NA

Prostate Cancer Early Detection Guideline Baseline screening Discussion of risks and benefits of screening DRE and PSA At age 40 no good consensus about this age.

Results of Initial Screening High risk groups Patients with baseline PSA.0.6 ng/ml, or African American, or Family history of prostate cancer especially at an early age Normal risk group Patients with baseline PSA of < 0.6 ng/ml No other high risk characteristics

Family History of Prostate Cancer Father, brother, or son with prostate cancer Diagnosed at an early age

African American Higher incidence and higher mortality in this population Evidence of specific genotype linked to increased risk of prostate cancer especially at a younger age

PSA Value Higher than Age Cohort Median 3x greater rate of prostate cancer if PSA > median for age Risk increases as PSA level increases above the median especially in younger patients Higher than median PSA is associated with higher risk of aggressive disease and higher risk of recurrence following local therapy.

PSA > Median for Age Group Age Range Median PSA Risk of Prostate Cancer within 5 Years with PSA < Median Risk of Prostate Cancer within 5 years with PSA Median 40-50 O.6-0.7 0.5% 7.3% 50-60 0.7-0.9 0.7% 8.1% Loeb, et al Urology, 2006

Stage Migration Prostate cancer is being diagnosed earlier More clinically insignificant cancers are being diagnosed (and treated) Fewer patients are being diagnosed with metastatic disease

Follow-up High Risk Patients: Annual follow-up with DRE and PSA non uniform consensus Normal Risk Patients: Repeat at age 45: If PSA < 0.6 ng/ml Offer regular screening at age 50 If PSA 0.6 ng/ml: Annual follow-up with DRE and PSA non uniform consensus