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Screening for Colorectal Cancer A 21 st Century Challenge Thomas Weber MD FACS Associate Professor of Surgery & Molecular Genetics Albert Einstein College of Medicine New York, New York

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Screening for Colorectal CancerA 21st Century Challenge

Thomas Weber MD FACSAssociate Professor of Surgery & Molecular

GeneticsAlbert Einstein College of Medicine

New York, New York

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“Colorectal Cancer”An Ironic Tragedy in Three Acts

Act I

“A Nation Ravaged”

Act II

“Victory In Our Grasp”

Act III

“Paradise Lost”

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Colorectal CancerAct I

“A Nation Ravaged”

• 148,000 cases anticipated for 2002*

• 55,000 deaths

• #1 solid tumor killer after lung cancer

• 10,400 cases in NYS

• 4000 deaths in NYS*ACS Cancer Statistics 2002

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Colorectal CancerAct I

“A Nation Ravaged”

• An equal opportunity killer• Equal rates of death for women and men• 1 in 20 Americans affected• 1 in 10 with affected 1st degree relative

*ACS Cancer Statistics 2002

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“A Nation Ravaged”

The Devil IS in the Details”

Colorectal Cancer Survival As A Function of Stage

at Diagnosis

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NCDB Colon Cancer Survival

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63% Stage III or IV55,000 Deaths

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“A Nation Ravaged”The Devil IS in the Details

Distribution of Stage at Diagnosis

Only 37% of Colorectal Cancers are diagnosed while still localized

(node negative).

63% have regional or distant metastatic disease at the time of

diagnosis.

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Colorectal CancerAct II

“Victory In Our Grasp”

• Screening for colorectal cancer removes pre-malignant lesions, promotes early stage diagnosis and saves lives.*

* Winawer et al. Gastroenterology 2003 124

* Selby et al. NEJM 1992 326:653-657

* Winawer et al. NEJM 1993 329:1977-81

* Newcomb et al. J Nat Can Inst 1992 84:1572-1575

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Act II“Victory In Our Grasp”

• Colorectal Cancer and Breast Cancer

• Two VERY different paradigms

• Mammography is principally directed at earliest stage INVASIVE lesions (DCIS aside).

• Endoscopic Colorectal surveillance REMOVES PREMALIGNANT LESIONS.

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Act II“Victory In Our Grasp”

• We have the tools!

• We have the case control and randomized evidence!

• Risk-benefit ratio is low!

• Cost is manageable!

• We have even achieved consensus!

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An IRONIC Tragedy

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Act III PARADISE LOST

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Act IIIParadise Lost

• “Based on data from the Behavioral Risk

Factor Surveillance System fewer than one in five adults reported having had an FOBT in the previous year and only 9.5% of adults reported having had both an FOBT test and flexible sigmoidoscopy during an interval recommended by the ACS.”*

• *CDC Morb Mortal Weekly Rep 1999;48:116-121

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Act IIIParadise Lost

• “Despite a consensus among expert groups on the effectiveness of screening for colorectal cancer, screening rates remain low.”*

* Winawer et al. Gastroenterology February 2003 124

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Act ThreeParadise Lost

• “Evidence Demonstrates that when a screening recommendation comes directly from the clinician, compliance with colorectal cancer screening can be quite high.”*

*CA Cancer Journal 2001 51: pg 49

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Act ThreeParadise Lost

• “Surveys of primary care providers and medical directors of managed care groups indicate a lack of preparedness to offer FOBT and flexible sigmoidoscopy”*

• “A recent report indicated medical directors were more likely to regard flexible sigmoidoscopy as an unreasonable expectation in a capitated plan“*

• “At this time economic and health care system disincentives to screening are impinging on CRC screeing efforts.*

*CA Cancer Journal 2001 51 38-75 CANCER

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Act ThreeParadise Lost

A Summary of the Tragedy

“Improvement depends on changes in patients attitudes, physicians behaviors, insurance

coverage, and the surveillance and reminder systems necessary to support screening

programs”*

* Winawer et al. Gastroenterology February 2003 124

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Epilogue

?

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We Write The Epilogue

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What Is The Current State-of-the-Art for Colorectal

Cancer Screening?

What is the best information that we have on this subject?

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Key Elements In Screening Average Risk Individuals*

Consensus on the First Step

• “Screening programs should begin by classifying the individual patient’s level of risk based on personal, family and medical history, which will determine the appropriate approach to screening that person”*

* Winawer et al. Gastroenterology February 2003 124

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Key Elements In Screening Average Risk Individuals*

• Men & Women 50 Years and Older• Stratify be Risk• Provide Options• Positive Screen => COLONOSCOPY• Cancer Detected => Definitive Therapy • Surveillance post polypectomy or surgery

* Winawer et al. Gastroenterology February 2003 124

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Why Is Risk Assessment So Important?

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The Impact of Family History on Colorectal Cancer Risk

• General population 6% 1 in 16

• 1 first degree relative 2-3 X

• 2 first degree relatives 3-4 X

• 1st degree < 50 years 3-4 X

• Multiple 1st degree 50%*

* Relative risk

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The First Step:Risk Assessment

Three Questions for Every Patient

• History of CRC or Adenomatous Polyp• Predisposing Illness? eg Ulcerative

Colitis• Family History: CRC or Polyps

How many?First degree?Age at diagnosis?

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Application of Risk Stratification

Three Questions for Every Patient• History of CRC or Adenomatous Polyp• Predisposing Illness? Eg Ulcerative Colitis• Family History: CRC or Polyps

How many?

First degree?

Age at diagnosis?• Answer is “NO” = Average Risk

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70-80% of Colorectal Cancer in the United States Occurs Among

Average Risk Individuals.

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70-80% of Colorectal Cancer in the United States Occurs Among

Average Risk Individuals

• For up to 80% of the CRC deaths sustained every year there is NO known predisposition clue!

• Rigorous Systematic Screening Protocol is the ONLY way we will save lives

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Outline

• Screening Recommendations and their scientific support for:

• Average Risk

• Increased Risk

• High Risk

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Screening RecommendationsAverage Risk Population

• Begin at age 50 for women and men

• Yearly FOBT

• Flexible sigmoidoscopy 5 year interval

• FOBT yearly, Flex Sig every 5 years

• Colonoscopy very 10 years

• Double-contrast every 5 years

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Why Is There a Range of Options?

• No single test is of unequivocal superiority.

• Choice increases the likelihood that screening will in fact occur.

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Yearly FOBT:Guaiac based with diet restriction or immunochemical with no restriction

Rational and Evidence

• Testing of 2 samples from 3 consecutive stools has been shown in 3 randomized controlled trials to reduce the risk of death from CRC

• Repeated annual testing can detect as many as 92% of cancers

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WARNING!

Only 1 in 3 individuals with a positive FOBT undergoes

colonoscopy!

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Flexible Sigmoidoscopy Every 5 Years

Rational and Evidence

• 4 case-controlled studies have reported reduced CRC mortality using flexible sigmoidoscopy.

• In the strongest study this reduction was 2/3rds for lesions within reach of the exam.

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Warning!

• There was no reduction in risk for lesions beyond the reach of the flex scope.

• 50 % of patients with advanced proximal colonic cancers had NO distal (within flex sig range) colonic neoplasms.

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Combined FOBT (yearly) and Flexible Sigmoidoscopy (5yrs)

• The effectiveness of the combination strategy has never been tested directly in a randomized trial.

• FOBT should be done first to minimize risks associated with multiple invasive procedures.

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Colonoscopy every 10 Years

Rational and Evidence

• Several lines of evidence support screening colonoscopy.

• Colonoscopy integral part of the FOBT trials that demonstrated a reduction in CRC mortality.

• Colonoscopy is diagnostic AND therapeutic.

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Colonoscopy every 10 Years

Rational and Evidence• There are no randomized controlled studies

evaluating whether colonoscopy alone reduces CRC mortality among individuals at average risk.

HOWEVER• 50 % of patients with advanced proximal

colonic cancers had NO distal (within flex sig range) colonic neoplasms.

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Double Contrast Barium EnemaEvery 5 Years

Rational and Evidence

• There are no randomized controlled trials evaluating the impact of DCBE on CRC mortality.

• DCBE sensitivity is significantly less than colonoscopy

• DCBE has no therapeutic option

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Outline

• Screening Recommendations and their scientific support for:

• Average Risk

• Increased Risk

• High Risk

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CRC Screening for Individuals at Increased Risk

• People with a first-degree relative with colon cancer or adenomatous polyps diagnosed < 60 years or 2 first degree relatives at any age should be advised to have screening colonoscopy at age 40 or 10 years earlier than the first CRC diagnosis, and repeat every 5 years.

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CRC Screening for Individuals at Increased Risk

• People with a first-degree relative with colon cancer or adenomatous polyps diagnosed > 60 years or 2 second degree relatives at any age should be advised to utilize same options as for average risk but begin at age 40.

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CRC Screening for Individuals at Increased Risk

Rational and Evidence

• Screening recommendations for increased risk individuals are based on the known effectiveness of available screening procedures and the observed increased risk among affected relatives.

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Outline

• Screening Recommendations and their scientific support for:

• Average Risk

• Increased Risk

• High Risk

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High Risk:Familial Adenomatous Polyposis:

FAP

• 100% CRC cancer risk.

• Flexible sigmoidoscopy at age 10-12.

• Genetic counseling & testing.

• Prophylactic surgery performed by an experienced provider team.

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High RiskHereditary Non-polyposis Colorectal

Cancer: HNPCC

• Colonoscopy every 1-2 years, beginning at age 20-25 years or 10 years younger than the earliest case in the family, whichever comes first.

• Supported by trials from the Netherlands and Finland by Vasen and Jarvinin respectively (Gastroenterology 2000; 118:829-834).

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What Now?

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Act IIIParadise Lost

• “Despite a consensus among expert groups on the effectiveness of screening for colorectal cancer, screening rates remain low.”*

* Winawer et al. Gastroenterology February 2003 124

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Elements Required for Improvement*

• Patient attitudes

• Physician behavior

• Insurance coverage

• Surveillance and Reminder systems

* Winawer et al. Gastroenterolgy 2003 124 #2

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Our Approach

“Partners in Prevention”

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Partners in Preventionof Colorectal Cancer

• Taking the initiative in mobilizing all of the components required for success.

• Patients

• Physicians

• Support systems

• Research

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Partners in Preventionof Colorectal Cancer

• Taking the initiative in mobilizing all of the components required for success.

• Patients > Risk Assessment

• Physicians > Guideline Clarification

• Support > Reminders

• Research > NIH & ACS

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Partners in PreventionStrategy

1. Risk Assessment

2. Appropriate Screening

3. Follow-up & Reminders

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Partners in PreventionStrategy

• General population outreach: AdvertisingEvents

• Advocacy groups• Academic medical & provider groups• Insurers• Employers• Trade Unions

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Patient & Provider Priority Number One:Risk Assessment

Early Age Risk Assessment

Average Risk Increased Risk High Risk

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How Does The Registry Work?

• We assess personal and family history of colorectal cancer AND adenomatous polyps

• RISK Assessment (ACS Guidelines)

• Screening & Recommendations

• Identify PROVIDER

• Access to research protocols

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Familial CRC RegistryObjectives

• Public Health

Secure higher rates of screening

Especially increased risk groups

• Population Genomics

Study populations for the next generation of studies.

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Registry Population Accrual Strategy

• Medical record retrospective review• Prospective

Surgical Admissions, Clinics, Admitting

etc• “Partners in Prevention”

Employee Health

Trade Unions

Faith Based Organizations

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The Future?

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Identifying Who is at RiskAmong the Negative History

Population?

• Selected Genetic Polymorphisms

• Predisposition Haplotypes & SNPS

• Novel gene discovery

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Partners is looking for Partners!

• NYS & NYC DOH

• NYC H&H

• Insurers

• Employee Health

• Trade Union

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Summary

• Colorectal Cancer remains a major public health challenge.

• We write the epilogue.

• Insurance industry support is crucial.

• Partners in Prevention is part of the solution.

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Thank You!