The New Grade A: USPSTF Updated Colorectal Cancer Screening Guidelines, What does it all mean?

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The New Grade A: USPSTF Updated Colorectal Cancer Screening Guidelines, What does it all mean? Robert A. Smith, PhD Cancer Control, Department of Prevention and Early Detection

American Cancer Society and United States Preventive Services Task Force Guidelines for CRC Screening, 2008 2

CRC Screening in Average Risk Adults: Update 2008 Recommendations in red represent differences Recommendation ACS, USMSTF, ACR USPSTF Stool Testing gfobt FIT mtsdna Annual screening with high sensitivity (HS) gfobt or FIT, or mtsdna every 3 years Low sensitivity gfobt not recommended Annual screening with high sensitivity gfobt or FIT sdna, insufficient evidence Flexible sigmoidoscopy Screening every 5 years Screening every 5 years, with annual gfobt or FIT is an option Screening every 5 years, with addition of gfobt or FIT every 3 years Colonoscopy Screening every 10 years Screening every 10 years CT Colonography Screening every 5 years Insufficient evidence (I)

On June 20, 2016, the USPSTF released updated CRC screening recommendations The recommendations covered colorectal cancer screening with FOBT (gfobt, FIT, and FIT-DNA), endoscopy (colonoscopy and flexible sigmoidoscopy), and CT colonography Two tests not endorsed in the draft recommendations released in 2015 (FIT-DNA and CT colonography) were endorsed in the 2016 final recommendations. JAMA June 21, 2016 Volume 315, Number 23

USPSTF CRC Screening Recommendation Statement In the current recommendation, instead of emphasizing specific screening approaches, the USPSTF has instead chosen to highlight that there is convincing evidence that colorectal cancer screening substantially reduces deaths from the disease among adults aged 50 to 75 years and that not enough adults in the United States are using this effective preventive intervention. JAMA June 21, 2016 Volume 315, Number 23

USPSTF CRC Screening Recommendations, 2016 How does these changes compare with the 2008 ACS guideline? ACS endorses screening Q 3 yrs. Same ACS does not emphasize combined FSIG/FOBT JAMA June 21, 2016 Volume 315, Number 23

AAFP CRC Screening Guidelines, 2016 While the USPSTF gave CRC Screening an A rating, the AAFP gave it a B rating. AAFP only recommends FIT, Flexible sigmoidoscopy, and colonoscopy

AAFP CRC Screening Guidelines, 2016 CTC and MT-sDNA are not recommended due to insufficient evidence on harms Age to stop is similar to the USPSTF

Annals of Internal Medicine, November 8, 2016

Annals of Internal Medicine, November 8, 2016

Benefits, Harms, and Burden of Colorectal Screening Strategies Over a Lifetime (1) Benefit: Life-years gained per 1000 individuals screened JAMA June 21, 2016 Volume 315, Number 23

Benefits, Harms, and Burden of Colorectal Screening Strategies Over a Lifetime (2) Benefit: CRC deaths averted per 1000 individuals screened JAMA June 21, 2016 Volume 315, Number 23

Benefits, Harms, and Burden of Colorectal Screening Strategies Over a Lifetime (3) Harms: Complications (gastrointestinal and cardiovascular events) of colorectal cancer screening and follow-up testing per 1000 individuals screened JAMA June 21, 2016 Volume 315, Number 23

Benefits, Harms, and Burden of Colorectal Screening Strategies Over a Lifetime (4) Harms: Lifetime No. of colonoscopies per 1000 individuals screened JAMA June 21, 2016 Volume 315, Number 23

Benefits, Harms, and Burdens of Recommended Screening Strategies Over a Lifetime Source: CISNET, 2015

Recommended Screening Tests ACS and USPSTF Colonoscopy High Sensitivity Fecal Occult Blood Testing High Sensitivity Guaiac Tests Fecal Immunochemical Tests Flexible Sigmoidoscopy (FSIG)* CT colonography* Stool DNA* *Highly limited utilization in US at present

Colonoscopy Allows direct visualization of entire colon lumen Screening, diagnostic and therapeutic 10 yr interval The most common screening test in US (>80%)

Influence of colonoscopic polypectomy on risk of death from colorectal cancer Colonoscopic polypectomy was associated with a 53% reduction in colorectal cancer mortality

Why Colonoscopy is NOT a gold standard screening test Evidence does not support best test or gold standard Colonoscopy misses ~ 10% of significant lesions in expert settings Wide variation in quality (when data are captured and available) More costly on a one-time basis Higher potential for patient injury than other tests

Quality Issues with Colonoscopy Poor pre-procedure documentation Poor prep Failure to reach the cecum Rapid withdrawal time Adverse events Over and under utilization of the procedure Highly variable reports Poor feedback Highly variable adenoma detection rate Interval cancers Most endoscopists are unaware of their numbers, since most facilities do not track their data.

Adenoma Detection Rate (ADR) ADR rate of detection of adenomatous polyps at screening colonoscopy in population age 50+ At least one adenoma should be found 30 percent of the time in men, and 20 percent of the time in women (25 percent composite) Studies indicate wide variation in ADR, even among clinicians in same practice ADR associated with adverse outcomes in a number of studies

ADR and Outcomes: Kaiser Data from 314,872 colonoscopies performed between January 1, 1998 and December 31, 2010 136 gastroenterologists To be included GI had to have completed > 300 colonoscopies and 75 or more screening examinations during the study period ADRs ranged from 7.4% to 52.5%. Corley et al. NEJM 2014: 370: 1298-1306

Hazard ratios for ADR and risk of advanced stage CRC, and fatal CRC Advance Stage CRC Fatal CRC

More Reasons Why Colonoscopy is NOT gold standard Greater patient requirements for successful completion Requires a bowel prep and facility visit, and often a pre-procedure specialty office visit Access Limited by insurance status, local resources Patient preference Many adults don t want an invasive test or a test that requires a bowel prep

Types of Stool Tests* A) Tests that detect blood (Fecal Occult Blood Tests) Two types Guaiac-based FOBT** Immunochemical (FIT) FOBT B) Tests that detect aberrant DNA One test (Cologuard) available in U.S. Cologuard is a multitarget CRC screening test Combines DNA mutation test with FIT Limited use at present * Appropriate only for those at average risk for CRC ** Performance influenced by whether the test is performed at home or in the clinic

Advantages of Stool Tests Less expensive No bowel preparation. Done in privacy at home. No need for time off work or assistance getting home after the procedure. Non-invasive no risk of pain, bleeding, perforation Limits need for colonoscopies required only if stool blood testing is abnormal.

Guaiac Tests Most common type in U.S. Solid evidence (3 RCT s) 30 year f/u (NEJM Oct 2013) Need specimens from 3 bowel movements Non-specific Results influenced by foods and medications Better sensitivity with newer versions (Hemoccult Sensa) Older forms (Hemoccult II) not recommended!

Single Panel FOBT Following Digital Rectal Exam Reasons to STOP single sample FOBT Not recommended by the manufacturer of any test Not recommended by any CRC screening guideline Lowest sensitivity of any CRC screening test, i.e., less than 5% for advanced neoplasia

Fecal Immunochemical Tests (FIT) Specific for human blood and for lower GI bleeding Results not influenced by foods or medications Some types require only 1 or 2 stool specimens Higher sensitivity than older forms of guaiac-based FOBT Costs more than guaiac tests (but higher reimbursement)

Gastroenterology 2016;-:1 21

33

Pooled sensitivity and specificity for FIT 79% sensitivity Ann Intern Med. 2014;160:171-181.

FIT Quality Issues All FIT are not created equal FDA clears guaiac FOBTs and FITs only for detection of blood no assessment of cancer detection capability is required Most FDA-cleared FITs have no published data on their performance for detection of CRC or adenoma Some tests are currently marketed as single sample tests with no performance data on this use FDA is updating clearance criteria

FITs With Published Data* Available in the US Name Hemoccult-ICT/Flexsure OBT Hemosure One Step InSure / ColoVantage OC-Sensor / OC FIT-CHEK OC-Auto Micro OC-Light Manufacturer Beckman-Coulter WHPM, Inc. Clinical Genomics Polymedco Polymedco Polymedco 36

PCP Perceptions of Screening Tests FOBT/FIT used, but: Effectiveness questioned by many clinicians Lack of knowledge re: performance of new vs. older forms of stool tests, other quality issues Colonoscopy viewed as the best screening test, but many patients face barriers or not willing Often recommended despite access or other challenges Focus on colonoscopy associated with low screening rates in a number of studies Patient preferences rarely solicited

Many Patients Prefer FOBT Randomized clinical trial in which 997 patients in the San Francisco PH care system received different recommendations for screening: Recommended Test Colonoscopy 38% FOBT 67% Colonoscopy or FOBT 69% Completed Screening Many patients will forgo screening if they are not offered an alternative to colonoscopy. (Inadomi et al. 2012)

Many Patients Prefer FOBT/FIT Diverse sample of 323 adults given detailed side-by-side description of FOBT and colonoscopy (DeBourcy et al. 2007) 53% preferred FOBT Almost half felt very strongly about their preference 212 patients at 4 health centers rated different screening options with different attributes (Hawley et al. 2008) 31% preferred FOBT 37% preferred colonoscopy Nationally representative sample of 2068 VA patients given brief descriptions of each screening mode (Powell et al. 2009) 29% preferred FOBT 37% preferred colonoscopy

Making the Best Use of Scarce Resources: Screening colonoscopy (refer 1,000 patients) Screening colonoscopy vs. FIT Represents 20 patients FIT testing (2,000 patients) Eligible population, referred Eligible population Patient refusal, no shows Patients with a positive FIT Slide courtesy of Dr. G.Coronado 1 cancer in 400-1000 colonoscopies 1 cancer in 20 colonoscopies

Stool DNA Test (sdna) Fecal occult blood tests detect blood in the stool which is intermittent and non-specific Colon cells are shed continuously Polyps and cancer cells contain abnormal DNA Stool DNA tests look for abnormal DNA from cells that are passed in the stool*

Multi-Target Stool DNA Test One test currently available (Cologuard) Combines tests for stool DNA markers associated with cancers and adenomas plus FIT

Cologuard Sample Collection Kit Rx only. Complete product labeling available at CologuardTest.com Cologuard Patient Guide. 2014.

Home Sample Collection Kit Steps 1 2 3 4 5 6 Rx only. Complete product labeling available at CologuardTest.com.

NEJM 2014

Cologuard FDA has cleared it for marketing as CRC screening test Every 3 year testing interval approved by FDA CMS has agreed to cover Cologuard for average risk Medicare beneficiaries age 50 85 yrs Medicare will reimburse ~ $500 q 3 yrs. for the test (price includes navigation component) Private insurance coverage limited All positive tests must be evaluated by colonoscopy Included in current ACS guideline

Cologuard No long term data on CRC outcomes No evidence for 3 year screening interval Concern that some DNA mutations associated with non-crc cancers Management of patients with positive Cologuard test and normal colonoscopy is uncertain Eligible for no cost sharing screening benefit but like other stool tests, if the test is positive, patients are subject to cost-sharing for follow up colonoscopy

Radiographic CRC Screening Tests Double Contrast Barium Enema CT Colonography, aka Virtual Colonoscopy

2-D View 3-D View Colonoscopy View

CTC to Screen for Colorectal Neoplasia in Asymptomatic Adults Prospective multi-center DoD trial of 1,233 asymptomatic adults

CTC Screening for Colorectal Neoplasia in Asymptomatic Adults Prospective multi-center DoD trial of 1,233 asymptomatic adults comparing tandem CT Colonography with Optical Colonoscopy Size Threshold: 6 mm 8 mm 10 mm By-Patient CTC Sensitivity 88.7% 93.9% 93.8% OC Sensitivity 92.3% 91.5% 87.5% CTC Specificity 79.6% 92.2% 96.0% Conclusion: CTC comparable to OC for detection of clinically relevant polyps

Results: For all samples, sensitivity of Epi procolon for CRC detection was 73.3% (95% CI 63.9 80.9%) and 68.0% (95% CI 58.2 76.5%) FIT. Specificity of the Epi procolon test was 81.5% (95% CI 75.5 86.3%) compared with 97.4% (95% CI 94.1 98.9%) for FIT. When test results for Epi procolon and FIT were combined, CRC detection was 88.7% at a specificity of 78.8%. Conclusions: At a sensitivity of 72%, the Epi procolon test is noninferior to FIT for CRC detection, although at a lower specificity. With negative predictive values of 99.8%, both methods are identical in confirming the absence of CRC. PLOS ONE www.plosone.org 1 June 2014 Volume 9 Issue 6 e98238

The Problem and a Path Ahead A Key Element of the FDA application for epi procolon was addressing the non-adherence challenge A third of US men and women remain unscreened 1 of 3 or ~ 35 million screening eligible women and men are not compliant with screening guidelines Choice of options increases participation Colonoscopy alone does not address the problem Additional options will enhance outcome Blood-based methods will expand the market Colonoscopy 35 million U.S. citizens are unscreened Incremental market opportunity > $1 Bn per year ww Additional options will enhance outcome

Conclusion What are the CRC Screening Challenges Today? This just in.what happens to the Affordable Care Act? Achieving 80% screening rate requires: Effective reminder systems and effective informed decision making Appropriate use of colonoscopy alternatives To spur growth, must educate PCPs on: Evidence of FOBT/FIT efficacy Stool test program quality features Importance of exploring patient preferences and offering options New and emerging test options

Conclusion What are the CRC Screening Challenges Today? Offering options: How many are too many? Access to colonoscopy for adults without insurance, or high deductible plans Community-based Links of Care Models Navigation Colonoscopy Quality Assurance Programs Endoscopists must track the ADR, and preferably the multiple ADR Measure quality on key indicators Have a plan for corrective action