tools you can use · •the webinar will be archived and posted on npc’s website in coming days....

TOOLS YOU CAN USE April 8, 2014

Academy of Managed Care Pharmacy

International Society for Pharmacoeconomics and Outcomes Research

National Pharmaceutical Council

Speakers

Bernadette Eichelberger, PharmD Director, Pharmacy Affairs, AMCP

Marc Berger, MD Vice President, Real World Data and Analytics, Pfizer

Brian Sweet, MBA Executive Director, U.S. Payer & Real World Evidence, AstraZeneca (Moderator)

Jennifer Graff, PharmD Director, Comparative Effectiveness Research, NPC

Dan Allen, PharmD Clinical Pharmacist Consultant, OmedaRx

Submit questions and

comments via the Questions

section in the Control Panel

To Submit Questions

How to Ask a Question

How to Ask a Question

Twitter

• Message @npcnow using #npcwebinar

• We also encourage you to tweet during the webinar using #npcwebinar

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Marc Berger, MD

Vice President, Real World Data and Analytics, Pfizer

AMCP/ISPOR/NPC CER Collaborative

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Part 1: Evaluate Quality of Individual Studies

•Prospective

•Retrospective

•Modeling

•Indirect Methods

Part 2: Synthesizing the Evidence Across Multiple Study Types

• RCT, Observational studies

Part 3: Assessing the Evidence by Decision Makers: A Toolkit

• Tools

• Educational Materials and Training

The Issues

• Pharmacy decision-makers (“users”) are uncertain to interpret CER evidence not derived from RCTs

– Inherent Causal Inference Challenge Due to Observational Nature

– Less Rigorous Regulatory Oversight

– Complex Statistical Modeling

– Heterogeneous Perspectives and Training

• The issues are growing more challenging

– More studies and more complex analytic approaches

Design Objectives

• Appraisal tools:

– Easy, fast, accurate, minimal skill required

– Help end users assess the quality, credibility, and relevance of studies

• Promote the use of non-RCT evidence in decision making

• Educational tools

Prospective and Retrospective Obs.

Studies

Indirect Treatment Comparison

Studies Modeling Studies

Evolution of the Tools

• Agreement on 2 main Categories

– Relevance (Are the results applicable?) • Generalizability/PICO

– Credibility (Can I trust the results?) • Validity

• Agreement on not to formally provide a score

– Concerns regarding “false precision”

– Concerns regarding “fatal flaws”

– Decision to ask rater to provide global assessment of each domain as either “sufficient” or “insufficient”

– Formal scoring would undermine the “educational” value of the tools

Examples of Questions

Retrospective/

Prospective

• Design

• Data

• Analysis

• Reporting

• Interpretation

• Conflicts of Interest

• 33 items

Modeling

• Validation

• External

• Verification

• Face

• Design

• Data

• Analysis

• Reporting

• Interpretation

• Conflicts of Interest

• 26 items

Indirect Treatment Comparisons

• Evidence Base

• Analysis

• Reporting

• Interpretation

• Conflict of Interest

• 15 items

Fig. 1

Source: Value in Health 2014; 17:143-156 (DOI:10.1016/j.jval.2013.12.011 )

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Step by Step Instructions

Evaluation History

www.cercollaborative.org

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Explanation/ Definitions

More Information Check Out the March 2014 Value in Health

• Editorial: Tools for Health Care Decision Making: Observational Studies, Modeling Studies, and Network Meta-Analyses

• A Questionnaire to Assess the Relevance and Credibility of Observational Studies to Inform Health Care Decision Making: An ISPOR-AMCP-NPC Good Practice Task Force Report

• Indirect Treatment Comparison/Network Meta-Analysis Study Questionnaire to Assess Relevance and Credibility to Inform Health Care Decision Making: An ISPOR-AMCP-NPC Good Practice Task Force Report

• Questionnaire to Assess Relevance and Credibility of Modeling Studies for Informing Health Care Decision Making: An ISPOR-AMCP-NPC Good Practice Task Force Report

Dan Allen, PharmD

Clinical Pharmacist Consultant, OmedaRx

Who is OmedaRx? • Stand-alone PBM wholly owned by Cambia Health

Solutions

– Formerly RegenceRx

– Cambia Health Solutions – BlueCross/Blue Shield franchise in Oregon, Washington, Idaho, Utah

– Full PBM services to the Regence family of health plans

• Provide formulary guidance and utilization management strategies to “Blues” and non-Blues plans nationwide

– Medication Reviews

– Medication Policies

– P&T Support

Why Implement ICER?

• Challenge: How do you systematically summarize separate clinical trials and available safety information?

• Institute for Clinical and Economic Review (ICER)

– Rating system evolved from earlier AHIP workgroup guided by insurers to meet needs for coverage decision-making

• Freely available, nationally vetted, meshes with current evaluation methods

Implementation • Extensive staff training

• In-service to clients’ P&T committees over multiple meetings

• Ongoing training

• Continuous quality improvement

• Decision tracking

• Developing custom formulary frameworks for each clients

The ICER Rating Matrix

High Certainty

D (Inferior)

C (Comparable)

B (Small/Modest

Benefit)

A (Moderate/

Large Benefit)

Moderate Certainty

I (Insufficient to determine)

P/I (Promising but Inconclusive)

Low Certainty

I (Insufficient to determine)

Negative Health Benefit

Comparable Health Benefit

Incremental Health Benefit

Substantial Health Benefit

The ICER Rating Matrix – Effect of Certainty

High Certainty

D (Inferior)

C (Comparable)

B (Small/Modest

Benefit)

A (Moderate/

Large Benefit)

Moderate Certainty

I (Insufficient to determine)

P/I (Promising but Inconclusive)

Low Certainty

I (Insufficient to determine)

Negative Health Benefit

Comparable Health Benefit

Incremental Health Benefit

Substantial Health Benefit

TE

Treatment Effect

Treatment Effect

OmedaRx ICER Process

Estimate certainty in the overall clinical

data

Estimate the magnitude of

net-health benefit

Make safety modification to point estimate

Identity “point estimate” on the

ICER matrix

Consideration for Using the ICER Matrix

• Most reviews involve two comparisons – against placebo and against existing therapies

• New therapies often lack direct comparative trials

– Compare the evidence synthesis of placebo-controlled data

• This process is always subject to peer review

– We challenge each other on our assessment of the evidence, our assessment of the standard of care, and our assessment of the safety profile

Finding Certainty of Benefit Certainty of

Benefit Definitions of Evidence

(ICER) Quantification of Studies

(OmedaRx)

High Certainty

Allows estimation for the relative potential chances / magnitude of net health benefit

≥1 high confidence study; consistent results OR ≥2 fair confidence studies with: • Consistent results • Possibly clinically meaningful endpoint

Moderate Certainty

Difficult to estimate the net health benefit with precision

≥1 high confidence study; consistent results OR ≥1 fair confidence study with: • Consistent results • Possibly clinically meaningful endpoint OR ≥2 low confidence studies with: • Consistent results • Possibly clinically meaningful endpoint

Low Certainty

Insufficient to allow assessment of the net health benefit

low confidence studies not meeting threshold for moderate certainty (defined above) OR ≥2 fair confidence studies with inconsistency in the results

Determining Magnitude of Health Benefit

High Certainty

D (Inferior)

C (Comparable)

B (Small/Modest

Benefit)

A (Moderate/

Large Benefit)

Moderate Certainty

I (Insufficient to determine)

P/I (Promising but Inconclusive)

Low Certainty

I (Insufficient to determine)

Negative Health Benefit

Comparable Health Benefit

Incremental Health Benefit

Substantial Health Benefit

Make Safety Modification to Point Estimate

Safety Conclusion Example

Estimate of Certainty Estimate of Benefit

Track record with proven advantages (over active comparator)

Track record with no new safety concerns

Insufficient track record

2013 New Medications: Overall Evidence and Clinical Trials Quality

High confidence (1)

1%

Fair confidence (11) 13%

Low confidence

(76) 86%

High certainty (1) 2%

Moderate certainty (17)

40%

Low certainty (17) 40%

Review in progress (8) 18%

Medications’ ICER

Evidence Synthesis

Individual Clinical

Trials

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Lessons Learned

• Successful clinical evidence synthesis is dependent on rigorous clinical evidence evaluation

• Agreed upon, uniform grading and synthesis guidelines important for maintaining quality across multiple reviewers

• Never allow the quantification guidelines to override professional judgement

Bernadette Eichelberger, PharmD

Director, Pharmacy Affairs, AMCP

AMCP/ISPOR/NPC CER Collaborative

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Part 1: Evaluate Quality of Individual Studies

•Prospective

•Retrospective

•Modeling

•Indirect Methods

Part 2: Synthesizing the Evidence Across Multiple Study Types

• RCT, Observational studies

Part 3: Assessing the Evidence by Decision Makers: A Toolkit

• Tools

• Educational Materials and Training

Additional Tools and Resources at www.cercollaborative.org

Summary Reports Can Be Downloaded in Word or Excel

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Register Today for the CER Certificate Program http://www.pharmacists4knowledge.org/cips/cer

CER Certificate Program Demo and Modules Available Today

Jennifer Graff, PharmD

Director, Comparative Effectiveness Research, NPC

CER Collaborative Tool Improves the Evidence Assessment Dialogue

• Clarity – Agreed upon elements of “good practice”

for conducting studies

– When evidence is considered = ROI for investing in further research

• Consistency – Evaluation of evidence in a similar fashion

at different times or different individuals or organizations

• Transparency – Need for evidence is considered for those

generating and using evidence

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CER Collaborative Improves Evidence Generation Certainty

• Began with good practices for research; goal is to ensure there is consistency in evidence evaluation

• Tools can be incorporated in study design, management, conduct and reporting processes

• Starting point for dialogue

– Feasibility of inclusion in a journal vs. on-line appendix vs. study report

CER Collaborative Continues the Dialogue to Improve Evidence Communication

• Framework for dialogue with managed market accounts and field based research groups

• Increase decision-maker awareness of all types of evidence

• May provide additional support for determining competent and reliable scientific evidence

Resources You Can Use https://members.npcnow.org/resources

Protocol and

Publication

Questionnaires

www.cercollaborative.org NPC Champion Slides

Implications for Industry

• Use familiar language of the decision-maker

• Ensure research meets good practice principles through eyes of reviewers

– Consider when designing research

– Review when finalizing publications

– Consider when communicating evidence to decision-makers

• Training

• Dialogue, dialogue, dialogue

Special Thanks to Work Groups Members Prospective Retrospective Indirect Treatment

Comparisons Modeling Synthesizing a Body of

Evidence

Dan Allen RegenceRx

Winnie Yang Blue Shield of

California

Sherry Andes Catamaran Cheryl Kaltz U. of Michigan

Lisa Cashman MedImpact

Karen Worley Humana

Eric Cannon SelectHealth

Jessica Daw UPMC Health Plan

Bimal Patel MedImpact

Jon Clouse OptumInsight

Scott Devine Merck

Kristijan Kahler Novartis

Joseph C. Cappelleri Pfizer

John Penrod Bristol-Myers Squibb

Jeff White WellPoint NextRX

John Graham Bristol-Myers Squibb

Nicole C. Quon Optimer

Vijay Joish Bayer

Hong Kan GlaxoSmithKline

Rahul Ganguly GlaxoSmithKline

Don Husereau U. Ottawa

William Crown Optuminsight Life

Sciences

Thomas Trikalinos Tufts Medical Center

David Eddy Archimedes Inc.

Bryan Luce PCORI

Dan Mullins U. Of Maryland

Michael Johnson U. of Houston

Georgia Salanti U. of Ioannina

Andy Briggs U. of Glasgow

Richard Willke Pfizer

Marc Berger (Chair) Pfizer

Bradley Martin (Chair)

U. of Arkansas

Jeroen Jansen (Chair)

Redwood Consulting

J. Jaime Caro (Chair)

United BioSource Corp.

Brian Sweet (Chair)

AstraZeneca

Helen Sherman (Chair)

Select Benefit Guidance

Questions?

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Q&A Panel

Bernadette Eichelberger, PharmD Director, Pharmacy Affairs, AMCP

Marc Berger, MD Vice President, Real World Data and Analytics, Pfizer

Brian Sweet, MBA Executive Director, U.S. Payer & Real World Evidence, AstraZeneca (Moderator)

Jennifer Graff, PharmD Director, Comparative Effectiveness Research, NPC

Dan Allen, PharmD Clinical Pharmacist Consultant, OmedaRx

Thank You

• The webinar will be archived and posted on NPC’s website in coming days.

• For further information, contact:

– Brian Sweet brian.sweet@astrazeneca.com

– Marc Berger marc.berger@pfizer.com

– Dan Allen dan.allen@omedarx.com

– Bernadette Eichelberger beichelberger@amcp.org

– Jennifer Graff jgraff@npcnow.org

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cercollaborative.org