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Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms. Using CTC v2.0 and CTCAE v3.0. Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms. Presentation Outline. AE Reporting Background/History AE Terminology Physician/Investigator Responsibility

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slide1

Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms

Using CTC v2.0 and CTCAE v3.0

presentation outline

Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms

Presentation Outline
  • AE Reporting Background/History
  • AE Terminology
  • Physician/Investigator Responsibility
  • AE Grade
  • AE Attribution
  • Locating AEs Terms
  • Use of ‘Other, Specify’
  • Summary
background and history

Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms

Background and History

Why is NCI stressing requirements for accurate, specific AE documentation and reporting?

  • It is the law – Federal Regulations
  • Required of all physicians who signthe FDA1572 investigator registration form
  • Ensures human subject safety
  • Facilitates accurate analysis of effects from investigational cancer interventions
nci requires ae reporting using ctc v2 0 ctcae v3 0 specific terms

Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms

NCI requires AE Reporting using CTC v2.0/CTCAE v3.0 Specific Terms

Background and History - continued

Within the scope of the CTC/CTCAE:

  • AE definition
  • AE grade (seriousness) assignment

Beyond the scope of CTC/CTCAE:

  • Attribution of AE
  • Interpretation of seriousness of AE
slide5

Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms

Background and History - continued

History of the Common Toxicity Criteria (CTC)

Since 1982, NCI CTC has been the standard for AE reporting in the oncology community.

Historical Timeline

1982

  • Adverse Drug Experience Reporting
  • Study Summaries
  • IND reports to FDA
  • Publications
  • Format:
    • 18 CATEGORIES
    • 49 AE Terms
    • Grades:
      • Grade 1 = Mild
      • Grade 2 = Moderate
      • Grade 3 = Severe
      • Grade 4 = Life-threatening
slide6

Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms

Background and History - continued

1997 -CTC Review Committee assembled to revise and expand CTC.

1998 - Introduced CTC v2.0

  • 24 CATEGORIES
  • ~300 AE Terms (Acute)
  • Specificity
  • Radiotherapy
  • Pediatrics
  • Appendices
    • RTOG/EORTG Late Radiation Morbidity Scoring Scheme
    • BMT Complex/Multi-component Event Scheme

NCI CTC v2.0 has become the worldwide standard dictionary for reporting acute AEs in cancer clinical trials and has been translated into several languages – NCI and Industry.

slide7

Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms

Background and History - continued

2002 -CTEP convened a CTC Development Team (CTCDT) consisting of independent disease and modality-specific cancer therapy experts and NCI representatives to oversee the creation of the Common Terminology Criteria Adverse Event (CTCAE) v3.0.

  • Update core criteria.
  • Expand to create comprehensive dictionary of AEs and grades applicable to all oncology clinical trials without regard to:
    • Chronicity
    • Modality
  • For criteria development, CTEP coordinated:
    • Late effects
    • Surgical
    • Pediatric workshops
  • CTCAE v3.0 is the first uniform and comprehensive dictionary of AE grading criteria available for use by all modalities.

2003 -Introduced CTCAE v3.0.

slide8

Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms

Adverse Events

Multiple clinical terms are used to convey the occurrence of an Adverse Event (AE):

  • Side effect
  • Acute effect or late effect
  • Complication
  • Toxicity
  • Morbidity, etc.

All terms essentially point to a change possibly caused by treatment.

slide9

Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms

Adverse Events - continued

  • An AE is any unfavorable or unintended:
    • Sign
    • Abnormal lab
    • Symptom
    • Disease
  • An AE is a unique representation of a specific event used for medical documentation and scientific analyses.
  • Each AE term is mapped to a MedDRA v6.0 term and code.
    • Same term and code used in Japan and the EU.
  • AEs can be:
    • Symptomatic or completely asymptomatic.
    • Clinically or radiographically detected.
    • Noted on laboratory studies or other testing.
slide10

Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms

Adverse Events - continued

What to report as an AE

  • The guideline for clinicians is to capture any effect from an intervention which may be deleterious.
  • Prudent adverse event reporting requires that only AEs that are mandated in protocols and clinically relevantpositives be documented.
slide11

Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms

Adverse Events - continued

There are multiple causes of AEs:

  • Pre-existing conditions
    • Hypertension
    • Diabetes
  • Concomitant medications
    • Anticoagulants
    • Steroids
  • Other causes
    • Transfusion reactions
    • Accidental injuries
  • Reporting and grading an AE simply reports that an event occurred and the seriousness of the event.
  • The clinician must assign attribution of the event, either to the intervention or something else.
slide12

Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms

Adverse Events - continued

Physician Responsibilities in Clinical Research

  • Must become familiar with the CTCAE Terms and Grades.
  • Responsible for documenting AEs that can be verified on audit.
  • Must document signs, symptoms, clinical findings, etc. as they appear.
  • Note: Realize documentation of AEs does not necessarily imply causality to intervention or error in administration.
slide13

Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms

Adverse Events - continued

Physician Responsibility Regarding Grade

  • Document at least descriptive terms found in definitions of Grades to enable CRAs easy identification of numeric Grade.
  • Document signs, symptoms, objective measures that characterize severity (Grade).

Refer to CTCAE descriptions of Grade.

slide14

Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms

Adverse Events - continued

Documenting Grade

  • Semi-colon indicates ‘or’ within the description of the Grade.
  • Em dash (—) indicates a Grade not applicable to the AE.

In the development of CTC/CTCAE careful consideration was given to including all descriptions of events that were considered “serious” or “life-threatening” (as defined in the FDA regulations) in Grade 3 and 4, respectively.

slide15

Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms

Adverse Events - continued

Documenting Grade

  • A patient need notexhibit all elements of a Grade description to be designated that Grade.
    • Example:
    • Induration/fibrosis (skin and subcutaneous tissue)
    • Grade 3:
    • Dysfunction interfering with ADL; very marked density, retraction or fixation

Read as “Dysfunction ….. OR very marked……”

    • Interpretation:
    • A patient with very marked density, retraction or fixation, but is able to perform ADLs, is Graded 3.

When a patient exhibits elements of multiple Grades, the highestGrade is to be assigned.

slide16

Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms

Adverse Events - continued

Physician Responsibility Regarding Attribution

  • Physicians are to document the relationship (ATTRIBUTION) of the protocol intervention to each event.
  • Designating an event as treatment related (or not) is done two ways:
    • 1. By the treating CLINICIAN:
      • Formal “assignment” per adverse event reporting form (“...unlikely, possibly, etc) at the time of clinical evaluation.
    • 2. By Investigators:
      • Later in aggregate data review and reporting by the Investigators.
slide17

Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms

Adverse Events - continued

Attribution Standards

  • Unrelated:

The Adverse Event is clearly not related to the investigational agent(s)

  • Unlikely:

The Adverse Event is doubtfully related to the investigational agent(s)

  • Possible:

The Adverse Event may be related to the investigational agent(s)

  • Probable:

The Adverse Event is likely related to the investigational agent(s)

  • Definite:

The Adverse Event is clearly related to the investigational agent(s)

slide18

Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms

Locating AE Terms - Introduction

The remainder of the presentation provides instruction to locate appropriate AE terms for use in AdEERS, CDUS, and other CTEP data systems.

Each section illustrates the steps used to find an AE using specific Common Toxicity Criteria v2.0 (CTC) and Common Terminology Criteria or Adverse Event v3.0 (CTCAE) examples.

slide19

Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms

Available Tools

The following are the tools available for determining correct AEs. Each correlates to a section within this presentation.

Section 1: CTCAE v3.0 Document Search

Section 2: CTCAE Dictionary and Index

Section 3: CTCAE Online Instructions and Guidelines

All tools are available from the CTEP Home Page at http://ctep.cancer.gov

slide20

Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms

Locating CTC/CTCAE Tools from the CTEP Home Page

  • Access the CTEP Home Page.
  • Scroll halfway down the page.
  • Click on the CTCAE v3.0 link.

The CTCAE v3.0 Web page displays.

slide21

Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms

Tools available from the CTCAE v3.0 Web page

The CTCAE v3.0 Web page provides links to the CTCAE v3.0 document and other related tools, including:

  • The CTCAE v3.0 Document
  • The CTCAE v3.0 Dictionary and Index
  • The CTCAE v3.0 Online Instructions and Guidelines
slide22

Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms

Section 1

Searching the CTCAE v3.0 Document

Access the CTCAE v3.0 Document PDF file from the Web.

Press CONTROL + F to open the Search Tool.

Note: The search tool may appear differently depending on the browser you use.

Enter the term you wish to search and click Search.

slide23

Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms

Section 1: Searching the CTCAE v3.0 Document - continued

The search returns six instances of the AE term.

Review all to select the most appropriate AE term and Grade.

slide24

Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms

Section 1: Searching the CTCAE v3.0 Document - continued

A search on the term ‘septic’ displays eight instances of the AE term.

See next slide to view the remaining terms.

slide25

Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms

Section 1: Searching the CTCAE v3.0 Document - continued

The term ‘non-septic’ will also match the search criteria and display.

slide26

Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms

Section 2

Searching the CTCAE Dictionary

The CTCAE Dictionary replaces the CTC Interactive Web Application and provides search capabilities for CTC v2.0 and CTCAE v3.0.

When opened, CTCAE v3.0 is displayed by default with the AE Short Names listed in alphabetical order.

slide27

Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms

  • To access the CTC v2.0 search page, click on the CTC v2.0 tab.
  • Click one of the alphabet buttons to limit the view alphabetically.
  • To view information related to an AE, click on the AE term.

The CATEGORY, full name, grade definitions and MedDRA codes, along with any supra-ordinate terms, remarks, and also consider information are displayed in the right panel.

  • To view Navigation Notes, hover the cursor over the icon or click the link.

Section 2: Searching the CTCAE Dictionary - continued

slide28

Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms

Section 2: Searching the CTCAE Dictionary - continued

Search by CATEGORY

To display the list of AEs by CATEGORY:

  • Click the drop down list arrow.

The list of CTCAE CATEGORIES display.

  • Click the CATEGORY.

Note: To revert to the alphabetical list, click ‘All Categories’ from the drop down list.

All AEs associated with the CATEGORY are displayed in alphabetical order.

slide29

Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms

Section 2: Searching the CTCAE Dictionary - continued

Search by Keyword

To search for a specific AE:

  • Enter the keyword within the Search for field.
  • Click the Literal button.

The term displays highlighted in blue.

In this example, Rash is also displayed as a consideration.

Click Rash.

The term ‘Pruritus’ is listed within the Grade 2 definition.

slide30

Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms

Section 2: Searching the CTCAE Dictionary - continued

Search by Index

To search for related AEs:

  • Enter the keyword within the Search for field.
  • Click the Index button.

Possible appropriate AEs are displayed.

Review all to select the most appropriate AE term and Grade.

slide31

Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms

Section 3

Searching the CTCAE Instructions and Guidelines

The CTCAE Instructions and Guidelines provides a wealth of information regarding the CTCAE and includes four methods to obtain information:

  • Contents (displays by default)
  • Index(narrow search)
  • Search(broad search)
  • Glossary
slide32

Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms

Section 3: Searching the CTCAE Instructions and Guidelines - continued

Search on Contents

To search using the Table of Contents:

  • From the left panel, click the chapter link. The chapter opens and displays all available topics.
  • Click the topic link. The topic displays in the right panel.
  • Topics may directly display information or provide links to information.

Display of related information.

slide33

Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms

Section 3: Searching the CTCAE Instructions and Guidelines - continued

Search on Index

To search using the Index function:

  • Click Index.
  • Either enter the keyword in the search field or scroll to the term.
  • Once the term is located, click the term within the Index list.
  • The topic where the term exists is displayed. It may be necessary to click other links to access the information.

Display of related information.

slide34

Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms

Section 3: Searching the CTCAE Instructions and Guidelines - continued

The Search Function

To search using the Search function:

  • Click Search.
  • Enter the keyword in the search field.
  • Click Go.

All topics that include a word(s) that match the keyword will display.

  • Locate and click the topic that best meets your information needs.The topic displays.

Display of related information.

slide35

Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms

Section 3: Searching the CTCAE Instructions and Guidelines - continued

The Glossary

To use the Glossary function:

  • Click Glossary.
  • Use the scroll bar to locate the term needed.
  • Click the term.

The term definition displays in the lower left panel.

slide36

Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms

How and When to use the ‘Other, Specify’ Mechanism for AE Reporting

    • In recognition that as science and cancer treatments continue to evolve and the potential for novel and unknown untoward affects to occur, the NCI has incorporated a mechanism into the CTC and CTCAE to capture these yet-to-be-defined events.
    • In the rare event that a suitable CTC or CTCAE term cannot be found, the NCI allows the submitter to report the appropriate verbatim term via the ‘Other, Specify’ mechanism.
  • The use of the ‘Other, Specify\' mechanism is an exception, not the rule.
    • To minimize overuse, CTEP, NCI will build rules into applications to flag and/or reject reports that take excessive advantage of the ‘Other, Specify’ mechanism. In addition, CTEP, NCI will closely scrutinize all AEs submitted as ‘Other, Specify’. The investigator will be required to correct and resubmit their report if a suitable CTC or CTCAE term is identified by CTEP, NCI staff.
slide37

Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms

How and When to use the ‘Other, Specify’ Mechanism for AE Reporting - continued

Using the ‘Other, Specify’ Mechanism

  • If a suitable CTC or CTCAE term is not available, the investigator must make a note to this affect in the source documentation.
  • The investigator must identify the most appropriate CTC or CTCAE CATEGORY to classify the event.
  • Within each CATEGORY is a CTC or CTCAE term ‘Other’ (i.e., ‘Cardiac Arrhythmia – Other’). The submitter must describe or ‘specify’ what the adverse event was. Descriptions must be explicit and provide sufficient detail to describe the event and should be as brief as possible (for example, two to four words).
  • Once the CTC or CTCAE CATEGORY ‘Other’ term has been selected and specified, the submitter must ‘Grade’ the event. The grade refers to the severity of the event. The general description of grades to be used for the ‘Other; Specify’ mechanism are as follows:
    • Grade 1 – Mild AE
    • Grade 2 – Moderate AE
    • Grade 3 – Severe AE
    • Grade 4 – Life threatening or disabling AE
    • Grade 5 – Death related to AE

For more information, see the Guidelines for CTC/CTCAE ‘Other, Specify’ from the CTC/CTCAE Home Page.

slide38

Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms

How and When to use the ‘Other, Specify’ Mechanism for AE Reporting - continued

Examples of inappropriate ‘Other, Specify’(CTC v2.0)

slide39

Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms

How and When to use the ‘Other, Specify’ Mechanism for AE Reporting - continued

Examples of inappropriate ‘Other, Specify’(CTC v2.0)

slide40

Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms

How and When to use the ‘Other, Specify’ Mechanism for AE Reporting - continued

Examples of inappropriate ‘Other, Specify’(CTCAE v3.0)

slide41

Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms

How and When to use the ‘Other, Specify’ Mechanism for AE Reporting - continued

Examples of inappropriate ‘Other, Specify’(CTCAE v3.0)

slide42

Responsible Adverse Event (AE) Reporting: Finding Appropriate AE Terms

How and When to use the ‘Other, Specify’ Mechanism for AE Reporting - continued

Summary: Using CTC v2.0/CTCAE v3.0

  • Use CTC v2.0 or CTCAE v3.0 to locate appropriate AE term.
  • Document the grade of the AE.
    • If a patient exhibits elements of multiple grades, assign the highest grade.
  • Assign attribution of the AE.
  • If a CTC or CTCAE term cannot be found using the different tools available, the ‘Other, Specify’ option should be used.
    • Grade and attribution must be assigned.
slide43

Contact the NCI CTEP Help Desk if further assistance is needed.

Phone: 888-CTEPHLP (1-888-283-7457)Fax: 301.948.2242E-mail: [email protected]

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