2022-01-10 - Cancer Synoptic Reporting Project Group Meeting

2022-01-10 - Cancer Synoptic Reporting Project Group Meeting

Cancer Synoptic Reporting Project Group

10 January 2022 at 17:30 UTC

Attendees @Scott Campbell @Ian Green @Paul @Stefan Dubois @Suzanne Santamaria @Nicola Ingram @Keng-Ling Wallin@laszlo @Daniel Karlsson @Thomas Ruediger. @Former user (Deleted) @Former user (Deleted)

@Elaine Wooler @r.dash

 

Discussion items

Item

Description

Owner

Notes

Action

Item

Description

Owner

Notes

Action

1

IHC

@Scott Campbell

  1. Confirm actions

  2. Background
    Two use cases:

    1. Prognostic stains - Primary cancer already determined.  Used for treatment decisions to be made.

      1. Pathologists knows where stain will/will not be expressed

      2. No need to declare location within cell that expresses the stain (nucleus, cytoplasm, membrane)

    2. Diagnostic stains - Used to differentiate between possible diagnoses.

      1. Where the protein is expressed informs the pathologist needed information to render a diagnosis.

      2. Need to declare location of protein expression in the cell.

 

Prognostic stain: 


This seems to be acceptable, in general.  JCA suggested the addition of a subtype of anatomical structure more reflective of cellular structure.

Diagnostic stain:

Discussion was robust with discussion surrounding specific meaning of the observable (i.e., what is being measured by the pathologist) vs. how the observable and observations are interpreted by the pathologist.  For example, IHC scoring of HER2 in breast is 0,1+,2+.  However, clinical interpretation of HER2+ tissue based on the 0,1+,2+ has changed.  0 and 1+ are now considered NEGATIVE for HER2 and 2+ is considered equivocal.

For purposes of the observable entity concepts as exemplified by IHC HER2, interpretation of results is separate from the observation.  Therefore, a separate observable entity OR clinical finding should be used to represent the interpretation of the IHC staining observation (ordinal scale) in such situations.  Observable entities will be created to represent FISH and other testing methods used to realize the final diagnosis/interpretation

@Scott Campbell to provide model examples of primary/met IHC

Also, focus to be on Synoptic vs. differential diagnostics.

2

Treatment effect

@Scott Campbell

Continue discussion:

What are we measuring when assessing "treatment effect"?  

Is this a histologic change?  Viability of tumor cells?

Briefly discussed, but general comments confer that this is a histologic feature property of measure.  Will address and confirm at next work group meeting

Did not discuss

3

Lymph nodes

@Scott Campbell

@Stefan Dubois

  1. Discuss approach to lymph node body structures and differences in naming/locations (example AJCC esophageal cancer vs. JES esophageal cancer)

2. Management of observables for lymph node involvement.  Example: 

Great discussion.  Assume site specific where clinically called for...use reference materials if provided.

4

AJCC update?

@Jim Case

Any updates that can be shared?

 

Meeting Files

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2022-Jan-10 by Scott Campbell

 

 

 

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