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Trastuzumab administered to patients with AJCC stage I (T1c) – III human epidermal growth factor receptor 2 (HER2) positive breast cancer who receive adjuvant chemotherapy

CBE ID
1858
Endorsement Status
1.1 New or Maintenance
Previous Endorsement Cycle
Is Under Review
No
Next Maintenance Cycle
Fall 2025
1.3 Measure Description

Percentage of female patients aged 18 and over with HER2/neu positive invasive breast cancer who are administered trastuzumab

        • 1.14 Numerator

          Patients for whom trastuzumab is administered within 12 months of diagnosis

        • 1.15 Denominator

          Female patients aged 18 and over with AJCC stage I (T1c) – III, HER2/neu positive breast cancer who receive chemotherapy

        • Exclusions

          Denominator Exclusions:
          o Patient transfer to practice after initiation of chemotherapy
          Denominator Exceptions:
          o Reason for not administering trastuzumab documented (e.g. patient declined, patient died, patient transferred, contraindication or other clinical exclusion, neoadjuvant chemotherapy or radiation therapy not complete)

        • OLD 1.12 MAT output not attached
          Attached
        • Most Recent Endorsement Activity
          Endorsed Cancer Fall Cycle 2019
          Initial Endorsement
          Last Updated
        • Steward
          American Society of Clinical Oncology
          Steward Organization POC Email
          Steward Organization Copyright

          The Measure is not clinical guidelines, does not establish a standard of medical care, and has not been tested for all potential applications.
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          Commercial uses of the Measure require a license agreement between the user and the American Society of Clinical Oncology (ASCO) and American Medical Association (AMA), [on behalf of the Physician Consortium for Performance Improvement® (PCPI®)] and prior written approval of ASCO, AMA, or PCPI. Neither ASCO, AMA, or PCPI, nor its members shall be responsible for any use of the Measures.
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          © 2020 American Medical Association and American Society of Clinical Oncology. All Rights Reserved. 
          Limited proprietary coding is contained in the Measure specification for convenience. Users of the proprietary code sets should obtain all necessary licenses from the owners of these code sets. ASCO, AMA, , PCPI and its members disclaim all liability for use or accuracy of any Current Procedural Terminology (CPT®) or other coding contained in the specification.
          CPT® contained in the Measures specifications is copyright 2004-2019 American Medical Association. LOINC® copyright 2004-2018 Regenstrief Institute, Inc. SNOMED CLINICAL TERMS (SNOMED CT®) copyright 2004-2018 College of American Pathologists. All Rights Reserved.

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                Conceptual model for risk adjustment
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                Conceptual model for risk adjustment
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