Strategies for Improving ERBB2 (HER2) Testing in NSCLC Within Community Settings - CME - Guideline Central

CME

Title
Strategies for Improving ERBB2 (HER2) Testing in NSCLC Within Community Settings
Link
Description
The pace at which targetable tumor-specific molecular alterations have been identified over the past decade have ushered in an era of precision oncology, yielding significant insights into the diversity of cancer, offering diagnostic and prognostic benefits, and guiding therapy selection. Indeed, guidelines emphasize that comprehensive biomarker testing should be conducted to identify actionable mutations in non-small-cell lung cancer (NSCLC), including ALK, EGFR, KRAS, MET, RET, and ERBB2 (HER2). These tests guide the selection of targeted therapies that can inhibit oncogenic pathways directly implicated in tumor growth and progression. However, comprehensive molecular testing continues to be underused, especially in community hospital settings. Underlying reasons are many and varied, and include lack of clinical knowledge, lack of multidisciplinary support in the interpretation of test results, shortcomings in tissue samples, lack of access to tests, reimbursement challenges, and turnaround times. Quality improvement (QI) programs are well suited to facilitate adoption of system-level solutions to improve guideline recommended testing of patients with NSCLC, including in patients with HER2 (ERBB2) mutations; To improve guideline recommended testing of patients with NSCLC, including in patients with HER2 (ERBB2) mutations, implementation-focused educational programs facilitating system- and process-related changes along with formalized training cascades are key to mitigating barriers. This interactive practice guide offers interventions for both team training and infrastructure building in a cost effective and high impact way. Learners can identify solutions most relevant to their scope of practice and areas of need. Don’t delay! Start improving your NSCLC biomarker testing to optimize treatment processes and practices now!
Target Audience
This activity is intended for multidisciplinary providers treating patients with NSCLC in the community cancer setting including thoracic oncologists, thoracic surgeons, medical oncologists, molecular pathologists, pulmonologists, oncology pharmacists, clinical pharmacists, patient navigators, tissue navigators, and other members of the multidisciplinary team.
Learning Objectives
  • Assess current NSCLC biomarker testing practices to confirm compliance with the latest guideline recommendations for a broad multi-panel approach
  • Develop strategies to mitigate challenges and barriers to standardizing ERBB2 (HER2) testing in all patients with advanced NSCLC
  • Establish multidisciplinary frameworks to interpret biomarker test findings prior to initiating first-line treatment and reassess again when initiating second-line treatment
Estimated Duration
150 minutes
Delivery Mode
Online
Format
Online Learning
Specialties
Oncology, Pulmonology, Thoracic Surgery
Disclosures and Disclaimers
The content for this activity was developed independently of any ineligible company. All materials are included with permission. The opinions expressed are those of the faculty and are not to be construed as those of the publisher or grantor(s). This educational activity was planned and produced in accordance with the ACCME Standards for Integrity and Independence in Accredited Continuing Education. Recommendations involving clinical medicine in a continuing medical education (CME/CE) activity must be based on evidence that is accepted within the profession of medicine as adequate justification for their indications and contraindications in the care of patients. All scientific research referred to, reported, or used in CME/CE in support or justification of a patient care recommendation must conform to the generally accepted standards of experimental design, data collection, and analysis. This CME/CE activity might describe the off-label, investigational, or experimental use of medications and/or devices that may exceed their FDA-approved labeling. Physicians should consult the current manufacturers’ prescribing information for these products. ACHL and The University of Chicago require the speaker to disclose that a product is not labeled for the use under discussion.
Accredited Providers
  • The University of Chicago Pritzker School of Medicine
  • Academy for Continued Healthcare Learning (ACHL)
Commercial Support
  • Boehringer Ingelheim Pharmaceuticals, Inc
Activity Expiration Date
April 1, 2027
Credit Information
Credit TypeUnits / Unit TypeBoard
AMA PRA Category 1 Credit2.5 CreditsACCME- Accreditation Council for Continuing Medical Education
You rely on Guideline Central for transparency

Guideline Central and select third party use “cookies” on this website to enhance the user experience.

This technology helps us gather statistical and analytical information to optimize the relevant content for you.

The user also has the option to opt-out which may have an effect on the browsing experience.