Activity Overview
PD-L1 expression defines which patients with metastatic triple-negative breast cancer (mTNBC) are candidates for first-line pembrolizumab. However, only about 4 of 10 patients meet the combined positive score threshold of 10, and expression can differ between a primary tumor and a metastatic site. For the rest, the first-line standard has moved from chemotherapy toward antibody-drug conjugates (ADCs): sacituzumab govitecan and datopotamab deruxtecan were both approved in 2026 for patients who are not candidates for PD-1/PD-L1 inhibitors, and sacituzumab govitecan plus pembrolizumab for PD-L1–positive disease. Both agents carry distinct toxicities that demand different monitoring, and the neutropenia-related deaths in ASCENT-03 occurred in patients without growth factor prophylaxis. As community oncologists navigate this landscape, accurate PD-L1 and germline BRCA1/2 testing, regimen selection by PD-L1 status and immunotherapy eligibility, and proactive toxicity management have become critical.
This Community Practice Connection™ program provides an in-depth review of PD-L1 testing and first-line treatment selection in mTNBC. This unique and engaging multimedia activity is ideal for the community-based clinician. It focuses on practical interpretation of clinical trial data and management strategies for PD-L1 and germline BRCA1/2 testing, first-line regimen selection by PD-L1 status and immunotherapy eligibility, and ADC toxicity in the community oncology setting.
Target Audience
This educational program is primarily directed toward community-based oncologists, nurses, nurse practitioners, advanced practice providers, and other health care professionals involved in the treatment of TNBC. The online enduring activity also extends to an international audience of oncology clinicians, with open-access availability via http://gotoper.com to practitioners outside the United States.
Learning Objectives
Upon successful completion of this activity, you should be better prepared to:
- Describe how PD-L1 testing impacts treatment planning and regimen selection in patients with newly diagnosed, metastatic, triple-negative breast cancer (mTNBC)
- Select appropriate frontline strategies for mTNBC based on PD-L1 status, immunotherapy eligibility, patient preferences, and evolving clinical evidence
- Apply practical approaches to toxicity management, patient communication, and workflow integration in community oncology settings

Neil M. Iyengar, MD
Associate Professor and Co-Director
Co-Director, Breast Oncology Program
Director, Cancer Survivorship Services
Winship Cancer Institute
Emory University
Atlanta, GA
Disclosures: Consultant/Advisor: Arvinas, AstraZeneca, BD Life Sciences, Daiichi Sankyo, Genentech/Roche, Gilead, Menarini-Stemline, Novartis, Pfizer, Puma, Seagen, TerSera Therapeutics; Speaker: Cardinal Health, Curio Sciences, DAVA Oncology, IntrinsiQ Health; Editorial Position: npj Breast Cancer, Oncology®; Equity/ Ownership: Complement Theory, The Bettering Company; Research Support (to institution): American Cancer Society, Breast Cancer Research Foundation, Conquer Cancer Foundation, Kat’s Ribbon of Hope, National Cancer Institute/National Institutes of Health; Contracted Research: Novartis, SynDevRx

Sara M. Tolaney, MD, MPH
Chief, Division of Breast Oncology
Dana-Farber Cancer Institute
Associate Professor of Medicine
Harvard Medical School
Boston, MA
Disclosures: Advisor, Consultant, Speaker, Honoraria Recipient: Aadi Bio, Aktis Oncology, Artios Pharma, Arvinas, AstraZeneca, Avenzo Therapeutics, Bayer, BeOne Medicines, Bicycle Therapeutics, BioNTech, Blueprint Medicines, Boehringer Ingelheim, Boundless Bio, Bristol Myers Squibb/SystImmune, Celcuity, Circle Pharma, Cullinan Oncology, Daiichi Sankyo, eFFECTOR, Eisai, Eli Lilly, Genentech/Roche, Gilead, Hengrui USA, Jazz Pharmaceuticals, Johnson & Johnson/Ambrx/Mersana, Launch Therapeutics, Menarini/Stemline, Merck, Natera, Novartis, Olema, Pfizer/Seagen, Reveal Genomics, Samsung Bioepis, Sumitovant Biopharma, Summit Therapeutics, Tango Therapeutics, Tempus, Zuellig Pharma; Grant/Research Funding: AstraZeneca, Bristol Myers Squibb, Daiichi Sankyo, Exelixis, Genentech/Roche, Gilead, Jazz Pharma, Lilly, Menarini/Stemline, Merck, NanoString Technologies, Novartis, OncoPep, Pfizer/Seagen
The staff of Physicians’ Education Resource®, LLC have no relevant financial relationships with ineligible companies.
PER® mitigated all conflicts of interest for faculty, staff, and planners before the start of this activity by using a multistep process.
Off-Label Disclosure and Disclaimer
This accredited continuing education activity was planned in accordance with the ACCME Standards for Integrity and Independence to ensure balance, objectivity, independence, and scientific rigor. Faculty were instructed to use generic names when possible and to base recommendations on the best available evidence. Proprietary product names may be referenced in clinical discussion for educational purposes only and do not imply endorsement.
This activity may include discussion of investigational, unapproved, or off‑label uses of drugs or devices. Learners are advised to consult prescribing information for products discussed. Content is provided for educational purposes only and is not a substitute for the independent clinical judgment of a health care professional. Learners are encouraged to critically evaluate the information presented and apply their own clinical judgment.
The views expressed are those of the individual faculty members and do not necessarily reflect the views of the accredited provider or any entity providing commercial support.
This activity may have used AI-assisted tools to support educational development. All content was reviewed and approved by qualified faculty or planners. The accredited provider retains full responsibility for accuracy, balance, and independence.

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