Launch Date
04/24/2023 at 4:00 am EST
Credit Amount
0.75
Credit Expires
04/24/2024
Despite promising, data-driven treatment recommendations for breast cancer posed by the National Comprehensive Cancer Network (NCCN), gaps in patient and provider education on available therapies remain. It is crucial for clinicians and patients to be wholly informed of treatment options as well as the similarities and differences between randomized clinical trials and real-world data, in order to lay the groundwork for shared decision making. By increasing provider and patient knowledge and thus enhancing the shared decision-making process, greater concordance between treatments offered and the guidelines can occur, leading to optimal patient outcomes.
In this 45-minute interactive CME Outfitters Snack, a diverse panel of expert faculty will discuss the evolving treatment landscape of metastatic breast cancer and how to integrate the latest clinical evidence, real world evidence, and treatment guideline recommendations to foster patient health literacy, shared-decision making, and individualized outcomes.
Supported by an educational grant from Pfizer Inc.
Physicians, nurse practitioners (NPs), physician associates (PAs), nurses, pharmacists, or other healthcare professionals involved in the care of patients with HR+/HER2- mBC. Patients and caregivers may also benefit from participating in this activity.
It is the policy of CME Outfitters, LLC, to ensure independence, balance, objectivity, and scientific rigor and integrity in all of their CE activities. Faculty must disclose to the participants any relationships with commercial companies whose products or devices may be mentioned in faculty presentations, or with the commercial supporter of this CE activity. CME Outfitters, LLC, has evaluated, identified, and mitigated any potential conflicts of interest through a rigorous content validation procedure, use of evidence-based data/research, and a multidisciplinary peer review process.
Dr. Hurvitz reports the following financial relationships:
Advisory Board: Ambrx; Amgen Inc.; Arvinas; AstraZeneca; Bayer AG; CytomX Therapeutics, Inc.; Daiichi-Sankyo, Inc.; Dantari; Dignitana; Eli Lilly and Company; G1-Therapeutics, Inc.; Genentech, Inc./Roche; Gilead Sciences, Inc.; Greenwich LifeSciences, Inc; GSK; Immunomedics; MacroGenics, Inc.; Novartis Pharmaceuticals Corporation; OBI Pharma; Orinove Inc.; Orum Therapeutics; Pfizer Inc.; Phoenix Molecular Designs; Pieris Pharmaceuticals, Inc.; Puma Biotechnology, Inc.; Radius Health, Inc.; Samumed; Sanofi; Seattle Genetics, Inc./Seagen Inc.; and Zymeworks Inc.
Ms. Rivers reports no financial relationships to disclose.
Dr. Tolaney reports the following financial relationships:
Consultant: 4D pharma plc; Aadi Biosciences; Arch Therapeutics, Inc.; AstraZeneca; Athenex, Inc.; Bayer; BeyondSpring Inc.; Blueprint Medicines Corporation; Bristol Myers Squibb Company; Certara, Inc.; Chugai Pharma USA, Inc.; CytomX Therapeutics, Inc.; Daiichi Sankyo, Inc.; Eisai Inc.; Eli Lilly and Company; Ellipses Pharma; Genentech, Inc./Roche; Gilead Sciences, Inc.; Infinity Therapeutics; Menarini/Stemline Therapeutics, Inc.; Merck & Co., Inc.; Mersana therapeutics; Myovant Sciences; Novartis Pharmaceuticals Corporation; Odonate Therapeutics, Inc.; OncoSec Medical Inc.; OncXerna Therapeutics, Inc.; Pfizer Inc.; Sanofi; Seattle Genetics; Inc.; Reveal Genomics; Umoja Biopharma; Zentalis Pharmaceuticals; Zetagen; and Zymeworks Inc.
Research Support (paid to institution): AstraZeneca; Bristol Myers Squibb Company; Cyclacel Pharmaceuticals, Inc.; Eisai Inc.; Exelixis, Inc.; Genentech, Inc./Roche; Gilead Sciences, Inc.; Lilly; Merck & Co., Inc.; NanoString; Nektar; Novartis Pharmaceuticals Corporation; Pfizer Inc.; Sanofi and Seattle Genetics, Inc.
Disclosures were obtained from the CME Outfitters, LLC staff: No disclosures to report:
Faculty of this CE activity may include discussions of products or devices that are not currently labeled for use by the FDA. The faculty have been informed of their responsibility to disclose to the audience if they will be discussing off-label or investigational uses (any uses not approved by the FDA) of products or devices.
Post-tests, credit request forms, and activity evaluations must be completed online (requires free account activation), and participants can print their certificate or statement of credit immediately (75% pass rate required). This website supports all browsers except Internet Explorer for Mac. For complete technical requirements and privacy policy, visit our Privacy & Confidentiality page.
Call us at 877.CME.PROS (877.263.7767).
SN-184-042423-02