What Now, What Next?
Appropriate Management of mUC

How I Practice: Treatment Landscape for mUC 

This activity is jointly provided by Partners for Advancing Clinical Education (PACE) and Bonum CE

This program has been supported by independent educational grants from Astellas, Gilead Sciences Inc., Merck Sharp & Dohme LLC, and Seagen.

Program Overview

Locally advanced or metastatic urothelial carcinoma (mUC) is an aggressive form of cancer with a poor prognosis, with a survival of 12–15 months with cisplatin-based combination chemotherapy, but only 3 to 6 months if left untreated. However, up to 50% of patients are ineligible to receive standard platinum-based treatment regimens due to the presence of comorbid conditions, and most who do receive treatment, eventually develop progressive disease. Recent developments have led to the approval of three new classes of agents that have vastly expanded treatment options for patients with mUC. With the expansion of the therapeutic armamentarium, the oncology care team is faced with interpreting a significant amount of new data, evolving guidelines, and nuanced considerations in clinic regarding practical application of these agents.

This series of CME-certified, social media-based activities will provide learners with information regarding new and evolving classes of therapies, updated guidelines in the US and EU, as well as information regarding treatment safety profiles and appropriate management of adverse events.

This activity, a X/Twitter-based How I Practice video focuses on the treatment landscape in first-, second- and subsequent-lines of therapy in metastatic disease.

Faculty

Petros Grivas, MD, PhD (program co-chair)
Professor
Clinical Research Division
Fred Hutch Cancer Center
Clinical Director, Genitourinary Cancers Program
Professor, Department of Medicine
Division of Oncology
University of Washington School of Medicine
Seattle, WA

Tian Zhang, MD, MHS (program co-chair)
Associate Professor
Director of Clinical Research
Division of Hematology and Oncology Department of Internal Medicine
UT Southwestern Medical Center
Dallas, TX

Target Audience

This program is intended for medical, surgical, radiation oncologists, urologists, fellows, trainees, oncology advance practice providers, oncology nurses, and oncology pharmacists caring for patients with mUC.

Learning Objectives

After completing this activity series, learners should be better able to:

  • DESCRIBE efficacy data regarding ICIs and other approved drug classes, including the use of maintenance  therapy in mUC.

  • SELECT appropriate treatment based on the latest recommendations from the National Comprehensive Cancer  Network’s preferred treatment regimens for mUC.

Disclosure of Relevant Financial Relationships

PACE requires every individual in a position to control educational content to disclose all financial relationships with ineligible companies that have occurred within the past 24 months. Ineligible companies are organizations whose primary business is producing, marketing, selling, re-selling, or distributing healthcare products used by or on patients.

All relevant financial relationships for anyone with the ability to control the content of this educational activity are listed below and have been mitigated according to PACE policies. Others involved in the planning of this activity have no relevant financial relationships.

 
  • Petros Grivas, MD, PhD (program co-chair)
    Consultant/Advisor/Speaker: Aadi Bioscience; Abbvie; AstraZeneca; Asieris Pharmaceuticals; Astellas Pharma; Bristol-Myers Squibb; Boston Gene; CG Oncology; Dyania Health; Fresenius Kabi, G1 Therapeutics; Gilead; Guardant Health; ImmunityBio; Janssen; Lucence Health; Merck KGaA; MSD; Pfizer; PureTech; Roche, SeaGen, Strata Oncology, Silverback Therapeutics

    Researcher: Acrivon Therapeutics; ALX Oncology; Bavarian Nordic; Bristol-Myers Squibb; Debiopharm; G1 Therapeutics; Genentech; Gilead; GlaxoSmithKline; Merck KGaA; Mirati Therapeutics; MSD; Pfizer; QED Therapeutics;

    Tian Zhang, MD, MHS (program co-chair)
    Consultant/Advisor/Speaker: Aravive, Astra Zeneca, Aveo Therapeutics, Bayer ,BMS, Caris, Eisai, Eli Lilly, EMD Serono, Exelixis, Gilead, Janssen, Merck, Pfizer, Sanofi Aventis, SeaGen

    Researcher: ALX Oncology, Astellas, Astra Zeneca, Eli Lilly, Janssen, Merck, Novartis, Pfizer

Joint Accreditation Statement

Joint Accreditation Statement
In support of improving patient care, this activity has been planned and implemented by Partners for Advancing Clinical Education (PACE) and Bonum CE. PACE is jointly accredited by the Accreditation Council for Continuing Medical Education (ACCME), the Accreditation Council for Pharmacy Education (ACPE), and the American Nurses Credentialing Center (ANCC), to provide continuing education for the healthcare team.

Physician Continuing Medical Education
PACE designates this enduring material for a maximum of 0.5 AMA PRA Category 1 Credit™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.

Instructions to Receive Credit & Fee Information

In order to receive credit for this activity, the participant must read the front matter, achieve a passing score of 75% on the post-test, complete the evaluation and application for credit form.

There is no fee to participate in this activity.

Disclosure of Unlabeled Use

This educational activity may contain discussion of published and/or investigational uses of agents that are not indicated by the FDA. The planners of this activity do not recommend the use of any agent outside of the labeled indications

The opinions expressed in the educational activity are those of the faculty and do not necessarily represent the views of any organization associated with this activity. Please refer to the official prescribing information for each product for discussion of approved indications, contraindications, and warnings.

Disclaimers

Participants have an implied responsibility to use the newly acquired information to enhance patient outcomes and their own professional development. The information presented in this activity is not meant to serve as a guideline for patient management. Any procedures, medications, or other courses of diagnosis or treatment discussed in this activity should not be used by clinicians without evaluation of patient conditions and possible contraindications on dangers in use, review of any applicable manufacturer’s product information, and comparison with recommendations of other authorities.

System Requirements

All Bonum CE digital activities require the following hardware/software to view and participate:

  • Internet connection (via PC or Mac desktop or laptop computer, tablet, mobile device, etc.)

  • PowerPoint and/or a PDF viewer may be required on some activities

We recommend a minimum of:

  • 128MB RAM

  • Processor speed of 500MHz or higher

  • 800x600 color monitor

  • Video or graphics card

  • Sound card and speakers

To actively participate in Bonum’s social media (SoMe)-based CME programs, learners will need to have an established account in good standing on that hosting SoMe site. Learners will need to be logged-in to the SoMe hosting platform.

For additional information about the accreditation of this activity, please visit https://www.partnersed.com

Release date: May 22, 2024
Expiration date: May 22, 2025
Estimated time to complete activity: 30 minutes