Wednesday, April 9, 2025, Denver, Colorado, 11:15 AM – 12:45 PM Mountain Time (1:15 PM – 2:45 PM Eastern Time)

Understanding the Current Paradigm and New Approaches: The Optimal Implementation of Antibody-Drug Conjugates in the Care of Patients with Cancer

A Complimentary NCPD Symposium Held During the 50th Annual ONS Congress

 

 

 

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Location
Hyatt Regency Denver
at Colorado Convention Center
650 15th Street
Denver, Colorado
Hotel Phone: (303) 436-1234

Program Schedule — Mountain Time
10:45 AM – 11:15 AM — Registration and Lunch
11:15 AM – 12:45 PM — Educational Meeting

Meeting Room
Centennial Ballroom DE (Third Floor)
Note, this meeting is in a different room from the other symposia in our series.
 
 
Faculty
Marianne J Davies, DNP, ACNP, AOCNP, FAAN
Program Manager, Care Signature
Oncology Service Line, Yale New Haven Health
Oncology Nurse Practitioner-Senior APP II
Yale Cancer Center
Smilow Cancer Hospital at Yale New Haven
Associate Professor
Yale University School of Nursing
New Haven, Connecticut

Edward B Garon, MD, MS
Professor
Director, Thoracic Oncology Program
Director, Signal Transduction and Therapeutics Research Program
David Geffen School of Medicine at UCLA
Jonsson Comprehensive Cancer Center
Los Angeles, California


Marissa Marti-Smith, DNP, APRN, AGNP-C, AOCNP
Nurse Practitioner
Texas Oncology-Baylor Charles A Sammons Cancer Center
Dallas, Texas

Heather McArthur, MD, MPH
Associate Professor
Department of Internal Medicine
Clinical Director, Breast Cancer Program
Komen Distinguished Chair in Clinical Breast Cancer Research
UT Southwestern Medical Center
Dallas, Texas



Meeting space has been assigned to provide a satellite symposium supported by AstraZeneca Pharmaceuticals LP and Daiichi Sankyo Inc during the Oncology Nursing Society’s (ONS) 50th Annual Congress, April 9-13, 2025 in Denver, Colorado. The Oncology Nursing Society’s assignment of meeting space does not imply product endorsement.
Program Schedule — Mountain Time
10:45 AM – 11:15 AM — Registration and Lunch
11:15 AM – 12:45 PM — Educational Meeting

MODULE 1: Rationale for the Use of Antibody-Drug Conjugates (ADCs) as Cancer Treatment

  • Rationale for conjugating monoclonal antibodies with cytotoxic drugs to form ADCs; theoretical improvement of chemotherapy efficacy while reducing systemic exposure and toxicity
  • Structural components, such as antibodies, linkers and cytotoxic payloads, of commercially available and investigational ADCs
  • Direct mechanism of antitumor activity of ADCs and other means by which they can elicit an antitumor effect, such as bystander killing

MODULE 2: Current and Future Role of ADCs in Cancer Therapy

  • FDA-approved indications for ADCs for various tumor types
  • Promising investigational ADCs in clinical development as anticancer therapy
  • Setting patient expectations regarding ADC efficacy and tolerability
  • Optimal timing for initiation of approved ADCs or consideration of a clinical trial evaluating 1 of these agents

MODULE 3: Cytopenias Associated with ADCs

  • Educating patients regarding the capacity of ADCs to cause acute chemotherapy-like side effects
  • Incidence and severity of neutropenia, thrombocytopenia and anemia with approved and investigational ADCs
  • Indications for prophylactic growth factor use for patients who are about to start treatment with an ADC
  • Appropriate monitoring of complete blood counts during ADC therapy; thresholds for dose modification, treatment interruption or discontinuation for patients experiencing cytopenias

MODULE 4: Gastrointestinal (GI) Adverse Events (AEs) Documented with ADCs

  • Rates of various GI issues, such as nausea, vomiting, diarrhea, constipation and abdominal pain, in patients receiving ADC therapy
  • Indications for prophylactic antiemetics and antidiarrheals for patients who are about to start treatment with an ADC
  • Role of nutritional counseling and diet modifications during ADC treatment
  • Potential advantages of complementary therapies, such as acupuncture and yoga, for managing GI side effects of ADCs, particularly for patients with anticipatory nausea

MODULE 5: Recognition and Management of Interstitial Lung Disease (ILD)/Pneumonitis Associated with ADCs

  • Pathophysiology of ILD/pneumonitis associated with ADCs; baseline risk factors for its development
  • Rates, severity and timing of ILD/pneumonitis in clinical trial experiences with various ADCs
  • Appropriate workup for patients suspected of experiencing therapy-related ILD/pneumonitis; strategies to distinguish drug-related pulmonary toxicity from other potential causes
  • Guidelines for treatment modifications and discontinuation for patients experiencing ILD/pneumonitis; indications for restarting ADC therapy after side-effect resolution
  • Utility of other supportive care measures, such as corticosteroids and oxygen supplementation, for patients experiencing ILD/pneumonitis

MODULE 6: Cardiovascular AEs with Select ADCs

  • Pathophysiology of cardiotoxicity associated with anti-HER2 therapies, including ADCs
  • Incidence of left ventricular dysfunction noted with HER2-targeted ADCs in clinical trial experiences
  • Appropriate monitoring of left ventricular ejection fraction (LVEF) at baseline and during treatment with HER2-targeted ADCs
  • Threshold for treatment interruption for patients experiencing LVEF decrease; indications for restarting HER2-targeted ADC therapy after recovery
  • Role of interdisciplinary coordination with cardiologists in monitoring for and managing cardiac toxicities associated with HER2-targeted ADCs

MODULE 7: Potential for Mucositis/Stomatitis with ADCs

  • Incidence and severity of mucositis/stomatitis with various approved and investigational ADCs
  • Counseling patients on the importance of oral hygiene during treatment with ADCs known to cause mucositis/stomatitis
  • Role of prescription steroid mouthwash, homemade mouth rinses, prophylactic antibiotics/antifungals and pain medications in treatment for patients who are at risk for or are experiencing mucositis/stomatitis
  • Dietary recommendations for patients experiencing mucositis/stomatitis

MODULE 8: Ocular Toxicities Associated with ADCs

  • Pathophysiology of ocular AEs associated with certain ADCs; spectrum, incidence and severity of ocular toxicities with different agents
  • Optimal patient counseling and education regarding signs of ocular toxicity and the importance of early reporting of symptoms
  • Guidelines for treatment modification for patients experiencing ocular complications of ADCs
  • Utility of other prophylactic and supportive care measures to mitigate and manage ocular toxicities
  • Importance of interdisciplinary coordination with eye-care professionals in the identification and management of treatment-related ocular AEs

MODULE 9: Other Toxicities Reported with 1 or More ADCs

  • Incidence and management of peripheral neuropathy associated with various ADCs
  • Rates of alopecia reported with ADC treatment; available strategies to reduce the incidence and severity of hair loss or limit its psychosocial effects, such as scalp-cooling methods and wigs or hair pieces
  • Available strategies to ameliorate the symptoms of rash and other cutaneous reactions associated with ADCs, such as antihistamines, topical steroids and emollients
  • Spectrum of other toxicities, such as fatigue, hemorrhage, effusion/edema and hyperglycemia, associated with 1 or more ADCs for cancer treatment

Target Audience
This activity has been designed to meet the educational needs of oncology nurses, nurse practitioners and clinical nurse specialists involved in the treatment of cancer.

Learning Objectives
Upon completion of this activity, participants should be able to

  • Consider the scientific justification for the use of ADCs as a therapeutic approach for patients with various tumor types, and recall the targets, structural components and mechanisms of activity of different clinically available and investigational agents in this class.
  • Appraise available clinical research data with novel ADCs for various cancers, and consider the current and potential role of these approaches in routine clinical care.
  • Appreciate the pathophysiology and severity of common and rare toxicities associated with ADCs employed in the treatment of different tumor types.
  • Understand the incidence of toxicities observed in pivotal trials evaluating novel ADCs, and educate patients about to commence therapy with these approaches regarding the potential development of these AEs and what to do if they are suspected.
  • Recall strategies commonly employed to identify, manage and mitigate resultant toxicities of anticancer treatment with ADCs, and use this information to appropriately intervene for patients in whom these side effects are suspected or diagnosed.
  • Understand the role of multidisciplinary specialists such as cardiologists, ophthalmologists and other medical professionals in the diagnosis and management of ADC-associated toxicities, and effectively educate patients regarding the potential need for and importance of specialty referral.

Accreditation Statement
Research To Practice is accredited as a provider of nursing continuing professional development by the American Nurses Credentialing Center’s (ANCC) Commission on Accreditation.

Credit Designation Statements
This educational activity for 1.5 contact hours is provided by Research To Practice.

This activity is awarded 1.5 ANCC pharmacotherapeutic contact hours.

Oncology Nursing Certification Corporation (ONCC)/Individual Learning Needs Assessment (ILNA) Certification Information
The program content has been reviewed by the Oncology Nursing Certification Corporation (ONCC) and is acceptable for recertification points. To review certification qualifications please visit https://researchtopractice.com/Meetings/ONS2025/ADCs/ILNA

Credit Form
To obtain a certificate of completion and receive credit for this event, nurses must attend the entire activity and return a completed Educational Assessment and Credit Form. A credit form link will be given to each participant as part of the meeting course materials.

Unlabeled/Unapproved Uses Notice
There is no implied or real endorsement of any product by Research To Practice or the American Nurses Credentialing Center.

Content Validation and Disclosures
Research To Practice (RTP) is committed to providing its participants with high-quality, unbiased and state-of-the-art education. Any individuals in a position to control the content of an accredited continuing education activity, including faculty, planners, reviewers and others, are required to disclose all relevant financial relationships with ineligible entities (commercial interests). All relevant conflicts of interest will have been mitigated prior to the commencement of this activity. In addition, all activity content is reviewed by RTP scientific staff and an external, independent reviewer for fair balance, scientific objectivity of studies referenced and patient care recommendations.

FACULTYMs Davies and Ms Marti-Smith have no relevant conflicts of interest to disclose. The following faculty reported relevant financial relationships with ineligible entities:

Dr GaronAdvisory Committees and Consulting Agreements: AbbVie Inc, Arcus Biosciences, ArriVent Biopharma, AstraZeneca Pharmaceuticals LP, Atreca, Black Diamond Therapeutics Inc, BridgeBio, Bristol Myers Squibb, EMD Serono Inc, Gilead Sciences Inc, Hookipa Pharma Inc, I-Mab Biopharma, LianBio, Lilly, Merck, Merus, Novartis, Nuvalent, Pfizer Inc, Regeneron Pharmaceuticals Inc, Sanofi, Seagen Inc, Sensei Biotherapeutics, Strata Oncology, Sumitomo Dainippon Pharma Oncology Inc, Summit Therapeutics, Synthekine; Contracted Research: ABL Bio, ArriVent Biopharma, AstraZeneca Pharmaceuticals LP, BridgeBio, Bristol Myers Squibb, Daiichi Sankyo Inc, EMD Serono Inc, Genentech, a member of the Roche Group, Gilead Sciences Inc, Iovance Biotherapeutics, Lilly, Merck, Mirati Therapeutics Inc, Novartis, Prelude Therapeutics, Regeneron Pharmaceuticals Inc, Synthekine, TILT Biotherapeutics; Sponsored Independent Medical Education: Daiichi Sankyo Inc; Travel: A2 Bio, Novartis. Additional faculty to be announced.

RESEARCH TO PRACTICE NCPD PLANNING COMMITTEE MEMBERS, STAFF AND REVIEWERS — Planners, scientific staff and independent reviewers for Research To Practice have no relevant conflicts of interest to disclose.

Supporters
This activity is supported by educational grants from AstraZeneca Pharmaceuticals LP and Daiichi Sankyo Inc.

Hyatt Regency Denver at Colorado Convention Center
650 15th Street
Denver, CO 80202
Hotel Phone: (303) 436-1234

Meeting Room
Centennial Ballroom DE (Third Floor)
Note, this meeting is in a different room from the other symposia in our series.

The Hyatt Regency Denver at Colorado Convention Center is the headquarters hotel for the 2025 ONS Congress and is adjacent to the Colorado Convention Center.

 

This activity has been designed to meet the educational needs of oncology nurses, nurse practitioners and clinical nurse specialists involved in the treatment of cancer.

There is no registration fee for this event. For the in-person symposium in Denver, preregistration is required as seating is limited.

NOTICE:
Registration for this event is independent of registration for the 2025 ONS Congress.

IN-PERSON Registration for clinicians in practice/healthcare professionals

I am a practicing physician, fellow, nurse or other healthcare provider involved in the treatment of cancer.

IN-PERSON Registration
for clinicians »
IN-PERSON Registration for other/industry professionals*

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IN-PERSON Registration
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WEBCAST Registration for all professionals

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