Thursday, April 27, 2023, San Antonio, Texas, 6:00 AM – 7:30 AM Central Time (7:00 AM – 8:30 AM Eastern Time)

What I Tell My Patients: Expert Insights into Patient Education on New Treatments and Clinical Trial Participation

Fifteenth Annual RTP Symposium Series Held During the Annual ONS Congress

Diffuse Large B-Cell Lymphoma

 
Location
Grand Hyatt San Antonio River Walk
600 E Market Street
San Antonio, TX 78205
Hotel Phone: (210) 224-1234

Program Schedule — Central Time
5:30 AM – 6:00 AM — Registration
6:00 AM – 7:30 AM — Breakfast Meeting

Meeting Room
Texas Ballroom (Salons A-C) – Fourth Floor


This event will also be webcast live.
Please see Registration tab for details.
There is no registration fee for this event. For the in-person symposium in San Antonio, preregistration is required as seating is limited.  
 
Faculty
Christopher R Flowers, MD, MS
Chair, Professor
Department of Lymphoma/Myeloma
The University of Texas
MD Anderson Cancer Center
Houston, Texas

Amy Goodrich, CRNP
Nurse Practitioner
The Sidney Kimmel Comprehensive Cancer Center
Johns Hopkins Medicine
Baltimore, Maryland


Robin Klebig, APRN, CNP, AOCNP
Hematology Outpatient APP Supervisor
Assistant Professor of Medicine
Nurse Practitioner, Lymphoma Group
Division of Hematology
Mayo Clinic
Rochester, Minnesota

Matthew Lunning, DO
Associate Professor
Medical Director, Cellular Therapy
Assistant Vice Chair of Research, Department
of Medicine
Assistant Vice Chancellor for Clinical Research
Fred and Pamela Buffett Cancer Center
University of Nebraska Medical Center
Omaha, Nebraska

Moderator
Neil Love, MD
Research To Practice
Miami, Florida


Meeting space has been assigned to provide a satellite symposium supported by ADC Therapeutics, Genentech, a member of the Roche Group, Genmab US Inc and AbbVie Inc, and Incyte Corporation during the Oncology Nursing Society’s (ONS) 48th Annual Congress, April 26–30, 2023 in San Antonio, Texas. The Oncology Nursing Society's assignment of meeting space does not imply product endorsement.
Program Schedule — Central Time
5:30 AM – 6:00 AM — Registration
6:00 AM – 7:30 AM — Educational Breakfast Meeting

What I Tell My Patients About ...

The Similarities and Differences Between Diffuse Large B-Cell Lymphoma (DLBCL) and Other Forms of Lymphoma

  • Various subtypes of non-Hodgkin lymphoma; biologic and clinical characteristics of DLBCL
  • Potential for cure in the treatment of DLBCL versus other subtypes of non-Hodgkin lymphoma
  • Relevance of cell of origin and implications for prognosis and treatment
  • Historical approaches to the management of newly diagnosed DLBCL; current role of chemoimmunotherapy

The Potential Role of Polatuzumab Vedotin as a Component of Up-Front Treatment for DLBCL

  • Structural components and mechanism of antitumor activity of polatuzumab vedotin
  • Published results with polatuzumab vedotin in combination with R-CHP for previously untreated DLBCL; effectiveness of this regimen in various subgroups (eg, cell of origin, IPI score, bulk of disease)
  • Tolerability of polatuzumab vedotin-based therapy in the up-front setting; comparison to the experience in relapsed disease
  • Upcoming FDA review and potential role of polatuzumab vedotin as a component of up-front therapy for newly diagnosed DLBCL

The Current Role of Polatuzumab Vedotin in Therapy for Relapsed/Refractory (R/R) DLBCL

  • Long-term research findings with polatuzumab vedotin in combination with bendamustine/rituximab (BR) for patients with R/R DLBCL
  • Selection and sequencing of polatuzumab vedotin/BR among other evidence-based options
  • Appropriate use of polatuzumab vedotin for patients with R/R disease for whom chimeric antigen receptor (CAR) T-cell therapy is planned
  • Spectrum, frequency and severity of toxicities reported with polatuzumab vedotin in R/R DLBCL

The Role of Tafasitamab/Lenalidomide in DLBCL Management

  • Biologic rationale for targeting CD19 in DLBCL
  • Mechanism of action of tafasitamab and rationale for combining it with lenalidomide
  • Published clinical trial and real-world findings with tafasitamab/lenalidomide for R/R DLBCL
  • Patient selection for tafasitamab/lenalidomide and appropriate integration into treatment algorithms

Side Effects and the Practical Implementation of Tafasitamab/Lenalidomide Therapy

  • Dose and schedule of tafasitamab/lenalidomide; frequency of infusion reactions and role of premedication
  • Spectrum and frequency of toxicities associated with tafasitamab/lenalidomide, such as infection and myelosuppression; optimal monitoring and management approaches
  • Duration of treatment with tafasitamab/lenalidomide; rationale for stopping lenalidomide but continuing tafasitamab

Loncastuximab Tesirine and Its Use in DLBCL Management

  • Structural components and mechanism of action of loncastuximab tesirine
  • Principal efficacy and safety findings with loncastuximab tesirine for patients with R/R DLBCL
  • FDA-approved indication for and current role of loncastuximab tesirine for patients with R/R DLBCL

Tolerability and Other Practical Considerations with Loncastuximab Tesirine

  • Incidence and severity of common adverse reactions, including laboratory abnormalities, observed with loncastuximab tesirine
  • Frequency of myelosuppression and recommended monitoring of blood cell counts in patients receiving loncastuximab tesirine
  • Pathophysiology of effusion and edema associated with loncastuximab tesirine; indications for diagnostic imaging and intervention
  • Cutaneous toxicity, including photosensitivity reactions, experienced with loncastuximab tesirine; counseling patients about dermatologic consultation and limiting sun exposure

The Efficacy and Safety of CAR T-Cell Therapy in DLBCL

  • Mechanism of action of CAR T-cell therapy; similarities and differences among available CAR T-cell platforms targeting CD19
  • Long-term follow-up from clinical trials evaluating the efficacy and safety of axicabtagene ciloleucel, tisagenlecleucel and lisocabtagene maraleucel for DLBCL that has relapsed on or after multiple lines of therapy
  • Available results with CAR T-cell therapy as second-line treatment for patients with DLBCL
  • Spectrum, frequency and severity of class-effect (eg, cytokine release syndrome [CRS], neurotoxicity) and other toxicities with CAR T-cell therapy

Bispecific Antibodies and Their Potential Role in Therapy for DLBCL

  • Mechanism of action of CD20 x CD3 bispecific antibodies under investigation for R/R DLBCL, such as glofitamab, epcoritamab and odronextamab
  • Pivotal clinical trial results with glofitamab, epcoritamab and odronextamab for patients with multiregimen-relapsed DLBCL
  • Potential role of CD20 x CD3 bispecific antibodies in DLBCL management; optimal sequencing relative to other evidence-based options
  • Potential practical advantages of bispecific antibodies over CAR T-cell therapy because of their “off-the-shelf” nature

Tolerability and Other Practical Considerations with CD20 x CD3 Bispecific Antibodies

  • Routes of administration and dosing schedules of various CD20 x CD3 bispecific antibody platforms under investigation
  • Incidence, severity and time course of CRS, neurotoxicity and other side effects with CD20 x CD3 bispecific antibodies; recommended monitoring, mitigation and management protocols
  • Feasibility of administering bispecific antibodies in the community-based setting

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 diffuse large B-cell lymphoma (DLBCL).

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

  • Appraise published Phase III clinical trial data documenting the benefit of CD79b-targeted therapy as a component of first-line treatment for DLBCL, and consider the implications for current clinical management.
  • Review pivotal clinical trial findings leading to the FDA approval of other novel compounds with unique mechanisms of action for relapsed/refractory DLBCL, and recognize patients for whom treatment with these approaches would be appropriate.
  • Develop an understanding of the mechanisms of action of and available data with bispecific antibodies targeting CD20 x CD3 in patients with DLBCL, and evaluate the potential clinical role of these agents.
  • Appreciate the side effects associated with available and emerging therapies for DLBCL, and formulate supportive care strategies to minimize and manage these toxicities.
  • Recall ongoing studies evaluating novel agents and strategies for DLBCL, and counsel appropriate patients regarding the potential benefits of trial participation.

Accreditation Statement
Research To Practice (RTP) 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 RTP.

This activity is awarded 1.5 ANCC pharmacotherapeutic contact hours.

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 emailed to participating nurses within 3 business days of the activity.

Oncology Nursing Certification Corporation (ONCC)/Individual Learning Needs Assessment (ILNA) Certification Information
The program content has been reviewed by the ONCC and is acceptable for recertification points. Learners must apply for NCPD credit to utilize this program for ONCC certification or renewal. https://www.researchtopractice.com/Meetings/ONS2023/DLBCL/ILNA

Unlabeled/Unapproved Uses Notice
There is no implied or real endorsement of any product by RTP or the ANCC.

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 Goodrich and Ms Klebig have no relevant conflicts of interest to disclose. The following faculty reported relevant financial relationships with ineligible entities:

Dr FlowersConsulting Agreements: AbbVie Inc, Bayer HealthCare Pharmaceuticals, BeiGene Ltd, Celgene Corporation, Denovo Biopharma, Epizyme Inc, Genentech, a member of the Roche Group, Genmab US Inc, Gilead Sciences Inc, Janssen Biotech Inc, Karyopharm Therapeutics, Pharmacyclics LLC, an AbbVie Company, Seagen Inc, Spectrum Pharmaceuticals Inc; Contracted Research: 4D Pharma PLC, AbbVie Inc, Acerta Pharma — A member of the AstraZeneca Group, Adaptimmune, Allogene Therapeutics, Amgen Inc, Bayer HealthCare Pharmaceuticals, Celgene Corporation, Cellectis, EMD Serono Inc, Genentech, a member of the Roche Group, Gilead Sciences Inc, Guardant Health, Iovance Biotherapeutics, Janssen Biotech Inc, Kite, A Gilead Company, MorphoSys, Nektar, Novartis, Pfizer Inc, Pharmacyclics LLC, an AbbVie Company, Sanofi, Takeda Pharmaceuticals USA Inc, TG Therapeutics Inc, Xencor, ZIOPHARM Oncology Inc; Nonrelevant Financial Relationship: Burroughs Wellcome Fund, Cancer Prevention and Research Institute of Texas (CPRIT Scholar in Cancer Research), Eastern Cooperative Oncology Group, National Cancer Institute. Dr LunningConsulting Agreements: AbbVie Inc, Acrotech Biopharma, ADC Therapeutics, Astellas, AstraZeneca Pharmaceuticals LP, Bristol-Myers Squibb Company, Caribou Biosciences Inc, CRISPR Therapeutics, Daiichi Sankyo Inc, EUSA Pharma, Fate Therapeutics, Genentech, a member of the Roche Group, Genmab US Inc, Instil Bio, Ipsen Biopharmaceuticals Inc, Janssen Biotech Inc, Kite, A Gilead Company, Loxo Oncology Inc, a wholly owned subsidiary of Eli Lilly & Company, Miltenyi Biotec, MorphoSys, Novartis, Nurix Therapeutics Inc, Pharmacyclics LLC, an AbbVie Company, Regeneron Pharmaceuticals Inc, Sanofi, Seagen Inc, Takeda Pharmaceuticals USA Inc, TG Therapeutics Inc; Contracted Research: Bristol-Myers Squibb Company, Curis Inc.

MODERATORDr Love is president and CEO of Research To Practice. Research To Practice receives funds in the form of educational grants to develop CME activities from the following companies: AbbVie Inc, Adaptive Biotechnologies Corporation, ADC Therapeutics, Agios Pharmaceuticals Inc, Alexion Pharmaceuticals, Amgen Inc, Array BioPharma Inc, a subsidiary of Pfizer Inc, Astellas, AstraZeneca Pharmaceuticals LP, Aveo Pharmaceuticals, Bayer HealthCare Pharmaceuticals, BeiGene Ltd, BeyondSpring Pharmaceuticals Inc, Blueprint Medicines, Boehringer Ingelheim Pharmaceuticals Inc, Bristol-Myers Squibb Company, Celgene Corporation, Clovis Oncology, Coherus BioSciences, CTI BioPharma Corp, Daiichi Sankyo Inc, Eisai Inc, Elevation Oncology Inc, EMD Serono Inc, Epizyme Inc, Exact Sciences Corporation, Exelixis Inc, Five Prime Therapeutics Inc, Foundation Medicine, G1 Therapeutics Inc, Genentech, a member of the Roche Group, Genmab US Inc, Gilead Sciences Inc, Grail Inc, GSK, Halozyme Inc, Helsinn Healthcare SA, ImmunoGen Inc, Incyte Corporation, Ipsen Biopharmaceuticals Inc, Janssen Biotech Inc, administered by Janssen Scientific Affairs LLC, Jazz Pharmaceuticals Inc, Karyopharm Therapeutics, Kite, A Gilead Company, Kronos Bio Inc, Lilly, Loxo Oncology Inc, a wholly owned subsidiary of Eli Lilly & Company, MEI Pharma Inc, Merck, Mersana Therapeutics Inc, Mirati Therapeutics Inc, Natera Inc, Novartis, Novartis Pharmaceuticals Corporation on behalf of Advanced Accelerator Applications, Novocure Inc, Oncopeptides, Pfizer Inc, Pharmacyclics LLC, an AbbVie Company, Puma Biotechnology Inc, Regeneron Pharmaceuticals Inc, Sanofi, Seagen Inc, Servier Pharmaceuticals LLC, SpringWorks Therapeutics Inc, Stemline Therapeutics Inc, Sumitomo Dainippon Pharma Oncology Inc, Taiho Oncology Inc, Takeda Pharmaceuticals USA Inc, TerSera Therapeutics LLC, Tesaro, A GSK Company, TG Therapeutics Inc, Turning Point Therapeutics Inc, Verastem Inc, and Zymeworks Inc.

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 ADC Therapeutics, Genentech, a member of the Roche Group, Genmab US Inc and AbbVie Inc, and Incyte Corporation.

Grand Hyatt San Antonio River Walk
600 E Market Street
San Antonio, TX 78205
Hotel Phone: (210) 224-1234

Meeting Room:
Texas Ballroom (Salons A-C) – Fourth Floor

The Grand Hyatt San Antonio is the headquarters hotel for the 2023 ONS Congress and is conveniently connected to the Henry B González 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 diffuse large B-cell lymphoma.

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IN-PERSON registration
Thank you for your interest in our NCPD program taking place in San Antonio, Texas. At this time online preregistration for in-person is closed for this event. LIMITED SEATS ARE STILL AVAILABLE FOR THIS SESSION. Our onsite registration desk will be open at 5:30 AM Central Time on Thursday, April 27th. If you are interested in attending, please visit our registration desk located outside the Texas Ballroom (Salons A-C) – Fourth Floor of the Grand Hyatt San Antonio River Walk hotel which is connected to the Henry B Gonzalez Convention Center.

If you have any questions, please feel free to contact us via email at Meetings@ResearchToPractice.com.

Please note, onsite registration does not guarantee seating and participation in meal service and will be based on availability.

LIVE WEBCAST registration open to all professionals

Please note we will stream this event over Zoom. After registering you will receive a separate confirmation from Zoom with the viewing instructions.

Registration for Webcast »

Registration for groups
If you are registering a group (more than 1 person) for this event, please contact us at Meetings@ResearchToPractice.com or (800) 233-6153.
To ensure seating and meal service, please check in at our onsite registration desk at least 30 minutes before the start of the meeting. We cannot guarantee seating after the start of the program.

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Research To Practice fully complies with the legal requirements of the ADA. If you are in need of assistance (ie, physical, dietary, et cetera), please contact us prior to the event at (800) 233-6153.