Explore the information below to find out about the Program schedule and content, which is outlined by day and in chronological order. Session descriptions and presenter information will be added as confirmed and received. The Program is subject to change.
Click here to download the Program at a Glance.
Click on the links below to go directly to any of the following days:
Wednesday
April 2, 2025
Explore an innovative approach to BTKi patient management in this on-demand symposium led by Christine Peragine (Pharmacist Lead, Oral Anticancer Medication Program at Sunnybrook Odette Cancer Centre). This session introduces the BTKi Patient Optimization Tool, a new digital resource co-developed with eight Canadian healthcare professionals. Designed to streamline patient management and empower clinicians, this tool provides an interactive solution for delivering comprehensive and optimized care to patients undergoing BTKi therapy.
This session will:
• Highlight how the BTKi Patient Optimization Tool can enhance patient care
• Provide actionable strategies for using the tool to identify, assess, and manage common BTKi side effects effectively
• Demonstrate how the tool integrates seamlessly into clinical workflows, supporting your practice and improving patient outcomes
Sponsored by BeiGene
Thursday
April 3, 2025
Additional fees apply. Click here for more information about the Workshop.
Additional fees apply. Click here for more information about the Workshop.
Program Overview
This symposium will enable Canadian pharmacists involved in the management of relapsed/refractory Multiple Myeloma (RRMM) to determine the optimal patient selection and management strategies for triple class-exposed patients receiving bispecific antibodies, with a focus on administration in the Community setting.
Learning Objectives
This symposium aims to:
• Explore patient selection for bispecific antibodies for the management of relapsed/refractory Multiple Myeloma (RRMM) in Canada
• Share best practices for the optimal management of adverse events associated with bispecific antibodies for Multiple Myeloma
• Consider the role of the pharmacist to support patient management and the delivery of bispecific antibodies for Multiple Myeloma within the Community setting
Sponsored by Johnson & Johnson
Join us for an engaging symposium addressing market challenges and innovative solutions for managing hazardous drugs. Explore practical strategies for implementing advanced technologies, including regulatory insights, user success stories, and real-world challenges. Highlights include live showcases of a state-of-the-art robotic system integrating closed-system drug transfer devices (CSTDs), discussions on vapor containment, and drug sterility innovations. Learn from renowned speakers with global experience in oncology pharmacy, offering invaluable perspectives and insights. Gain actionable knowledge to drive informed decisions and elevate safety and efficiency in your pharmacy.
Sponsored by Simplivia
Friday
April 4, 2025
Presentation Summary
Disaster preparedness is essential for minimizing the impact of health emergencies, ensuring continuity of care, and safeguarding vulnerable populations. Effective preparedness requires coordinated planning, rapid response, and resilient health systems to address the complex challenges posed by emergencies. Oncology pharmacy plays a critical role in such scenarios, given the vulnerability of cancer patients and the reliance on uninterrupted, specialized care. This keynote will highlight the pivotal role of disaster preparedness in mitigating health crises and explore how oncology pharmacy can contribute to emergency planning and response.
Embark on an enlightening journey into the vital domain of disaster preparedness led by Dr. Kaitlyn Watson, B. Pharmacy (Hons), PhD, a disaster pharmacy researcher and Founder & CEO of Disaster Pharmacy Solutions. The focus encompasses exploring the evolving role of pharmacy during crises, acquiring actionable approaches for effective disaster preparedness, and uncovering tailored self-care strategies and disaster response approaches designed specifically for oncology pharmacy personnel.
Learning Objectives
At the end of the session, participants will be able to:
1. Explain the importance of disaster preparedness for health emergencies.
2. Describe roles and responsibilities for oncology pharmacy in health emergencies.
Presentation Summary:
This session is an introduction to statistics and is suitable for anyone with little or no statistics background. It will start with the fundamentals and utilize practical examples that are applicable and relevant to oncology. The attendees will learn to differentiate between descriptive statistics and inferential statistics. An overview of common statistical analyses used in oncology will be presented. The session will conclude with a discussion on how to present data effectively.
Learning Objectives:
At the end of this program, participants will be able to:
1. Differentiate between different data types and how to best summarize data based on the data type.
2. Identify the appropriate statistical analysis based on data type.
3. Present data in a meaningful way that can be used to support clinical and/or policy decisions.
4. Participants will be able to take the learnings from this session to develop suitable methodology for research studies in oncology.
Six Abstract Platform Presentations
Presentation Summary
The presentation will include a brief overview of the workload to show the how busy the oncology pharmacy is at a national hospital in Kenya.
It will also highlight the main challenges pharmacists face integrating research in their work -African perspective. Then highlight the major challenges from the Kenyan perspective based on a national hospital.
The better part of the presentation will be a discussion on the strategies implemented based on the challenges faced to better integrate research in our day-to-day oncology pharmacy practice. This will include a brief explanation of the reasons for the specific strategies and their outcomes.
Learning Objectives
1. To identify challenges that a pharmacist may face when integrating research into a busy practice.
2. Develop an understanding of some strategies that have been used to integrate research into a busy practice.
3. To learn how to evaluate outcome of implemented strategies.
Theme: Oncology Pharmacy Variability around the World
Saturday
April 5, 2025
Concepts of EDI and Initiatives in Oncology Pharmacy
Presentation Summary
This presentation explores the risks linked to the use of commercial monoclonal antibodies in hospitals, with a focus on the impact of in-hospital handling and pneumatic tube transport. It details the methodology used to assess the effects of transport on five commonly used drugs and presents key findings. Attendees will gain insights into how transport and handling conditions can affect drug integrity and will learn approaches to assess these risks, ensuring the safety and efficacy of monoclonal antibody treatments in hospital settings.
Learning Objectives
By the end of this presentation, participants will understand the key risks associated with the transport and handling of monoclonal antibodies within hospital settings.
• Attendees will gain insights into assessing the comprehensiveness of research methodologies used to evaluate the impact of pneumatic tube transport on monoclonal antibodies.
• Participants will learn about the stability outcomes of five commonly used monoclonal antibodies after pneumatic tube transport.
• Attendees will be equipped to critically evaluate and improve handling and transport protocols for monoclonal antibodies in their own hospitals.
Presentation Summary:
This talk will explore how real-world evidence from the Australasian Longitudinal Cohort Study and Biobank (AURORA) and other international real-world cohorts is shaping regulatory decision-making and drug approvals while enhancing treatment decision-making in lung cancer. The presentation will address key topics such as the role of molecularly guided treatment selection, disparities between real-world and clinical trial outcomes, insights from repeat biopsy strategies, and the impact of drug sequencing on clinical outcomes. The discussion will emphasize the use of longitudinal data to inform personalized treatment strategies, optimize therapy selection and sequencing, and improve outcomes for patients, with a focus on oncogene driven lung cancers.
Learning Objectives:
• Understand the importance of real-world evidence in advancing therapeutic strategies and informing regulatory decisions in lung cancer.
• Recognize disparities between real-world and clinical trial outcomes and their implications for clinical practice.
• Evaluate the role of repeat biopsy in tracking molecular changes and guiding treatment decisions.
• Explore the impact of drug sequencing approaches on long-term clinical outcomes in lung cancer management.
Presentation Summary:
Clinical research offers patients with various diseases the opportunity to access innovatives medicines. Clinical studies have different inclusion and exclusion criteria and are not always an option for patients with intractable diseases. This is when Expanded Access and Compassionate Use become an opportunity for free access to innovative treatments. In Brazil, these programs are governed by a specific resolution (RDC), which regulates their implementation and oversight. This presentation will focus on exploring this resolution.
Learning Objectives:
By the end of this session, participants will be able to know:
• Difference between expanded access and compassionate use
• Brazilian scenario
• Role of the pharmacist in this context
Presentation Summary
With the increasingly impressive survival rates in pediatric oncology, it has become even more imperative to ensure that survivors of childhood cancers enjoy healthy lives as adults. Mitigation or prevention of known late effects of treatment such as cardiotoxicity and ototoxicity will be discussed. Evidence to support the use of prophylaxis under specific circumstances and the attendant controversies will be summarized. Interventions currently under study to prevent late treatment effects will be presented.
Learning Objectives
By the end of this presentation attendees will be able to:
• Recall the clinical circumstances where cardiotoxicity and ototoxicity can be effectively and safely minimized in pediatric patients with cancer
• Evaluate the risks and benefits of interventions aimed at preventing cardiotoxicity and ototoxicity
• Identify interventions that may prove to be effective in preventing cardiotoxicity and ototoxicity
Presentation Summary
Retrospective, prospective and naturalistic studies all provide compelling evidence that genetic variation affects the way people respond to drugs. Currently, reactive, and pre-therapeutic single-gene PGx tests are increasingly applied in clinical practice for several indications, such as DPYD testing in oncology. Moreover, specific recommendations on how to tailor drug treatment based on genetic test results are available from the Dutch Pharmacogenetics Working Group (DPWG) and Clinical Pharmacogenetics Implementation Consortium (CPIC) for a large number of drugs. In addition to pre-therapeutic testing for a single gene, pharmacogenomic panel-based testing represents a new model for precision medicine. While several small studies indicated a panel approach is indeed favourable, the Ubiquitous Pharmacogenomics Consortium recently completed the PREemptive Pharmacogenomic testing for prevention of Adverse drug Reactions (PREPARE) study. In this presentation, the results and experiences from PREPARE as well as the next steps for moving PGx testing from promise to practice will be discussed.
Learning Objectives
Participants of this seminar will learn:
1. About the Dutch Pharmacogenetics Working Group Guidelines and how they support PGx testing
2. About the efforts and results of the Ubiquitous Pharmacogenomics (www.upgx.eu) consortium to implement PGx testing in Europe
3. How panel-based PGx testing may help to reduce the risk for adverse drug events
Presentation Summary
This lecture will highlight evidence and gaps in the literature which describe the relationship between pharmacogenomics and health disparities in pediatric cancer patients.
Learning Objectives
• Define the role of health equity science in the study of pharmacogenomics
• Describe the relationship between pharmacogenomics and health disparities
• Propose opportunities to apply the use of pharmacogenomics to minimize health disparities
Presentation Summary:
5-Fluorouracil (5FU) is the backbone of anticancer treatment in many solid tumours, with approx. 2 million people are treated with 5FU each year. Studies have shown that approx. ~40-60% of patients were underdosed, and ~10-20% were overdosed, when dosed based on body surface area (BSA). 5FU has a narrow therapeutic index and marked intra-patient pharmacokinetic variability, which is partially explained by PGx. The success of implementing upfront PGx program for DPYD genotyping in clinical oncology practice to prevent serious and fatal 5FU toxicities was proven feasible. However, concerns with upfront PGx dose reductions especially for DPYD intermediate metabolisers, may compromise 5FU efficacy, leading to poorer cancer outcomes. Hence, the use of TDM should be considered to supplement PGx testing, to guide dose modifications to dose 5FU safely and effectively in cancer patients. This presentation will showcase final and interim results from prospective, multisite clinical trials (PREDICT 5FU and PRECISION) respectively, with applied PGx and TDM in clinical oncology practice.
Learning Objectives:
1. Understand the evidence and challenges for integrating 5FU therapeutic drug monitoring (TDM) into routine clinical oncology practice.
2. Explore the integration of pharmacogenetics (PGx) and TDM testing (including peripheral and finger prick sampling) as part of clinical practice (results from PREDICT 5FU and PRECISION multisite clinical trials).
3. Examine the challenges with upfront dose reduction for DPYD intermediate metabolisers according to PGx testing and how TDM was utilised to dose escalate according to area under the curve (AUC) Level(s).
Sunday
April 6, 2025
11:00-11:20 - Discussion 1
11:30-11:50 - Discussion 2
Note: The list of Round Table Discussion topics will be confirmed later.
11:00-11:20 Interest Groups:
- Pediatric Pharmacy Meet Up
- Pharmacy Technicians & Assistants Meet Up: Drug Access Navigation
11:30-11:50 Interest Groups:
- Pharmacy Technicians & Assistants Meet Up: Ergonomics during Compounding
- Heme and Transplant and Cellular Therapy Meet Up: CAR T-cell Therapy Implementation and Pearls
Pharmacists will gain knowledge and understanding of the impact of innovative biosimilars and generics and how they contribute to health equity, both locally and globally.
Learning Objectives:
1. To provide a high-level overview of health equity, inclusion and accessibility in oncology, in Canada and globally.
2. To understand the role of innovative biosimilars and generics in improving health equity in Canada.
3. To showcase how various Canadian oncology pharmacists/pharmacy teams innovate in their institution to improve education, efficiency, and interprofessional programs.
4. Health equity call to action.
Sponsored by Apobiologix
The symposium will showcase unique and state-of-the-art Canadian pharmacist-led models of care for breast cancer patients. The wealth of experience and implementation toolkit shared with the ISOPP CAPhO 2025 delegates will demonstrate the importance and distinctive position of pharmacists in oncology in the breast cancer patients journey.
Sponsored by Novartis
Monday
April 7, 2025
Additional fees apply. Click here to for more information about the Masterclass.
Additional fees apply. Click here to for more information about the Masterclass.