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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.
Would you like to get a sneak peek about what is in store for you? Listen to Tina Crosbie, Symposium Chair, discussing the ISOPP CAPhO 2025 Program in the latest episode of the CAPhO Connections Podcast.
Click here to see the Program at a Glance.
Click on the links below to go directly to any of the following days:
Thursday
March 27, 2025
This session offers a comprehensive understanding of induced menopause addressing its causes, symptoms, like hot flashes and mood swings, along with potential complications such as cardiovascular and cognition issues. Pharmacists will gain insights into pharmacological and non-pharmacological therapies, including lifestyle modifications, to manage menopause symptoms. The session will also focus on counseling strategies and monitoring approaches to optimize patient care.
Learning Objectives:
- Understand chemo-induced menopause
- Recognize common symptoms and complications associated with induced menopause in cancer patients
- Recommend pharmacological and non-pharmacological therapies to alleviate induced menopause symptoms
- Confidently counsel and monitor therapies and symptoms to support and enhance overall health and well-being of patients
Sponsored by Organon

The presentation provides guidance on managing multiple myeloma, particularly in cases of relapse or refractory disease. A range of therapeutic options are available to patients including established treatments such as stem cell transplantation, immunomodulatory agents, and anti-CD38 antibodies.
Additionally, newer therapies such as bispecific T-cell therapy (BiTE), CAR-T cellular therapy, and antibody-drug conjugates will be reviewed. The presentation also addresses the management of side effects specifically associated with BiTE and CAR-T therapies.
Sponsored by Natco Pharma (Canada) Inc.
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

Join us for Tackling TKI Toxicities Together: A Fireside Chat on Advanced RCC Treatment, an on-demand symposium focused on managing adverse events associated with TKI therapy in advanced RCC. Expert panelists, including an oncologist, pharmacist, and a patient, will dive into the challenges of TKI-related toxicities, offering strategies for effective management. Attendees will gain insights into the patient and pharmacist's role in improving patient adherence, including the importance of dose individualization and monitoring for optimal outcomes. Through a real-life example and an interactive fireside chat, participants will leave with practical tips for enhancing TKI therapy management in aRCC care.
Learning Objectives:
1. Understand Overlapping Toxicities of IO/TKI Combinations: Learn about the toxicities from combining IO therapies and TKIs in RCC treatment and strategies for managing them.
2. Enhance the Pharmacist’s Role in Access and Adherence: Explore how pharmacists ensure patient access to therapies and support adherence through education and management.
3. Implement Dose Individualization and Monitoring: Develop skills in dose adjustments and monitoring to optimize outcomes, focusing on managing side effects and differences between IO therapies and TKIs.
Cliquez ici pour en savoir plus.
Sponsored by Ipsen Biopharmaceuticals Canada
This sponsored symposium will feature pharmacists from St. James’s Hospital (Dublin, Ireland), Onkologikoa (San Sebastián, Spain), Fred Hutchinson Cancer Center (Seattle, USA), and Arthur Child Comprehensive Cancer Centre (Calgary, Canada) sharing their experiences with IV automation in oncology compounding. The session will explore the adoption and use of automation to enhance patient safety, reduce staff exposure, and streamline pharmacy workflows. Topics include user training and qualification, drugs produced by automated systems, and future perspectives on IV automation. Join us to gain valuable insights into the advancements and challenges in this critical area of oncology pharmacy.
Sponsored by Healthmark Services Ltd.

Session Summary
The GU oncology treatment landscape is growing increasingly innovative and complex with an increasing number of therapeutic options becoming available for patient treatment, both alone as single agents, as well as in various combinations of multiple agents. While these innovations in care are improving patient outcomes, they also come with patient management complexities that require a team approach to patient management.
Learning Objectives
At the end of this session, and using case-based learning scenarios, participants will be able to:
1. REVIEW and EVALUATE the impact of recent practice changing data in genitourinary (GU) oncology, (RCC), highlighting the implications for treatment and patient care.
2. EXPLAIN and RECOGNIZE actionable strategies for pharmacy professionals to enhance the cancer care experience by optimizing patient management and addressing the unique side effects and needs stemming from novel GU oncology therapies.
3. EXAMINE multidisciplinary collaborative practice models that empower pharmacists to lead in patient care, highlighting real-world examples and best practices that can improve the patient experience and overall care delivery.
Featuring experts Chelsea Normore and Matthew Young. This session covers recent practice-changing data in genitourinary (GU) oncology, with a focus on bladder cancer and renal cell carcinoma (RCC), and its impact on treatment and patient care. It emphasizes actionable strategies for pharmacy professionals to optimize cancer care, manage patients effectively, and address the unique side effects of novel GU oncology therapies. Additionally, it explores multidisciplinary collaborative practice models, presenting real-world examples and best practices that enable pharmacists to lead in patient care and improve overall care delivery.
Sponsored by Merck

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

Learning Objectives:
• Discuss the future role of immunotherapies in the treatment of B-ALL
• Outline the implementation of novel therapies into frontline B-ALL regimens
• Highlight the crucial role of pharmacists in recognizing and managing potential adverse effects associated with novel therapies for B-ALL
Sponsored by Amgen Canada Inc.
Join us on Thursday, April 3, from 15:30 to 16:30 for an engaging symposium: "Innovative Technologies for Safe and Economical Handling of Hazardous Drugs: New Frontiers in Automation, CSTD Vapor Containment, and Drug Sterility in the Modern Pharmacy"
Key Highlights:
• Live Case Studies: Explore a state-of-the-art robotic chemo automation system integrating closed-system drug transfer devices (CSTDs).
• In-Depth Discussions: Dive into vapor containment and drug sterility innovations that are redefining safety standards.
• Expert Insights: Hear from globally recognized speakers in oncology pharmacy, sharing valuable perspectives and solutions.
Gain practical knowledge to make informed decisions and improve safety and efficiency in pharmacy workflows.
Why Choose Chemfort®?
Chemfort®, the only drug-binding mechanical barrier CSTD, offers a vial-to-vein solution that ensures a closed workflow. It minimizes exposure to hazardous drugs while maintaining drug sterility. Tested with real cytotoxic drugs, Chemfort® has been proven effective for vapor containment and is compatible with all known hazardous drugs. Simplivia products have been chosen by healthcare professionals as the most user-friendly.
Simplivia is trusted by over 5,000 hospitals worldwide, offering a comprehensive range of solutions tailored for nurses and oncology pharmacists, including Chemfort®, Chemfort® Closed Administration, and Automated SmartCompounders, which are revolutionizing the compounding process.
Join us for an insightful and engaging symposium—we can’t wait to see you there!
Sponsored by Simplivia HealthCare

This case-based session will explore the management of patients with metastatic breast cancer receiving antibody–drug conjugates (ADCs). The presentation will include a clinical resource designed by a multidisciplinary faculty to support nurses and pharmacists in the care of patients receiving ADCs. The presenting faculty will review the resource and discuss proactive monitoring and toxicity management strategies for trastuzumab emtansine, trastuzumab deruxtecan, and sacituzumab govitecan, demonstrating how this print tool can be employed in routine clinical practice.
LEARNING OBJECTIVES
Upon completion of this activity, participants should be able to:
- Understand key differences between the safety profiles of antibody–drug conjugates (ADCs) currently approved by Health Canada for the treatment of metastatic breast cancer, including trastuzumab emtansine, trastuzumab deruxtecan, and sacituzumab govitecan
- Integrate proactive monitoring strategies during the routine care of patients receiving ADCs
- Collaborate with the multidisciplinary team for timely management of ADC-related toxicities
Sponsored by AstraZeneca Canada and Daiichi Sankyo Canada
Friday
April 4, 2025
Following the initial use of PARP inhibitors in ovarian cancer, their role has expanded to include treatment of several early and later stage cancers including breast, prostate and pancreatic cancer. This case-based session will bring together practitioners with experience in managing patients receiving PARP inhibitors to discuss practical strategies for optimizing the benefits of treatment through proactive toxicity management. The presenters will review the CANO-endorsed PARP Inhibitor Clinical Resource and application of this tool in routine practice.
LEARNING OBJECTIVES
At the end of the session, participants will be able to:
- Explain the role of PARP inhibitor therapy in the treatment of breast, prostate, and ovarian cancers
- Understand the similarities and differences in the clinical management of patients with different solid tumours who are receiving PARP inhibitor therapy
- Implement proactive and reactive toxicity management strategies from the CANO-endorsed PARP Inhibitor Clinical Resource to optimize tolerability and clinical benefit from PARP inhibitor therapy
Sponsored by AstraZeneca Canada.
Presentation Summary
Pharmacists can play an important role in delivering culturally responsive patient-centered care. Cultural competence in pharmacy practice can enhance cross-cultural communication skills, help to break down potential barriers, augment medication therapy management recommendations, and bridge gaps in effective patient care strategies. Customer-owned, relationship-based health care requires effective, open communication and demonstrates respect for cultural values. This presentation will explore strategies in Indigenous health care and traditional healing methods that augment Western biomedical treatment approaches. By building trust and relationships with patients and families, pharmacists can help navigate the complexities in cancer care, improve medication adherence, and enhance health outcomes for diverse patient populations.
Learning Objectives
By the end of the session, participants will be able to:
1. Explain the role culturally responsive approaches in pharmacy practice when working in communities outside of your culture, including Indigenous communities.
2. Compare traditional healing practices with Western biomedical approaches, highlighting differences and similarities.
3. Explore how cultural competence in pharmacy practice can enhance cross-cultural communication skills and ensure respectful, inclusive, patient-centered interactions.
4. Identify clinical pearls from an Alaska Native-owned and operated health care system’s approach to cancer care.
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 will explore practical strategies for improving environmental sustainability in oncology pharmacy practice, focusing on emissions reduction, pharmaceutical waste minimization, and plastic reduction. A panel of experts will share real-world approaches, including sustainable procurement and product selection, other opportunities to reduce pharmaceutical cytotoxic pollution within practice, and an overarching discussion on sustainability in oncology pharmacy. Attendees will gain actionable insights on how to implement greener practices in their own settings while outlining how patient and public safety and planetary health are significantly linked through oncology pharmacy practice. The session will conclude with an interactive discussion, encouraging participants to identify and overcome barriers to sustainability in their practice.
Learning Objectives
By the end of this session, participants will be able to:
• Recognize and explain how oncology pharmacists can consider climate change and planetary health more broadly within clinical practice.
• Identify at least three key environmental impacts of oncology pharmacy practice
• Analyze potential barriers and solutions to greener oncology practice
Common challenges are faced in multiple myeloma care, both from a resource standpoint and from a patient experience standpoint. Addressing these by providing solutions is key to sustaining/enhancing our healthcare system and improving patient outcomes and quality of life.
Learning Objectives:
• Understand the role of pre-medication in multiple myeloma and areas for improvement.
• Discuss current challenges in dose scheduling concerning clinic and patient burden.
• Discuss new dosing administration protocols for multiple myeloma therapies.
Sponsored by Sanofi
• Opportunities for Pharmacogenomic-Driven Medication Optimisation in Cancer Care: Early Insights from the Multicentre Australian PRECISION Trial – Marliese Alexander
• Descriptive Analysis of the Use of Pembrolizumab Alone or in Combination with Lenvatinib in the Treatment of Endometrial Cancer in Four University Hospitals in Quebec, Canada – Nathalie Letarte
• Magnesium Supplementation for Cisplatin-Induced Magnesium Wasting: A Scoping Review – Wendi Lin
• Technical Practices in Oncology Pharmacy in Brazil: Insights from the SOBRAFO 2024 Analysis – Tiago Castro
• Hazardous Drug Locking Capacity of Activated Carbon-Based CSTD: 3 Approaches – Elana Slutsky Smith
• Quantifying Pharmacy Human Resources required to deliver Comprehensive Ambulatory Oncology Clinical Pharmacy Key Performance Indicator based care for patients receiving Take Home Cancer Drugs – Jason Wentzell
Presentation Summary
Older and unfit patients with haematological malignancies frequently have complex care needs which can lead to worse outcomes. Frailty, cognitive impairment, polypharmacy, socio-economic issues, and co-morbidities are common, and can lead to increased treatment toxicity, admissions, and higher rates of mortality.
Early identification of these complex care needs is vital to optimally manage this patient population and ensure best treatment outcomes.
Empowering pharmacists with tools to assess risk and deliver personalised treatment is crucial for an ageing population, living longer with blood cancers.
Learning Objectives
- Recognise the holistic needs of older or unfit patients
- Define at least 5 assessment tools available for use in clinical practice
- Recognise the impact of frailty and geriatric assessments on risk and treatment stratification in clinical practice
- Evaluate clinical trial data in context of applicability to real world older and unfit patients
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. Develop suitable methodology for oncology research studies based on the data types and statistical analysis discussed.
Presentation Summary
Oncology pharmacy is a high-risk, fast-paced, and resource-intensive field, where pharmacists juggle complex responsibilities, including patient safety, treatment optimization, and medication management. These demands often leave little time and resources for research, making its integration into daily workflows challenging. This presentation examines the linear workflow of hospital pharmacy and the barriers it creates for research. By shifting to a Lean workflow, pharmacists can seamlessly integrate research without disrupting essential operations. The F.I.V.E² model provides a structured approach to overcoming these challenges. Through real-world examples, including COVID-19 crisis research, we will showcase how research can thrive in a busy oncology setting.
Learning Objectives
By the end of the session participants will be able to:
1. Identify key barriers preventing research integration in oncology pharmacy workflows and their impact on patient care.
2. Analyze how the traditional linear workflow limits research opportunities and how shifting to a Lean model can enhance efficiency.
3. Apply the F.I.V.E² model to develop and implement small-scale research projects within a busy clinical setting.
4. Evaluate the impact of integrating research into daily practice by measuring improvements in workflow, patient outcomes, and team engagement.
5. Explore real-world examples of research conducted in an oncology pharmacy department during the COVID-19 pandemic and extract key takeaways for future implementation.
Presentation Summary
Cytomegalovirus is one of the most important infections that occur after allogeneic hematopoietic stem cell transplantation, and an increasing number of reports indicate that cytomegalovirus is a potentially important pathogen in patients treated with newer pharmacotherapies for hematologic malignancies. This presentation will focus on the pathogenesis of cytomegalovirus, strategies to prevent cytomegalovirus, as well as evidence-based recommendations for treatment of cytomegalovirus in patients with hematologic malignancies.
Learning Objectives
By the end of this presentation, participants will be able to:
• Explain the pathogenesis of cytomegalovirus (CMV) in patients with hematologic malignancies and after hematopoietic stem cell transplantation.
• Identify approaches to prevent CMV after hematopoietic stem cell transplantation.
• Describe current pharmacotherapies to manage CMV.
Presentation Summary
Have you ever wondered what oncology pharmacy service levels are being provided from different countries around the world? For the first time ever, a global review of oncology pharmacy services was undertaken via a survey of ISOPP Global Leaders. Hear from the panel who were the research team behind this important body of work that will be used to assist in facilitating professional development and oncology pharmacy advancement, by connecting countries with mentoring opportunities, resources, and providing a benchmark and possible future state of oncology pharmacy services!
Learning Objectives
By the end of the session, delegates should be able to:
• Describe different oncology pharmacy service levels
• Describe the knowledge required for delivering these service levels
• Identify which countries have a protected title for pharmacist, pharmacy technician, and oncology pharmacist and the advantages of having protected titles
• Evaluate the resources available in their country that can be shared and would be useful to share with the ISOPP community and the advantages of sharing these resources
Every day oncology pharmacy professionals make a difference in the lives of cancer patients around the world. ISOPP and CAPhO recognize members’ achievements in the field of oncology pharmacy through their awards. Join us on Friday, April 4 at 15:00 for the Oncology Pharmacy Around the World session in the Lecture Hall to acknowledge and celebrate the recipients of ISOPP’s Helen McKinnon Award and CAPhO’s Larry Broadfield Distinguished Service Award and FCAPhO Award.
Additional awards will be recognized at the ISOPP and CAPhO AGMs and Closing Remarks.
17:00-17:10
Introduction
Flay Charbonneau, RPh, BScPharm
17:10 – 17:45
“Exposure Assessment and Health Effects in Oncology Workers: Making the Case for Evidence Based Safe Handling”
Dr. Melissa A. McDiarmid, MD,MPH, DABT
17:45 – 18:20
2024 NIOSH Hazardous Drug List-Let’s roll up our sleeves.
Fred Massoomi, Pharm.D, BCSCP, FASHP
18:20-18:30
Discussion
Visit the Networking Events page for more details.
Saturday
April 5, 2025
Learning Objectives:
- Discover insights into hazardous drug (HD) exposure risks, current safe handling guidelines, and the NIOSH vapor containment performance protocol’s history for evaluation of CSTDs.
- Review the recent study results that evaluated the performance of seven CSTD brands.
- Gain practical tips for enhancing safety protocols and minimizing HD exposure risks.
- Don’t miss the interactive Q&A session for an engaging discussion.
Sponsored by BD

Presentation summary
This presentation will first start off with a patient care example that includes a racist encounter with a pharmacist and the long-term effects of it, then we will move into EDI and why it is important (the effects of racism and microaggressions in accessing health care). Then I will speak about definitions and understanding concepts in EDI. Then to close it off I will speak about how all of us have probably been some sort of "ism" (racism sexism) or -phobic (transphobic, homophobic) and how we can avoid it.
Learning Objectives
By the end of this session, participants will be able to:
1. Define EDI: list the core concepts of equity, diversity, inclusion and trauma informed care
2. Explore Research Findings: Examine recent EDI Research from BOPA, with insights on the perception of EDI principles and challenges in the workplace
3. Identify Barriers and Biases: Identify common obstacles to EDI, including unconscious bias and systemic inequities
4. Describe how ISOPP is integrating EDI principles within the organization
Presentation Summary
The rapid advancements in artificial intelligence are revolutionizing oncology, offering exciting opportunities for improved patient care. However, this progress comes with significant challenges and safety concerns that must be addressed. Join us as we explore the promising yet intricate landscape of AI in oncology, balancing innovation with critical risk management to ensure optimal outcomes for patients.
Learning objectives
1. By the end of this presentation, participants will be able to:
2. Identify and discuss three specific benefits of integrating AI in oncology practice.
3. Identify and discuss three specific risks associated with AI integration in oncology practice.
4. Explain the significance of continuously monitoring AI models and provide a detailed description of model drift.
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 be able to:
• Identify the key risks associated with the transport and handling of monoclonal antibodies within hospital settings.
• Assess the comprehensiveness of research methodologies used to evaluate the impact of pneumatic tube transport on monoclonal antibodies.
• Describe the stability outcomes of five commonly used monoclonal antibodies after pneumatic tube transport.
• Critically evaluate and propose improvements to 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 innovative 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:
• Differentiate between expanded access and compassionate use
• Describe Brazilian scenario related to expanded access and compassionate use
• Explain the role of the pharmacist in this context
Presentation Summary
Cancer-associated thrombosis (CAT) is a leading cause of morbidity and mortality, yet uptake of thromboprophylaxis remains suboptimal, especially in the ambulatory setting. This session will review recent evidence shaping the evolving guideline recommendations for CAT prevention, and examine risk assessment tools to identify patients who may benefit. Considerations for anticoagulation selection and real-world barriers to implementation will be explored, focusing on the pharmacist’s role in leading strategies to drive improved, risk-based thromboprophylaxis. We will also take a big picture view of current global practice patterns, highlighting the need for benchmarking. Expect practical takeaways and actionable insights to preventing CAT in oncology care.
Learning objectives
By the end of this presentation, participants will be able to:
1. Interpret the current evidence – summarise recent key clinical trials and their impact on guidelines updates for the prevention of cancer-associated thrombosis (CAT)
2. Apply risk assessment models – discuss the utility and limitations of risk stratification tools to assess patients with cancer who may benefit from thromboprophylaxis
3. Compare anticoagulation options – evaluate the efficacy, safety, and practical considerations of different antithrombotics used for primary prophylaxis in patients with cancer
4. Address barriers to implementation – identify common real-world challenges to integrating risk-directed thromboprophylaxis in cancer care
5. Develop pharmacist-led interventions – propose strategies for pharmacists to enhance uptake of primary thromboprophylaxis via multidisciplinary collaboration
Presentation Summary
This presentation will offer an overview of the significance of serum asparaginase activity monitoring. It will provide a review of consensus recommendations for monitoring serum asparaginase activity as well as literature highlighting the variability in therapeutic drug monitoring practices. Additionally, the pharmacokinetic differences between pegaspargase and the newest pegylated formulation, calaspargase pegol, will be discussed.
Learning objectives
By the end of the session, participants will be able to:
• Recognize the importance and identify reasons for therapeutic drug monitoring of different asparaginase formulations
• Describe the consensus recommendations for monitoring serum asparaginase activity (SAA)
• Analyze and compare differences in the pharmacokinetic profile and rates of adverse effects of pegaspargase and calaspargase pegol
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
By the end of this session participants will be able to:
1. Describe the Dutch Pharmacogenetics Working Group Guidelines and how they support PGx testing
2. Recognise the efforts and results of the Ubiquitous Pharmacogenomics (www.upgx.eu) consortium to implement PGx testing in Europe
3. Identify how panel-based PGx testing may help to reduce the risk for adverse drug events
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
SOBRAFO has been working in educational activities since its creation in 2001. The first SOBRAFO EXPERIENCE was held in 2023 in the city of São Paulo and represented not just a course in handling oncology drugs, but also an opportunity for professionals in the field to exchange knowledge and experiences. At the unique Brazil Training Simulation Facility for Oncology Drug Preparation, participants go through all the stages of the oncology drug preparation process with technical and scientific support, which adds value to daily practice. More than 60 pharmacists have already taken part in this immersive experience.
1. Outline the creation history and educational objectives of SOBRAFO EXPERIENCE training project in Brazil
2. Describe the structure of SOBRAFO EXPERIENCE simulation facility at the headquarters in São Paulo
3. Present the results of the SOBRAFO EXPERIENCE from the perspective of the participating pharmacists.
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
By the end of this session, participants will be able to:
• 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
This session will introduce the new education pathway that is supporting recruitment and retention of staff within Pharmacy Technical service environments within the UK. It will also outline the creation of the educational course that is supporting the workforce to ensure there are future leaders for these services, whilst meeting the demands of the Lord Carter report for expansion of the provision to meet demand, enhance patient care and support the technical services team with career pathways and educational opportunities.
Learning objectives
By the end of this session, participants will be able to:
• Outline the novel education opportunities undertaken in the UK and the career pathway trajectory.
• Describe how these courses meet the legislative and regulatory guidelines for safe production of medicines.
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:
By the end of this session participants will be able to:
1. Describe the evidence and challenges for integrating 5FU therapeutic drug monitoring (TDM) into routine clinical oncology practice.
2. Explain 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. Identify 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).
In this dynamic and interactive symposium, a multidisciplinary panel of experts will discuss the latest advances in subcutaneous immunotherapy in oncology. Through short presentations of relevant data, panel discussions, interactive polling sessions, and a question-and-answer period, participants will review safety and efficacy data for SC IO formulations, understand their role in the current healthcare environment, and gain practical tips regarding the implementation and administration of these therapeutic options.
Learning objectives
• Evaluate the latest advances in SC IO therapy applications across multiple tumour types
• Understand the potential impact of SC IO therapy in healthcare utilization and services
• Increase expertise in the safe administration of SC oncology drugs in different care settings
Sponsored by Bristol Myers Squibb
CAPhO members are invited to join CAPhO’s Annual General Meeting either in person or virtually. CAPhO will unveil its 2025 to 2028 Strategic Plan, request approval of two Bylaw changes, present awards and introduce you to the incoming Board of Directors. Join the meeting for a chance to win complimentary registration to CAPhO Conference 2026.
CAPhO members, log in as a member and visit CAPhO’s Community Centre to review the Agenda, last year’s AGM Minutes, Committee Chair reports and the Bylaw Amendment document.
ISOPP members are invited to join ISOPP’s Annual General Meeting either in person or virtually. ISOPP will update you on the progress of ISOPP’s activities, share future plans, present awards and introduce the incoming Secretariat. Visit the ISOPP Website and log in as a member to review 2024 AGM Minutes, 2025 AGM Agenda and Annual Report 2024 in the Society Documents under My Dashboard.
The Global Town Hall is an opportunity for members of the oncology pharmacy community to ask questions, discuss issues, share ideas, get updates and learn more about ISOPP Society’s initiatives. Submit your questions in advance using the following link: 2025ISOPPAGM. You may also ask questions during the Town Hall.
The objective of this symposium is to discuss the change management involved with setting up a dose banding program, with an operational focus.
This session will be moderated by Flay Charbonneau, Pharmacy Manager, Sunnybrook Health Sciences Centre.
Format:
• Three panelists will each deliver a 15 min overview (with slides) of their dose banding program/journey.
• Followed by 15-30 mins of panel discussion questions.
• Remainder of the time will be filled Q&A from audience.
Sponsored by Baxter Corporation

Click here for more information about the Reception.
Sunday
April 6, 2025
Join us for an engaging symposium offering insights into the latest developments in lung and urothelial cancers through informative presentations, panel discussions, and interactive Q&A sessions. This session will feature a panel of pharmacists sharing expert perspectives and practical tips on patient counseling, as well as the monitoring and management of adverse events related to first-line treatments for ALK-positive non-small cell lung cancer (NSCLC) and locally advanced/metastatic urothelial cancer (la/mUC).
After attending this symposium, participants will be able to:
• Describe the changing first-line treatment landscape in locally advanced/metastatic urothelial cancer (la/mUC)
• Implement practical strategies to identify and manage adverse events in patients treated with immunotherapy with or without an antibody-drug conjugate (ADC) for la/mUC
• Counsel patients regarding adverse events associated with first-line treatment options for ALK-positive non-small cell lung cancer (NSCLC)
• Appropriately monitor patients treated with ALK inhibitors for ALK-positive NSCLC and manage associated toxicities
Breakfast will be served and barista available from 6:30am - 7:00am
Sponsored by Pfizer Canada
• AI-Driven Optimization of Cytotoxic Drug Compounding: Reducing Chemotherapy Wastage and Promoting Sustainability in Healthcare – Lita Chew
• Evaluating the impact of a pharmacist-led venetoclax ramp-up clinic for chronic lymphocytic leukemia patients: a retrospective chart review – Adrian de Boer
• Cost Effectiveness of Rituximab Biosimilar IV vs SC for R-CHOP Regimen in an Ontario Hospital Setting – Shayna Pan
• Reduction in carbon dioxide emissions to a dose-rounding policy: an estimate for 8 monoclonal antibodies and antibody-drug conjugates across 6 BC Regional Cancer Centres – Jennifer Suess
Presentation Summary
Over the past few years, it has been common to see headlines in the UK media such as ‘The Systemic Anti-Cancer Treatment (SACT) Capacity Crisis in the NHS’ and ‘Cancer care still lags behind other countries’. These headlines reflect the experiences of cancer multidisciplinary teams (MDTs) across the country, who are working incredibly hard every day to deliver high-quality care to patients. Among the advantageous initiatives enabled by MDT collaboration and SACT development is decentralised care – whether this is a homecare model, a hub and spoke model or utilisation of primary care. This session will explore Care Closer to Home and how this can be a potential model to improve patient care but also help with the SACT crisis in the NHS and beyond.
Learning Objectives
By the end of the lecture, participants will be able to:
1. Define what "Cancer Care Closer to Home" means and identify at least three key benefits of delivering cancer care in local communities.
2. List and describe at least five key strategies for implementing cancer care closer to home, as demonstrated through an interactive Q&A session.
3. Identify local healthcare facilities or services that could be expanded to offer cancer care services, given the existing resources and information.
4. Recognize how providing cancer care closer to home can improve patient outcomes, enhance access to care, and reduce healthcare costs in their communities
For oncology pharmacists that want to become researchers, it can be daunting to get started. This round table will discuss approaches to successfully obtaining grants, preparing manuscripts for publication, and dealing with the peer review process.
Leadership in pharmacy is not just about titles; it’s about influence and impact on patient care. This session will explore how pharmacists can take initiative, influence decisions, and drive patient-centered improvements within healthcare teams and systems, regardless of their official role.
This round table discussion will provide an opportunity for attendees to ask questions about how to perform high-quality reviews for scientific journals.
11:00-11:20 Interest Groups:
- Pediatric Pharmacy Meet Up - Katie Lacaria
- Pharmacy Technicians & Assistants Meet Up: Drug Access Navigation - Alan Birch
11:30-11:50 Interest Groups:
- Pharmacy Technicians & Assistants Meet Up: Ergonomics during Compounding - Amy Laflin
- Hematology and Transplant and Cellular Therapy Meet Up: CAR T-cell Therapy Implementation and Pearls - Katie Lacaria
Whether it is for patients, students, or colleagues, oncology pharmacy professionals are often called upon to develop or participate in educating others. But without formal training as teachers, how do we know if we do this well? This round table will facilitate the sharing of best practices and evidence-based approaches for teaching among participants and review evaluation strategies that can be utilized to determine whether education is effective.
Are you a pharmacist new to oncology pharmacy? Join us for an engaging roundtable discussion for early-career (less than 5 years) oncology pharmacists to foster connections and share valuable experiences. This collaborative space will encourage peer support and the exchange for insights to enhance professional growth in the oncology pharmacy field.
Electronic medical record (EMR) outages disrupt critical cancer treatments, leading to delays and enormous medication safety risks. This session provides a starting point for oncology teams to understand the potential impacts of downtime, learn how to develop basic backup procedures for accessing treatment plans and documenting care manually, and establish quick communication strategies to maintain continuity. Designed as a practical introduction, this session will help participants take the first steps toward improving readiness for unexpected system failures.
Let's talk social media and oncology IRL! Join our roundtable discussion to explore how social media platforms can help develop meaningful connections with healthcare professionals and patients. We'll share practical strategies for engagement, support, and effective communication.
Presentation summary
The roles and responsibilities of pharmacists and pharmacy technicians in Canada and the UK will be compared and contrasted. Panel members will highlight the educational requirements and qualifications for practice in each country. The benefits of scope expansion and practicing to full scope will be discussed along with limitations of practicing to full or expanded scope. Panel members will offer strategies that can be used to expand scope or implement a full scope of practice in various settings.
Learning Objectives
By the end of the session, participants will be able to:
• Describe how oncology pharmacists can directly contribute to anticancer medication prescribing practices to improve patient safety, enhance patient satisfaction and provide optimal patient care.
• Identify at least two tasks that pharmacy technicians can take over to alleviate pharmacists' time spent on administrative and operational duties, allowing them to focus on clinical responsibilities.
• Recognize the potential benefits of practicing to full scope in oncology, including reducing delays in treatment, improving care coordination, and reducing physician and nurse workload.
• Leave the session with at least one actionable strategy they can propose to their organizations for expanding pharmacy technician responsibilities or increasing the clinical roles of oncology pharmacists.
Interested in learning more about health equity in Canada and innovations in oncology? Please join us at the Apobiologix Symposium on Sunday, April 6th, from 1:00pm-2:30pm!
Titled “The role of innovative biosimilars and generics in improving health equity + 2025 HOPE Awards”, the session will begin with exploring the current state of health equity in the Canadian oncology landscape. Flay Charbonneau, Oncology Pharmacy Director at Sunnybrook Hospital, will then share the transformative impact of innovative generics and biosimilars in oncology. Lastly, recent projects that drive innovations in oncology will be celebrated with presentations from the winners of the 5th Annual HOPE Awards.
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.
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.
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.
Learning Objectives:
- Discuss best-practices in the implementation of a pharmacist-led model of care in breast cancer, including presentation of a Canadian toolkit
- Describe evidence-based medicine and best practices around patient management processes and clinical management of early and advanced breast cancer
- Examine existing models from Canada using case-based scenarios
Sponsored by Novartis Canada

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.