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POGO > Blog > Clinical Trials
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Stopping Cancer Cell Evasion with Immune Therapies

Posted on November 22, 2018 by Jamie Irvine


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Presentation Description:
How can the immune system be modified and engaged to target cancer cells? This is a priority of basic science research and all phases of clinical trials with the goal of improving survival for the most challenging to cure pediatric cancers. Caring for patients receiving new immunotherapies and their families requires new knowledge of how immunotherapies work, and based on this mechanism what and when unique side effects might be expected. This brief quick hit session will describe why immunotherapies might work against pediatric cancer cells with case examples highlighting new agents in current clinical trials.

Speaker:
Sue Zupanec
, MN, NP Pediatrics
Nurse Practitioner, Leukemia & Lymphoma
The Hospital for Sick Children

Sue Zupanec is a Nurse Practitioner in the Hematology/Oncology Program at the Hospital for Sick Children. In her clinical practice Sue provides care to children and teens with a diagnoses of Leukemia or Lymphoma and their families.

Sue currently serves as the Education Sub Committee Chair on the Nursing Steering Committee for the Children’s Oncology Group and is an executive committee member for the Garron Family Cancer Center.

 

Posted in 2018 Pre-Symposium Nursing Seminar | Tagged 2018 pre-symposium, Clinical Trials, immunotherapies, nursing

2018 POGO Symposium on Childhood Cancer

Posted on November 22, 2018 by Jamie Irvine


The 2018 POGO Multi-Disciplinary Symposium on Childhood Cancer – Precision Medicine in Pediatric Oncology – examined clinical and scientific advances in precision medicine and explored how those advances are impacting the diagnosis and treatment of cancer in children.

Over 250 delegates representing a variety of disciplines attended the conference.

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Click on the session titles below to view presentations that POGO has permission to share. 

PLENARY SESSIONS

Precision Medicine in the Pediatric Oncology Clinic: From Feasibility to Clinical Impact
Katherine Janeway, MDMD, MMSc

Precision Medicine – A Paradigm Shift?
Ian F. Tannock, CM, MD, PhD, DSc
Uri Tabori, MD

Thinking Practically: Delivery of Care Considerations for New Agents
Karen Fung, MSW, RSW
Tara McKeown, RN MN NP-Paediatrics

Ethics and Consent in the Age of Precision Medicine – Forging a Path Forward
Steven Joffe, MD, MPH

Select Poster Presentations
Alexandra Zorzi, MD, FRCPC
Andrew Shuen, PhD Candidate, MD, FRCPC
Lauren Mulrooney
, Nursing Student (3rd year)
Valli Subasri, MSc candidate (Medical Biophysics)
Nicole Espinosa, BScH Candidate (Life Sciences)
Mohammad R. Alqudimat, PhD Student (Nursing)
Marta Wilejto, Assistant Professor Paediatric Hematology/Oncology
Sarah Naraine, Fourth Year Nursing Student
Ceilidh Eaton Russell, PhD
Jill Furzer, PhD candidate (health economics)

Targeted and Traditional Agents: Can We Reduce Side Effects Using Pharmacogenomic and Endogenous Biomarkers?
Richard B. Kim, MD, FRCPC

The Future of Immunotherapy, CAR-T and Beyond
Shannon L. Maude, MD, PhD

WORKSHOPS

The Evolution of Clinical Trials in Canada
Rebecca Deyell, MD, MSc, FRCPC
Josh Silvertown, PhD, MBA, MSM
Patrick Sullivan

PROFYLE/KiCS: The ABCs of Precision Medicine in Canada
Alexandra Zorzi, MD
Anita Villani, MD, MSc, FRCPC
Andrea Cote, RN, BScN

CAR-T Cell Therapy in Ontario: Opportunities and Challenges
Joerg Krueger, MD
Stacey Marjerrison, MD, MSc, FRCPC
Colleen Callahan, RN, MSN, CRN

Posted in 2018 Symposium, Education for Health Professionals | Tagged 2018 symposium, CAR-T, Clinical Trials, consent, diagnos, ethics, genetics, pharmacology, precision therapy, psychosocial, side effects

Thinking Practically: Delivery of Care Considerations for New Agents

Posted on November 22, 2018 by Jamie Irvine


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Presentation Description: 
Sequencing a tumour, identifying molecular targets and pinpointing the appropriate drug or clinical trial, is merely step one of a complex and intense process for health teams and patients/families. Once a drug has been identified, what are the practical considerations that health teams need to consider in order to deliver optimal care to the patient? This session, led by a Social Worker and Patient Navigator of the SickKids NAIT (New Agents and Innovative Therapy) Program and a Nurse Practitioner in the Neuro-Oncology division at SickKids, will provide a thorough dissemination and discussion of the many challenges that need to be anticipated and addressed once a patient has been matched with a drug/trial.

Speakers:
Karen Fung
, MSW, RSW
Social Worker
The Hospital for Sick Children

Karen Fung is a social worker in the solid tumour section of the Haematology/Oncology Program at SickKids, and works part-time as a patient navigator in the New Agent and Innovative Therapy (NAIT) Program. As a social worker, Karen provides assessment and counselling to children and youth, and their families, through the trajectory of the illness to enhance coping and capacity. In her role as the patient navigator in the early phase clinical trials program, Karen has been assisting in the development of the NAIT Program, as well as collaborating with the primary stakeholders and the children and their families from across Canada to help them gain better access to new and innovative clinical trials.

Tara McKeown, RN MN NP-Paediatrics
Nurse Practitioner Neuro-Oncology Team
The Hospital for Sick Children
Adjunct Lecturer, Lawrence S. Bloomberg, Faculty of Nursing
University of Toronto

Tara McKeown completed a Bachelor of Science degree at the University of Western Ontario and then went on to complete a Bachelor of Science in Nursing at the University of Toronto. She worked at the Hospital for Sick Children inpatient Haematology/Oncology inpatient ward as a Registered Nurse for five years and during that time completed a Master of Nursing with Nurse Practitioner in the child stream. Tara has worked as the Nurse Practitioner with the Neuro Oncology team at the Hospital for Sick Children since Jan 2013. She also retains adjunct appointment as an Adjunct Lecturer for the Lawrence S. Bloomberg Faculty of Nursing at the University of Toronto. Tara has worked closely with the New Agents and Innovative Therapy team at Sick Kids as new drugs, treatments and side effect management is emerging for the Neuro Oncology population.

Posted in 2018 Symposium | Tagged 2018 symposium, Clinical Trials

The Evolution of Clinical Trials in Canada

Posted on November 22, 2018 by Jamie Irvine


VIEW THE PRESENTATION*

* Josh Silvertown’s presentation slides not included

Presentation Description:
Clinical trial design is complex and not without challenges, particularly in the pediatric context. This workshop brings together medical and industry experts to share their unique perspectives on the challenges and opportunities of designing molecularly targeted clinical trials in Canada. This interactive workshop will feature a case study on larotrectinib, a selective TRK inhibitor that is showing early promise in the treatment of pediatric solid tumours.

Speakers:
Rebecca Deyell, MD, MSc, FRCPC
Pediatric Oncologist /Hematologist and Clinician Investigator
BC Children’s Hospital and Research Institute

Dr. Deyell is a pediatric oncologist/hematologist and clinician investigator at BC Children’s Hospital and Research Institute. She is a co-leader of the BC Pediatric Precision OncoGenomics Study (PedsPOG) and of the Clinical Node for the national PRecision Oncology For Young peopLE (PROFYLE) program. She leads the Developmental Therapeutics Program in pediatric oncology/hematology in BC, and participates in the national C17 DVL network.

Josh Silvertown, PhD, MBA, MSM (slides unavailable)
Senior Manager, Medical Affairs Strategist (Oncology)
Bayer Canada

Josh Silvertown is the Senior Manager, Medical Affairs Strategist (Oncology) for Bayer Canada, leading medical affairs for TRK fusion cancer therapies. Prior to this role, Josh was Medical Scientific Advisor (Hematology) for Bayer Canada, leading medical affairs for the hemophilia portfolio.

Before joining Bayer, Josh worked in executive roles for Toronto-based companies focused on the development and commercialization of drug (Armour Therapeutics) and diagnostic device (Quantum Dental Technologies) products. Josh also worked at AXON Clinical Research, Manhattan, as the Director of Scientific Affairs and Business Development. He spent three years as an NSERC Post-Doctoral Fellow conducting prostate cancer research at the Ontario Cancer Institute in Toronto. He holds a PhD in Biomedical Sciences and an Honours BSc in Molecular Biology and Genetics from the University of Guelph. Josh is a graduate of the Richard Ivey School of Business at Western University where he completed an MBA as a Canadian Institutes of Health Research “Science to Business” Fellow.

Josh is an Action Canada Fellow (2004), a “Top 40 Under 40” by the Medical Device and Diagnostic Industry (2012), and a Meritorious Service Medal recipient from the Governor General (2017). Josh is the author of over 30 scientific journal publications and an inventor on 23 issued and pending patents.

Patrick Sullivan
Childhood Cancer Advocate

Patrick Sullivan is a passionate childhood cancer advocate, the President and a Founder of the Team Finn Foundation, and Co-Founder of Ac2orn. Patrick became an advocate after his twin son Finn was diagnosed with rhabdomyosarcoma in 2007 and heard the word “incurable” for the first time in May 2008. His desire to make a change in cancer research is in part an effort to pay an un-payable debt to his son Finn and to “change the stories” of other Finns.

Patrick participates in several national and international initiatives. His roles include Founder of Ac2orn (Advocacy for Canadian Children Oncology Research Network), Chair of the Bio-CanRX Cancer Stakeholder Alliance, member of the AACR Pediatric Cancer Working Group, Director of Childhood Cancer Canada, Director of Coast to Coast Against Cancer Foundation, Director on the Canadian Cancer Research Alliance, Co-Lead of the Terry Fox Research Profyle initiative, member of the CTCG Lay Representative Committee, and Lead Advocate on the St. Baldrick’s/Stand Up to Cancer Immunogenomics Dream Team.

By profession, Patrick is a securities and corporate-commercial litigator and one of the founding partners of Taylor Veinotte Sullivan Barristers. Patrick is the proud father of three remarkable children, Baird, Sarah and Finn, and would do almost anything for the simple pleasure of holding Finn’s hand again.

Posted in 2018 Symposium | Tagged 2018 symposium, Clinical Trials

Workshop – Clinical Trials and Adverse Effects in the Satellite Setting: Toxicity Grading, OCREB, and More

Posted on May 30, 2017 by Jamie Irvine

VIEW THE PRESENTATION

Presentation Description:
Clinical trials remain the most critical tool to improve outcome in paediatric cancer. This workshop will review current regulatory and ethics regulations and preview the upcoming roll out of the Ontario Cancer Research Ethics Board (OCREB) to satellite care. Interactive case discussions will highlight important elements of reporting adverse events that occur on study. Furthermore, the session will include a preview of a variety of upcoming OCREB trials and an open discussion of research challenges in the satellite context.

Speakers:
Sarah Alexander, MD
Clinical Director, Haematology/Oncology, The Hospital for Sick Children, Toronto, ON

Sarah Alexander is the clinical director of the Division of Haematology/ Oncology at SickKids. She is a member of the leukemia and lymphoma section. Her research is focused on infectious complications of chemotherapy and strategies for the treatment of children with non-Hodgkin lymphoma. She has been working with POGO, OCREB and leads from the other centres on optimizing the system for regulatory compliance and REB oversight for patients enrolled on clinical trials who receive care at tertiary and satellite centres.

Paul Gibson, MD, FRCPC
Pediatric Oncologist, Children’s Hospital, London Health Sciences Centre (LHSC), London, ON
Medical Officer, Pediatric Oncology Group of Ontario
Assistant Professor, Western University, London, ON

Paul Gibson is a graduate of Queen’s University’s Medical School. He completed pediatric residency training at B.C. Children’s Hospital prior to subspecialty training at The Hospital for Sick Children. He joined the Section of Pediatric Haematology and Oncology at Children’s Hospital full time in 2010. He has served as Physician Lead in the LHSC Computerized Provider Order Entry and PowerChart Oncology projects. Dr. Gibson has served as Medical Officer of the Pediatric Oncology Group of Ontario (POGO) since 2015. His role with POGO includes medical support of the POGO Satellite program and a member of the executive oversight committee of the provincial pediatric oncology planning process.

Posted in 2017 Satellite Education Day | Tagged 2017 Satellite Education Day, Clinical Trials, side effects

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