Discover what you can learn on our Precision Oncology online learning library. Explore resources compiled of both ONS and external content such as practice tools, courses, case studies, webinars, podcasts, websites, and more.
The ONS Genomics Advisory Board invites you to share your stories, ideas, or needs in relation to integrating genomics into cancer care. Submit your questions, comments and thoughts for consideration by the Genomics Advisory Board.
The ONS Genomics Advisory Board was established in May 2019 to guide the development of genomic education and practice resources for oncology nurses. Cancer care is in the midst of a massive paradigm shift. The cancer care workforce, both current and future, is under-prepared for the rapid application of genomic discoveries and the changes needed in cancer care delivery. We want to assure that the current and next generation of oncology nurses know the science, can apply the latest evidence in practice, and translate this information to patients and families.
Advisory Board Members
Kathleen Calzone, PhD, RN, AGN-BC, FAAN
Kelliann C. Fee-Schroeder, BSN, RN, OCN®
Patricia Friend PhD, APRN-CNS, AOCNS®, AGN-BC
Suzanne Mahon, RN, DNSc AOCN®, AGN-BC
Mary L. Schmitt, MS, APRN, FNP-BC, AOCNP
Katie Slane, MSN, AGPCNP-BC, AOCNP
Subject Matter Expert Contributors
Kerensa Marty, RN MSN/Ed OCN
Jessica Pforr, MSN, NP-C, AOCNP®
Kathy Pratt, BSN, RN, OCN, CBCN, ONN-CG
Meaghan Ryan, MSN, FNP-BC
Ilene Lattimer BSN, OCN, CCRC
ONS is looking for nurses with expertise in genomics! Apply for various opportunities to get involved depending on expertise and availability.
Genomic technologies are rapidly being integrated into cancer care. Genetic/genomic tests are applied across the cancer care continuum for risk identification, risk reduction and cancer prevention, diagnosis and treatment. Oncology nurses must be knowledgeable about the different types of technologies/tests including when and how they are used so they can navigate patients and families through the maze of precision oncology.
Earn 1 NCPD ILNA categories: Scientific Basis, Professional, Disease-Related Biology, and Basic Concepts and Indications for Transplantation
Learners will find genomics included in varying detail depending on the course they are completing. Some examples are Cancer Biology, ONS/ONCC Chemotherapy and Immunotherapy Certificate Course, Immunotherapy in Cancer Treatment, A Primer on the Role of the Immune System, and many more!
Suzanne Mahon, RN, DNSc, AOCN®, AGN-BC, professor at Saint Louis University in internal medicine and the school of nursing, joins Chris Pirschel to discuss direct-to-consumer genetic testing, what it means to patients and providers, and how oncology nurses can help their patients understand genetic testing. (Podcast: 31 minutes)
ONS member Patricia Friend, PhD, APRN-CNS, AOCNS®, AGN-BC, associate professor and program director for the Marcella Niehoff School of Nursing at Loyola University in Chicago, IL, joins ONS’s Erin Dickman, MS, RN, OCN®, to discuss the different applications of genetics and genomics, what oncology nurses need to know about genomics, and much more. (Podcast: 39 minutes)
ONS member Suzanne Mahon, RN, DNSc, AOCN®, AGN-BC, clinical nurse specialist and professor at Saint Louis University in Missouri, joins Chris Pirschel, ONS staff writer, to discuss her ONS Congress presentation on hereditary cancer genetics, collaborating with genetic professionals, and how genetic testing influences cancer prevention and care. (Podcast: 50 minutes)
Navigating Genomics and Its Effect on Cancer Care
ONS member Celeste Adams, RN, BSN, MBA, nurse navigator at Intermountain Healthcare in Salt Lake City, UT, and member of the ONS Intermountain Chapter, and Kathleen Wiley, RN, MSN, AOCNS®, director of oncology nursing practice at ONS, discuss how nurse navigators can help patients and caregivers understand genomic advancements, how someone’s genes affect cancer prevention and treatment, and the impact that genomics testing can have on a patient’s quality of life. (Podcast: 29 minutes)
In a recent survey, we asked ONS members what they wanted to know more about as it relates to genomics. In these short videos, members of our Genomics Advisory Board answer those questions and topics that were identified through that survey.
Pedigree construction is an important component of cancer risk assessment and comprehensive genetic care. Pedigrees must be updated and re-evaluated on a regular basis. Complete pedigrees are needed to select genetic tests and interpret genetic testing results accurately, as well as to enroll patients and families in research and variant reclassification studies to advance the science of genetics. Identified barriers to pedigree construction and assessment are described with implications for nursing practice.
Review the extensive list of genomics articles published in CJON and ONF. Two distinguished and evidence-based publications.
ONS Voice has published over 75 articles on the topic of genomics in cancer care. Review the library of articles. Highlighted articles and information:
“Genetics versus genomics: Is there a difference? Does it even matter? There is, and it does. In our era of precision medicine, also referred to as individualized or genomic medicine, being able to differentiate the terms is a first step in establishing a foundational understanding of what they mean for cancer care from prevention to treatment.
“What Is the Difference Between the Techniques?”
Some highlights from the genome report include:
The average cancer genome is driven by four or five cancer-causing mute.
This ONS Voice article describes how every cancer diagnosis is as individualized and unique as the person receiving it.
The ONS Genomics Taxonomy is compiled of 89 foundational genomic terms categorized into six groups that provide standardized genomic language for oncology nursing practice and promotes understanding of genomic concepts that reflect the state of the science.
The ONS Advisory Board has selected additional genomics information and resources from respected authorities across the web, review that collection in the drop-down below.
The G3C (Global Genetics and Genomics Community) learning portal presents a bilingual collection of interactive cases that demonstrate how genetics and genomics link to health and illness. G3C is free to all users and encourages students and practicing healthcare providers to address the multi-dimensional needs of patients through various self-guided, video-taped "patient-provider" interview simulations.
Oncology focused cases include Gabe, Grace, Jeff and Maria, Luis, and Tom
This document identifies essential genetic and genomic competencies for individuals prepared at the graduate level in nursing. These competencies apply to anyone functioning at the graduate level in nursing, including but not limited to advanced practice registered nurses (APRNs), clinical nurse leaders, nurse educators, nurse administrators, and nurse scientists.
This document identifies the minimum knowledge and skill a nurse needs to be prepared to deliver competent genetic and genomic focused nursing care.
A resource for nurse educators and administrators interested in integrating genomic competency into nursing practice. Content provided includes:
Jackson Labs offer ‘free’ and ‘for pay’ CNE and CME educational modules and mini courses for all healthcare providers related to genomics and applications in practice. Topics include:
Learn more about genomics, using the genome to treat cancer, blood tests to detect cancer, family risk and additional resources.
PMA specializes in communicating precision medicine to lay professional audiences, providing scientifically sound, unbiased information to promote the responsible use of genomics in medicine. ‘Free’ and ‘For Pay’ CME/CNE education opportunities are available.
Interested in learning the basics of genetics? The University of Utah's Genetics Science learning Center provides a wide range of resources and short-engaging videos to help you learn about the basics of genetics, traits, DNA, chromosomes, genes, inheritance, and more.
Patient friendly website for patients with colorectal cancer to understand their biomarkers and what that means for their treatment
A website geared for those with hereditary breast, ovarian and related cancers. Learn about genes and cancer, signs of hereditary cancer, genetic counseling, types of genetic tests and what results mean for patients and their and families.
Patient-friendly videos on precision medicine, targeted therapies, inherited cancers and biomarkers are featured. Companion downloadable PDFs are provided. In addition to precision oncology resources, free patient education publications on other cancer topics are available to download in multiple languages including English, Spanish, Chinese, Korean, Russian, and Vietnamese.