Emotional and financial impact of the inability to become biological parents can be devastating for young people living with cancer
TORONTO, April 24, 2017 /CNW/ - The Canadian Partnership Against Cancer (the Partnership) has released a report on Canadian adolescents and young adults (AYAs) – aged 15 to 39 – living with cancer. The report identified fertility as a primary concern for men and women in this group, and that the emotional and financial impact of the inability to become biological parents, as a result of cancer treatment, can be devastating to individuals and their families.
"Loss of fertility as a complication of cancer therapy is important, specifically to adolescents and young adults. Many who survive cancer but find themselves infertile, experience damage to their aspirations and identity, made all the worse if they feel that they weren't made aware of the risks of infertility nor of opportunities to preserve fertility prior to cancer therapy," said Dr. Paul Grundy, Expert Lead of Pediatric, AYA Oncology at the Partnership. "This whole issue dubbed 'oncofertility,' has generally not been given appropriate attention by our healthcare system, perhaps in the face of the more life-threatening diagnosis of cancer, but survivors tell us that these long-term challenges are very important."
Adolescents and Young Adults with Cancer: A System Performance Report provides data on the burden fertility clinics would experience if all AYAs with cancer were referred for fertility counselling, and includes insights from AYA cancer patients on fertility concerns following a cancer diagnosis. During treatment for cancer, patients receive therapies that are toxic to the ovaries and testes, and can lead to problems with fertility.1 This is significant for young patients who are all within the reproductive age range.
"The cancer diagnosis was easier to accept than I could have hoped. My reality was that I had the disease and I felt lucky to have treatment options, but the pain I felt when hearing that treatment may leave me infertile is impossible to describe," said Bronwen Garand-Sheridan, cancer survivor. "What was worse was the lack of psychological support provided after receiving this news. Our health system must do a better job of preparing the cancer patient for the news of infertility."
For young women with cancer, procedures such as egg harvesting are intensive procedures to perform in a potentially unwell patients. Egg harvesting can take upwards of two weeks and may delay the start of treatment. It also comes with a significant financial burden averaging more than $10,000.
Key opportunities and challenges outlined in the report include:
- Interviews with AYAs diagnosed with cancer identified fertility as a major source of distress prior to treatment.
- Fertility preservation is an option for young people with cancer and concerned about their reproductive health, but it is affected by the limited number of specialized in-vitro fertilization (IVF) clinics in Canada.
- It is estimated that if all women aged 15-39 with cancer, in Canada, were referred for fertility consultations (e.g., to discuss egg harvesting), fertility clinics could see an increase from 103 patients per clinic per year in Ontario to 230 in Alberta, with all other provinces falling within this range. This would be a burden for clinics which treat all women (including those without cancer).
- Data are not available in Canada on how well informed young men and women with cancer are on fertility issues, and on how many are referred to (or actually see) a fertility specialist. These are areas to be explored in future reports.
"Most fertility clinics get very few referrals for AYAs with cancer, suggesting that the majority are not being referred for counselling," said Dr. Anne Katz, Sexuality Counselor at CancerCare Manitoba. "We need to identify gaps in care and steps to be taken to ensure equitable access to fertility preservation counselling and services for young men and women with cancer across the country."
In addition to oncofertility, Adolescents and Young Adults with Cancer provides information on incidence rates and trends, and distribution of cancer types among AYAs in Canada. It also includes other unique aspects of the AYA cancer journey including: mental health and psychosocial needs; medical needs during diagnosis, treatment, and survivorship; impact of cancer on employment and professional development; and challenges with AYA involvement in research and clinical trials.
"We are pleased to see this type of research being done looking at the cancer experience of adolescents and young adults in Canada, particularly in the area of oncofertility," said Britt Andersen, Executive Director of the Terry Fox Foundation. "The better we can understand the mental and emotional trauma experienced by this group during their cancer journey, the better we can improve outcomes for these cancer survivors who have many years ahead of them."
A full copy of the report is available at systemperformance.ca.
Data on oncofertility was obtained from the Childhood and Adolescent Young Adult Cancer Survivors Research Program (CAYACS), BC Cancer Agency, Cancer Care Manitoba, Pediatric Oncology Group of Ontario (POGO)'s database POGOnis, IWK Health Centre, and Janeway Children's Health and Rehabilitation Centre.
About AYAs with cancer in Canada
Over 7,000 Canadians aged 15-39 are diagnosed with cancer every year.2 The underlying biology of specific cancers changes during the AYA years, so risk factors, genetic makeup and clinical behaviour are closely linked to age at diagnosis.3 For many AYA cancers, this translates to a more advanced stage at presentation, more aggressive histological or genetic subtypes and poorer outcomes. Adolescence and young adulthood is a period of key developmental milestones that are fundamental to a person's overall well-being for the rest of their life. These milestones include the development of values and personal identity, formation of strong personal relationships and attaining financial independence.4,5 Cancer means additional challenges during this period of development.6-11
About the Canadian Partnership Against Cancer
The Canadian Partnership Against Cancer works with Canada's cancer community to reduce the burden of cancer on Canadians. Grounded in and informed by the experiences of those affected by cancer, the organization works with partners to support multi-jurisdictional uptake of evidence that will help to optimize cancer control planning and drive improvements in quality of practice across Canada. Through sustained effort and a focus on the cancer continuum, the organization supports the work of the collective cancer community in achieving long-term population outcomes: reduced incidence of cancer, less likelihood of Canadians dying from cancer, and an enhanced quality of life of those affected by cancer. For more information, visit www.partnershipagainstcancer.ca
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SOURCE Canadian Partnership Against Cancer
or to arrange interviews, please contact: Nick Williams, Communications Officer, Media Relations, Canadian Partnership Against Cancer, 416-915-9222, x5799 (office); 647-388-9647 (mobile), [email protected]
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