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Addressing the Lifelong Challenges of Childhood Cancer Survivors
Late Effects of TreamentAllArticle

Addressing the Lifelong Challenges of Childhood Cancer Survivors

Surviving childhood cancer can be a lifelong challenge: up to 75% of childhood cancer survivors must deal with late effects of their cancer and treatments. Next to keeping the balance between dealing with late-effects and adapting to a life "after cancer" many childhood cancer survivors also face the reality of inadequate or nonexisting follow-up care. Because cure is not enough, patient advocates depict why it is important to #RaiseYourHands4Survivors!

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Surviving childhood cancer can be a lifelong challenge: up to 75% of childhood cancer survivors must deal with the late effects of their cancer and treatments. Next to keeping the balance between dealing with late-effects and adapting to a life “after cancer” many childhood cancer survivors also face the reality of inadequate or nonexisting follow-up care. Because cure is not enough, patient advocates depict why it is important to #RaiseYourHands4Survivors!

Being cured does not always mean “being well.” Up to 75% of survivors deal with late effects. Keeping the balance between coping and living life to the fullest can be a life-long challenge.

There is a worldwide lack of structure for psychosocial and medical follow-up care. They need to be developed.

Survivors need comprehensive and age-appropriate information about the risks they can expect due to their cancer and treatments, what to do about their late effects, and where to turn to.

More research must be carried out to reduce late effects and optimize long-term care.

Continue reading · Late Effects of TreamentOutcome Indicators Make Quality of Life After Pediatric Cancer MeasurableThe focus of childhood cancer treatment is to achieve a cure for all patients. With improving survival rates, the emphasis has shifted towards assessing long-term health outcomes as a measure of quality care. The International Childhood Cancer Outcome Project involved various stakeholders, including survivors, pediatric oncologists, medical, nursing, and paramedical care providers, as well as psychosocial and neurocognitive care providers. They collaborated to develop a set of core outcomes for different types of childhood cancers, allowing for outcome-based evaluation of childhood cancer care. Through surveys and online focus groups, unique candidate outcome lists were created for 17 types of childhood cancer. A two-round Delphi survey involving 435 healthcare providers from 68 institutions resulted in the selection of four to eight physical core outcomes and three aspects of quality of life per pediatric cancer subtype. These core outcomes, measured through various instruments, provide valuable information to patients, survivors, and healthcare providers, enabling assessment of institutional progress and comparisons with other facilities.

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