Young people with cancer have suffered from not being recognized as
either children or adult patients. The lack of an adequate number
of centres, properly equipped for teenage cancer care, is
acknowledged worldwide. Yet their needs, both physically and
psychologically, are perhaps the most acute of all.
Now, this book, based on an international conference hosted by
the Teenage Cancer Trust, addresses the issues surrounding care of
the adolescent with cancer more completely than ever before.
Some chapters provide practical information from leading
specialists on managing and treating the specific tumours affecting
this group whilst others present discussions by psychologists,
nurses and other healthcare professionals on the many lifestyle
issues that confront teenagers with cancer. Finally and maybe, most
importantly, contributions from patients and carers give an insight
into what it feels like to have the disease while growing into
adulthood.
With its insight into the problems, and guidance on best
practice, this book will be welcomed by all professionals and
carers who work with young people with cancer.
Mục lục
1 A right not a privilege!.
Part 1 Patterns and perspectives.
2 Patterns of incidence of cancer in teenagers and young adults:
implications for aetiology.
3 Lack of participation of older adolescents and young adults
with cancer in clinical trials: impact in the USA.
4 Adolescents and cancer: perspectives from France.
5 Care of teenagers with cancer: a North American
perspective.
Part 2 Advances.
6 Leukaemia.
7 Advances in treatment for non-Hodgkin’s lymphoma.
8 Hodgkin’s disease and adolescents – the lost
tribe?.
9 Adolescent CNS tumours: my brain has damaged my life.
10 Ewing’s sarcoma.
11 Advances in osteosarcoma.
12 Osteosarcoma and surgery.
Part 3 Survivorship.
13 Subfertility in adolescents with cancer: who is at risk and
what can be done?.
14 Body image.
15 The impact of cancer on adolescents and their families.
16 Resilience in survivors of teenage cancer: a life-adaptive
approach.
17 Surviving with scars: the long-term psychosocial consequences
of teenage cancer.
Part 4 Palliation.
18 Whose dying is it anyway? Palliative care in adolescence.
19 The parent’s perspective of teenage cancer.
Part 5 Controversies.
20 Who should care for young people with cancer?.
21 Patterns of care for teenagers and young adults with cancer:
is there a single blueprint of care?.
22 Managing professional relationships across the services.
23 The next 10 years in biomedical science and care for
teenagers and young adults with cancer
Giới thiệu về tác giả
Tim Eden, Christie Hospital Nhs Trust, UK
Ronald Barr, Children’s Hospital, Department of Pediatrics,
Ontario, Canada
Archie Bleyer, University of Texas, UTMD Anderson Cancer Center,
Texas, USA
Myrna Whiteson, Chair of Teenage Cancer Trust, UK
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