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Sökning: onr:"swepub:oai:lup.lub.lu.se:ac6d7acd-aa15-4b9e-b101-cf03232625dd" > Surveillance for la...

Surveillance for late effects in childhood cancer survivors

Landier, Wendy (författare)
University of Alabama
Skinner, Roderick (författare)
University of Newcastle upon Tyne
Wallace, W. Hamish (författare)
Royal Hospital for Sick Children, Edinburgh
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Hjorth, Lars (författare)
Lund University,Lunds universitet,Sena effekter efter barncancerbehandling,Forskargrupper vid Lunds universitet,Late effects after childhood cancer treatment,Lund University Research Groups,Skåne University Hospital
Mulder, Renée L. (författare)
Academic Medical Center of University of Amsterdam (AMC)
Wong, F. Lennie (författare)
City of Hope National Medical Center
Yasui, Yutaka (författare)
St Jude Children´s Research Hospital, Memphis
Bhakta, Nickhill (författare)
St Jude Children´s Research Hospital, Memphis
Constine, Louis S. (författare)
University of Rochester
Bhatia, Smita (författare)
University of Alabama
Kremer, Leontien C. (författare)
Academic Medical Center of University of Amsterdam (AMC)
Hudson, Melissa M. (författare)
St Jude Children´s Research Hospital, Memphis
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 (creator_code:org_t)
2018
2018
Engelska 7 s.
Ingår i: Journal of Clinical Oncology. - 0732-183X. ; 36:21, s. 2216-2222
  • Forskningsöversikt (refereegranskat)
Abstract Ämnesord
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  • Many childhood cancer survivors carry a significant risk for late morbidity and mortality, a consequence of the numerous therapeutic exposures that contribute to their cure. Focused surveillance for late therapy-related complications provides opportunities for early detection and implementation of health-preserving interventions. The substantial body of research that links therapeutic exposures used during treatment of childhood cancer to adverse outcomes among survivors enables the characterization of groups at the highest risk for developing complications related to specific therapies; however, methods available to optimize screening strategies to detect these therapy-related complications are limited. Moreover, the feasibility of conducting clinical trials to test screening recommendations for childhood cancer survivors is limited by requirements for large sample sizes, lengthy study periods, prohibitive costs, and ethical concerns. In addition, the harms of screening should be considered, including overdiagnosis and psychological distress. Experts in several countries have developed guideline recommendations for late effects surveillance and have collaborated to harmonize these recommendations internationally to enhance long-term follow-up care and quality of life for childhood cancer survivors. Methods used in these international efforts include systematic literature searches, development of evidence-based summaries, rigorous evaluation of the evidence, and formulation of consensus-based surveillance recommendations for each late complication. Alternate methods to refine recommendations, such as cumulative burden assessment and risk prediction and cost-effectiveness modeling, may provide novel approaches to guide survivorship care in this vulnerable population and, thus, represents a worthy objective for future international survivorship collaborations.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

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