Genetic testing for the risk of developing late effects among survivors of childhood cancer: Consumer understanding, acceptance, and willingness to pay

被引:6
|
作者
Georgiou, Gabrielle [1 ,2 ]
Wakefield, Claire E. [1 ,2 ]
McGill, Brittany C. [1 ,2 ]
Fardell, Joanna E. [1 ,2 ]
Signorelli, Christina [1 ,2 ]
Hanlon, Lucy [1 ,2 ]
Tucker, Kathy [3 ,4 ]
Patenaude, Andrea F. [5 ,6 ]
Cohn, Richard J. [1 ,2 ]
机构
[1] Univ New South Wales, Discipline Paediat, Sch Womens & Childrens Hlth, Univ New South Wales Med, Sydney, NSW, Australia
[2] Sydney Childrens Hosp, Kids Canc Ctr, Behav Sci Unit Proudly Supported Kids Canc Fdn, Randwick, NSW, Australia
[3] Prince Wales Hosp, Hereditary Canc Clin, Dept Med Oncol, Randwick, NSW, Australia
[4] Univ New South Wales, Prince Wales Clin Sch, Sydney, NSW, Australia
[5] Dana Farber Canc Inst, Dept Psychosocial Oncol & Palliat Care, Boston, MA 02115 USA
[6] Harvard Med Sch, Dept Psychiat, Boston, MA USA
关键词
attitudes; cancer; decision making; genetic testing; oncology; pediatrics; personalized medicine; understanding; ATTITUDES; KNOWLEDGE; MEDICINE; OUTCOMES; MOTHERS; HEALTH;
D O I
10.1002/cncr.30119
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUNDGenetic testing to determine cancer survivors' risk of developing late effects from their cancer treatment will be increasingly used in survivorship care. This 2-stage study with 64 survivors of childhood cancer and their parents investigated the preferences and acceptability of testing among those who may be at risk of developing late effects. METHODSThe first stage (Stage 1) identified the most commonly perceived benefits and concerns regarding genetic testing for the risk of late effects among 24 participants. In Stage 2, during interviews, 20 survivors (55% of whom were female; mean age, 26.0 years [range, 18-39 years]; standard deviation [SD], 0.80) and 20 parents (55% of whom were male; mean age of child survivor, 14.2 years [range, 10-19 years]; SD, 0.79) rated the 7 most common benefits and concerns from those identified in Stage 1. Interviews were transcribed verbatim and analyzed. Decisional balance ratios were calculated by dividing the participants' average concerns scores with the average benefits scores. RESULTSGenetic testing for late effects was highly acceptable: 95% of participants leaned toward testing, and the majority (65.9%) would pay up to Australian $5000. The majority (97.2%) reported it was acceptable to wait for up to 6 months to receive results, and to be offered testing immediately after treatment or when the survivor reached adulthood (62.9%). Survivors and parents had a highly positive decisional balance (Mean (M), 0.5 [SD, 0.38] and M, 0.5 [SD, 0.39], respectively), indicating that perceived benefits outweighed concerns. CONCLUSIONSAlthough to our knowledge clinical efficacy has yet to be clearly demonstrated, survivors and parents described positive interest in genetic testing for the risk of developing late effects. Perceived benefits outweighed harms, and the majority of participants would be willing to pay, and wait, for testing. Cancer 2016. (c) 2016 American Cancer Society. Cancer 2016;122:2876-2885. (c) 2016 American Cancer Society
引用
收藏
页码:2876 / 2885
页数:10
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