CDKN2A/p16 genetic test reporting improves early detection intentions and practices in high-risk melanoma families

被引:54
作者
Aspinwall, Lisa G. [1 ]
Leaf, Samantha L. [1 ]
Dola, Erin R. [3 ]
Kohlmann, Wendy [3 ]
Leachman, Sancy A. [2 ,3 ]
机构
[1] Univ Utah, Dept Psychol, Salt Lake City, UT 84112 USA
[2] Univ Utah, Dept Dermatol, Salt Lake City, UT 84112 USA
[3] Univ Utah, Huntsman Canc Inst, Salt Lake City, UT 84112 USA
关键词
D O I
10.1158/1055-9965.EPI-08-0010
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Genetic testing for melanoma has yet to enter routine clinical use because of the scarcity of available data on the effect of test reporting. A prospective study of 59 members of Utah CDKN2A/p16 mutation-positive pedigrees was conducted to establish the effect of CDKN2A/p16 genetic test reporting on melanoma early detection intentions and behaviors (total body skin examination and skin self-examination) in a high-risk population. Behavioral assessments were made at baseline, immediately after CDKN2A/p16 test reporting and counseling, and at 1-month follow-up (42 participants). Baseline screening practices were poor relative to current recommendations, especially among participants without a personal history of melanoma. Changes from baseline practice were evaluated in three groups of participants (CDKN2A/p16(+) with history of melanoma, CDKN2A/p16(+) without melanoma history, and CDKN2A/p16(-)). Across multiple measures, test reporting caused CDKN2A/p16 mutation carriers without a melanoma history to improve to the level of adherence reported by participants with a melanoma history, without decreasing compliance of the CDKN2A/p16(-) group. Compared with baseline, CDKN2A/p16(+) participants without a melanoma history reported greater intention to obtain total body skin examinations (P < 0.0001), increased intentions and adherence to skin self-examination recommendations (P < 0.01 and P < 0.001, respectively), and increased number of body sites examined at 1 month (P < 0.002); further, 55% reported adopting a new screening behavior at follow-up. Test reporting also improved skin self-examination adherence among CDKN2A/p16(-) participants (P < 0.03). The finding that CDKN2A/p(16) test reporting enhances compliance with early detection measures among CDKN2A/p16(+) participants without diminishing the compliance of CDKN2A/p16(-) participants suggests a favorable risk-benefit ratio for melanoma genetic testing in high-risk patients.
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收藏
页码:1510 / 1519
页数:10
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