Psychosocial outcomes and interventions among cancer survivors diagnosed during adolescence and young adulthood (AYA): a systematic review

被引:198
作者
Barnett, Marie [1 ]
McDonnell, Glynnis [2 ,3 ]
DeRosa, Antonio [2 ]
Schuler, Tammy [2 ,4 ]
Philip, Errol [5 ]
Peterson, Lisa [2 ]
Touza, Kaitlin [6 ]
Jhanwar, Sabrina [2 ]
Atkinson, Thomas M. [2 ]
Ford, Jennifer S. [2 ]
机构
[1] Columbia Univ, Med Ctr, New York, NY USA
[2] Mem Sloan Kettering Canc Ctr, Dept Psychiat & Behav Sci, 641 Lexington Ave,7th Floor, New York, NY 10022 USA
[3] St Johns Univ, Dept Psychol, Queens, NY USA
[4] Assoc Behav & Cognit Therapies, New York, NY USA
[5] Notre Dame Lab Psychooncol Res, Notre Dame, IN USA
[6] Indiana Univ Purdue Univ, Indianapolis, IN 46202 USA
基金
美国国家卫生研究院;
关键词
Adolescent; Cancer survivorship; Literature review; Neoplasms; Young adult; QUALITY-OF-LIFE; BREAST-CANCER; HEALTH-STATUS; IMPACT; NEEDS; EXPERIENCES; PROGRAM; CARE; CHILDHOOD; ONLINE;
D O I
10.1007/s11764-016-0527-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A cancer diagnosis during adolescence or young adulthood (AYA; defined as ages 15-39) generates unique medical and psychosocial needs as developmental milestones are simultaneously impacted. Past research highlights that AYAs' experiences and psychosocial outcomes are different, and more research and attention is needed. We aimed to identify and synthesize literature regarding psychosocial outcomes, unique needs, and existing psychosocial interventions pertaining to individuals diagnosed with cancer exclusively during AYA, and to highlight areas for future research. A systematic literature search was conducted using MEDLINE (via PubMed), EMBASE, Cochrane, Web of Science, and PsycINFO (via OVID). Grey literature was searched using key term variations and combinations. Overall, 15,301 records were assessed by two independent reviewers, with 38 studies meeting inclusion criteria. Data synthesis of the 38 articles was organized by four main themes based on quality of life and survivorship: physical well-being (7 studies), psychological well-being (8 studies), social well-being (9 studies), and survivorship care (14 studies). The paucity of studies for such broad inclusion criteria highlights that this population is often combined or subsumed under other age groups, missing needs unique to these AYAs. AYA cancer survivors' experiences are nuanced, with interacting variables contributing to post-treatment outcomes. AYAs require age-appropriate and flexible care, informational needs and treatment-related education that foster autonomy for long-term survivorship, as well as improved follow-up care and psychological outcomes. By incorporating these findings into practice, the informational and unmet needs of AYAs can be addressed effectively. Education and programming is lacking specific and general subject matter specific to AYAs, incorporating ranging needs at different treatment stages.
引用
收藏
页码:814 / 831
页数:18
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