Novel Clinician-Lead Intervention to Address Fear of Cancer Recurrence in Breast Cancer Survivors

被引:20
|
作者
Liu, Jia [1 ,2 ,3 ,4 ,5 ]
Butow, Phyllis [2 ,3 ]
Bui, Kim T. [6 ]
Serafimovska, Anastasia [2 ]
Costa, Daniel S. J. [7 ,8 ]
Kiely, Belinda E. [5 ]
Hui, Mun N. [3 ]
Goodwin, Annabel [5 ]
McNeil, Catriona M. [3 ]
Beith, Jane M. [2 ,3 ]
机构
[1] Crown Princess Mary Canc Ctr, Westmead, NSW, Australia
[2] Univ Sydney, Psychooncol Cooperat Res Grp, Camperdown, NSW, Australia
[3] Chris OBrien Lifehouse, Camperdown, NSW, Australia
[4] Blacktown Canc Ctr, Blacktown, NSW, Australia
[5] Western Sydney Univ, Campbelltown, NSW, Australia
[6] Concord Repatriat Gen Hosp, Concord Canc Ctr, Concord, Australia
[7] Pain Management Res Inst, St Leonards, NSW, Australia
[8] Univ Sydney, Sch Psychol, Camperdown, NSW, Australia
关键词
VALIDATION;
D O I
10.1200/OP.20.00799
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PURPOSE: Fear of cancer recurrence (FCR) affects 50%-70% of cancer survivors. This multicenter, single-arm study sought to determine the participant-rated usefulness of an oncologist-delivered FCR intervention. METHODS: Women who completed treatment for early breast cancer (could be receiving endocrine therapy) with baseline FCR > 0 were invited to participate. FCR was measured using a validated 42-item FCR Inventory. The brief oncologist-delivered intervention entailed (1) FCR normalization; (2) provision of personalized prognostic information; (3) recurrence symptoms education, (4) advice on managing worry, and (5) referral to psycho-oncologist if FCR was high. FCR, depression, and anxiety were assessed preintervention (T0), at 1 week (T1), and 3 months (T2) postintervention. The primary outcome was participant-rated usefulness. Secondary outcomes included feasibility and efficacy. RESULTS: Five oncologists delivered the intervention to 61/255 women invited. Mean age was 58 +/- 12 years. Mean time since breast cancer diagnosis was 2.5 +/- 1.3 years. Forty-three women (71%) were on adjuvant endocrine therapy. Of 58 women who completed T1 assessment, 56 (97%) found the intervention to be useful. FCR severity decreased significantly at T1 (F = 18.5, effect size = 0.39, P < .0001) and T2 (F = 24, effect size = 0.68, P < .0001) compared with baseline. There were no changes in unmet need or depression or anxiety. Mean consultation length was 22 minutes (range, 7-47 minutes), and mean intervention length was 8 minutes (range, 2-20 minutes). The intervention was perceived as useful and feasible by oncologists. CONCLUSION: A brief oncologist-delivered intervention to address FCR is useful and feasible, and has preliminary efficacy in reducing FCR. Plans for a cluster randomized trial are underway.
引用
收藏
页码:351 / E784
页数:12
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