CIFeR: A novel Clinician-lead Intervention to address Fear of cancer Recurrence (FCR) in breast cancer survivors.

Authors

Jia (Jenny) Liu

Jia Liu

Psycho-Oncology Co-operative Research Group, Camperdown, Australia

Jia Liu , Kim Tam Bui , Anastasia Serafimovska , Belinda Emma Kiely , Mun Ngah Hui , Annabel Goodwin , Catriona M. McNeil , Daniel SJ Costa , Phyllis Butow , Jane McNeil Beith

Organizations

Psycho-Oncology Co-operative Research Group, Camperdown, Australia, Concord Cancer Centre, Concord, Australia, Concord Cancer Centre, Concord, NSW, Australia, The Chris O'Brien Lifehouse, Camperdown, Australia, Concord Clinical School, University of Sydney, NSW, Australia, Pain Management Research Institute, St Leonards, Australia

Research Funding

Other Foundation
Sydney Breast Cancer Foundation, AVANT Foundation

Background: FCR affects 50-70% of cancer survivors. There are no validated oncologist-delivered FCR interventions. This multicentre, single-arm study sought to determine the helpfulness, feasibility and efficacy of an oncologist-delivered FCR intervention. Methods: Women were invited to participate if they had completed local treatment, chemotherapy and/or HER2 targeted therapy for early stage breast cancer and had a FCR score >0 on the 42-item FCR Inventory. The brief intervention, delivered by their medical oncologist at routine follow-up, entailed 1) FCR normalisation; 2) provision of personalised prognostic information; 3) take-home education sheet on recurrence symptoms; and 4) advice on managing worry. Consultations were audio-recorded. FCR, need for help, depression and anxiety were assessed before the intervention (T0), and at one week (T1) and three months (T2) after the intervention. Satisfaction with the intervention was assessed at T1. The primary outcome was participant-rated helpfulness. Secondary outcomes included feasibility (response rate, time taken for intervention) and efficacy. Results: Five oncologists delivered the intervention to 61 women (255 women invited; response rate 24%). The mean age was 57 ± 13 years. The mean time since breast cancer diagnosis was 2.5 ± 1.3 years. Forty-three (72%) were on adjuvant hormonal therapy. Overall, 58 women (95%) found the intervention helpful and 59 (98%) would recommend it to others. FCR severity, and the proportion of women with clinically significant FCR decreased significantly over time. There were no significant changes in unmet need, depression, or anxiety. Forty (66%) of consultations were recorded. Mean consultation length was 22 minutes (range 12-37 minutes) and mean intervention length was 9 minutes (3-20 minutes). The intervention was perceived as useful and feasible by oncologists, all of whom have used components of the intervention to help manage FCR in other breast cancer patients. Conclusions: A brief oncologist-delivered intervention to address FCR is helpful and feasible, and has shown preliminary efficacy in reducing FCR. Plans for an implementation study amongst oncologists in Australia are underway. Clinical trial information: ACTRN12618001615279.

T0 (n=61)T1 (n=52)T2 (n=33)P-value
FCR Severity (mean ± SD)1
15.5 ± 6.313.3 ± 5.810.9 ± 4.6p<0.00012
p<0.00012
Proportion with clinically significant FCR (≥13)139 (64%)27 (52%)12 (36%)p=0.0163
p=0.0063

1Measured using the severity subscale of 42-item validated FCR Inventory 2Repeated measures ANOVA 3McNemar’s test (exact significance)

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Abstract Details

Meeting

2020 ASCO Virtual Scientific Program

Session Type

Poster Session

Session Title

Symptoms and Survivorship

Track

Symptom Science and Palliative Care

Sub Track

Psychosocial and Communication Research

Clinical Trial Registration Number

ACTRN12618001615279

Citation

J Clin Oncol 38: 2020 (suppl; abstr 12115)

DOI

10.1200/JCO.2020.38.15_suppl.12115

Abstract #

12115

Poster Bd #

403

Abstract Disclosures

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