Patient and Provider Web-Based Decision Support for Breast Cancer Chemoprevention: A Randomized Controlled Trial

Author:

Crew Katherine D.123ORCID,Bhatkhande Gauri2ORCID,Silverman Thomas4ORCID,Amenta Jacquelyn1ORCID,Jones Tarsha5ORCID,McGuinness Julia E.13ORCID,Mata Jennie13ORCID,Guzman Ashlee13ORCID,He Ting6ORCID,Dimond Jill7ORCID,Tsai Wei-Yann38ORCID,Kukafka Rita349ORCID

Affiliation:

1. 1Department of Medicine, Vagelos College of Physicians and Surgeons, Columbia University Irving Medical Center, New York, New York.

2. 2Department of Epidemiology, Mailman School of Public Health, Columbia University Irving Medical Center, New York, New York.

3. 3Herbert Irving Comprehensive Cancer Center, Columbia University Irving Medical Center, New York, New York.

4. 4Department of Biomedical Informatics, Vagelos College of Physicians and Surgeons, Columbia University Irving Medical Center, New York, New York.

5. 5Christine E. Lynn College of Nursing, Florida Atlantic University, Boca Raton, Florida.

6. 6Department of Biomedical Informatics and Data Sciences, Johns Hopkins University, Baltimore, Maryland.

7. 7Sassafras Collective, Ann Arbor, Michigan.

8. 8Department of Biostatistics, Mailman School of Public Health, Columbia University Irving Medical Center, New York, New York.

9. 9Department of Sociomedical Sciences, Mailman School of Public Health, Columbia University Irving Medical Center, New York, New York.

Abstract

Abstract Significant underutilization of breast cancer chemoprevention remains, despite guidelines stating that physicians should recommend chemoprevention with antiestrogen therapy to high-risk women. We randomized women, ages 35 to 75 years, who met high-risk criteria for breast cancer, without a personal history of breast cancer or prior chemoprevention use, to standard educational materials alone or combined with a web-based decision aid. All healthcare providers, including primary care providers and breast specialists, were given access to a web-based decision support tool. The primary endpoint was chemoprevention uptake at 6 months. Secondary outcomes included decision antecedents (perceived breast cancer risk/worry, chemoprevention knowledge, self-efficacy) and decision quality (decision conflict, chemoprevention informed choice) based upon patient surveys administered at baseline, 1 and 6 months after randomization. Among 282 evaluable high-risk women enrolled from November 2016 to March 2020, mean age was 57 years (SD, 9.9) and mean 5-year invasive breast cancer risk was 2.98% (SD, 1.42). There was no significant difference in chemoprevention uptake at 6 months between the intervention and control groups (2.1% vs. 3.5%). Comparing the intervention and control arms at 1 month, there were significant differences among high-risk women in accurate breast cancer risk perceptions (56% vs. 39%, P = 0.017), adequate chemoprevention knowledge (49% vs. 27%, P < 0.001), mean decision conflict (34.0 vs. 47.0, P < 0.001), and informed choice (41% vs. 23%, P = 0.003). These differences were no longer significant at 6 months. Although our decision support tools did not result in a significant increase in chemoprevention uptake, we did observe improvements in decision antecedents and decision quality measures. Prevention Relevance: In this randomized controlled trial of decision support for 300 high-risk women and 50 healthcare providers, we did not observe a significant increase in chemoprevention uptake, which remained low at under 5%. However, these decision support tools may increase knowledge and informed choice about breast cancer chemoprevention.

Funder

NIH

NCI

National Center for Advancing Translational Sciences

Publisher

American Association for Cancer Research (AACR)

Subject

Cancer Research,Oncology

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