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Randomized Controlled Trial
. 2025 Aug 1;117(8):1593-1604.
doi: 10.1093/jnci/djaf067.

A randomized study of 2 risk assessment models for individualized breast cancer risk estimation

Affiliations
Randomized Controlled Trial

A randomized study of 2 risk assessment models for individualized breast cancer risk estimation

Adrià López-Fernández et al. J Natl Cancer Inst. .

Abstract

Background: Estimating breast cancer risk involves quantifying genetic and non-genetic factors. This supports health interventions and risk communication to ensure adherence to screening recommendations. This study evaluated the change in risk estimation when incorporating breast density and polygenic risk score (PRS) into the baseline cancer risk assessment and compared the efficacy of 2 risk-assessment delivery models.

Methods: This 2-step study included 663 healthy women with a family history of breast cancer in which no pathogenic variants were identified. First, breast density and PRS were added to the baseline risk assessment for all participants. A randomized intervention study compared 2 delivery models (in-person vs pre-recorded video) for risk assessment in women at moderate or average risk. All tests were 2-sided.

Results: Breast density and PRS reclassified the risk group into 33% of the participants, with only 5% reclassified as high-risk. After disclosure of their estimated multifactorial risk, 65% of women aligned their risk perception with their estimated risk, compared to 47% at baseline (P < .05). No statistically significant differences were found in the primary endpoint cancer worry, mean = 10.2 (SD = 3.1) vs 10.1 (2.7), between delivery models. In-person delivery had slightly better psychological outcomes (excluding the primary outcome) and higher satisfaction, though few participants in the video group sought in-person clarification.

Conclusions: Incorporating breast density and PRS into risk assessments led to substantial reclassification, with 1 in 5 women facing de-escalated surveillance. Personalized assessments improve objective perceptions alignment. A model using a pre-recorded video-based model matches in-person delivery for moderate and average-risk women and is scalable for population-level implementation.

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Conflict of interest statement

A.C.A. is listed as the creator of the BOADICEA model, which has been licensed by the Cambridge Enterprise (University of Cambridge). The other authors have no conflicts of interest to declare.

Figures

Figure 1.
Figure 1.
CONSORT flow diagram of participant stratification by risk group and subsequent randomization for delivery of risk assessment.
Figure 2.
Figure 2.
Change in 10-y BC risk stratification after addition of breast density and PRS to non-genetic risk factors of the 395 participants with all data available. BC = breast cancer; BD = breast density; PRS = Polygenic Risk Score.
Figure 3.
Figure 3.
Rate of adequacy between subjective BC risk perception and objective BC risk estimation before and after individualized BC risk assessment visit.
Figure 4.
Figure 4.
Psychological scores after BC risk assessment according to risk category and delivery model. (A) Change in Cancer Worry Scale. (B) State-Trait Anxiety scale: state scores are represented. (C) MICRA total scores. (D) MICRA distress. (E) MICRA uncertainty. (F) Decisional conflict. CWS = Cancer Worry Scale; MICRA = Multidimensional Impact of Cancer Risk Assessment Questionnaire.
Figure 5.
Figure 5.
Comparison of delivery models in terms of quality of information and satisfaction with delivery model (average and moderate risk).

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