Abstract

BackgroundBreast cancer is the most commonly diagnosed malignancy in women. Mastectomy and breast-conserving surgery (BCS) have equivalent survival for early stage breast cancer. However, each surgery has different benefits and harms that women may value differently. Women of lower socioeconomic status (SES) diagnosed with early stage breast cancer are more likely to experience poorer doctor-patient communication, lower satisfaction with surgery and decision-making, and higher decision regret compared to women of higher SES. They often play a more passive role in decision-making and are less likely to undergo BCS. Our aim is to understand how best to support women of lower SES in making decisions about early stage breast cancer treatments and to reduce disparities in decision quality across socioeconomic strata.MethodsWe will conduct a three-arm, multi-site randomized controlled superiority trial with stratification by SES and clinician-level randomization. At four large cancer centers in the United States, 1100 patients (half higher SES and half lower SES) will be randomized to: (1) Option Grid, (2) Picture Option Grid, or (3) usual care. Interviews, field-notes, and observations will be used to explore strategies that promote the interventions’ sustained use and dissemination. Community-Based Participatory Research will be used throughout. We will include women aged at least 18 years of age with a confirmed diagnosis of early stage breast cancer (I to IIIA) from both higher and lower SES, provided they speak English, Spanish, or Mandarin Chinese. Our primary outcome measure is the 16-item validated Decision Quality Instrument. We will use a regression framework, mediation analyses, and multiple informants analysis. Heterogeneity of treatment effects analyses for SES, age, ethnicity, race, literacy, language, and study site will be performed.DiscussionCurrently, women of lower SES are more likely to make treatment decisions based on incomplete or uninformed preferences, potentially leading to poorer decision quality, quality of life, and decision regret. This study hopes to identify solutions that effectively improve patient-centered care across socioeconomic strata and reduce disparities in decision and care quality.Trial registrationNCT03136367 at ClinicalTrials.govProtocol version: Manuscript based on study protocol version 2.2, 7 November 2017.

Highlights

  • Breast cancer is the most commonly diagnosed malignancy in women

  • If this study shows the advantage of the Option Grid and/or Picture Option Grid, dissemination of those interventions could improve decision quality, knowledge, quality of life, and other outcomes while promoting informed treatment choice irrespective of socioeconomic status (SES) and health literacy, compared to usual care

  • We anticipate that findings could be reproduced and the intervention(s) adopted by clinicians in clinical practice to rapidly improve delivery of care

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Summary

Introduction

Breast cancer is the most commonly diagnosed malignancy in women. Mastectomy and breastconserving surgery (BCS) have equivalent survival for early stage breast cancer. Women of lower socioeconomic status (SES) diagnosed with early stage breast cancer (I to IIIA) report significantly poorer communication with their clinicians, lower knowledge of breast cancer surgery options, higher uptake of mastectomy, and worse cancer-related and patient-centered health outcomes compared to women of higher SES [3,4,5,6,7,8,9,10,11]. They tend to receive breast cancer care that deviates from established clinical guidelines (e.g., inconsistent use of radiation after breast conserving surgery) [4, 10]. The exact impact of these factors remains unclear [20, 21]

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