RecruitingNot ApplicableNCT02620852

Women Informed to Screen Depending on Measures of Risk (Wisdom Study)

Enabling a Paradigm Shift: A Preference-Tolerant RCT of Personalized vs. Annual Screening for Breast Cancer (Wisdom Study)


Sponsor

University of California, San Francisco

Enrollment

100,000 participants

Start Date

Aug 31, 2016

Study Type

INTERVENTIONAL

Conditions

Summary

Most physicians still use a one-size-fits-all approach to breast screening in which all women, regardless of their personal history, family history or genetics (except BRCA carriers) are recommended to have annual mammograms starting at age 40. Mammograms benefit women by detecting cancers early when they are easier to treat, but they are not perfect. Recent news stories have discussed some of the potential harms: large numbers of positive results that cause stressful recalls for additional mammograms and biopsies. With the current screening approach, half of the women who undergo annual screening for ten years will have at least one false positive biopsy. Potentially more important are cancer diagnoses for growths that might never come to clinical attention if left alone (called "overdiagnosis"). This can lead to unnecessary treatment. Even more concerning is evidence that up to 20% of breast cancers detected today may fall into the category of "overdiagnosis." The WISDOM 1.0 study compares annual screening with a risk-based breast cancer screening schedule, based upon each woman's personal risk of breast cancer. The investigators have designed the study to be inclusive of all, so that even women who might be nervous about being randomly assigned to receive a particular type of care (a procedure that is typical in clinical studies) will still be able to participate by choosing the type of care they receive. For participants in the risk-based screening arm, each woman will receive a personal risk assessment that includes her family and medical history, breast density measurement and tests for genes (mutations and variations) linked to the development of breast cancer. Women who have the highest personal risk of developing breast cancer will receive more frequent screening, while women with a lower personal risk would receive less frequent screening. No woman will be screened less than is recommended by the USPSTF breast cancer screening guidelines. If this study is successful, women will gain a realistic understanding of their personal risk of breast cancer as well as strategies to reduce their risk, and fewer women will suffer from the anxiety of false positive mammograms and unnecessary biopsies. The investigators believe this study has the potential to transform breast cancer screening in America. Starting in Spring 2023, WISDOM's design shifted to remove the randomized option, but will continue with the preference/self-selection option for participation (WISDOM 2.0). Participants will therefore continue to choose their study arm (Personalized or Annual) rather than have the option to be randomized. This study design change was made after review of the WISDOM 1.0 data by an independent monitoring committee, which indicates that personalized screening does not cause harm. WISDOM 2.0 has also lowered the eligibility to ages 30-74. Women ages 30-39 will only be offered to join the Personalized Arm.


Eligibility

Sex: FEMALEMin Age: 30 YearsMax Age: 74 Years

Plain Language Summary

Simplified for easier understanding

This trial is studying whether personalizing breast cancer screening schedules based on each woman's individual risk level leads to better outcomes than a one-size-fits-all approach. You may be eligible if: you identify as female; you are between 30 and 74 years old; and you live in the United States. You may NOT be eligible if: you have already been diagnosed with breast cancer or ductal carcinoma in situ (an early form of breast cancer); you have had a double mastectomy as a preventive measure; you are unable to give consent; or you do not speak English or Spanish. Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

OTHERComplete a health questionnaire

Complete a health history questionnaire.

DEVICEProvide a saliva sample for genetic testing

Provide a saliva sample for testing of 9 genes and a panel of single nucleotide polymorphisms (SNPs) that influence breast cancer risk

OTHERScreening advice based on a comprehensive risk assessment

Receive a screening schedule recommendation

OTHERScreening advice based on a basic risk assessment

Receive a screening schedule recommendation


Locations(11)

University of Alabama at Birmingham

Birmingham, Alabama, United States

University of California Irvine

Irvine, California, United States

University of California Los Angeles

Los Angeles, California, United States

University of California Davis

Sacramento, California, United States

University of California San Diego

San Diego, California, United States

University of California San Francisco

San Francisco, California, United States

TopLine MD Alliance

Miami, Florida, United States

University of Chicago

Chicago, Illinois, United States

Louisiana State University

New Orleans, Louisiana, United States

Weill Cornell Medicine

New York, New York, United States

Edith Sanford Breast Center

Sioux Falls, South Dakota, United States

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NCT02620852


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