Comparison of Breast Cancer Screening With Dual-Energy Contrast-Enhanced Spectral Mammography to Digital Breast Tomosynthesis in Women With Dense Breasts (Contrast Mammography Imaging Screening Trial
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 2,032
- 试验地点
- 13
- 主要终点
- Cancer Detection Rate
研究概览
简要总结
The over-arching goal of the Contrast-Enhanced Spectral Mammography Imaging Screening Trial (CMIST) is to determine if dual-energy contrast-enhanced spectral mammography (CESM) can detect more cancers with fewer false positives than digital breast tomosynthesis (DBT) in women with dense breasts.
Aim 1: To evaluate the performance of CESM compared to DBT at baseline for breast-cancer screening in women with dense breasts.
Aim 2: To evaluate the performance of CESM compared to DBT at the 1-year follow up for breast-cancer screening in women with dense breasts.
详细描述
The Contrast-Enhanced Spectral Mammography Imaging Screening Trial (CMIST), which will be managed by the American College of Radiology (ACR), Center for Research and Innovation (CRI), seeks to determine if dual-energy contrast-enhanced spectral mammography (CESM) screening provides more accurate cancer detection compared to digital breast tomosynthesis (DBT) in women with dense breasts.
Year 0 Visit:
All women aged 45 to 74 years of age known mammographically dense breasts, as reported on their most recent prior mammogram who are scheduled for a routine annual screening DBT will be offered CESM in addition to DBT. Baseline imaging (Year 0) will be performed within 30 days after participant registration. Standard DBT screening views followed by standard CESM screening views will be performed on the same day and prior to any additional workup.
Year 1 Visit (12 Months ±2 Months After Year 0 Imaging):
Standard DBT screening views followed by standard CESM screening views will be performed on the same day and prior to any additional workup.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Diagnostic
- 盲法
- None
盲法说明
Two independent readers at each institution participating in the trial will be assigned the task of either interpreting the results of the DBT images or the CESM images: one reader will read only the DBT images, while the other will read only the CESM images. Both individuals will be blinded to the results of the other modality, and the readers may not discuss their findings before both finalize their interpretations and complete the requisite CRFs.
入排标准
- 年龄范围
- 45 Years 至 74 Years（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •1. Women must have mammographically dense breasts, ACR BI-RADS® lexicon categories c or d (heterogeneous or extreme fibroglandular tissue) on their most recent prior screening.
- •2. Women agree to not undergo whole breast screening ultrasound for the duration of the trial until the year 2 standard of care imaging.
- •3. Women must not have symptoms or signs of benign or malignant breast disease (e.g., bloody, or clear nipple discharge, breast lump, focal breast pain).
- •4. Women must be able to undergo intravenous (IV) administration of iodinated contrast (e.g., no contraindication to intravenous contrast administration for Omnipaque [iohexol], and no known allergy-like reaction to iodine or moderate or severe allergic reactions to one or more allergens as defined by the American College of Radiology [ACR]: https://www.acr.org/-/media/ACR/files/clinical-resources/contrast_media.pdf).
- •5. Women must not be pregnant or breast-feeding. All females of childbearing potential who are uncertain if they could be pregnant or may be pregnant or as per local site standard of practice in women undergoing DBT and CESM must have a negative blood test or urine pregnancy test prior to Omnipaque (iohexol) administration. A female of childbearing potential is any woman, regardless of sexual orientation, sexual identity or whether they have undergone tubal ligation, who meets the following criteria: 1) has not undergone a hysterectomy or bilateral oophorectomy; or 2) has not been naturally postmenopausal for at least 24 consecutive months (i.e., has had menses at any time in the preceding 24 consecutive months).
- •6. Women of childbearing potential must be strongly advised to use an accepted and effective method of contraception or to abstain from sexual intercourse for the following year until the Year 1 DBT and CESM studies are performed.
排除标准
- •1. Women currently undergoing treatment for breast cancer, or planning surgery for a high-risk lesion (ADH, ALH, LCIS, papilloma, radial scar).
- •2. Women who have had the following are not eligible:
- •a mammogram less than 11 months prior to study entry.
- •screening breast ultrasound within 11 months prior to study entry.
- •breast MRI less than 36 months prior to study entry.
- •contrast-enhanced spectral mammography less than 36 months prior to study entry.
- •molecular breast imaging (MBI) less than 36 months prior to study entry.
- •breast prosthetic implants (silicone or saline).
- •suspected of being at high-risk for breast cancer, as defined by the ACS breast MR screening recommendations (lifetime risk of ≥20%-25%) unless they are unable to undergo an MRI. (Reference Appendix I)
- •a history of sickle cell disease.
- •3. Women with known or suspected renal impairment. Requirements for glomerular filtration rate (GFR) determination prior to IV iodinated contrast administration are determined by local site standard practice. Criteria that should be considered include, but are not limited to, the following:
- •Age >60 years old
- •History of renal disease, including dialysis, kidney transplant, single kidney, renal cancer, and renal surgery
- •History of hypertension requiring medical therapy
- •History of diabetes mellitus
- •Use of metformin or metformin-containing drug combinations
- •4. Women who are pregnant, breast feeding, or planning to become pregnant from screening until 30 days after the last administration of Omnipaque (iohexol).
- •5. Large breasted women that require multiple images per standard view of the breast (Tiling) as determined by their most recent mammogram.
研究组 & 干预措施
DBT and CESM Diagnostic Imaging in Women with Dense Breasts
Interventional Diagnostic
干预措施: Dual-Energy Contrast-Enhanced Spectral Mammography (CESM) (Diagnostic Test)
结局指标
主要结局
Cancer Detection Rate
时间窗: Year 0
The cancer detection rate (CDR) at the participant level at Year 0. This measure will be evaluated for CESM and DBT
Recall Rate
时间窗: 1 Year
The recall rate for participants at Year 1, which will be estimated for each imaging modality separately.
次要结局
未报告次要终点