跳至主要内容
临床试验/NCT07111728
NCT07111728招募中不适用

Multimodal Hyperspectral Imaging and Raman Spectroscopy for Intraoperative Assessment of Breast Tumor Resection Margins

Istituti Clinici Scientifici Maugeri SpA1 个研究点 分布在 1 个国家目标入组 104 人开始时间: 2025年10月6日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
104
试验地点
1
主要终点
Sensitivity and specificity of Spectra-BREAST system margin status prediction

研究概览

简要总结

Breast-conserving surgery (lumpectomy) aims to remove cancer while preserving healthy tissue, but up to 20% of patients require a second operation because cancer cells remain at the edge (margin) of the removed tissue. The Spectra-BREAST study evaluates a new optical device that combines hyperspectral imaging (HIS) and Raman spectroscopy (RS) with artificial-intelligence analysis to quickly assess the entire surface of excised breast specimens during surgery. By flagging areas at risk of positive margins in real time, the device may help surgeons remove any remaining cancer in a single procedure.

In this prospective, single-arm diagnostic study, surgeons will use the Spectra-BREAST system on freshly resected breast tissue from up to 99 women undergoing lumpectomy for invasive carcinoma or ductal carcinoma in situ. First, the device's cancer-detection algorithms will be trained on 74 specimens with known pathology. Then, in a separate group of patients, the fully integrated device will be tested on all six faces of each lumpectomy specimen and its predictions will be compared against the gold-standard histopathology margin assessment. Key measures include the sensitivity and specificity of the device's margin predictions, the time needed to generate results, and the device's usability in a clinical setting.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Histologically confirmed diagnosis of ductal carcinoma in situ (B5a) or invasive breast carcinoma (B5b) on pre-operative core needle biopsy
  • Scheduled to undergo breast-conserving surgery (lumpectomy)
  • Able and willing to provide written informed consent

排除标准

  • Pre-operative histologic or cytologic diagnosis of a benign breast lesion (B2/C2)
  • Initial diagnosis of advanced (stage III/IV) or metastatic breast carcinoma, or indication for neoadjuvant chemotherapy
  • Neurocognitive disorders that would impair comprehension of the study procedures or consent process
  • Concurrent pregnancy or breastfeeding

研究组 & 干预措施

DCIS breast cancer

干预措施: Spectra-BREAST system in DCIS Breast Cancer (Diagnostic Test)

Invasive Breast Cancer

干预措施: Spectra-BREAST system in Invasive Breast Cancer (Diagnostic Test)

结局指标

主要结局

Sensitivity and specificity of Spectra-BREAST system margin status prediction

时间窗: Within 21 days after surgery (latest expected receipt of the final pathology report).

Proportion of resection faces correctly classified by the Spectra-BREAST device as "positive margin" or "negative margin" when compared to gold-standard postoperative histopathology. Sensitivity and specificity will both be calculated independently in Invasive Breast Cancer and in DCIS breast cancer across all specimens in the validation cohort.

次要结局

  • Concordance of HSI-only versus combined HSI + RS predictions(During Spectra-BREAST procedure)
  • Time from specimen removal to Spectra-BREAST system result(Per specimen, measured intraoperatively)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Fabio Corsi

Prof.

Istituti Clinici Scientifici Maugeri SpA

研究点 (1)

Loading locations...

相似试验