Mapping breast cancer therapy with circulating tumor cells: The expert perspective

被引:0
作者
Gerratana, Lorenzo [1 ,2 ]
Gianni, Caterina [3 ,4 ]
Nicolo, Eleonora [3 ]
Pontolillo, Letizia [3 ,5 ]
Bidard, Francois-Clement [6 ]
Reduzzi, Carolina [3 ]
Cristofanilli, Massimo [3 ]
机构
[1] IRCCS, NCI, Dept Med Oncol, CRO Aviano, Aviano, Italy
[2] Univ Udine, Dept Med, Udine, Italy
[3] Weill Cornell Med, Dept Med, Div Hematol Oncol, Liquid Biopsy Platform, New York 10065, NY USA
[4] IRCCS Ist Romagnolo Studio Tumori IRST Dino Amador, Med Oncol & Breast Unit, Med Oncol Dept, Meldola, Forli Cesena, Italy
[5] Univ Cattolica Sacro Cuore, Dept Translat Med & Surg, Thorac Surg, Rome, Italy
[6] Paris Saclay Univ, Inst Curie, Dept Med Oncol, UVSQ, St Cloud, France
关键词
Breast cancer; Circulating tumor cells; Precision medicine; Liquid biopsy; POOLED ANALYSIS; CHEMOTHERAPY; SURVIVAL;
D O I
10.1016/j.breast.2025.104463
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Circulating tumor cells (CTCs) have emerged as a key prognostic biomarker for breast cancer, with their role becoming more pronounced in metastatic cases. In metastatic breast cancer, having five or more CTCs per 7.5 mL of blood is linked to poorer survival and more aggressive disease, marking it as stage IVaggressive. Conversely, fewer than five CTCs per 7.5 mL of blood indicates a less aggressive, stage IVindolent disease. Additionally, molecular CTCs characterization provides a real-time snapshot of tumor biology, capturing its temporal and spatial variability and providing insights into tumor behavior. Beyond their role in predicting outcomes, CTCs can help guide treatment intensity as shown in clinical trials like the STIC trial, offering a new way to tailor therapy alongside other liquid biopsy biomarkers such as circulating tumor DNA. The aim of our review is to focus on both enumeration and phenotyping of CTCs and examine how CTC-guided strategies can improve treatment tailoring and patient outcomes. We also explore the potential for integrating CTCs with other biomarkers, such as circulating tumor DNA, and discuss how innovative biomarker-driven clinical trial designs could further advance personalized treatment strategies.
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收藏
页数:6
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