- Sun, Na;
- Yang, Yingying;
- Miao, Hui;
- Redublo, Peter;
- Liu, Hongtao;
- Liu, Wenfei;
- Huang, Yen-Wen;
- Teng, Pai-Chi;
- Zhang, Ceng;
- Zhang, Ryan Y;
- Smalley, Matthew;
- Yang, Peng;
- Chou, Shih-Jie;
- Huai, Kevin;
- Zhang, Zhicheng;
- Lee, Yi-Te;
- Wang, Jasmine J;
- Wang, Jing;
- Liang, Icy Y;
- Zhang, Tiffany X;
- Zhang, Dongyun;
- Liang, Li;
- Weiss, Paul S;
- Posadas, Edwin M;
- Donahue, Timothy;
- Hecht, J Randolph;
- Allen-Auerbach, Martin S;
- Bergsland, Emily K;
- Hope, Thomas A;
- Pei, Renjun;
- Zhu, Yazhen;
- Tseng, Hsian-Rong;
- Heaney, Anthony P
Circulating tumor cell (CTC) clusters are present in cancer patients with severe metastasis, resulting in poor clinical outcomes. However, CTC clusters have not been studied as extensively as single CTCs, and the clinical utility of CTC clusters remains largely unknown. In this study, we aim sought to explore the feasibility of NanoVelcro Chips to simultaneously detect both single CTCs and CTC clusters with negligible perturbation to their intrinsic properties in neuroendocrine tumors (NETs). We discovered frequent CTC clusters in patients with advanced NETs and examined their potential roles, together with single NET CTCs, as novel biomarkers of patient response following peptide receptor radionuclide therapy (PRRT). We observed dynamic changes in both total NET CTCs and NET CTC cluster counts in NET patients undergoing PRRT which correlated with clinical outcome. These preliminary findings suggest that CTC clusters, along with single CTCs, offer a potential non-invasive option to monitor the treatment response in NET patients undergoing PRRT.