Jingwen Zheng, Hao Chen, Hongyun Zhang, Zhifen Wu, Lixiang Ye, Jianxi Ke, Feize Li, Ning Liu, Yongsheng Liu, Maochun Hong
Cancer remains a global health challenge, with current postoperative adjuvant therapies for advanced solid tumors being limited by therapeutic resistance, off-target effects, and insufficient treatment monitoring. Here, we report a rational design of a novel tumor-targeted 177 Lu-labeled lanthanide nanoradiopharmaceutical called 177 Lu-LnNRP@HER2 (namely, NaGdF 4:Yb@NaErF 4:Tm@NaYF 4:Yb/ 177 Lu@NaYF 4 @DSPE-PEG-HER2). This nanoradiopharmaceutical is engineered to enable precision postoperative β-radiotherapy in combination with real-time radiation-free prognosis monitoring. The unique multilayer structure of 177 Lu-LnNRP@HER2 simultaneously facilitates tumor-selective β-particle irradiation through stably labeled 177 Lu for eliminating residual tumor cells and provides strong upconversion/near-infrared-II (UC/NIR-II) fluorescent signals for intraoperative tumor margin delineation and postoperative monitoring. In an orthotopic gastric tumor model, 177 Lu-LnNRP@HER2 demonstrates significant postoperative therapeutic efficacy and real-time prognosis monitoring capability, achieving an 84% suppression of recurrence, an 88.6% reduction in metastasis, and a 2.6-fold increase in median survival. Multimodal analyses, including high-resolution cell imaging, flow cytometry, and transcriptomics, reveal that the excellent antitumor activity of 177 Lu-LnNRP@HER2 is mainly attributed to the DNA damage and reactive oxygen species elevation arising from the proximity-targeted β-particle irradiation of tumor cell nuclei and mitochondria. These findings address a key gap in the field by synchronizing targeted radionuclide therapy with integrated real-time monitoring, thus promising a new paradigm for precision oncology.