Wenpeng Huang, Xinyao Sun, Yutong Liang, Jason C Mixdorf, Qi Yang, Jonathan W Engle, Xiaoyan Xiao, Liming Li, Lei Kang, Weibo Cai
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ImmunoPET imaging with [<sup>89</sup>Zr]Zr-DFO-Trodelvy was performed at multiple time points to evaluate <i>in vivo</i> targeting. Additionally, tumor tissues from tumor-bearing mice were analyzed by immunofluorescence.</p><p><strong>Results: </strong>The radiochemical yield of [<sup>89</sup>Zr]Zr-DFO-Trodelvy was >90%, with radiochemical purity exceeding 99%. Trop2 expression was high in HT1376 cells and low in T24 cells. ImmunoPET imaging demonstrated effective visualization of tumors in HT1376 models as early as 6 h post-injection, with tumor uptake reaching peak at 48 h (16.33 ± 0.90 %ID/g), followed by a gradual decline. In contrast, T24 tumors showed significantly lower uptake (6.20 ± 0.99 %ID/g, <i>P</i> = 0.0005). Co-injection with 2 mg of unlabeled Trodelvy significantly reduced tumor uptake in HT1376 models (4.50 ± 0.51 %ID/g, <i>P</i> = 0.0004), confirming target specificity. At 48 h, a high tumor-to-background ratio was observed, indicating selective accumulation in tumor tissue.</p><p><strong>Conclusions: </strong>[<sup>89</sup>Zr]Zr-DFO-Trodelvy enables precise immunoPET imaging of bladder cancer models with high Trop2 expression, demonstrating specific and sustained tumor accumulation. These findings highlight the potential of this imaging approach for the noninvasive assessment of Trop2 expression.</p>","PeriodicalId":7572,"journal":{"name":"American journal of nuclear medicine and molecular imaging","volume":"15 3","pages":"87-96"},"PeriodicalIF":1.8000,"publicationDate":"2025-06-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12267092/pdf/","citationCount":"0","resultStr":"{\"title\":\"[<sup>89</sup>Zr]Zr-DFO-Trodelvy immunoPET for noninvasive Trop2 imaging in bladder cancer.\",\"authors\":\"Wenpeng Huang, Xinyao Sun, Yutong Liang, Jason C Mixdorf, Qi Yang, Jonathan W Engle, Xiaoyan Xiao, Liming Li, Lei Kang, Weibo Cai\",\"doi\":\"10.62347/KKEE6954\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Purpose: </strong>The Trop2-targeting antibody-drug conjugate (ADC), sacituzumab govitecan (Trodelvy<sup>TM</sup>), demonstrates significant therapeutic efficacy in targeting Trop2-expressing tumors. In this study, we utilized immunoPET imaging to assess Trop2 expression in bladder cancer models using [<sup>89</sup>Zr]Zr-DFO-Trodelvy.</p><p><strong>Materials and methods: </strong>Trop2 expression levels in bladder cancer cell lines were measured using flow cytometry and immunofluorescence staining. Radiolabeling of DFO-Trodelvy with <sup>89</sup>Zr was carried out in Na<sub>2</sub>CO<sub>3</sub> buffer at pH 7 (37°C, 1.5 h). ImmunoPET imaging with [<sup>89</sup>Zr]Zr-DFO-Trodelvy was performed at multiple time points to evaluate <i>in vivo</i> targeting. Additionally, tumor tissues from tumor-bearing mice were analyzed by immunofluorescence.</p><p><strong>Results: </strong>The radiochemical yield of [<sup>89</sup>Zr]Zr-DFO-Trodelvy was >90%, with radiochemical purity exceeding 99%. Trop2 expression was high in HT1376 cells and low in T24 cells. ImmunoPET imaging demonstrated effective visualization of tumors in HT1376 models as early as 6 h post-injection, with tumor uptake reaching peak at 48 h (16.33 ± 0.90 %ID/g), followed by a gradual decline. In contrast, T24 tumors showed significantly lower uptake (6.20 ± 0.99 %ID/g, <i>P</i> = 0.0005). Co-injection with 2 mg of unlabeled Trodelvy significantly reduced tumor uptake in HT1376 models (4.50 ± 0.51 %ID/g, <i>P</i> = 0.0004), confirming target specificity. At 48 h, a high tumor-to-background ratio was observed, indicating selective accumulation in tumor tissue.</p><p><strong>Conclusions: </strong>[<sup>89</sup>Zr]Zr-DFO-Trodelvy enables precise immunoPET imaging of bladder cancer models with high Trop2 expression, demonstrating specific and sustained tumor accumulation. 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引用次数: 0
摘要
目的:靶向trop2的抗体-药物偶联物(ADC) sacituzumab govitecan (TrodelvyTM)在靶向表达trop2的肿瘤中显示出显著的治疗效果。在本研究中,我们使用[89Zr]Zr-DFO-Trodelvy免疫pet成像技术评估膀胱癌模型中Trop2的表达。材料与方法:采用流式细胞术和免疫荧光染色法检测膀胱癌细胞株中Trop2的表达水平。用89Zr在Na2CO3缓冲液中,在pH 7(37°C, 1.5 h)下对DFO-Trodelvy进行放射性标记。用[89Zr]Zr-DFO-Trodelvy在多个时间点进行免疫pet成像以评估体内靶向性。此外,用免疫荧光法分析荷瘤小鼠的肿瘤组织。结果:[89Zr]Zr-DFO-Trodelvy的放射化学产率为90%,放射化学纯度超过99%。Trop2在HT1376细胞中高表达,在T24细胞中低表达。免疫pet成像显示HT1376模型早在注射后6 h就能有效显示肿瘤,48 h时肿瘤摄取达到峰值(16.33±0.90% ID/g),随后逐渐下降。相比之下,T24肿瘤的摄取明显降低(6.20±0.99% ID/g, P = 0.0005)。在HT1376模型中,共注射2 mg未标记的Trodelvy显著降低肿瘤摄取(4.50±0.51% ID/g, P = 0.0004),证实了靶特异性。48 h时,观察到较高的肿瘤与背景比,表明肿瘤组织中选择性积累。结论:[89Zr]Zr-DFO-Trodelvy能够对Trop2高表达的膀胱癌模型进行精确的免疫pet成像,显示肿瘤特异性和持续性的积累。这些发现强调了这种成像方法在无创性评估Trop2表达方面的潜力。
[89Zr]Zr-DFO-Trodelvy immunoPET for noninvasive Trop2 imaging in bladder cancer.
Purpose: The Trop2-targeting antibody-drug conjugate (ADC), sacituzumab govitecan (TrodelvyTM), demonstrates significant therapeutic efficacy in targeting Trop2-expressing tumors. In this study, we utilized immunoPET imaging to assess Trop2 expression in bladder cancer models using [89Zr]Zr-DFO-Trodelvy.
Materials and methods: Trop2 expression levels in bladder cancer cell lines were measured using flow cytometry and immunofluorescence staining. Radiolabeling of DFO-Trodelvy with 89Zr was carried out in Na2CO3 buffer at pH 7 (37°C, 1.5 h). ImmunoPET imaging with [89Zr]Zr-DFO-Trodelvy was performed at multiple time points to evaluate in vivo targeting. Additionally, tumor tissues from tumor-bearing mice were analyzed by immunofluorescence.
Results: The radiochemical yield of [89Zr]Zr-DFO-Trodelvy was >90%, with radiochemical purity exceeding 99%. Trop2 expression was high in HT1376 cells and low in T24 cells. ImmunoPET imaging demonstrated effective visualization of tumors in HT1376 models as early as 6 h post-injection, with tumor uptake reaching peak at 48 h (16.33 ± 0.90 %ID/g), followed by a gradual decline. In contrast, T24 tumors showed significantly lower uptake (6.20 ± 0.99 %ID/g, P = 0.0005). Co-injection with 2 mg of unlabeled Trodelvy significantly reduced tumor uptake in HT1376 models (4.50 ± 0.51 %ID/g, P = 0.0004), confirming target specificity. At 48 h, a high tumor-to-background ratio was observed, indicating selective accumulation in tumor tissue.
Conclusions: [89Zr]Zr-DFO-Trodelvy enables precise immunoPET imaging of bladder cancer models with high Trop2 expression, demonstrating specific and sustained tumor accumulation. These findings highlight the potential of this imaging approach for the noninvasive assessment of Trop2 expression.
期刊介绍:
The scope of AJNMMI encompasses all areas of molecular imaging, including but not limited to: positron emission tomography (PET), single-photon emission computed tomography (SPECT), molecular magnetic resonance imaging, magnetic resonance spectroscopy, optical bioluminescence, optical fluorescence, targeted ultrasound, photoacoustic imaging, etc. AJNMMI welcomes original and review articles on both clinical investigation and preclinical research. Occasionally, special topic issues, short communications, editorials, and invited perspectives will also be published. Manuscripts, including figures and tables, must be original and not under consideration by another journal.