Trop2-targeted PET/CT imaging with 68Ga-MY6349 improves diagnostic accuracy and influences clinical management in breast cancer.

IF 14.9 1区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Theranostics Pub Date : 2026-07-13 eCollection Date: 2026-01-01 DOI:10.7150/thno.136704
Lingyu Yu, Liang Zhao, Ru Zeng, Yonghui Su, Zhenyu Wu, Shan Yu, Yin Li, Hao Fu, Wei Guo, Yining Sun, Hannan Gao, Long Sun, Hua Wu, Feng Ye, Fan Wang, Haojun Chen
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引用次数: 0

Abstract

Rationale: Trophoblast cell-surface antigen 2 (Trop2) is an essential therapeutic target in breast cancer, yet non-invasive methods for assessing its expression and predicting response to Trop2-directed antibody-drug conjugates (ADCs) remain limited. We aimed to evaluate the diagnostic accuracy of 68Ga-MY6349 positron emission tomography/computed tomography (PET/CT) in patients with breast cancer and assess its impact on clinical decision-making. Methods: We prospectively enrolled 73 patients with suspected or confirmed breast cancer who underwent both 68Ga-MY6349 and 18F-fluorodeoxyglucose (18F-FDG) PET/CT from December 2024 to April 2025. Lesion-based diagnostic performance was compared using histopathology and follow-up imaging as reference standards. Treatment decisions were recorded before and after 68Ga-MY6349 PET/CT. Serial 68Ga-MY6349 PET/CT was performed to assess the early metabolic response in three patients with triple-negative breast cancer receiving sacituzumab tirumotecan. Results: 68Ga-MY6349 PET/CT identified more malignant lesions (564 vs. 436) and fewer false positives (2 vs. 40) than 18F-FDG PET/CT. In the initial-staging cohort (n = 30), 68Ga-MY6349 PET/CT led to TNM stage upgrades in 6/30 patients (20%) and treatment modifications in 4/30. In the restaging cohort (n = 43), clinical management was altered in 5/43 patients (12%) owing to the identification of additional metastatic lesions or rectification of false-positive findings via 68Ga-MY6349 PET/CT. 68Ga-MY6349 PET/CT yielded higher overall tumor uptake (median maximum standardized uptake value (SUVmax), 5.9 vs. 4.1; P < 0.001) and improved lesion conspicuity, particularly in lymph node and metastatic lesions. Exploratory analysis in three patients receiving Trop2-ADC therapy showed that early changes in 68Ga-MY6349 uptake after two treatment cycles were concordant with the subsequent clinical response. Conclusions: 68Ga-MY6349 PET/CT demonstrated superior diagnostic performance to 18F-FDG PET/CT in breast cancer staging and diagnosis, directly influencing therapeutic strategies. Preliminary findings from the triple-negative breast cancer cases suggest that early changes in SUVmax may be associated with the treatment response to Trop2-targeted ADC therapy, warranting further prospective validation in larger patient populations.

68Ga-MY6349靶向trop2的PET/CT成像提高了乳腺癌的诊断准确性并影响了临床管理。
理由:滋养细胞表面抗原2 (Trop2)是乳腺癌的重要治疗靶点,然而评估其表达和预测对Trop2导向的抗体-药物偶联物(adc)反应的非侵入性方法仍然有限。我们旨在评估68Ga-MY6349正电子发射断层扫描/计算机断层扫描(PET/CT)对乳腺癌患者的诊断准确性,并评估其对临床决策的影响。方法:我们前瞻性地招募了73例疑似或确诊乳腺癌患者,这些患者于2024年12月至2025年4月期间接受了68Ga-MY6349和18f -氟脱氧葡萄糖(18F-FDG) PET/CT检查。以组织病理学和随访影像作为参考标准,比较基于病变的诊断表现。记录68Ga-MY6349 PET/CT前后的治疗决定。采用68Ga-MY6349系列PET/CT评估3例接受舒妥珠单抗替鲁莫替康治疗的三阴性乳腺癌患者的早期代谢反应。结果:与18F-FDG PET/CT相比,68Ga-MY6349 PET/CT鉴别出更多恶性病变(564对436),假阳性较少(2对40)。在初始分期队列(n = 30)中,68Ga-MY6349 PET/CT导致6/30例患者(20%)的TNM分期升级,4/30例患者的治疗改变。在重新分期队列(n = 43)中,由于通过68Ga-MY6349 PET/CT发现了额外的转移性病变或纠正了假阳性结果,有5/43(12%)的患者改变了临床管理。68Ga-MY6349 PET/CT显示更高的整体肿瘤摄取(最大标准化摄取值中位数(SUVmax), 5.9 vs 4.1;P < 0.001),并改善了病变的显著性,尤其是淋巴结和转移性病变。对三名接受Trop2-ADC治疗的患者的探索性分析显示,两个治疗周期后68Ga-MY6349摄取的早期变化与随后的临床反应一致。结论:68Ga-MY6349 PET/CT在乳腺癌分期和诊断方面优于18F-FDG PET/CT,直接影响治疗策略。来自三阴性乳腺癌病例的初步研究结果表明,SUVmax的早期变化可能与trop2靶向ADC治疗的治疗反应有关,需要在更大的患者群体中进一步进行前瞻性验证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Theranostics
Theranostics MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
25.40
自引率
1.60%
发文量
433
审稿时长
1 months
期刊介绍: Theranostics serves as a pivotal platform for the exchange of clinical and scientific insights within the diagnostic and therapeutic molecular and nanomedicine community, along with allied professions engaged in integrating molecular imaging and therapy. As a multidisciplinary journal, Theranostics showcases innovative research articles spanning fields such as in vitro diagnostics and prognostics, in vivo molecular imaging, molecular therapeutics, image-guided therapy, biosensor technology, nanobiosensors, bioelectronics, system biology, translational medicine, point-of-care applications, and personalized medicine. Encouraging a broad spectrum of biomedical research with potential theranostic applications, the journal rigorously peer-reviews primary research, alongside publishing reviews, news, and commentary that aim to bridge the gap between the laboratory, clinic, and biotechnology industries.
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