Gupta Santosh, Fernandez Luisa, Bourdon David, Hamid Anis A, Pasam Anupama, Lam Ernest, Wenstrup Richard, Sandhu Shahneen
Translational Research and Assay Development, Epic Sciences, San Diego, California - USA.
Department of Medical Oncology, University of Melbourne, Melbourne, Victoria - Australia.
J Circ Biomark. 2024 Feb 21;13:1-6. doi: 10.33393/jcb.2024.2636. eCollection 2024 Jan-Dec.
For patients with mCRPC, PSMA-targeted radioligand treatment has significantly improved the clinical outcome. A blood-based liquid biopsy assay for recognizing PSMA protein expression on circulating tumor cells may be beneficial for better informing therapeutic decision-making and identifying the patients most likely to benefit from PSMA-targeted radioligand therapy.
Using high-throughput imaging and digital AI pathology algorithms, a four-color immunofluorescence assay has been developed to find PSMA protein expression on CTCs on a glass slide. Cell line cells (LNCaP/PC3s/22Rv1) spiked into healthy donor blood were used to study the precision, specificity, sensitivity, limit of detection, and overall accuracy of the assay. Clinical validation and low-pass whole-genome sequencing were performed in PSMA-PET-positive patients with high-risk mCRPC (N = 24) utilizing 3 mL of blood.
The PSMA CTC IF assay achieved analytical specificity, sensitivity, and overall accuracy above 99% with high precision. In the clinical validation, 76% (16/21) of the cases were PSMA positive with CTC heterogeneity, and 88% (21/24) of the patients contained at least one conventional CTC per milliliter of blood. Thirty-six low-pass-sequenced CTCs from 11 individuals with mCRPC frequently exhibited copy number increases in and and losses in , and locus.
The analytical validation utilizing Epic Sciences' liquid biopsy CTC platform demonstrated the potential to detect PSMA protein expression in CTCs from patients with mCRPC. This assay is positioned as an effective research tool to evaluate PSMA expression, heterogeneity, and therapeutic response in many ongoing clinical studies to target tumors that express PSMA.
对于转移性去势抵抗性前列腺癌(mCRPC)患者,靶向前列腺特异性膜抗原(PSMA)的放射性配体治疗显著改善了临床结局。一种基于血液的液体活检检测方法,用于识别循环肿瘤细胞上的PSMA蛋白表达,可能有助于更好地指导治疗决策,并确定最有可能从靶向PSMA的放射性配体治疗中获益的患者。
利用高通量成像和数字人工智能病理学算法,开发了一种四色免疫荧光检测方法,以在载玻片上检测循环肿瘤细胞(CTC)上的PSMA蛋白表达。将细胞系细胞(LNCaP/PC3s/22Rv1)加入健康供体血液中,用于研究该检测方法的精密度、特异性、灵敏度、检测限和总体准确性。对24例高危mCRPC的PSMA-PET阳性患者采集3 mL血液进行临床验证和低通量全基因组测序。
PSMA CTC免疫荧光检测方法具有高精度,分析特异性、灵敏度和总体准确性均高于99%。在临床验证中,76%(16/21)的病例PSMA呈阳性,存在CTC异质性,88%(21/24)的患者每毫升血液中至少含有一个传统CTC。来自11例mCRPC患者的36个低通量测序的CTC经常表现出 和 基因座的拷贝数增加以及 和 基因座的缺失。
利用Epic Sciences公司的液体活检CTC平台进行的分析验证表明,该方法具有检测mCRPC患者CTC中PSMA蛋白表达的潜力。在许多正在进行的针对表达PSMA肿瘤的临床研究中,该检测方法被定位为一种评估PSMA表达、异质性和治疗反应的有效研究工具。