O'Neill Allison F, Dearling Jason L J, Wang Yuchuan, Tupper Tanya, Sun Yanping, Aster Jon C, Calicchio Monica L, Perez-Atayde Antonio R, Packard Alan B, Kung Andrew L
Authors' Affiliations: Department of Pediatric Oncology, Dana-Farber Cancer Institute, Boston Children's Hospital, and Harvard Medical School; Division of Nuclear Medicine and Molecular Imaging, Department of Radiology, Boston Children's Hospital, and Harvard Medical School; Lurie Family Imaging Center, Dana-Farber Cancer Institute; Department of Pathology, Brigham and Women's Hospital, and Harvard Medical School; Department of Pathology, Boston Children's Hospital, and Harvard Medical School, Boston, Massachusetts; and Department of Pediatrics, Columbia University Medical Center, New York.
Clin Cancer Res. 2014 Feb 1;20(3):678-87. doi: 10.1158/1078-0432.CCR-13-1660. Epub 2013 Nov 11.
Ewing sarcoma is a tumor of the bone and soft tissue characterized by diffuse cell membrane expression of CD99 (MIC2). Single-site, surgically resectable disease is associated with an excellent 5-year event-free survival; conversely, patients with distant metastases have a poor prognosis. Noninvasive imaging is the standard approach to identifying sites of metastatic disease. We sought to develop a CD99-targeted imaging agent for staging Ewing sarcoma and other CD99-expressing tumors.
We identified a CD99 antibody with highly specific binding in vitro and labeled this antibody with (64)Cu. Mice with either subcutaneous Ewing sarcoma xenograft tumors or micrometastases were imaged with the (64)Cu-labeled anti-CD99 antibody and these results were compared with conventional MRI and 2[18F]fluoro-2-deoxy-D-glucose-positron emission tomography (FDG-PET) imaging.
(64)Cu-labeled anti-CD99 antibody demonstrated high avidity for the CD99-positive subcutaneous tumors, with a high tumor-to-background ratio, greater than that demonstrated with FDG-PET. Micrometastases, measuring 1 to 2 mm on MRI, were not detected with FDG-PET but were readily visualized with the (64)Cu-labeled anti-CD99 antibody. Probe biodistribution studies demonstrated high specificity of the probe for CD99-positive tumors.
(64)Cu-labeled anti-CD99 antibody can detect subcutaneous Ewing sarcoma tumors and metastatic sites with high sensitivity, outperforming FDG-PET in preclinical studies. This targeted radiotracer may have important implications for the diagnosis, surveillance, and treatment of Ewing sarcoma. Similarly, it may impact the management of other CD99 positive tumors.
尤因肉瘤是一种发生于骨和软组织的肿瘤,其特征为CD99(MIC2)在细胞膜上弥漫性表达。单发病灶且可手术切除的疾病患者5年无事件生存率良好;相反,发生远处转移的患者预后较差。非侵入性成像检查是识别转移病灶部位的标准方法。我们试图开发一种针对CD99的成像剂,用于尤因肉瘤及其他表达CD99的肿瘤的分期。
我们鉴定出一种在体外具有高度特异性结合能力的CD99抗体,并用(64)Cu对该抗体进行标记。使用(64)Cu标记的抗CD99抗体对皮下接种尤因肉瘤异种移植瘤或微转移灶的小鼠进行成像,并将结果与传统MRI及2-[18F]氟-2-脱氧-D-葡萄糖-正电子发射断层扫描(FDG-PET)成像进行比较。
(64)Cu标记的抗CD99抗体对CD99阳性皮下肿瘤显示出高亲和力,肿瘤与背景比值高,高于FDG-PET。MRI显示大小为1至2毫米的微转移灶,FDG-PET未检测到,但(64)Cu标记的抗CD99抗体很容易将其显示出来。探针生物分布研究表明该探针对CD99阳性肿瘤具有高度特异性。
(64)Cu标记的抗CD99抗体能够高灵敏度地检测皮下尤因肉瘤肿瘤及转移部位,在临床前研究中表现优于FDG-PET。这种靶向放射性示踪剂可能对尤因肉瘤的诊断、监测及治疗具有重要意义。同样,它可能会影响其他CD99阳性肿瘤的治疗。