Dutour Aurelie, Josserand Veronique, Jury Delphine, Guillermet Stephanie, Decouvelaere Anne Valerie, Chotel Franck, Pointecouteau Thomas, Rizo Philippe, Coll Jean Luc, Blay Jean Yves
Department of Clinical Sciences, Centre Léon Berard, Lyon, France; Centre de Recherche en Cancerologie, UMR, INSERM, U1052-Equipe 11-CLB, Lyon, France.
Institut National de la Santé et de la Recherche Médicale (INSERM), Unité 823, Institut Albert Bonniot, Grenoble, France; Université Joseph Fourier (UJF), Grenoble, France.
Bone. 2014 May;62:71-8. doi: 10.1016/j.bone.2014.02.004. Epub 2014 Feb 14.
Tumor size and location along with efficacy of pre-operative imaging are limiting factors for optimal surgical excision for osteosarcoma. Our general hypothesis is that targeting αvβ3 integrin-rich osteosarcoma neoangiogenesis should provide improved delivery of diagnostic compounds and assist surgeons intra operatively using near-infrared imaging techniques. We evaluated in an orthotopic metastatic osteosarcoma in rats the potential of AngioStamp™ targeting αvβ3 integrins and detected intra operatively by near infrared (NIR) illumination (Fluobeam™) as a novel, intra operative imaging technique. To determine the potential of this association in improving tumor and metastasis detection, we compared the quality and sensitivity of tumor/metastasis margin delineation and tumor resection using intra-operative NIR imaging to the ones guided by pre-operative imaging (i.e., MRI subsequently confirmed by histopathological analysis). Chemotherapy being essential in osteosarcoma treatment, we evaluated the capacity of AngioStamp™ to specifically localize to the tumor after chemotherapy treatment. We showed a significantly lesser extent of healthy tissue resection after surgical excision when assessing tumor margin intra operatively using AngioStamp™/Fluobeam™ association compared to pre-operative MRI post-operatively confirmed by histopathological analysis (p<0.01). Importantly, intra-operative NIR illumination of lungs revealed more metastases than were detected by CT Scan or under intra-operative white light examination (p<0.01). Importantly, chemotherapy did not alter AngioStamp™ tumor specific targeting nor the sensitivity of tumor detection. Our preclinical data confirm the potential of intra-operative imaging for improved primary tumor and lung metastasis excision. Based on these promising results, we now propose to evaluate this approach as a mean to improve surgical excision while maintaining tumor control in other sarcoma or tumors overexpressing αvβ3 integrins.
肿瘤大小和位置以及术前成像的效果是骨肉瘤实现最佳手术切除的限制因素。我们的总体假设是,靶向富含αvβ3整合素的骨肉瘤新生血管生成应能改善诊断化合物的递送,并在术中借助近红外成像技术协助外科医生。我们在大鼠原位转移性骨肉瘤模型中评估了AngioStamp™靶向αvβ3整合素并通过近红外(NIR)照明(Fluobeam™)在术中检测的潜力,将其作为一种新型的术中成像技术。为了确定这种联合在改善肿瘤和转移灶检测方面的潜力,我们将术中NIR成像引导下的肿瘤/转移灶边缘勾勒和肿瘤切除的质量与敏感性,与术前成像(即随后经组织病理学分析证实的MRI)引导下的情况进行了比较。化疗在骨肉瘤治疗中至关重要,我们评估了化疗后AngioStamp™特异性定位于肿瘤的能力。与术后经组织病理学分析证实的术前MRI相比,当使用AngioStamp™/Fluobeam™联合在术中评估肿瘤边缘时,我们发现手术切除后健康组织的切除范围明显更小(p<0.01)。重要的是,术中对肺部进行近红外照明发现的转移灶比CT扫描或术中白光检查发现的更多(p<0.01)。重要的是,化疗并未改变AngioStamp™对肿瘤的特异性靶向,也未改变肿瘤检测的敏感性。我们的临床前数据证实了术中成像在改善原发性肿瘤和肺转移灶切除方面的潜力。基于这些有前景的结果,我们现在提议评估这种方法,作为在其他过表达αvβ3整合素的肉瘤或肿瘤中改善手术切除同时维持肿瘤控制的手段。