Paoloni Melissa C, Tandle Anita, Mazcko Christina, Hanna Engy, Kachala Stefan, Leblanc Amy, Newman Shelley, Vail David, Henry Carolyn, Thamm Douglas, Sorenmo Karin, Hajitou Amin, Pasqualini Renata, Arap Wadih, Khanna Chand, Libutti Steven K
Comparative Oncology Program, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland, USA.
PLoS One. 2009;4(3):e4972. doi: 10.1371/journal.pone.0004972. Epub 2009 Mar 30.
Under the direction and sponsorship of the National Cancer Institute, we report on the first pre-clinical trial of the Comparative Oncology Trials Consortium (COTC). The COTC is a novel infrastructure to integrate cancers that naturally develop in pet dogs into the development path of new human drugs. Trials are designed to address questions challenging in conventional preclinical models and early phase human trials. Large animal spontaneous cancer models can be a valuable addition to successful studies of cancer biology and novel therapeutic drug, imaging and device development.
METHODOLOGY/PRINCIPAL FINDINGS: Through this established infrastructure, the first trial of the COTC (COTC001) evaluated a targeted AAV-phage vector delivering tumor necrosis factor (RGD-A-TNF) to alphaV integrins on tumor endothelium. Trial progress and data was reviewed contemporaneously using a web-enabled electronic reporting system developed for the consortium. Dose-escalation in cohorts of 3 dogs (n = 24) determined an optimal safe dose (5x10(12) transducing units intravenous) of RGD-A-TNF. This demonstrated selective targeting of tumor-associated vasculature and sparing of normal tissues assessed via serial biopsy of both tumor and normal tissue. Repetitive dosing in a cohort of 14 dogs, at the defined optimal dose, was well tolerated and led to objective tumor regression in two dogs (14%), stable disease in six (43%), and disease progression in six (43%) via Response Evaluation Criteria in Solid Tumors (RECIST).
CONCLUSIONS/SIGNIFICANCE: The first study of the COTC has demonstrated the utility and efficiency of the established infrastructure to inform the development of new cancer drugs within large animal naturally occurring cancer models. The preclinical evaluation of RGD-A-TNF within this network provided valuable and necessary data to complete the design of first-in-man studies.
在美国国立癌症研究所的指导和赞助下,我们报告了比较肿瘤试验联盟(COTC)的首次临床前试验。COTC是一种新型的基础设施,旨在将宠物狗自然发生的癌症纳入新型人类药物的研发路径。试验旨在解决传统临床前模型和早期人体试验中具有挑战性的问题。大型动物自发癌症模型可以为癌症生物学和新型治疗药物、成像及设备开发的成功研究提供有价值的补充。
方法/主要发现:通过这一既定的基础设施,COTC的首次试验(COTC001)评估了一种靶向腺相关病毒噬菌体载体,该载体可将肿瘤坏死因子(RGD-A-TNF)递送至肿瘤内皮细胞上的αV整合素。使用为该联盟开发的基于网络的电子报告系统同步审查试验进展和数据。对3只狗(n = 24)的队列进行剂量递增,确定了RGD-A-TNF的最佳安全剂量(5×10¹²转导单位静脉注射)。这表明通过对肿瘤和正常组织进行连续活检评估,RGD-A-TNF可选择性靶向肿瘤相关血管系统并避免对正常组织造成损伤。在14只狗的队列中,以确定的最佳剂量重复给药,耐受性良好,并通过实体瘤疗效评价标准(RECIST)使两只狗(14%)的肿瘤出现客观消退,六只狗(43%)病情稳定,六只狗(43%)病情进展。
结论/意义:COTC的首次研究证明了既定基础设施在大型动物自然发生癌症模型中为新癌症药物研发提供信息的实用性和效率。在此网络内对RGD-A-TNF进行的临床前评估为完成首次人体研究的设计提供了有价值且必要的数据。