Engineered imaging nanoparticles for real-time detection of cancer in the tumor b

工程成像纳米颗粒用于实时检测肿瘤中的癌症

• 批准号: 8716696
• 负责人: W David Lee
• 金额: $ 20.74万
• 依托单位: LUMICELL, INC.
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-09-27 至 2015-01-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8716696
• 关键词: Academic Medical Centers; Address; Adenocarcinoma; Animals; Beds; Biopsy; Breast Sarcoma; Cancer Detection; Cancer Patient; Canis familiaris; Carcinoma; Cathepsins; Clinical; Clinical Research; Clinical Trials; Colon; Colon Carcinoma; Colonoscopy; Conduct Clinical Trials; Data; Dermatologic; Detection; Development; Drug Kinetics; Dyes; Engineering; Excision; FDA approved; Failure; General Hospitals; Genetically Engineered Mouse; Goals; Health Care Costs; Histocompatibility Testing; Histopathology; Hospitals; Human; Image; Imaging Device; Imaging technology; Label; Lead; Lesion; Light; Malignant - descriptor; Malignant Neoplasms; Malignant neoplasm of lung; Marketing; Massachusetts; Metric; Modeling; Modification; Motivation; Mus; Neoplasm Metastasis; New Agents; Normal tissue morphology; Operative Surgical Procedures; Patients; Performance; Phase; Phase I Clinical Trials; Pilot Projects; Rattus; Recruitment Activity; Recurrence; Repeat Surgery; Residual Cancers; Risk; Risk Factors; Savings; Schools; Sensitivity and Specificity; Signal Transduction; Site; Skin Cancer; Small Business Innovation Research Grant; Surgical Pathology; Technology; Testing; Time; Toxic effect; Toxicity Tests; Toxicology; Translating; Tumor Tissue; Universities; Veterinary Medicine; Work; base; cancer cell; cancer surgery; cancer therapy; cancer type; cost; design; improved; intraoperative imaging; lung cancer screening; malignant breast neoplasm; mathematical model; medical specialties; meetings; mouse model; nanoparticle; neoplastic cell; novel; prevent; programs; public health relevance; research study; sarcoma; screening; tumor

DESCRIPTION (provided by applicant): The overall goal of this application is to evaluate new imaging agents for (1) real-time detection of residual cancer in the tumor bed during surgery in primary colon and lung cancers in mice to eliminate or significantly reduce the need for repeat surgeries and local recurrence, and (2) guiding resection surgeries in canine patients with naturally occurring cancer. In a pilot study, we will also test our imaging technology to improve the detection of lesions during routine colonoscopy examination. Failure to remove cancer cells during surgery is a leading risk factor for local tumor recurrence and subsequent reoperation. Rates of secondary surgeries because of positive margins range between 10-50% depending on cancer type, grade and anatomical site. For colon cancer screening, many small lesions go undetected that are only found after progressing into malignant carcinomas. Furthermore, even for larger carcinomas, colonoscopy using white light will not identify these 22% of the time. Thus, a technology that can assess whether tumor cells have been adequately removed during surgery or can identify colon lesions with higher efficiency will have a major impact on cancer therapy worldwide as more than two million people undergo cancer surgery every year. During the SBIR Phase I work, Lumicell developed several imaging agents by using our novel mathematical model to predict their performance across species. The goal was to develop high-performance, lower cost imaging agents to satisfy the needs for colon cancer screening and eventually skin cancer surgeries. These imaging agents are based upon the design of our lead candidate for sarcoma and breast cancer indications, LUM015, which has been approved by the FDA to start first-in-human clinical trials with our clinical collaborators at Duke University Medical Center. Based upon modifications to LUM015, the new imaging agents cost about 66% less to manufacture with improved yields. After testing them in our baseline mouse model for breast cancer, these new agents proved equal or better performance than LUM015. A lower cost imaging agent is mandatory for entry into several of our new target markets and will be an additional offering for the other markets. For Phase II, we propose in Aims 1 and 2 to evaluate the performance of these imaging agents in state-of-the-art genetically engineered mouse models for lung cancer and colon cancer with our collaborators at Duke University and Massachusetts General Hospital. In Aim 3, we will move forward with the selected lead candidate (based upon results from Aims 1 and 2) into a veterinary clinical trial conducted at Duke/Veterinary Specialty Hospital of the Carolinas and Tufts University Cummings School of Veterinary Medicine. Canine patients suffering from any type of cancer will be recruited to evaluate the performance of the lead candidate in naturally occurring cancers. Aim 4 is focused on reaching the endpoint of this proposal: submit an IND to support a Phase I clinical trial for colon and lung cancer surgeries and colon cancer screening using our new lead candidate.

描述(申请人提供)：本申请的总体目标是评估新的显像剂，用于(1)实时检测手术过程中肿瘤床上残留的癌症，以消除或显著减少再次手术和局部复发的需要，以及(2)指导自然发生癌症的犬患者的切除手术。在一项初步研究中，我们还将测试我们的成像技术，以提高在常规结肠镜检查中对病变的检测。手术中未能清除癌细胞是局部肿瘤复发和随后再次手术的主要风险因素。根据肿瘤类型、分级和解剖部位的不同，切缘阳性的二次手术率在10-50%之间。对于结肠癌筛查，许多小病变没有被发现，只有在发展成恶性肿瘤后才能发现。此外，即使对于较大的癌，使用白光的结肠镜检查也无法在22%的时间内发现这一点。因此，一项能够评估手术中肿瘤细胞是否被充分移除或能够更高效地识别结肠病变的技术将对全球的癌症治疗产生重大影响，因为每年有200多万人接受癌症手术。在SBIR第一阶段的工作中，Lumicell通过使用我们新的数学模型来预测它们的跨物种性能，开发了几种成像剂。其目标是开发高性能、低成本的显像剂，以满足结肠癌筛查以及最终皮肤癌手术的需求。这些显像剂是基于我们的肉瘤和乳腺癌适应症的主要候选药物LUM015的设计，LUM015已被FDA批准与我们在杜克大学医学中心的临床合作者一起开始首个人类临床试验。基于对LUM015的改进，新的成像剂的制造成本降低了约66%，产量有所提高。在我们的乳腺癌基线小鼠模型中测试它们后，这些新的药物被证明与LUM015的性能相同或更好。较低成本的显像剂是进入我们几个新目标市场的必备产品，将是其他市场的额外产品。对于第二阶段，我们在AIMS 1和2中建议与我们在杜克大学和马萨诸塞州总医院的合作者一起，在最先进的肺癌和结肠癌基因工程小鼠模型中评估这些显像剂的性能。在目标3中，我们将与选定的主要候选人(基于目标1和2的结果)一起进入在卡罗莱纳州杜克/兽医专科医院和塔夫茨大学卡明斯兽医学院进行的兽医临床试验。患有任何类型癌症的犬类患者将被招募来评估主要候选者在自然发生癌症方面的表现。AIM 4专注于达到该提案的终点：提交IND以支持结肠癌和肺癌手术的I期临床试验，以及使用我们新的领先候选方案进行结肠癌筛查。