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Toll样受体配体CB101联合低分割放射治疗犬头颈癌的安全性和可行性的初步评估:一项试点研究。

Preliminary evaluation of the safety and feasibility of toll-like receptor ligand CB101 combined with hypofractionated radiation therapy in canine head and neck cancer: a pilot study.

作者信息

Ghanian Audrey, DiBona June, Duda Lili, Xu Xiaowei, Lukens John Nicholas, Pearce Tillman, Ehrhardt Michael, Rook Alain, Durham Amy, Maity Amit, Flesner Brian

机构信息

University of Pennsylvania, Philadelphia, USA.

Curebiotech, Inc. Philadelphia, Philadelphia, PA, USA.

出版信息

Vet Oncol. 2025;2(1):18. doi: 10.1186/s44356-025-00031-6. Epub 2025 Aug 4.

Abstract

Radiation therapy (RT) is a common treatment modality for dogs with locally advanced head and neck tumors. Most dogs experience a clinical benefit secondary to RT, however, long term remissions are rare. This study evaluates the feasibility and safety profile of intratumoral CBC101 (a proprietary hydrogel-based injectable resiquimod formulation), a toll-like receptor (TLR) 7/8 agonist with immunomodulatory properties, when used in combination with radiation therapy. Three dogs with histologically confirmed head/neck cancers were prospectively enrolled. A baseline CT scan was performed. Dogs received palliative radiation therapy (8 Gy × 4) in conjunction with intratumoral CB101. A follow-up CT scan was performed at week 12 to assess tumor response and to evaluate for metastatic disease. Intratumoral CB101 was well-tolerated, feasible, and produced minimal adverse effects. Only one grade 1 adverse event was attributable to CB101; all other adverse events were expected radiation therapy side effects. The data obtained from this preliminary study will be used for further investigation into appropriate dosing and timing of intratumoral resiquimod or other TLRs, with eventual escalation into phase II and III clinical trials.

摘要

放射治疗(RT)是局部晚期头颈肿瘤犬的常见治疗方式。大多数犬因放疗获得临床益处,然而,长期缓解罕见。本研究评估了瘤内注射CBC101(一种基于水凝胶的可注射瑞喹莫德专利制剂)联合放射治疗时的可行性和安全性,CBC101是一种具有免疫调节特性的Toll样受体(TLR)7/8激动剂。前瞻性纳入了3只经组织学确诊的头颈癌犬。进行了基线CT扫描。犬接受姑息性放射治疗(8 Gy×4)联合瘤内注射CB101。在第12周进行随访CT扫描以评估肿瘤反应并评估是否有转移性疾病。瘤内注射CB101耐受性良好、可行且产生的不良反应最小。仅1例1级不良事件归因于CB101;所有其他不良事件均为预期的放疗副作用。从这项初步研究中获得的数据将用于进一步研究瘤内瑞喹莫德或其他TLR的合适剂量和给药时间,并最终逐步开展II期和III期临床试验。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c1e/12318883/838adff3e86c/44356_2025_31_Fig1_HTML.jpg

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