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Intra-arterial cetuximab for the treatment of recurrent unresectable head and neck squamous cell carcinoma

机译:动脉内甲磺酸纤维素用于治疗反复性的不可切除头颈鳞状细胞癌

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Importance: Management of recurrent head and neck squamous cell carcinoma is a common and challenging clinical problem in head and neck oncology. Objective: Here we present the first reported case of super-selective intra-arterial (SSIA) microcatheter based local delivery of cetuximab for head and neck cancer. This technical report describes the techniques used to deliver the SSIA dose of cetuximab, as well as the patient outcome. Design: This technical report is part of an ongoing Phase I Clinical Trial Setting: The New York Head and Neck Institute (NYHNI) is a full-service otolaryngology and neurosurgery department at Lenox Hill Hospital, part of the Northwell Health System. The NYHNI serves a diverse patient population with a wide range of head and neck diseases in a tertiary hospital setting. Intervention: SSIA Cetuximab Participant: A patient presents to our clinic with recurrent unresectable squamous cell carcinoma of the nasopharynx. He is recruited into the first cohort of a phase I clinical trial to assess the safety of SSIA cetuximab, dose starting at 100mg/m2. Adjuvant chemoradiation therapy is also given. Main Outcome(s) and Measures: Safety, as measured by toxicity of SSIA cetuximab. Results: SSIA Cetuximab has been demonstrated to be a safe and feasible procedure in this technical report. Conclusions and Relevance: This case illustrates technical feasibility and a very preliminary assessment of the safety of a novel delivery of a biologic agent for squamous cell carcinoma of the head and neck, which is part of an ongoing phase I clinical trial.
机译:重要性:经常性头部和颈鳞状细胞癌的管理是头部和颈部肿瘤学中的常见而挑战性临床问题。目的:在这里,我们提出了第一个报告的超选择性动脉内(SSIA)微直升基于局部递送的尾癌,用于头部和颈部癌症。本技术报告描述了用于递送SSIA剂量的西妥昔单抗以及患者结果的技术。设计:本技术报告是正在进行的阶段临床试验环境的一部分:纽约头部和颈部研究所(NYHNI)是北京河山医院的一部分耳鼻喉科和神经外科部门,是诺韦尔卫生系统的一部分。 Nyhni在第三节医院环境中提供了多种患者人口,具有各种各样的头部和颈部疾病。干预:SSIA Cetuximab参与者:患者与鼻咽的反复性的不可切除的鳞状细胞癌提供给我们的诊所。他被招募进入第一阶段临床试验的队列,以评估SSIA西汀昔单抗的安全性,以100mg / m 2开始的剂量。还给予佐剂化学疗法。主要结果和措施:安全,含有SSIA Cetuximab的毒性。结果:SSIA Cetuximab已被证明是本技术报告中的安全可行的程序。结论和相关性:这种情况说明了技术可行性和对头部和颈部鳞状细胞癌生物剂的新递送安全性的非常初步的评估,这是临床试验的一部分。

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