## Abstract ## Background. Treatment of head and neck squamous cell carcinoma (HNSCC) addresses the primary tumor and the lymphatic drainage. Modalities for the neck are neck dissection and/or radiation therapy. In most cases, the neck is treated by the modality that seems more appropriate for the
Radioimmunotherapy in patients with head and neck squamous cell carcinoma: Initial experience
β Scribed by David R. Colnot; Jasper J. Quak; Jan C. Roos; Remco de Bree; Abraham J. Wilhelm; Gordon B. Snow; Guus A. M. S. van Dongen
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- English
- Weight
- 186 KB
- Volume
- 23
- Category
- Article
- ISSN
- 1043-3074
- DOI
- 10.1002/hed.1078
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
Background
Despite improvements in locoregional treatment of stages III/IV squamous cell carcinoma of the head and neck (HNSCC), local and distant failure rates remain high. An effective adjuvant therapy is required for these patients. Among novel approaches is radioimmunotherapy, in which monoclonal antibodies (MAbs) are used for selective delivery of radiation to tumor cells.
Methods
The suitability of ^186^Reβlabeled chimeric MAb U36 (^186^ReβcMAb U36) for radioimmunotherapy was evaluated in a phase I study, with radiation dose escalating steps of 11, 27, and 41 mCi/m^2^. Tumor targeting was monitored with a gamma camera, and the maximum tolerated dose was established in 13 patients with recurrent or metastatic disease.
Results
Administrations were well tolerated, and excellent targeting of tumor lesions was seen. Myelotoxicity was the only toxicity observed, resulting in doseβlimiting toxicity in two patients treated with 41 mCi/m^2^. The MTD was established at 27 mCi/m^2^. A marked reduction in tumor size was observed in two patients, another showed stable disease for 6 months.
Conclusions
Radioimmunotherapy with ^186^ReβcMAb U36 seems to be well tolerated, with bone marrow being the doseβlimiting organ. The observation of antitumor effects is encouraging for further development of radioimmunotherapy for HNSCC. Β© 2001 John Wiley & Sons, Inc. Head Neck 23: 559β565, 2001.
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