Phase I trial with the CD44v6-targeting immunoconjugate bivatuzumab mertansine in head and neck squamous cell carcinoma

• Published in: Oral oncology 2008-09, Vol.44 (9), p.823-829
• Main Authors: Riechelmann, Herbert, Sauter, Alexander, Golze, Wolfram, Hanft, Gertraud, Schroen, Carsten, Hoermann, Karl, Erhardt, Thomas, Gronau, Silke
• Format: Article
• Language: English
• Subjects: Aged; Antibodies; Antibodies, Monoclonal - administration & dosage; Antibodies, Monoclonal - adverse effects; Antibodies, Monoclonal, Humanized; Biological and medical sciences; Carcinoma, Squamous Cell - complications; Carcinoma, Squamous Cell - drug therapy; Carcinoma, Squamous Cell - immunology; Clinical trials; Dose-Response Relationship, Drug; Female; Head and neck neoplasms; Head and Neck Neoplasms - complications; Head and Neck Neoplasms - drug therapy; Head and Neck Neoplasms - immunology; Hematology, Oncology and Palliative Medicine; Humans; Hyaluronan Receptors - immunology; Immunoconjugates - administration & dosage; Immunoconjugates - adverse effects; Immunomodulators; Infusions, Intravenous; Male; Maximum Tolerated Dose; Maytansine; Maytansine - administration & dosage; Maytansine - adverse effects; Maytansine - analogs & derivatives; Medical sciences; Middle Aged; neoplasm; Otolaryngology; Otorhinolaryngology (head neck, general aspects and miscellaneous); Otorhinolaryngology. Stomatology; Patient Selection; Pharmacology. Drug treatments; Treatment Outcome; Tumors
• ISSN: 1368-8375; 1879-0593
• DOI: 10.1016/j.oraloncology.2007.10.009

Summary CD44v6 is a tumor associated antigen abundantly expressed in head and neck squamous cell carcinomas (HNSCC) and in normal squamous epithelium. The immunoconjugate bivatuzumab mertansine (BIWI 1) consists of a highly potent antimicrotubule agent coupled to a monoclonal antibody against CD44v6. The maximum tolerated dose (MTD), safety and efficacy of BIWI 1 administered IV in patients with HNSCC has not been determined. In a clinical phase I trial, adult patients with recurrent or metastatic HNSCC were treated intravenously with BIWI 1. Starting with 25 mg/m2 , the dose was escalated in steps of 25 mg/m2 until dose limiting toxicity was observed. Six women and 25 men were included. The MTD was 300 mg/m2 . Twelve patients were treated with at least the MTD. The principal toxic effects were maculopapular rashes, focal blister formation and skin exfoliation. Three patients had partial responses at doses of 200, 275 and 325 mg/m2 . The concept that bivatuzumab can direct mertansine activity to CD44v6 expressing tumors was confirmed. Although CD44v6 was abundantly expressed in all tumors, the response to BIWI 1 was variable. Binding to CD44v6 on skin keratinocytes mediated serious skin toxicity with a fatal outcome in a parallel trial, which led to the termination of the development program of bivatuzumab mertansine and the present study.