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Intraperitoneal bispecific antibody (HEA125xOKT3) therapy inhibits malignant ascites production in advanced ovarian carcinoma
Author(s) -
Marmé Alexander,
Strauß Gudrun,
Bastert Gunther,
Grischke EvaMaria,
Moldenhauer Gerhard
Publication year - 2002
Publication title -
international journal of cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.475
H-Index - 234
eISSN - 1097-0215
pISSN - 0020-7136
DOI - 10.1002/ijc.10562
Subject(s) - ascites , medicine , ovarian carcinoma , chemotherapy , carcinoma , antibody , ovarian cancer , peritoneal cavity , gastroenterology , cancer research , immunology , cancer , surgery
Abstract Bispecific antibody HEA125xOKT3 was shown to redirect T lymphocytes toward carcinoma cells and to induce tumor cell lysis in vitro . Preclinical studies have demonstrated that tumor‐associated lymphocytes (TAL) derived from malignant ascites can be used as effector cells with a high efficacy and without prior stimulation. These data provided the rationale for a clinical trial to investigate whether bsAb HEA125xOKT3 is also able to induce tumor cell lysis in vivo and can be used for local treatment of malignant ascites arising from ovarian carcinoma. Ten ovarian carcinoma patients presenting with malignant ascites resistant to chemotherapy were enrolled in the study. They received weekly intraperitoneal injections of 1 mg bsAb diluted in 500 ml NaCl solution to allow homogeneous antibody distribution within the peritoneal cavity. All patients responded clinically well to the therapy. Eight patients experienced a complete and 2 patients a partial reduction of ascites production. A decrease or stabilization of tumor marker CA125 was detected in the sera of 8 patients. Only WHO Grade I and II toxicity was observed including mild fever, chills and allergic eczema. Thus, intraperitoneal application of bsAb HEA125xOKT3 appears to be an easy and cost effective palliative treatment for ovarian carcinoma with recurrent ascites that leads to a substantially increased quality of life for the patients. During therapy TNF‐α concentrations raised markedly in the ascites fluid whereas VEGF and sFLT‐1 ascites levels declined. This indicates that not only T cell‐mediated tumor cell lysis but also changes in vascular permeability due to downregulation of VEGF and its receptors might be responsible for the beneficial therapeutic effect. © 2002 Wiley‐Liss, Inc.