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Vaccination of Patients with Advanced Ovarian Carcinoma with the Anti-Idiotype ACA125

Immunological Response and Survival (Phase Ib/II)

¹ Center of Obstetrics and Gynecology, University of Marburg, Marburg, Germany; ² CellControl Biomedical Laboratories AG, Martinsried, Germany; ³ Center of Obstetrics and Gynecology, University of Tuebingen, Tuebingen, Germany; ⁴ Städtische Kliniken Frankfurt a.M./Höchst, Frauenklinik, Frankfurt, Germany; ⁵ Center of Obstetrics and Gynecology, University of Ulm, Ulm, Germany; ⁶ Dr. Horst-Schmidt-Kliniken Wiesbaden, Department for Gynecology, Wiesbaden, Germany; and ⁷ Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, New York

ABSTRACT

Purpose: A Phase I/IIb multicenter study was conducted to evaluate the safety and immunogenicity of the anti-idiotypic antibody vaccine ACA125 that functionally imitates the tumor antigen CA125 in 119 patients with advanced ovarian carcinoma. A preliminary report on the initial 42 patients demonstrated safety and immunogenicity.

Experimental Design: Using the complete intention-to-treat population (n = 119) who received a mean of 9.7 ACA125 applications, survival was analyzed with respect to immunological responses.

Results: In 81 patients (68.1%), a specific anti-anti-idiotypic antibody (Ab3) response could be induced. Additionally, the development of CA125-specific antibodies (Ab1') and antibody-dependent cell-mediated cytotoxicity of CA125-positive tumor cells was observed in 50.4% and 26.9% of patients, respectively. The median survival of all patients was 19.4 months (range, 0.5–56.1 months). Ab3-positive patients showed a significantly longer survival (median, 23.4 months; P < 0.0001) as compared with Ab3-negative patients (median, 4.9 months). A positive Ab3 response remained associated with longer survival when controlling for other prognostic factors including FIGO (International Federation of Gynecologists and Obstetricians) stage, response to and type of first-line chemotherapy, number of previous treatments, or concomitant antitumor therapy. With regard to safety, repeated vaccination was well tolerated. No serious adverse events related to the application of ACA125 occurred.

Conclusions: Although the uncontrolled design of this study prevents definitive conclusions with respect to subgroups, the data support a relationship between Ab3 response and survival time. Thus, the need for further randomized, controlled clinical trials to establish efficacy of the vaccine ACA125 seems to be indicated.

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