Intraperitoneale Therapie des Ovarialkarzinoms mit T-Lymphozyten, präinkubiert mit bispezifischen monoklonalen Antikörpern und Interleukin-2

Background Ovarian cancer refractory to chemotherapy has a very poor prognosis and no standard treatment options. In a phase I–II study patients with recurrent disease restricted to the peritoneal cavity received intraperitoneal (i.p.) immunotherapy with interleukin-2 (IL-2) and autologous T-cells redirected by bispecific monoclonal antibodies (bs-MAb). Methods A bs-MAb with on the one hand specificity for ovarian cancer cells (the folate binding site MOv 18) and for the CD3 activation site on T-lymphocytes on the other, was produced in large quantities. Lymphocytes, obtained from the patient prior to debulking surgery, were cultured ex vivo and preincubated with the bs-Mab OC/TR (Ovarian Cancer-T cell Receptor) before i.p. administration. IL-2 was given i.p. every 12 hours at a dose of 600.000 IU. The first 4 days increasing numbers of T-cells were administered (106–109 cells), on days 7–11 and 28–32, 109 redirected T-cells were administered each day. Evaluation for tumor response was done by laparotomy 6 weeks after i.p. treatment. Results 11 patients entered the protocol; 10 were evaluable for toxicity; 3 had extracavitary progression without signs of i.p. progression, but were not explored. Therefore in 7 patients i.p. tumor response was evaluated by laparotomy: i.p. CRs were observed in 2 patients, in 1 however there was concurrent PD in retroperitoneal lymph nodes; furthermore 2PRs, 1 SD and 2 PDs were observed. Toxicity was mild, limited to grade 2 fever, abdominal discomfort, tenderness, bloating, and grade 1–2 nausea. Conclusions Immunotherapy with T-cells redirected by bs-Mabs in ovarian cancer has therapeutic potential and should be explored further.