Tumor Regression in Cancer Patients by Very Low Doses of a T Cell–Engaging Antibody

Ralf C. Bargou(Universität Ulm), Eugen Leo(Universität Ulm), Gerhard Zugmaier(Universität Ulm), Matthias Klinger(Universität Ulm), Mariele Goebeler(Universität Ulm), Stefan Knop(Universität Ulm), Richard Noppeney(Universität Ulm), Andreas Viardot(Universität Ulm), Georg Heß(Universität Ulm), Martin Schüler(Universität Ulm), Hermann Einsele(Universität Ulm), Christian Brandl(Universität Ulm), Andreas Wolf(Universität Ulm), Petra Kirchinger(Universität Ulm), Petra Klappers(Universität Ulm), Margit Schmidt(Universität Ulm), Gert Riethmüller(Universität Ulm), Carsten Reinhardt(Universität Ulm), Patrick A. Baeuerle(Universität Ulm), Peter Kufer(Universität Ulm)
Science
August 14, 2008
Cited by 1,073

Abstract

Previous attempts have shown the potential of T cells in immunotherapy of cancer. Here, we report on the clinical activity of a bispecific antibody construct called blinatumomab, which has the potential to engage all cytotoxic T cells in patients for lysis of cancer cells. Doses as low as 0.005 milligrams per square meter per day in non-Hodgkin's lymphoma patients led to an elimination of target cells in blood. Partial and complete tumor regressions were first observed at a dose level of 0.015 milligrams, and all seven patients treated at a dose level of 0.06 milligrams experienced a tumor regression. Blinatumomab also led to clearance of tumor cells from bone marrow and liver. T cell-engaging antibodies appear to have therapeutic potential for the treatment of malignant diseases.


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