Zr-89-labeled Bispecific T-cell Engager AMG 211 PET Shows AMG 211 Accumulation in CD3-rich Tissues and Clear, Heterogeneous Tumor UptakeMoek, K. L., Waaijer, S. J. H., Kok, I. C., Suurs, F. V., Brouwers, A. H., Menke-van der Houven van Oordt, C. W., Wind, T. T., Gietema, J. A., Schröder, C. P., Mahesh, S. V. K., Jorritsma-Smit, A., Lub-de Hooge, M. N., Fehrmann, R. S. N., de Groot, D-J. & de Vries, E. G., 15-Jun-2019, In : Clinical Cancer Research. 25, 12, p. 3517-3527 12 p.
Research output: Contribution to journal › Article › Academic › peer-review
Purpose: Biodistribution of bispecific antibodies in patients is largely unknown. We therefore performed a feasibility study in 9 patients with advanced gastrointestinal adenocarcinomas to explore AMG 211 biodistribution (also known as MEDI-565), an approximately 55 kDa bispecific T-cell engager (BiTE (R)) directed against carcinoembryonic antigen (CEA) on tumor cells and cluster of differentiation 3 (CD3) on T-cells.
Experimental Design: Zr-89-labeled AMG 211 as tracer was administered alone or with cold AMG 211, for PET imaging before and/ or during AMG 211 treatment.
Results: Before AMG 211 treatment, the optimal imaging dose was 200-mg Zr-89-AMG 211 + 1,800-mg cold AMG 211. At 3 hours, the highest blood pool standardized uptake value (SUV) mean was 4.0, and tracer serum half-life was 3.3 hours. CD3-mediated uptake was clearly observed in CD3-rich lymphoid tissues including spleen and bone marrow (SUVmean 3.2 and 1.8, respectively), and the SUVmean decreased more slowly than in other healthy tissues. Zr-89-AMG 211 remained intact in plasma and was excreted predominantly via the kidneys in degraded forms. Of 43 visible tumor lesions, 37 were PET quantifiable, with a SUVmax of 4.0 [interquartile range (IQR) 2.7-4.4] at 3 hours using the optimal imaging dose. The tracer uptake differed between tumor lesions 5-fold within and 9-fold between patients. During AMG 211 treatment, tracer was present in the blood pool, whereas tumor lesions were not visualized, possibly reflecting target saturation.
Conclusions: This first-in-human study shows high, specific Zr-89-AMG 211 accumulation in CD3-rich lymphoid tissues, as well as a clear, inter-and intraindividual heterogeneous tumor uptake.
|Number of pages||12|
|Journal||Clinical Cancer Research|
|Early online date||11-Feb-2019|
|Publication status||Published - 15-Jun-2019|
- NORMAL ORGAN WEIGHTS, II-THE-BRAIN, CARCINOEMBRYONIC ANTIGEN, CLINICAL-PHARMACOLOGY, ANTIBODY CONSTRUCTS, BLINATUMOMAB, EXPRESSION, BITE(R), CANCER, BIODISTRIBUTION