How to obtain the image‑derived blood concentration from 89Zr‑immuno‑PET scans

ABSTRACT

Background

PET scans using zirconium-89 labelled monoclonal antibodies (⁸⁹Zr-mAbs), known as ⁸⁹Zr-immuno-PET, are made to measure uptake in tumour and organ tissue. Uptake is related to the supply of ⁸⁹Zr-mAbs in the blood. Measuring activity concentrations in blood, however, requires invasive blood sampling. This study aims to identify the best delineation strategy to obtain the image-derived blood concentration (IDBC) from ⁸⁹Zr-immuno-PET scans.

Methods

PET imaging and blood sampling of two ⁸⁹Zr-mAbs were included, ⁸⁹Zr-cetuximab and ⁸⁹Zr-durvalumab. For seven patients receiving ⁸⁹Zr-cetuximab, PET scans on 1-2 h, 2 and 6 days post-injection (p.i.) were analysed. Five patients received three injections of ⁸⁹Zr-durvalumab. The scanning protocol for the first two injections consisted of PET scanning on 2, 5 and 7 days p.i. and for the third injection only on 7 days p.i. Blood samples were drawn with every PET scan and the sample-derived blood concentration (SDBC) was used as gold standard for the IDBC. According to an in-house developed standard operating procedure, the aortic arch, ascending aorta, descending aorta and left ventricle were delineated. Bland-Altman analyses were performed to assess the bias (mean difference) and variability (1.96 times the standard deviation of the differences) between IDBC and SDBC.

Results

Overall, the activity concentration obtained from the IDBC was lower than from the SDBC. When comparing IDBC with SDBC, variability was smallest for the ascending aorta (20.3% and 17.0% for ⁸⁹Zr-cetuximab and ⁸⁹Zr-durvalumab, respectively). Variability for the other regions ranged between 17.9 and 30.8%. Bias for the ascending aorta was – 10.9% and – 11.4% for ⁸⁹Zr-cetuximab and ⁸⁹Zr-durvalumab, respectively.

Conclusion

Authors

Wijngaarden, Jessica E.; Ahbari, Amina; Pouw, Johanna E.E.; Greuter, Henri N.J.M.; Bahce, Idris; Zwezerijnen, Gerben J.C.; Vugts, Danielle J.; van Dongen, Guus A.M.S.; Boellaard, Ronald; Menke-van der Houven van Oordt, C. Willemien; Huisman, Marc C.