Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/33287
Title: PD-L1 PET imaging in patients with NSCLC: Preliminary results of the ImmunoPET Phase 0 study.
Austin Authors: Hegi-Johnson, Fiona;Rudd, Stacey E;Wichmann, Christian W;Akhurst, Tim;Roselt, Peter;Sursock, Sandra;Trinh, Jenny;John, Thomas ;Devereux, Lisa;Donnelly, Paul S;Hicks, Rodney J;Scott, Andrew M ;Steinfort, Daniel;Fox, Stephen;Blyth, Benjamin;Parakh, Sagun ;Hanna, Gerard G;Callahan, Jason;Burbury, Kate;MacManus, Michael
Affiliation: Radiation Oncology, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.
School of Chemistry and Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, Melbourne, Victoria, Australia.
Olivia Newton-John Cancer Research Institute
Sir Peter MacCallum Department of Oncology, The University of Melbourne, Melbourne, Victoria, Australia; Cancer Imaging, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.
Cancer Imaging, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.
Sir Peter MacCallum Department of Oncology, The University of Melbourne, Melbourne, Victoria, Australia.
Radiation Oncology, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.
Sir Peter MacCallum Department of Oncology, The University of Melbourne, Melbourne, Victoria, Australia; The Department of Medicine, St Vincent's Medical School, University of Melbourne, Melbourne, Victoria, Australia.
School of Chemistry and Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, Melbourne, Victoria, Australia.
The Department of Medicine, St Vincent's Medical School, University of Melbourne, Melbourne, Victoria, Australia; The Department of Medicine, Central Medical School, the Alfred Hospital, Monash University, Melbourne, Victoria, Australia.
Olivia Newton-John Cancer Research Institute, Melbourne, Victoria, Australia; School of Cancer Medicine, La Trobe University, Melbourne, Victoria, Australia; Department of Molecular Imaging and Therapy, Austin Health, and The University of Melbourne, Melbourne, Victoria, Australia.
Sir Peter MacCallum Department of Oncology, The University of Melbourne, Melbourne, Victoria, Australia; Anatomical Pathology, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.
School of Cancer Medicine, La Trobe University, Melbourne, Victoria, Australia.
Molecular Imaging and Therapeutic Nuclear Medicine, Cancer Imaging, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.
Haematology, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.
Issue Date: 1-Nov-2023
Date: 2023
Publication information: International Journal of Radiation Oncology, Biology, Physics 2023-11-01; 117(3)
Abstract: ImmunoPET is a multicenter, single arm, phase 0-1 study of 89Zr-DFO-Sq-durvalumab (89Zr-durvalumab), a novel PET tracer, designed to interrogate the expression of PD-L1 in patients with NSCLC. Clinically relevant findings from phase 0 are presented here. Phase 0 was designed to investigate tracer biodistribution and safety in patients with metastatic NSCLC with PD-L1 expression >25%. After 60MBq/70kg 89Zr-durvalumab infusion, PET/CT images were acquired at days 0, 1, 3 or 5 ± 24h. Baseline FDG PET/CT was performed prior to PD-L1 PET imaging. All five patients recruited to phase 0 completed the full imaging protocol. The only reported adverse event was a transient asymptomatic increase in respiratory rate. At the time of PD-L1 imaging, two patients were in complete remission on FDG-PET after treatment with osimertinib and pembrolizumab; neither showed PD-L1 tracer uptake in previous tumor sites. All three patients with active tumor had received radiotherapy to some or all disease sites prior to PD-L1 imaging. With the exception of a single disease site, specific uptake of 89Zr-durvalumab uptake was seen in tumours, with increasing uptake in tumor seen up to Day 5 post-injection. Patient 1, who had multiple metastases, including brain and bone, showed more intense 89Zr-durvalumab uptake in recently irradiated bone lesions than un-irradiated lesions and uptake was also observed in treated brain metastases.. One patient, who experienced rapid growth of a single lung lesion that had acquired resistance to pembrolizumab, showed no significant 89Zr-durvalumab in that lesion, despite recent radiotherapy. In patient 5, 89Zr-durvalumab uptake was observed in the viable rim of a large, recently irradiated adrenal oligometastasis. 89Zr- durvalumab imaging was safe and detected known viable tumor at multiple sites. Recently irradiated tumours showed the highest uptake and in another, a single site of immunotherapy resistant disease showed minimal tracer uptake. PD-L1 imaging may have utility in patients with NSCLC treated with radiotherapy.
URI: https://ahro.austin.org.au/austinjspui/handle/1/33287
DOI: 10.1016/j.ijrobp.2023.05.019
ORCID: 
Journal: International Journal of Radiation Oncology, Biology, Physics
PubMed URL: 37406824
ISSN: 1879-355X
Type: Journal Article
Appears in Collections:Journal articles

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