Nanoreporter PET predicts the efficacy of anti-cancer nanotherapy

The application of nanoparticle drug formulations, such as nanoliposomal doxorubicin (Doxil), is increasingly integrated in clinical cancer care. Despite nanomedicine’s remarkable potential and growth over the last three decades, its clinical benefits for cancer patients vary. Here we report a non-i...

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Published inNature communications Vol. 7; no. 1; pp. 11838 - 8
Main Authors Pérez-Medina, Carlos, Abdel-Atti, Dalya, Tang, Jun, Zhao, Yiming, Fayad, Zahi A., Lewis, Jason S., Mulder, Willem J. M., Reiner, Thomas
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 20.06.2016
Nature Publishing Group
Nature Portfolio
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Summary:The application of nanoparticle drug formulations, such as nanoliposomal doxorubicin (Doxil), is increasingly integrated in clinical cancer care. Despite nanomedicine’s remarkable potential and growth over the last three decades, its clinical benefits for cancer patients vary. Here we report a non-invasive quantitative positron emission tomography (PET) nanoreporter technology that is predictive of therapeutic outcome in individual subjects. In a breast cancer mouse model, we demonstrate that co-injecting Doxil and a Zirconium-89 nanoreporter ( 89 Zr-NRep) allows precise doxorubicin (DOX) quantification. Importantly, 89 Zr-NRep uptake also correlates with other types of nanoparticles’ tumour accumulation. 89 Zr-NRep PET imaging reveals remarkable accumulation heterogeneity independent of tumour size. We subsequently demonstrate that mice with >25 mg kg −1 DOX accumulation in tumours had significantly better growth inhibition and enhanced survival. This non-invasive imaging tool may be developed into a robust inclusion criterion for patients amenable to nanotherapy. Nanoparticle drug formulations are currently used as cancer treatment but the response in patients is highly variable. Here, the authors developed a Zirconium-89 nanoreporter able to predict using PET, therapeutic accumulation and efficacy of anti-cancer nanoparticle drug formulations when co-injected in a murine breast cancer model.
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ISSN:2041-1723
2041-1723
DOI:10.1038/ncomms11838