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    Home»Health»Researchers Develop New Approach to Personalized Cancer Treatment
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    Researchers Develop New Approach to Personalized Cancer Treatment

    By Laurie Callahan, Society of Nuclear Medicine and Molecular ImagingMarch 1, 2018No Comments3 Mins Read
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    Researchers Develop New Approach to Personalized Cancer Treatment
    Representative whole-body PET (maximal intensity projection) images of kidneys and spleen 90 minutes post injection of 18F-BMS-986192 only (left) and of 18F-BMS-986192 and co-administration of 1 mg/kg BMS-986192 in the same monkey (center). Representative anti-PD-L1 immunohistochemistry of healthy monkey spleen tissue (right). Credit: D Donnelly et al., Bristol-Myers Squibb Pharmaceutical Research and Development, Princeton, N.J.

    Researchers have developed a same-day, noninvasive positron emission tomography (PET)-based imaging approach to assess PD-L1 positive tumors, and the study is presented in the featured article of The Journal of Nuclear Medicine’s March issue.

    A healthy immune system strikes a delicate balance between eradicating infections and cancers and not overreacting to damage one’s own tissue. Immune checkpoints help control the immune response, but tumors exploit these checkpoint pathways by expressing special proteins that evade antitumor immune responses. One major checkpoint inhibitor pathway is the PD-1 pathway, and its ligand is PD-L1.

    In this study, the PD-L1 ligand, which enables cancer to evade a person’s immune system, has been successfully targeted for the first time with a fluorine-18 (18F)-labeled PD-L1 radioligand. Until now, efforts to predict response to treatments targeting PD-1 or PD-L1 have typically been limited to the evaluation of a single patient biopsy sample.

    “This approach represents an opportunity for physicians to noninvasively assess all of a patient’s tumors for PD-L1 expression with a single PET scan and timely readout,” explains David J. Donnelly, Ph.D., at Bristol-Myers Squibb Research and Development in Princeton, New Jersey. “This may help guide treatment decisions and assess treatment response, to help identify the right treatment for the right patient at the right time and right dose.”

    For the study, an anti-PD-L1 adnectin (an engineered, target-binding protein) was labeled with 18F to generate 18F-BMS-986192, which was then evaluated in mice bearing bilateral PD-L1(-) and PD-L1(+) subcutaneous tumors. 18F-BMS-986192 was also evaluated for distribution, binding, and radiation dosimetry in the healthy cynomolgus monkey. The results of the study demonstrate the feasibility of the approach, and the radiation dosimetry estimates indicate that the tracer is safe to administer in human studies. Clinical studies are now underway to measure PD-L1 expression in human tumors.

    Reference: “Synthesis and Biologic Evaluation of a Novel 18F-Labeled Adnectin as a PET Radioligand for Imaging PD-L1 Expression” by David J. Donnelly, R. Adam Smith, Paul Morin, Daša Lipovšek, Jochem Gokemeijer, Daniel Cohen, Virginie Lafont, Tritin Tran, Erin L. Cole, Martin Wright, Joonyoung Kim, Adrienne Pena, Daniel Kukral, Douglas D. Dischino, Patrick Chow, Jinping Gan, Olufemi Adelakun, Xi-Tao Wang, Kai Cao, David Leung, Samuel J. Bonacorsi and Wendy Hayes, 1 March 2018, Journal of Nuclear Medicine.
    DOI: 10.2967/jnumed.117.199596

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    Cancer Medicine Molecular Biology Society of Nuclear Medicine and Molecular Imaging
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