作者
Neeta Pandit-Taskar, Michael A Postow, Matthew D Hellmann, James J Harding, Christopher A Barker, Joseph A O’Donoghue, Martha Ziolkowska, Shutian Ruan, Serge K Lyashchenko, Frank Tsai, Michael Farwell, Tara C Mitchell, Ron Korn, William Le, Jason S Lewis, Wolfgang A Weber, Deepak Behera, Ian Wilson, Michael Gordon, Anna M Wu, Jedd D Wolchok
发表日期
2020/4/1
期刊
Journal of Nuclear Medicine
卷号
61
期号
4
页码范围
512-519
出版商
Society of Nuclear Medicine
简介
Immunotherapy is becoming the mainstay for treatment of a variety of malignancies, but only a subset of patients responds to treatment. Tumor-infiltrating CD8-positive (CD8+) T lymphocytes play a central role in antitumor immune responses. Noninvasive imaging of CD8+ T cells may provide new insights into the mechanisms of immunotherapy and potentially predict treatment response. We are studying the safety and utility of 89Zr-IAB22M2C, a radiolabeled minibody against CD8+ T cells, for targeted imaging of CD8+ T cells in patients with cancer.
Methods
The initial dose escalation phase of this first-in-humans prospective study included 6 patients (melanoma, 1; lung, 4; hepatocellular carcinoma, 1). Patients received approximately 111 MBq (3 mCi) of 89Zr-IAB22M2C (at minibody mass doses of 0.2, 0.5, 1.0, 1.5, 5, or 10 mg) as a single dose, followed by PET/CT scans at approximately 1–2, 6–8, 24, 48, and 96 …
引用总数
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