Niaz Muhammad O, Sun Michael, Ramirez-Fort Marigdalia K, Niaz Muhammad J
Internal Medicine, Sharif Medical City Hospital, Lahore, PAK.
Internal Medicine, Weill Cornell Medicine, New York, USA.
Cureus. 2020 Feb 26;12(2):e7107. doi: 10.7759/cureus.7107.
Prostate cancer is the most common non-cutaneous cancer in men in the United States and is the second most common cause of cancer deaths after lung cancer in men. Despite all advances in the field of prostate cancer imaging and treatment, currently, it is sub-optimally responsive to all available treatment options. Radioimmunotherapy with a monoclonal antibody (mAb), J591, has shown promising results in the treatment of prostate cancer. J591 is a deimmunized mAb that targets the extracellular domain of prostate-specific membrane antigen (PSMA), a surface-bound and internalizing glycoprotein that is upregulated in prostate cancer. Phase I/II clinical trials have shown accurate tumor targeting, biochemical and radiographic responses, and increased overall survival in patients with mCRPC with tolerable, predictable, and reversible myelotoxicity. Ongoing studies focus on improving the therapeutic index of radiolabeled J591. Herein, the literature on published clinical trials involving therapeutic J591 conjugated to b-emitter, lutetium-177 for mCRPC, is sequentially reviewed.
前列腺癌是美国男性中最常见的非皮肤癌,也是男性癌症死亡的第二大常见原因,仅次于肺癌。尽管前列腺癌成像和治疗领域取得了所有进展,但目前,它对所有可用治疗方案的反应都不尽人意。用单克隆抗体(mAb)J591进行放射免疫治疗在前列腺癌治疗中已显示出有前景的结果。J591是一种去免疫的单克隆抗体,靶向前列腺特异性膜抗原(PSMA)的细胞外结构域,PSMA是一种表面结合且可内化的糖蛋白,在前列腺癌中上调。I/II期临床试验已显示在mCRPC患者中肿瘤靶向准确、有生化和影像学反应,以及总生存期延长,且有可耐受、可预测和可逆的骨髓毒性。正在进行的研究集中于提高放射性标记J591的治疗指数。在此,对已发表的涉及用于mCRPC的与β发射体镥-177偶联的治疗性J591的临床试验文献进行了顺序回顾。