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Sipuleucel-T:抗肿瘤疫苗开发的原型。

Sipuleucel-T: Prototype for development of anti-tumor vaccines.

机构信息

Moffitt Cancer Center and Research Institute, 12902 Magnolia Drive, Tampa, FL 33612, USA.

出版信息

Curr Oncol Rep. 2011 Apr;13(2):112-9. doi: 10.1007/s11912-011-0152-5.

Abstract

Prostate cancer immunotherapy officially debuted with the recent FDA approval of Sipuleucel-T. The novel trend of cancer immunotherapy relies on the identification of particular tumor-associated antigens, like prostatic acid phosphatase (PAP). Sipuleucel-T consists of autologous dendritic cells activated in vitro with recombinant fusion protein PA2024, PAP-linked to granulocyte-macrophage colony-stimulating factor. Sipuleucel-T represents a prototype for the development of cancer vaccines. Preclinical and clinical data as well as landmark studies for the existing narrow chemotherapy alternatives and early immunotherapy trials will be discussed. The pivotal trial demonstrated a 4.1-month difference of median survival, but with no effect on time to progression in asymptomatic or minimally symptomatic metastatic castrate-resistant patients. Several immunologic effects were observed in the treated population, including antibody and T cell-specific activity to P2024 and PAP. With all new therapies the extent of clinical and objective benefits versus encountered limitations should be evaluated. This review highlights the events and decisions in the process of the development of Sipuleucel-T. We discuss how this successful immunotherapy outcome challenges us to use it as a starting point for variations to or try to amplify practical anticancer progress within the antitumor vaccine paradigm.

摘要

前列腺癌免疫疗法随着最近 FDA 批准 Sipuleucel-T 的使用而正式问世。癌症免疫疗法的新趋势依赖于特定肿瘤相关抗原的识别,如前列腺酸性磷酸酶 (PAP)。Sipuleucel-T 由体外激活的自体树突状细胞与重组融合蛋白 PA2024 组成,PAP 与粒细胞-巨噬细胞集落刺激因子相连。Sipuleucel-T 代表了癌症疫苗开发的原型。将讨论临床前和临床数据以及现有的窄化疗替代方案和早期免疫治疗试验的里程碑式研究。关键试验表明,中位生存期差异为 4.1 个月,但对无症状或轻度症状转移性去势抵抗性患者的无进展时间没有影响。在治疗人群中观察到几种免疫效应,包括针对 P2024 和 PAP 的抗体和 T 细胞特异性活性。对于所有新疗法,都应评估临床和客观益处与遇到的局限性之间的程度。这篇综述强调了 Sipuleucel-T 开发过程中的事件和决策。我们讨论了这种成功的免疫治疗结果如何挑战我们将其用作变体的起点,或试图在抗肿瘤疫苗范式内放大实际抗癌进展。

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