Department of Oncology, Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins University, 1650 Orleans Street, Baltimore, MD 21231, USA.
Curr Opin Urol. 2010 May;20(3):241-6. doi: 10.1097/MOU.0b013e3283381793.
Considerable progress has been made in prostate cancer immunotherapy over the last year, and two agents have completed phase III testing. This review will discuss the most promising immune-directed strategies in development for prostate cancer, outlining interventions that mitigate tumor-induced tolerance and highlighting several combination immunotherapy approaches.
A pivotal phase III study using Sipuleucel-T, an autologous prostatic acid phosphatase (PAP)-loaded dendritic cell immunotherapy, in men with metastatic castration-resistant prostate cancer (CRPC) demonstrated a survival advantage over placebo. By contrast, two phase III studies of GVAX, an allogeneic tumor cell vaccine, in a similar patient population failed to show a survival benefit of GVAX or GVAX/docetaxel over standard docetaxel/prednisone. Other strategies currently in clinical development include the ProstVac poxviral vaccine, a PAP-encoding DNA vaccine, and immune checkpoint inhibitory approaches.
Although Sipuleucel-T may receive FDA approval for patients with metastatic CRPC, challenges remain in identifying immunotherapy strategies that overcome immune tolerance, especially when disease burden is substantial. An emerging paradigm focuses on using immunotherapy together with checkpoint antagonists or in combination with conventional therapies in patients with early-stage disease. Such approaches are likely to yield optimal results, but must carefully be explored in well designed phase II studies before moving forward.
过去一年,前列腺癌免疫疗法取得了重大进展,有两种药物已完成 III 期临床试验。本文将讨论目前开发中最有前途的免疫靶向策略,概述减轻肿瘤诱导免疫耐受的干预措施,并强调几种联合免疫治疗方法。
一项使用前列腺酸性磷酸酶(PAP)负载树突状细胞免疫疗法 Sipuleucel-T 的关键 III 期研究表明,与安慰剂相比,转移性去势抵抗性前列腺癌(CRPC)患者的生存时间有优势。相比之下,两项针对同种异体肿瘤细胞疫苗 GVAX 的 III 期研究未能显示 GVAX 或 GVAX/多西他赛比标准多西他赛/泼尼松更能改善生存时间。目前处于临床开发阶段的其他策略包括 ProstVac 痘病毒疫苗、PAP 编码 DNA 疫苗和免疫检查点抑制方法。
虽然 Sipuleucel-T 可能会获得 FDA 批准用于转移性 CRPC 患者,但在识别克服免疫耐受的免疫疗法策略方面仍存在挑战,尤其是在疾病负担较大的情况下。一个新出现的范例侧重于将免疫疗法与检查点拮抗剂联合使用,或在早期疾病患者中与常规疗法联合使用。这些方法可能会产生最佳结果,但必须在进一步推进之前,通过精心设计的 II 期研究进行仔细探索。