Simons Jonathan W, Sacks Natalie
Winship Cancer Institute, Emory University, Atlanta, GA 30322, USA.
Urol Oncol. 2006 Sep-Oct;24(5):419-24. doi: 10.1016/j.urolonc.2005.08.021.
New approaches to therapeutics of advanced prostate cancer are urgently needed. GVAX (granulocyte-macrophage colony-stimulating factor [GM-CSF] gene transduced irradiated prostate cancer vaccine cells) offers the possibility that "host versus prostate cancer" immune responses can be generated in prostate cancer patients. Critical components involve the dendritic cell loading of candidate prostate cancer lymph node metastasis and candidate bone metastasis antigens derived from irradiated prostate cancer whole cells. GM-CSF acts at the vaccination site to enhance activation dendritic cells and antigen presentation to both the B-cell and T-cell arms of the immune system. GVAX preclinically-in both rat and transgenic prostate cancer models-has antitumor activity which has informed early clinical trial designs. Clinical investigations reviewed in this report suggest that vaccination is safe and immune tolerance can be broken against prostate cancer. Multi-institutional phase III investigation is currently underway to evaluate the impact of allogeneic prostate GVAX cellular immunotherapy on time to progression and overall survival in hormone refractory prostate cancer.
迫切需要针对晚期前列腺癌的新治疗方法。GVAX(粒细胞巨噬细胞集落刺激因子[GM-CSF]基因转导的经照射的前列腺癌疫苗细胞)为在前列腺癌患者中产生“宿主抗前列腺癌”免疫反应提供了可能性。关键组成部分包括用源自经照射的前列腺癌全细胞的候选前列腺癌淋巴结转移抗原和候选骨转移抗原负载树突状细胞。GM-CSF在疫苗接种部位起作用,以增强树突状细胞的活化以及向免疫系统的B细胞和T细胞分支呈递抗原。在大鼠和转基因前列腺癌模型的临床前研究中,GVAX均具有抗肿瘤活性,这为早期临床试验设计提供了依据。本报告中综述的临床研究表明,接种疫苗是安全的,并且可以打破对前列腺癌的免疫耐受。目前正在进行多机构III期研究,以评估异体前列腺GVAX细胞免疫疗法对激素难治性前列腺癌进展时间和总生存期的影响。