Fusi Alberto, Procopio Giuseppe, Della Torre Silvia, Ricotta Riccardo, Bianchini Gianpaolo, Salvioni Roberto, Ferrari Leonardo, Martinetti Antonia, Savelli Giordano, Villa Sergio, Bajetta Emilio
Medical Oncology Unit B, National Institute for the Study and the Treatment of Tumors, Milan, Italy.
Tumori. 2004 Nov-Dec;90(6):535-46. doi: 10.1177/030089160409000601.
Prostate cancer represents one of the most important health problems in industrialized countries. It is the second leading cause of cancer-related death in the United States. Therapeutic options are different according to the stage of the disease at the diagnosis. Patients with localized disease may be treated with surgery or radiation, whereas the treatment for patients with a metastatic disease is purely palliative. Hormonal treatment represents the standard therapy for stage IV prostate cancer, but patients ultimately become unresponsive to androgen ablation and are classified as hormone-refractory prostate cancer patients. The molecular mechanisms involved in progression in hormone resistance are characterized by mutations, down and up-regulation in the androgen receptor gene, mutations in p53 and over-expression of Bcl2 and other alterations in genes and in gene expression. The important thing is that we understand these mechanisms to define potential therapeutic agents for the treatment of hormone-refractory prostate cancer patients. Conventional options for patients with hormone-refractory prostate cancer include secondary hormone therapy, radiotherapy and cytotoxic chemotherapy. The commonest antineoplastic agents are mitoxantrone, estramustine and taxanes. Despite an improvement in the palliative benefit, none of these agents has demonstrated a beneficial impact on the overall survival of patients. Therefore, there is no standard therapy for these patients, thus we need new approaches which should be studied in clinical trials. The evaluation and incorporation of new agents into current treatment regimens could have a role in the treatment of hormone-refractory prostate cancer, but their efficacy has not yet been demonstrated.
前列腺癌是工业化国家最重要的健康问题之一。它是美国癌症相关死亡的第二大原因。根据诊断时疾病的阶段,治疗选择有所不同。局限性疾病患者可接受手术或放疗,而转移性疾病患者的治疗则纯属姑息性治疗。激素治疗是IV期前列腺癌的标准疗法,但患者最终会对雄激素剥夺产生耐药性,被归类为激素难治性前列腺癌患者。激素抵抗进展中涉及的分子机制表现为雄激素受体基因的突变、下调和上调、p53突变以及Bcl2过表达和其他基因及基因表达改变。重要的是我们要了解这些机制,以确定治疗激素难治性前列腺癌患者的潜在治疗药物。激素难治性前列腺癌患者的传统治疗选择包括二线激素治疗、放疗和细胞毒性化疗。最常用的抗肿瘤药物是米托蒽醌、雌莫司汀和紫杉烷。尽管姑息治疗效果有所改善,但这些药物均未对患者的总生存期产生有益影响。因此,这些患者没有标准治疗方法,所以我们需要在临床试验中研究新的方法。评估新药物并将其纳入当前治疗方案可能对激素难治性前列腺癌的治疗有作用,但其疗效尚未得到证实。