Shibata Hiroyuki
Dept. of Clinical Oncology, IDAC, Tohoku University, Japan.
Gan To Kagaku Ryoho. 2009 Jun;36(6):918-22.
Cancer of unknown primary(CUP)is a malignant disease with metastases such as lymph nodes, lung or liver metastasis, and without an identified primary site. CUP constitutes 5% of all human malignant diseases. CUPs are divided into two sub-groups, favorable and unfavorable, based on their clinical output. In the unfavorable group, platinumbased CUPs or those combined with taxane regimens have been examined in phase II trials and practically conducted with high frequency. However, no standard regimens have thus far been established. Chemotherapy based on the primary site is not applicable for the treatment of CUP. It is very difficult to apply any regimens without information on the primary sites. To resolve this problem, molecular diagnostic technologies using a gene expression profiling platform to identify the primary site of CUP are now applied. Primary site-dependent chemotherapy could be conducted in accordance with the result of the molecular diagnosis of the primary site. On the other hand, the idea that the unfavorable group is an independent entity of malignancy is supported. The unfavorable CUPs might have a common molecular mechanism. Identification of the underlying mechanism that is specific to the unfavorable CUP may be a clue to develop a novel treatment for CUP.
原发灶不明的癌症(CUP)是一种恶性疾病,伴有淋巴结、肺或肝转移等转移灶,且原发部位未明确。CUP占所有人类恶性疾病的5%。根据临床结果,CUP分为两个亚组,预后良好组和预后不良组。在预后不良组中,铂类CUP或联合紫杉烷方案的CUP已在II期试验中进行研究,并在实际应用中具有较高的频率。然而,迄今为止尚未建立标准方案。基于原发部位的化疗不适用于CUP的治疗。在没有原发部位信息的情况下应用任何方案都非常困难。为了解决这个问题,现在应用了使用基因表达谱平台来识别CUP原发部位的分子诊断技术。可以根据原发部位的分子诊断结果进行基于原发部位的化疗。另一方面,预后不良组是一个独立的恶性实体这一观点得到了支持。预后不良的CUP可能有共同的分子机制。识别预后不良CUP特有的潜在机制可能是开发CUP新疗法的线索。