Department of medical oncology, Centre Oscar Lambret, 3 rue Combemale, 59020 Lille cedex, France.
Crit Rev Oncol Hematol. 2012 Nov;84(2):213-23. doi: 10.1016/j.critrevonc.2012.03.003. Epub 2012 Apr 11.
Carcinomas of unknown primary (CUP) approximately represent 2-3% of all adult cancers. Various clinicopathological subsets of CUP have been identified, which may be treated with tailored approaches. Nevertheless, 80% of CUP do not fall into these subsets. Even when at least 4 prognostic models have been developed and validated in independent patient cohorts, there is no consensus or reliable guidance for estimating the prognosis of these "unfavourable" CUP. Consequently, targeting patients who benefit from palliative chemotherapy is difficult. Thirty-eight phase II trials were published between 1997 and 2011; a systematic analysis of these trials did not allow the recommendation of any of the tested regimens as a standard of care. Currently, there is only one published phase III clinical trial (Paclitaxel/carboplatin/etoposide versus gemcitabine/irinotecan); without significant difference between both regimens. Thus, with the promise of molecular profiling, we are waiting for a large collaborative clinical trial that validates the concept of targeted treatment in this population of patients with "unfavourable" CUP.
原发灶不明的癌(CUP)约占所有成人癌症的 2-3%。已经确定了 CUP 的各种临床病理亚组,这些亚组可以采用针对性的方法进行治疗。然而,80%的 CUP 不属于这些亚组。即使已经在独立的患者队列中开发和验证了至少 4 种预后模型,对于这些“不利”CUP 的预后评估仍没有共识或可靠的指导。因此,很难确定哪些患者可以从姑息化疗中获益。1997 年至 2011 年期间发表了 38 项 II 期临床试验;对这些试验的系统分析不支持任何一种已测试方案作为标准治疗。目前,只有一项发表的 III 期临床试验(紫杉醇/卡铂/依托泊苷与吉西他滨/伊立替康);两种方案之间没有显著差异。因此,随着分子谱分析的出现,我们正在等待一项大型合作临床试验,以验证针对“不利”CUP 患者的靶向治疗这一概念。