Italiano Antoine
Department of Medical Oncology, Centre Régional de Lutte contre le Cancer Antoine Lacassagne, Canceropôle PACA, Nice, France.
Oncology. 2006;70(3):161-7. doi: 10.1159/000093092. Epub 2006 May 3.
Colorectal cancer (CRC) is the second leading cause of cancer death in the western world. Even with the significant improvement in traditional chemotherapy, there remain limitations with this treatment. One of the most promising new targets in the treatment of CRC is the epithelial growth factor receptor (EGFR). Agents that inhibit the EGFR have demonstrated clinical activity as single agents and in combination with chemotherapy and the most promising of these agents is cetuximab, which blocks the binding of EGF and transforming growth factor-alpha (TGF-alpha) to EGFR. Thus, the finding that monoclonal antibodies against EGFR caused a response in patients, and reversed resistance to chemotherapy, was exciting news. However, expression of EGFR did not correlate with clinical benefit. Clearly, the search for markers of response to treatment against EGFR must go on.
在西方世界,结直肠癌(CRC)是癌症死亡的第二大主要原因。即使传统化疗有了显著改善,但这种治疗仍存在局限性。治疗CRC最有前景的新靶点之一是表皮生长因子受体(EGFR)。抑制EGFR的药物已显示出作为单一药物以及与化疗联合使用时的临床活性,其中最有前景的药物是西妥昔单抗,它可阻断表皮生长因子(EGF)和转化生长因子-α(TGF-α)与EGFR的结合。因此,抗EGFR单克隆抗体在患者中引起反应并逆转化疗耐药性这一发现是令人振奋的消息。然而,EGFR的表达与临床获益并无关联。显然,针对EGFR治疗反应标志物的探索必须继续。