Leroy Xavier, Edeline Julien, Rioux-Leclercq Nathalie
Pôle de pathologie, CHRU, Lille cedex, France.
Ann Pathol. 2011 Dec;31(6):466-71. doi: 10.1016/j.annpat.2011.10.004. Epub 2011 Nov 29.
The medical treatment of renal-cell carcinoma, and of its most frequent histologic subtype, the clear cell renal-cell carcinoma, has been changed by the emergence of targeted therapies. The development of these drugs has been made possible by more precise knowledge of molecular mechanisms involved in the carcinogenesis of these tumors. Three molecular pathways may be involved in clear cell renal-cell carcinoma: VHL/HIF/VEGF, PI3K/AKT/mTOR and MAPKinases pathways. These antiangiogenic therapies are approved for the treatment of advanced and metastatic clear cell renal-cell carcinoma. In metastatic disease, pathologists have significant and different implications: 1) in tumor biopsy, only the diagnosis of clear cell renal-cell carcinoma implies the prescription of antiangiogenic drugs, and 2) after targeted therapies, pathologists must evaluate the therapeutic effects on tumor. Consensus on macroscopic and histologic reports are needed by pathologists.
靶向治疗的出现改变了肾细胞癌及其最常见的组织学亚型——透明细胞肾细胞癌的医学治疗方式。对这些肿瘤致癌过程中所涉及分子机制的更精确了解使得这些药物得以研发。透明细胞肾细胞癌可能涉及三种分子途径:VHL/HIF/VEGF、PI3K/AKT/mTOR和丝裂原活化蛋白激酶途径。这些抗血管生成疗法已被批准用于治疗晚期和转移性透明细胞肾细胞癌。在转移性疾病中,病理学家有重要且不同的职责:1)在肿瘤活检中,只有透明细胞肾细胞癌的诊断意味着需要开具抗血管生成药物,2)在靶向治疗后,病理学家必须评估对肿瘤的治疗效果。病理学家需要就宏观和组织学报告达成共识。