Curr Opin Oncol. 2011 Mar;23(2):177-82. doi: 10.1097/CCO.0b013e3283436e8c.
Targeted anticancer agents are associated with frequent skin side-effects. Several kinase inhibitors have been implicated in the appearance of borderline and malignant skin tumors such as keratoacanthomas and squamous cell carcinomas. The purpose of this review is to discuss the mechanisms as well as the management and implications of this unexpected side-effect.
Recent findings suggest that these skin neoplasms are due to RAF inhibition and that they are more frequent and arise earlier after treatment initiation with the more specific and potent RAF inhibitors than with the multikinase and pan-RAF inhibitor sorafenib. Biological results show that RAF inhibition induces paradoxical activation of the MAPK (mitogen-activated protein kinase) signaling pathway in cells that do not carry BRAF mutation.
This review discusses the various mechanisms that could be implicated in the appearance of skin tumors during the course of anti-RAF treatments as well as the implications of these findings for clinical practice and future drug development. The unexpected emergence of tumors during the course of anticancer therapies is a concern that stimulates an active field of research in the aim of understanding the underlying mechanisms and preventing if possible skin tumor initiation.
靶向抗癌药物常伴有皮肤副作用。一些激酶抑制剂与角化棘皮瘤和鳞状细胞癌等交界性和恶性皮肤肿瘤的发生有关。本文的目的是讨论这些意外副作用的发生机制、处理方法和意义。
最近的研究结果表明,这些皮肤肿瘤是由于 RAF 抑制引起的,与多激酶和泛 RAF 抑制剂索拉非尼相比,更特异和强效的 RAF 抑制剂起始治疗后皮肤肿瘤发生更频繁,出现更早。生物学研究结果表明,RAF 抑制在不携带 BRAF 突变的细胞中诱导 MAPK(丝裂原活化蛋白激酶)信号通路的反常激活。
本文综述了在 RAF 治疗过程中皮肤肿瘤发生的各种可能机制,以及这些发现对临床实践和未来药物研发的意义。在癌症治疗过程中肿瘤意外出现是一个令人关注的问题,激发了对潜在机制的深入研究,以期能够预防皮肤肿瘤的发生。