Baumann Michael, Krause Mechthild
Department of Radiation Oncology, Medical Faculty and University Hospital Carl Gustav Carus, University of Technology, 01307 Dresden, Germany.
Radiother Oncol. 2004 Sep;72(3):257-66. doi: 10.1016/j.radonc.2004.07.007.
Inhibition of the epidermal growth factor receptor (EGFR) is a fastly developing field in preclinical and clinical cancer research. This review presents the current status of knowledge and discusses radiobiological mechanisms which may underly the efficacy of EGFR inhibitors combined with irradiation.
Preclinical and clinical results on combined targeting of the EGFR and irradiation from the literature and from this laboratory are reviewed. Focus is given to the radiobiological rationale of this approach and to endpoints of experimental radiotherapy.
Overexpression of the EGFR is associated with decreased local tumour control after radiotherapy, especially when the overall treatment time is long. Inhibition of the EGFR either alone or in combination with irradiation decreases the growth rate of tumours expressing this receptor. Preclinical data provide proof-of-principle that local tumour control may be improved by combining irradiation with C225 mAb. In a randomised phase III clinical trial, simultaneous irradiation and treatment with the EGFR antibody Cetuximab (Erbitux; C225) in head and neck cancer patients resulted in significantly improved locoregional tumour control and survival compared to curative irradiation alone. Acute skin reactions increased in the experimental arm. The underlying mechanisms of enhanced radiation effects of combined EGFR inhibition with irradiation and of the partly conflicting results in different studies are poorly understood. There is increasing evidence, that important intertumoral heterogeneity in the response to EGFR inhibition alone and combined with irradiation exists, which appears to be at least partly dependent on specific mutations of the receptor as well as of molecules that are involved in the intracellular signal transduction pathway.
Further investigations at all levels of the translational research chain exploring the mechanisms of EGFR inhibition in the context of radiotherapy are needed to fully exploit the potential of such combinations and to develop predictive tests that direct their use.
表皮生长因子受体(EGFR)抑制是临床前和临床癌症研究中一个快速发展的领域。本综述介绍了当前的知识现状,并讨论了可能是EGFR抑制剂联合放疗疗效基础的放射生物学机制。
综述了文献及本实验室关于EGFR联合放疗的临床前和临床结果。重点关注这种方法的放射生物学原理以及实验性放疗的终点。
EGFR的过表达与放疗后局部肿瘤控制率降低有关,尤其是当总治疗时间较长时。单独或联合放疗抑制EGFR可降低表达该受体的肿瘤的生长速率。临床前数据提供了原理证明,即联合放疗与西妥昔单抗(C225)可能改善局部肿瘤控制。在一项随机III期临床试验中,头颈部癌患者同时接受放疗和EGFR抗体西妥昔单抗(爱必妥;C225)治疗,与单纯根治性放疗相比,局部区域肿瘤控制和生存率显著提高。试验组急性皮肤反应增加。EGFR抑制联合放疗增强放射效应的潜在机制以及不同研究中部分相互矛盾的结果尚不清楚。越来越多的证据表明,单独及联合放疗时对EGFR抑制的反应存在重要的肿瘤间异质性,这似乎至少部分取决于受体以及参与细胞内信号转导途径的分子的特定突变。
需要在转化研究链的各个层面进一步开展研究,探索放疗背景下EGFR抑制的机制,以充分发挥此类联合治疗的潜力,并开发指导其应用的预测性检测方法。