All authors: University of Wisconsin School of Medicine and Public Health, Madison, WI.
J Clin Oncol. 2014 Sep 10;32(26):2886-93. doi: 10.1200/JCO.2014.55.1366. Epub 2014 Aug 11.
The development of molecular targeted therapeutics in oncology builds on many years of scientific investigation into the cellular mechanics of malignant transformation and progression. The past two decades have brought an accelerating pace to the clinical investigation of new molecular targeted agents, particularly in the setting of metastatic disease. The integration of molecular targeted agents into phase III clinical trial design has lagged in the curative treatment setting, particularly in combination with established therapeutic modalities such as radiation. In this review, we discuss the interaction of radiation and molecular targeted therapeutics. The dynamics of cellular and tumor response to radiation offer unique opportunities for beneficial interplay with molecular targeted agents that may go unrecognized with conventional screening and monotherapy clinical testing of novel agents. By using epidermal growth factor receptor (EGFR) as a primary example, we discuss recent clinical studies that illustrate the potential synergy of molecular targeted agents with radiation and highlight the clinical value of such interactions. For various molecular targeted agents, their greatest clinical impact may rest in combination with radiation, and efforts to facilitate systematic investigation of this approach appear highly warranted.
肿瘤分子靶向治疗的发展是基于多年来对恶性转化和进展的细胞机制的科学研究。在过去的二十年中,新的分子靶向药物的临床研究步伐加快,特别是在转移性疾病的治疗中。将分子靶向药物整合到 III 期临床试验设计中在根治性治疗中滞后,特别是与放射等已确立的治疗方式联合应用时。在这篇综述中,我们讨论了放射与分子靶向治疗的相互作用。细胞和肿瘤对放射的反应动力学为与分子靶向药物进行有益的相互作用提供了独特的机会,如果仅使用常规筛选和新型药物的单药临床测试可能会忽略这些机会。我们以表皮生长因子受体(EGFR)为例,讨论了最近的临床研究,这些研究说明了分子靶向药物与放射的潜在协同作用,并强调了这种相互作用的临床价值。对于各种分子靶向药物,它们最大的临床影响可能在于与放射的联合应用,因此有必要努力促进对此类方法的系统研究。