Sedlaczek O, Grüllich C, Röthke M, Schlemmer H-P, Kauczor H-U
Diagnostische und Interventionelle Radiologie, Universitätsklinik Heidelberg, Im Neuenheimer Feld 110, 69120, Heidelberg, Deutschland.
Radiologe. 2013 Apr;53(4):329-35. doi: 10.1007/s00117-012-2428-7.
CLINICAL/METHODOLOGICAL ISSUE: In antineoplastic chemotherapy classical cytostatic drugs are increasingly being supplemented by antibodies and so-called targeted therapies. In addition to the antineoplastic effect and general intolerance quite characteristic morphological changes can often be found and identified by the radiologist. The distinction between findings indicating side effects versus tumor progression or an infectious etiology is essential.
Classical antineoplastic chemotherapy interacts with DNA and RNA synthesis, DNA repair or the mitosis process. In contrast modern targeted anticancer therapies act at the level of signal transduction pathways.Localized, organ-related changes are related to the metabolic characteristics of organs or anatomical features such as the properties of the local blood-tissue barrier. Toxicity associated findings often resemble fulminant tumor progression.
In new targeted anti-cancer therapies toxicity often occurs in a non-cumulative way; therefore, morphological changes are often precursors of the manifestation of clinical toxicity.
Oncological radiology requires increasingly active interdisciplinary dialogue in order to delineate morphological correlates of organ toxicity against tumor progression and initiate appropriate therapeutic measures.
临床/方法学问题:在抗肿瘤化疗中,经典的细胞毒性药物越来越多地被抗体和所谓的靶向治疗所补充。除了抗肿瘤作用和一般不耐受性外,放射科医生常常能发现并识别出相当典型的形态学变化。区分表明副作用与肿瘤进展或感染病因的发现至关重要。
经典的抗肿瘤化疗与DNA和RNA合成、DNA修复或有丝分裂过程相互作用。相比之下,现代靶向抗癌疗法作用于信号转导通路水平。局部的、与器官相关的变化与器官的代谢特征或解剖学特征有关,如局部血组织屏障的特性。与毒性相关的表现常常类似于暴发性肿瘤进展。
在新的靶向抗癌疗法中,毒性通常以非累积的方式出现;因此,形态学变化常常是临床毒性表现的先兆。
肿瘤放射学需要越来越积极的跨学科对话,以便区分器官毒性与肿瘤进展的形态学关联,并启动适当的治疗措施。