Bijlsma Maarten F, van Laarhoven Hanneke W M
Laboratory for Experimental Oncology and Radiobiology, Center for Experimental Molecular Medicine, Academic Medical Center, University of Amsterdam, Meibergdreef 9, 1105AZ, Amsterdam, The Netherlands.
Cancer Metastasis Rev. 2015 Mar;34(1):97-114. doi: 10.1007/s10555-014-9541-1.
A nearly universal feature of pancreatic ductal adenocarcinoma (PDAC) is an extensive presence of activated stroma. This stroma is thought to aid in various tumor-promoting processes and hampers response to therapy. Here, we aim to evaluate the evidence that supports this role of the stroma in PDAC with functional experiments in relevant models, discuss the clinical trials that have aimed to target the stroma in this disease, and examine recent work that explains why these clinical trials based on stroma-targeting strategies have thus far not achieved the expected success. We systematically searched PubMed through August 2014 with no restrictions to identify published peer-reviewed research articles assessing the effect of targeting the stroma on tumor growth or metastases in preclinical animal models. Five hundred and thirty articles were extracted of which 31 were included in the analysis. Unfortunately, due to the large variety in models and outcome measures, we could not perform a meta-analysis of our data. We find that despite an abundance of positive outcomes reported in previous studies on stroma targeting, a strong discrepancy exists with the outcomes of clinical trials and the more recent preclinical work that is in line with these trials. We explain the incongruities by the duration of stroma targeting and propose that chronic stroma targeting treatment is possibly detrimental in the treatment of this disease.
胰腺导管腺癌(PDAC)几乎一个普遍特征是存在广泛的活化基质。这种基质被认为有助于各种肿瘤促进过程,并妨碍对治疗的反应。在此,我们旨在通过相关模型中的功能实验评估支持基质在PDAC中发挥此作用的证据,讨论旨在针对该疾病基质的临床试验,并审视近期的研究工作,这些工作解释了为何基于基质靶向策略的这些临床试验迄今未取得预期成功。我们在2014年8月前系统检索了PubMed,无限制地识别已发表的同行评审研究文章,这些文章评估了在临床前动物模型中靶向基质对肿瘤生长或转移的影响。提取了530篇文章,其中31篇纳入分析。遗憾的是,由于模型和结局指标种类繁多,我们无法对数据进行荟萃分析。我们发现,尽管先前关于基质靶向的研究报告了大量阳性结果,但临床试验结果与符合这些试验的近期临床前研究结果存在强烈差异。我们通过基质靶向的持续时间来解释这些不一致性,并提出长期基质靶向治疗在该疾病治疗中可能有害。