Avigad Smadar, Yaniv Isaac
Molecular Oncology, Felsenstein Medical Research Center, Schneider Children's Medical Center of Israel, Sackler Faculty of Medicine, Tel Aviv University, Petah-Tikva, Israel.
Future Oncol. 2006 Oct;2(5):659-65. doi: 10.2217/14796694.2.5.659.
The concepts of tailored therapy according to genetic profiling and response based on minimal residual disease evaluation during therapy are attracting increasing interest in modern clinical oncology. Children with acute lymphoblastic leukemia are being stratified to various treatment arms with different intensities according to the genetic characteristics of their leukemia and their response to therapy as measured by real-time polymerase chain reaction. Our ability to quickly identify patients with Ewing sarcoma who have a poor prognosis, and to offer them aggressive therapeutic modalities, such as stem cell transplantation, may result in an improved cure rate. Based on the knowledge gained by gene expression profiling and gene silencing techniques we can expect the emergence of new specific drugs that will target malignant cells without causing damage to normal tissue, resulting in improved cancer therapy.
根据基因谱进行个性化治疗以及在治疗期间基于微小残留病评估进行反应评估的概念,在现代临床肿瘤学中引起了越来越多的关注。急性淋巴细胞白血病患儿正根据其白血病的基因特征以及通过实时聚合酶链反应测量的对治疗的反应,被分层到不同强度的各种治疗组。我们快速识别预后不良的尤因肉瘤患者并为他们提供积极治疗方式(如干细胞移植)的能力,可能会提高治愈率。基于基因表达谱分析和基因沉默技术所获得的知识,我们有望出现新的特异性药物,这些药物将靶向恶性细胞而不损害正常组织,从而改善癌症治疗。