Patel Shreyaskumar R
Department of Sarcoma Medical Oncology, The University of Texas M.D. Anderson Cancer Center, 1515 Holcombe Boulevard, Box 450, Houston 77030, USA.
Curr Oncol Rep. 2002 Jul;4(4):299-304. doi: 10.1007/s11912-002-0005-3.
The field of oncology is experiencing a paradigm shift from broad-spectrum cytotoxic therapies to more specific molecularly based targeted therapies. The activity of imatinib mesylate in chronic myelogenous leukemia and gastrointestinal stromal tumors (GIST) has reinforced our faith in translational research and its potential impact on the cure of cancer and improvement in quality of life for patients. This breakthrough has been particularly exciting for the field of sarcoma and for patients with advanced GIST, for whom no other effective therapy was available. Unfortunately, as is becoming increasingly clear, cancer is a very complex problem with multiple mechanisms and pathways that function either independently or interdependently enabling cell survival. We are therefore far away from having solved the problem. Attempts at refining the currently available therapeutic armamentarium to maximize the therapeutic index (dose intensification with growth factor support) must continue in parallel with laboratory-based research identifying critical targets to be inhibited or blocked. Identification of new agents with some activity, such as gemcitabine and ecteinascidin (ET-743), is also of paramount importance.
肿瘤学领域正在经历一场范式转变,从广谱细胞毒性疗法转向更具针对性的基于分子的靶向疗法。甲磺酸伊马替尼在慢性粒细胞白血病和胃肠道间质瘤(GIST)中的活性增强了我们对转化研究的信心,以及其对癌症治愈和患者生活质量改善的潜在影响。这一突破对于肉瘤领域以及晚期GIST患者来说尤其令人兴奋,因为此前他们没有其他有效的治疗方法。不幸的是,越来越明显的是,癌症是一个非常复杂的问题,有多种独立或相互依赖发挥作用以实现细胞存活的机制和途径。因此,我们离解决这个问题还很遥远。在基于实验室的研究确定要抑制或阻断的关键靶点的同时,必须继续努力完善目前可用的治疗手段,以最大限度地提高治疗指数(通过生长因子支持进行剂量强化)。鉴定具有一定活性的新药物,如吉西他滨和埃博霉素(ET-743),也至关重要。