Hayon Tamar, Dvilansky Alexander, Shpilberg Ofer, Nathan Ilana
Department of Clinical Biochemistry, Faculty of Health Sciences, Ben-Gurion University, Beer Sheva, Israel.
Leuk Lymphoma. 2003 Nov;44(11):1957-62. doi: 10.1080/1042819031000116607.
The MTT-based assay relies upon the cellular reduction of tetrazolium salts to their intensely colored formazans. The test is easy to perform in hematological malignancies and is adaptable for high throughput of samples, although there are some minor limitations in its application resulting from metabolic interference. This class of assays are highly accurate for predicting drug resistance, whereas their predictive value for drug sensitivity depends on the type of disease and drug or drug combination used. They have been found to predict clinical response to fludarabine FLD in B-CLL and were useful for predetermining clinical potential of a single drug or drug combination in AML patients. Extensive studies with ALL patients have supported their advantage for selecting effective drug treatment of the disease. To conclude, pretreatment chemosensitivity assays may help in the selection of chemotherapeutic drugs with the greatest likelihood for clinical effectiveness, and in the exclusion of uneffective therapy. This can lead to improved disease management, response, survival and use of financial resources.
基于MTT的检测方法依赖于细胞将四唑盐还原为颜色深的甲臜。该检测在血液系统恶性肿瘤中易于操作,适用于高通量样本检测,尽管其应用存在一些由代谢干扰导致的小局限。这类检测在预测耐药性方面高度准确,而其对药物敏感性的预测价值取决于疾病类型以及所用药物或药物组合。已发现它们可预测B细胞慢性淋巴细胞白血病(B-CLL)患者对氟达拉滨(FLD)的临床反应,并且有助于预先确定急性髓系白血病(AML)患者中单一药物或药物组合的临床潜力。对急性淋巴细胞白血病(ALL)患者的广泛研究支持了它们在选择该疾病有效药物治疗方面的优势。总之,预处理化疗敏感性检测可能有助于选择最有可能产生临床疗效的化疗药物,并排除无效治疗。这可改善疾病管理、反应、生存率以及财政资源的利用。