Department of Stem Cell Transplantation, University Cancer Center Hamburg (UCCH), Hamburg, Germany.
Cancer Treat Rev. 2010 Dec;36(8):637-46. doi: 10.1016/j.ctrv.2010.05.002. Epub 2010 Jun 8.
A decade ago, gene expression profiling (GEP) was successfully introduced in haematological research. Considering the heterogeneity of haematological malignancies, the growing arsenal of compounds, allowing targeted therapy, e.g. in myelodysplastic syndromes (MDS) or chronic myeloid leukaemia (CML), and the more differentiated indication to allogeneic stem cell transplantation, routine diagnostic procedures would highly benefit from an introduction of this novel methodology: by now, the majority of genetically defined leukaemia subtypes has been accurately reproduced on the basis of distinct gene expression patterns by various independent research groups. Moreover, classification of histomorphologically overlapping lymphoma subentities (e.g. Burkitt lymphoma and diffuse large B-cell lymphoma, DLBCL), was considerably improved by GEP. Beyond that, differential gene expression has provided the basis for assays being able to predict prognosis of individual patients as well as the response to specific treatment approaches, e.g. to lenalidomide in MDS. In a high proportion of Philadelphia positive acute lymphoblastic leukaemia (ALL) patients, prognostically adverse deletions of the IKZF1 gene coding for a specific transcription factor were identified with GEP analysis, which revealed new insights in the clinical variability of this disorder. Given these advantages of GEP, the introduction of this methodology in current diagnostic algorithms of haematological malignancies should further be validated in clinical studies.
十年前,基因表达谱(GEP)在血液学研究中成功引入。考虑到血液恶性肿瘤的异质性,靶向治疗的化合物种类不断增加,例如在骨髓增生异常综合征(MDS)或慢性髓性白血病(CML)中,以及异基因干细胞移植的指征更加明确,常规诊断程序将从这种新方法的引入中受益匪浅:到目前为止,大多数基于不同基因表达模式的遗传定义的白血病亚型已由多个独立的研究小组准确重现。此外,GEP 极大地改善了组织形态学重叠的淋巴瘤亚群(例如伯基特淋巴瘤和弥漫性大 B 细胞淋巴瘤,DLBCL)的分类。除此之外,差异基因表达为能够预测个体患者预后以及对特定治疗方法(例如 MDS 中的来那度胺)反应的检测提供了基础。在相当比例的费城阳性急性淋巴细胞白血病(ALL)患者中,通过 GEP 分析鉴定出预后不良的 IKZF1 基因缺失,该基因编码特定转录因子,这为该疾病的临床变异性提供了新的见解。鉴于 GEP 的这些优势,应在临床研究中进一步验证将这种方法引入血液恶性肿瘤的当前诊断算法。