Shih L Y, Chiu W F, Lee C T
Department of Internal Medicine, Chang Gung Memorial Hospital, Chang Gung Medical College, Taipei, Taiwan, Republic of China.
Leukemia. 1991 Dec;5(12):1092-8.
The in vitro culture growth of marrow granulocyte-macrophage progenitors (CFU-GM assay) was studied in 102 consecutive patients with newly diagnosed primary myelodysplastic syndrome (MDS) to determine its diagnostic utility and prognostic value. There were 18 patients with refractory anemia (RA), eight RA with ringed-sideroblast (RARS), 30 RA with excess of blasts (RAEB), 18 chronic myelomonocytic leukemia (CMML), and 28 RAEB in transformation (RAEB-T). Patients with MDS had a significantly lower number of GM colonies and a significantly higher cluster to colony ratio than those of normal controls and patients with cytopenias of other causes. Six in vitro growth patterns were observed; 85% of patients with MDS showed various abnormal growth patterns, and 42% of all MDS patients exhibited a leukemic growth pattern at diagnosis. None of the 40 patients with cytopenias of other causes had a leukemic type growth. A leukemic growth pattern was rarely observed in patients with RA and RARS (4%), but was common in other subgroups (57%). The distribution of various growth patterns was not statistically different among patients with RAEB, CMML, and RAEB-T. Thirty-six patients developed acute leukemia during the follow-up period. The MDS patients with leukemic type growth were at increased risk of rapid progression to acute leukemia, and they also had a shorter survival time than patients with a non-leukemic pattern. These results showed that simply scoring the number of CFU-GM is of limited value for the diagnosis and the prediction of prognosis of MDS, whereas the in vitro marrow culture growth pattern is of prognostic significance independently of the FAB classification. It is concluded that the in vitro growth pattern of marrow CFU-GM is helpful in diagnosing patients with MDS as well as in predicting their clinical outcome.
对102例新诊断的原发性骨髓增生异常综合征(MDS)患者连续进行研究,以确定体外培养的骨髓粒系巨噬系祖细胞(CFU-GM检测)的生长情况及其诊断效用和预后价值。其中难治性贫血(RA)患者18例,环形铁粒幼细胞性难治性贫血(RARS)患者8例,原始细胞过多的难治性贫血(RAEB)患者30例,慢性粒-单核细胞白血病(CMML)患者18例,转化中的RAEB(RAEB-T)患者28例。与正常对照及其他原因导致血细胞减少的患者相比,MDS患者的GM集落数量显著减少,集簇与集落比值显著升高。观察到六种体外生长模式;85%的MDS患者表现出各种异常生长模式,42%的MDS患者在诊断时表现出白血病样生长模式。40例其他原因导致血细胞减少的患者均无白血病样生长。RA和RARS患者很少出现白血病样生长模式(4%),但在其他亚组中很常见(57%)。RAEB、CMML和RAEB-T患者的各种生长模式分布无统计学差异。36例患者在随访期间发生了急性白血病。具有白血病样生长模式的MDS患者快速进展为急性白血病的风险增加,且其生存时间也短于非白血病样模式的患者。这些结果表明,单纯对CFU-GM数量进行评分对MDS的诊断和预后预测价值有限,而体外骨髓培养生长模式具有独立于FAB分类的预后意义。结论是,骨髓CFU-GM的体外生长模式有助于诊断MDS患者并预测其临床结局。