Vaughan W P, Civin C I, Weisenburger D D, Karp J E, Graham M L, Sanger W G, Grierson H L, Joshi S S, Burke P J
Department of Internal Medicine, University of Nebraska Medical Center, Omaha 68105.
Leukemia. 1988 Oct;2(10):661-6.
Thirty-one cases of acute leukemia with blast cells greater than or equal to 70% positive for the hematopoietic stem cell Ag, CD34 (MY10, HPCA-1), were identified from the University of Nebraska Medical Center and The Johns Hopkins Oncology Center over an 18-month period. Fourteen of the cases were classified as early B-lineage ALL, 3 cases were other ALL subtypes, and 14 of the cases were ANLL. Five of the 17 cases of ALL expressed one or more myeloid-associated surface Ags, 3 ANLL cases expressed CD10 (CALLA, J5), and T-lymphoid Ags were present in 12 of 31 cases (1 T-cell ALL, 3 of 16 B-lineage ALL cases, and 8 of 14 ANLL cases). Eleven of 12 CD34+ ALL cases studied had abnormal karyotypes; only 7 of 12 CD34+ ANLL cases studied had abnormal karyotypes, and 3 of these were CD10+ ANLL. Six cases were Ph1 positive, including the one mature B cell ALL, 4 early B-lineage ALL, and 1 CD10+ ANLL case. Good and poor prognosis subgroups of high frequency of expression of CD34 leukemias could be identified, generally, as would have been predicted by previously defined criteria. Thus, of the 10 Ph1-negative early B-lineage ALL patients, 9 achieved CR (90%). At the other extreme, the CR rate of CD10- ANLL was 4 of 11 (36%). The leukemias characterized by greater than or equal to 70% of cells positive for CD34 form a relatively undifferentiated subset of the leukemias which may show features associated with more than one lineage, and if CD10- and myeloid morphology, may respond poorly to therapy.
在内布拉斯加大学医学中心和约翰霍普金斯肿瘤中心18个月的时间里,共识别出31例急性白血病患者,其原始细胞中造血干细胞抗原CD34(MY10,HPCA - 1)阳性率大于或等于70%。其中14例被分类为早期B系急性淋巴细胞白血病,3例为其他急性淋巴细胞白血病亚型,14例为急性非淋巴细胞白血病。17例急性淋巴细胞白血病中有5例表达一种或多种髓系相关表面抗原,3例急性非淋巴细胞白血病表达CD10(CALLA,J5),31例中有12例存在T淋巴细胞抗原(1例T细胞急性淋巴细胞白血病,16例B系急性淋巴细胞白血病中的3例,14例急性非淋巴细胞白血病中的8例)。研究的12例CD34 +急性淋巴细胞白血病中有11例核型异常;研究的12例CD34 +急性非淋巴细胞白血病中只有7例核型异常,其中3例为CD10 +急性非淋巴细胞白血病。6例为Ph1阳性,包括1例成熟B细胞急性淋巴细胞白血病、4例早期B系急性淋巴细胞白血病和1例CD10 +急性非淋巴细胞白血病病例。通常可以按照先前定义的标准识别出CD34白血病高表达频率的预后良好和不良亚组。因此,10例Ph1阴性早期B系急性淋巴细胞白血病患者中有9例获得完全缓解(90%)。在另一个极端,CD10 -急性非淋巴细胞白血病的完全缓解率为11例中的4例(36%)。以CD34阳性细胞大于或等于70%为特征的白血病形成了白血病中一个相对未分化的亚组,可能表现出与多个谱系相关的特征,如果是CD10 -且具有髓系形态,则对治疗反应可能较差。