Bonhomme J, Solary E, Caillot D, d'Athis P, Carli P M, Guy H
Laboratoire d'Hématologie, Hôpital du Bocage, Dijon, France.
Nouv Rev Fr Hematol (1978). 1987;29(4):225-30.
In 164 B cell chronic lymphocytic leukemias, surface membrane immunoglobulin (SmIg) phenotype has been determined on lymphocytes from 158 patients (mean age = 66 years, sex ratio = 1.43) to examine the prognostic significance of cell marker phenotype. Correlation of clinical stages of the disease according to Rai and Binet and SmIg phenotype emphasized the absence of the SmIgG phenotype, suggesting more mature cells, at stage C according to Binet (11 of 13 being stage A) and at stage III or IV according to Rai. The majority of SmIg phenotypes was SmIgM +/- D. Survival curves according to SmIg heavy or light chain phenotypes did not emphasize a prognostic significance of cell marker phenotype. Peripheral lymphocytosis over 50,000/microliter correlated with a worse prognosis regardless of clinical staging and SmIg phenotype.
在164例B细胞慢性淋巴细胞白血病患者中,已对158例患者(平均年龄 = 66岁,性别比 = 1.43)的淋巴细胞进行了表面膜免疫球蛋白(SmIg)表型测定,以研究细胞标志物表型的预后意义。根据Rai和Binet分期的疾病临床分期与SmIg表型的相关性强调,在Binet分期的C期(13例中有11例为A期)以及Rai分期的III期或IV期,不存在提示细胞更成熟的SmIgG表型。大多数SmIg表型为SmIgM +/- D。根据SmIg重链或轻链表型绘制的生存曲线并未凸显细胞标志物表型的预后意义。无论临床分期和SmIg表型如何,外周血淋巴细胞计数超过50,000/微升均与较差的预后相关。