Song Moo-Kon, Chung Joo-Seop, Lee Je-Jung, Yang Deok-Hwan, Kim In-Suk, Shin Dong-Hoon, Shin Ho-Jin
Department of Hematology-Oncology, School of Medicine, Pusan National University Hospital, Medical Research Institute, 1-10 Ami-dong, Gudeok-Ro 179, Seo-Gu, Busan, 602-739, Republic of Korea,
Int J Hematol. 2015 Feb;101(2):140-7. doi: 10.1007/s12185-014-1719-3. Epub 2014 Dec 12.
Approximately 10-25 % of patients with diffuse large B cell lymphoma (DLBCL) at the time of diagnosis exhibit bone marrow involvement (BMI). After introduction of rituximab, immunohistochemistry (IHC) markers lost to prognostic value in DLBCL patients. However, the specimens used have mainly been diagnostic tissues, not bone marrow (BM). It would thus be useful to determine the prognostic value of specific IHC markers of pathologic BM in DLBCL patients with BMI in the rituximab era. In the present study, a total of 580 DLBCL patients were analyzed 67 of whom had BMI. CD10, Bcl-6, MUM-1, Bcl-6 and Ki-67 dyeing on pathologic BM were applied. Bcl-2 positivity was more frequent in discordant BMI (P = 0.039) and high Ki-67 expression was more frequent in concordant BMI (P = 0.016). High Ki-67 expression independently predicted poor prognosis between the negative BMI group and each of the following BMI-positive groups: entire BMI (PFS, P < 0.001; OS, P < 0.001), concordant BMI (PFS, P = 0.024; OS, P = 0.007), and discordant BMI (PFS, P = 0.033; OS, P = 0.026). We found that Ki-67 expression in pathologic BM is a novel significant prognostic parameter of worse prognosis in DLBCL patients with BMI in the rituximab era.
在弥漫性大B细胞淋巴瘤(DLBCL)患者中,约10%-25%在诊断时即表现出骨髓受累(BMI)。利妥昔单抗应用后,免疫组化(IHC)标志物在DLBCL患者中失去了预后价值。然而,所使用的标本主要是诊断组织,而非骨髓(BM)。因此,确定利妥昔单抗时代BMI的DLBCL患者病理BM中特定IHC标志物的预后价值将是有用的。在本研究中,共分析了580例DLBCL患者,其中67例有BMI。对病理BM进行了CD10、Bcl-6、MUM-1、Bcl-6和Ki-67染色。Bcl-2阳性在不一致的BMI中更常见(P = 0.039),高Ki-67表达在一致的BMI中更常见(P = 0.016)。在阴性BMI组与以下每个BMI阳性组之间,高Ki-67表达独立预测预后不良:整个BMI(无进展生存期,P < 0.001;总生存期,P < 0.001)、一致的BMI(无进展生存期,P = 0.024;总生存期,P = 0.007)和不一致的BMI(无进展生存期,P = 0.033;总生存期,P = 0.026)。我们发现,在利妥昔单抗时代,病理BM中的Ki-67表达是BMI的DLBCL患者预后较差的一个新的重要预后参数。