Department of Laboratory Medicine, National Cancer Center, Goyang-si, Gyeonggi-do, South Korea.
J Clin Pathol. 2013 May;66(5):420-5. doi: 10.1136/jclinpath-2012-201158.
Bone marrow involvement confers a poor prognosis in patients with diffuse, large, B-cell lymphoma (DLBCL). However, the prognostic significance of concordant and discordant bone marrow involvement in these cases differs. We analysed this further in patients treated with R-CHOP (rituximab plus cyclophosphamide, doxorubicin, vincristine and prednisone) at a single institute.
The cytomorphology of bone marrow involvement was evaluated in 632 patients who were diagnosed with DLBCL in primary tissues and had received R-CHOP therapy. Bone marrow trephine biopsies and clot sections were analysed, along with the immunohistochemical analysis of CD20, CD79a and CD3.
Bone marrow involvement was identified in 80 of our DLBCL patient subjects (12.7%). Of these, 32 (40%) showed discordant bone marrow involvement, and 48 (60%) showed concordant involvement. Kaplan-Meier survival analysis showed that progression-free survival and overall survival was poorer in the concordant group (p<0.001). Multivariate analysis, adjusted for the International Prognostic Index score, showed that concordant involvement was an independent predictor of progression-free survival (p<0.001) and overall survival (p=0.011). Discordant involvement was not a negative prognostic factor independent of the International Prognostic Index.
Prognostication based on bone marrow involvement cytomorphology is a useful indicator of progression-free survival and overall survival, independent of the International Prognostic Index score, in DLBCL patients. Accurate staging based on morphology should thus be included in bone marrow examinations of such cases.
弥漫性大 B 细胞淋巴瘤(DLBCL)患者骨髓侵犯预示预后不良。然而,这些病例中骨髓侵犯一致性和不一致性的预后意义不同。我们在单中心接受 R-CHOP(利妥昔单抗联合环磷酰胺、多柔比星、长春新碱和泼尼松)治疗的患者中进一步分析了这一点。
对 632 例经原发性组织诊断为 DLBCL 且接受 R-CHOP 治疗的患者的骨髓侵犯的细胞形态学进行了评估。分析了骨髓活检和凝血切片,并进行了 CD20、CD79a 和 CD3 的免疫组织化学分析。
在我们的 632 例 DLBCL 患者中,有 80 例(12.7%)发现骨髓侵犯。其中,32 例(40%)表现为不一致性骨髓侵犯,48 例(60%)表现为一致性侵犯。Kaplan-Meier 生存分析显示,一致性侵犯组无进展生存和总生存较差(p<0.001)。多变量分析,调整国际预后指数评分后,显示一致性侵犯是无进展生存(p<0.001)和总生存(p=0.011)的独立预测因素。不一致性侵犯不是独立于国际预后指数的不良预后因素。
基于骨髓侵犯细胞形态学的预后预测是 DLBCL 患者无进展生存和总生存的有用指标,独立于国际预后指数评分。因此,应在这些病例的骨髓检查中包括基于形态学的准确分期。