Ki67增殖指数、CD10和MUM1对滤泡性淋巴瘤的预后价值

Vu Minh Phuong, Le Thanh Vui, Kieu Van Oanh
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Results: Ki-67 PI levels were as follows: ≤ 20% in 14 patients, 21-40% in 6 patients, 41-60% in 4 patients, > 60% in 3 patients. A cut-off value of 60% revealed significantly different survival rates. OS, PFS in the Ki67 > 60% group decreased significantly for 5 years, and the difference was statistically significant (37.5% vs. 100%, p = 0.000; 0% vs. 66.7%, p = 0.016; respectively). The CD10 negative group had a less favorable outcome than the positive group in the OS rate at 5 years (72% vs. 100%, p = 0.049) and the PFS rate at 5 years (25.3% vs. 72.6%, p = 0.017). OS and PFS in the group with MUM1 positive/CD10 negative decreased significantly for 5 years than in the group without MUM1 positive/CD10 negative (4.7% vs. 100%, p = 0.002; 0% vs. 66.4%, p = 0.006; respectively). 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摘要

背景/目的:滤泡性淋巴瘤(滤泡性淋巴瘤)是一种无痛性淋巴瘤,其生存期较长。然而,也有患者在标准治疗后出现早期进展。方法:对27例FL患者进行福尔马林固定石蜡包埋活检组织进行Ki67、CD10和MUM1的免疫组化染色,并根据Ki67增殖指数(PI)水平对患者进行分组。分析存活时间,确定Ki67 PI的临界值。根据CD10、MUM1和MUM1阳性/CD10阴性情况将患者分为两组。结果:Ki-67 PI水平:≤20% 14例,21 ~ 40% 6例,41 ~ 60% 4例,bb0 ~ 60% 3例。60%的临界值显示了显著不同的存活率。Ki67 > 60%组OS、PFS连续5年显著下降,差异有统计学意义(37.5% vs. 100%, p = 0.000;0% vs. 66.7%, p = 0.016;分别)。CD10阴性组的5年OS率(72%比100%,p = 0.049)和5年PFS率(25.3%比72.6%,p = 0.017)均不及阳性组。5年期间,MUM1阳性/CD10阴性组的OS和PFS显著低于无MUM1阳性/CD10阴性组(4.7% vs. 100%, p = 0.002;0% vs. 66.4%, p = 0.006;分别)。结论:ki67bbb60 %、CD10阴性、MUM1阳性/ CD10阴性是FL的不良预后因素。
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Prognostic Value of the Ki67 Proliferation Index, CD10 and MUM1 in Follicular Lymphoma
Background/Purpose: Follicular lymphoma (FL) is an indolent lymphoma and is associated with a long survival time. However, there are patients who had an early progression after standard therapy. Our aim was to analyze the prognostic value of Ki67, CD10 and MUM1 expression in FL. Methods: Immunohistochemical staining for Ki67, CD10 and MUM1 was performed on formalin-fixed paraffin-embedded biopsy tissues from 27 patients with FL. Patients were grouped according to the levels of the Ki67 proliferation index (PI). Survival times were analyzed and the cut-off value for Ki67 PI was determined. The patients were also divided into groups according to the presence of CD10, MUM1and MUM1 positive/CD10 negative. Results: Ki-67 PI levels were as follows: ≤ 20% in 14 patients, 21-40% in 6 patients, 41-60% in 4 patients, > 60% in 3 patients. A cut-off value of 60% revealed significantly different survival rates. OS, PFS in the Ki67 > 60% group decreased significantly for 5 years, and the difference was statistically significant (37.5% vs. 100%, p = 0.000; 0% vs. 66.7%, p = 0.016; respectively). The CD10 negative group had a less favorable outcome than the positive group in the OS rate at 5 years (72% vs. 100%, p = 0.049) and the PFS rate at 5 years (25.3% vs. 72.6%, p = 0.017). OS and PFS in the group with MUM1 positive/CD10 negative decreased significantly for 5 years than in the group without MUM1 positive/CD10 negative (4.7% vs. 100%, p = 0.002; 0% vs. 66.4%, p = 0.006; respectively). Conclusion: Ki67 > 60%, CD10 negative, MUM1 positive/ CD10 negative are poor prognostic factors in FL.
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