Yang X, Chen S, Qi Y, Xu X Y, Guan X, Yang Y C, Liu Y X, Guo Y H, Gong W C, Gao Y N, Wang X H, Li W, Li L F, Fu K, Zhang H L, Meng B
Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer; Key Laboratory of Cancer Prevention and Therapy, Tianjin; Tianjin's Clinical Research Center of Cancer, Tianjin 300060, China Department of Pathology, Tianjin Medical University Cancer Institute andHospital, Tianjin 300060, China.
Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer; Key Laboratory of Cancer Prevention and Therapy, Tianjin; Tianjin's Clinical Research Center of Cancer, Tianjin 300060, China Department of Lymphoma, Tianjin Medical University Cancer Institute and Hospital, Tianjin 300060, China.
Zhonghua Xue Ye Xue Za Zhi. 2021 Jun 14;42(6):487-494. doi: 10.3760/cma.j.issn.0253-2727.2021.06.008.
To screen and analyze the prognostic protein biomarkers of DLBCL, and to explore their value in the prognostic evaluation. 163 cases of confirmed DLBCLs from January 2011 to December 2016 were collected with their clinical, pathological and follow-up data, which were all from our hospital. The expression of protein markers were tested using immunohistochemical staining (IHC) . The immune phenotypes independent of the International Prognostic Index (IPI) that affect overall survival (OS) and progression-free survival (PFS) of DLBCL were explored by COX regression model, and the effect of their co-expression on the prognosis were also analyzed. BCL6 negative (PFS: =1.652, 95% 1.030-2.649, =0.037) , P53 positive (OS: =1.842, 95% 1.008-3.367, =0.047) , and BCL2 strong positive expressions (S+) (OS: =2.102, 95% 1.249-3.537, =0.005; PFS: =2.126, 95% 1.312-3.443, =0.002) are adverse prognostic factors of DLBCL that are independent of IPI. BCL6(-) (PFS: =2.042, 95% 1.021-4.081, =0.043) , P53(+) (OS: =3.069, 95% 1.244-7.569, =0.015) and BCL2(S+) (OS: =2.433, 95% 1.165-5.082, =0.018; PFS: =3.209, 95% 1.606-6.410, =0.001) are adverse prognostic factors in the group of age≤60-year-old; in the group of IPI score 0-2, cases with BCL6(-) (OS: =2.467, 95% 1.322-4.604, =0.005; PFS: =2.248, 95% 1.275-3.965, =0.005) and BCL2(S+) (PFS: =2.045, 95% 1.119-3.735, =0.020) have worse prognosis. The co-expression of BCL6(-) and BCL2(S+) has significant influence on prognosis of DLBCL (=0.005 and <0.001) , in which BCL6(+)/non-BCL2(S+) (=86) has the best prognosis[3-year-OS (71.6±4.9) %, 3-year-PFS (67.0±5.1) %], and BCL6(-)/BCL2(S+) (=10) has the worst prognosis[3-year-OS (20.0±12.6) %, 3-year-PFS (10.0±9.5) %]; the co-expression of BCL6(-) and P53(+) has no significant influence on prognosis (=0.061 and =0.089) , however, those cases with BCL6(+)/P53(-) (=98) often get better prognosis[3-year-OS (70.6±4.7) %, 3-year-PFS (64.6±4.9) %] than others; the co-expression of P53(+) and BCL2(S+) has significant influence on prognosis of DLBCL (<0.001 and <0.001) , and P53(+)/BCL2(S+) (=5) has the worst prognosis (3-year-OS and 3-year-PFS are both 0) ; BCL2(S+) cases get shorter OS and PFS, regardless of the expression of BCL6 and P53. The expression and co-expression of BCL6 negative, P53 positive and BCL2(S+) have certain value in the prognostic evaluation of DLBCL, especially in the group of age≤60-year-old and IPI score 0-2.
筛选并分析弥漫性大B细胞淋巴瘤(DLBCL)的预后蛋白生物标志物,探讨其在预后评估中的价值。收集我院2011年1月至2016年12月确诊的163例DLBCL患者的临床、病理及随访资料。采用免疫组织化学染色(IHC)检测蛋白标志物的表达。通过COX回归模型探讨独立于国际预后指数(IPI)影响DLBCL总生存期(OS)和无进展生存期(PFS)的免疫表型,并分析其共表达对预后的影响。BCL6阴性(PFS:=1.652,95% 1.030 - 2.649,=0.037)、P53阳性(OS:=1.842,95% 1.008 - 3.367,=0.047)以及BCL2强阳性表达(S+)(OS:=2.102,95% 1.249 - 3.537,=0.005;PFS:=2.126,95% 1.312 - 3.443,=0.002)是独立于IPI的DLBCL不良预后因素。BCL6(-)(PFS:=2.042,95% 1.021 - 4.081,=0.043)、P53(+)(OS:=3.069,95% 1.244 - 7.569,=0.015)以及BCL2(S+)(OS:=2.433,95% 1.165 - 5.082,=0.018;PFS:=3.209,95% 1.606 - 6.410,=0.001)在年龄≤60岁组是不良预后因素;在IPI评分0 - 2组中,BCL6(-)(OS:=2.467,95% 1.322 - 4.604,=0.005;PFS:=2.248,95% 1.275 - 3.965,=0.005)和BCL2(S+)(PFS:=2.045,95% 1.119 - 3.735,=0.020)的患者预后较差。BCL6(-)与BCL2(S+)的共表达对DLBCL预后有显著影响(=0.005和<0.001),其中BCL6(+)/非BCL2(S+)(=86)预后最佳[3年总生存率(71.6±4.9)%,3年无进展生存率(67.0±5.1)%],而BCL6(-)/BCL2(S+)(=10)预后最差[3年总生存率(20.0±12.6)%,3年无进展生存率(10.0±9.5)%];BCL6(-)与P53(+)的共表达对预后无显著影响(=0.061和=0.089),然而,BCL6(+)/P53(-)(=98)的患者通常比其他患者预后更好[3年总生存率(70.6±4.7)%,3年无进展生存率(64.6±4.9)%];P53(+)与BCL2(S+)的共表达对DLBCL预后有显著影响(<0.001和<0.001),且P53(+)/BCL2(S+)(=5)预后最差(3年总生存率和3年无进展生存率均为0);无论BCL6和P53的表达情况如何,BCL2(S+)的患者总生存期和无进展生存期均较短。BCL6阴性、P53阳性及BCL2(S+)的表达及共表达在DLBCL预后评估中具有一定价值,尤其在年龄≤60岁组和IPI评分0 - 2组中。