Programmed death ligand 1 expression in diffuse large B cell lymphoma: correlation with clinicopathological prognostic factors.

IF 2.1 Q3 ONCOLOGY
Eman Mohamad Ibrahim, Sherine Refat, Shaimaa El-Ashwah, Maryan Waheeb Fahmi, Afaf Taha Ibrahiem
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引用次数: 0

Abstract

Background: The prognostic value of the level of programmed death ligand 1 (PD-L1) expression in non-Hodgkin lymphoma (NHL) is still debatable. This study examined the effect of the level of PD-L1 expression on the clinicopathological characteristics and prognosis of diffuse large B cell lymphoma (DLBCL).

Methods: A retrospective study was conducted on formalin-fixed paraffin-embedded tissue blocks of one hundred de novo DLBCL patients diagnosed from 2013 to 2016. PD-L1 expression was defined by a modified Combined-Positive Score (CPS) and their medical records were reviewed to collect their clinical, laboratory and radiological data, treatment, and outcome.

Results: The included patients were aged from 23 to 85 years and treated by rituximab- cyclophosphamide, doxorubicin, oncovin, prednisone (R-CHOP); 49% were males; 85% of the cases were presented at Ann Arbor stages III, IV; 33% of patients were seropositive for HCV and 87% of cases were presented with intermediate and high IPI. All included cases expressed PD-L1 using modified CPS. 27% of patients showed low PD-L1 expression (≥ 5% to < 50% of total tumor cellularity) while 73% of patients showed high PD-L1expression (≥ 50% of total tumor cellularity). High PD-L1 expression is statistically correlated with advanced stage (p 0.01), high IPI score (p 0.017), high incidence of stationary and progressive disease (p 0.002) and high incidence of relapse (p value 0.01). Five-year disease-free survival (DFS) was 29% for patients with high PD-L1 expression compared with 84.8% for patients with low PD-L1 expression (p 0.001).

Conclusions: This study suggests that high PD-L1 expression in DLBCL is associated with aggressive clinicopathological features and a decreased response to R-CHOP. The level of PD-L1 expression could be an independent predictor of DFS of DLBCL. More research is mandatory to standardize the cutoff value and scoring methods.

程序性死亡配体1在弥漫性大B细胞淋巴瘤中的表达:与临床病理预后因素的相关性
背景:程序性死亡配体1 (PD-L1)表达水平在非霍奇金淋巴瘤(NHL)中的预后价值仍有争议。本研究探讨PD-L1表达水平对弥漫性大B细胞淋巴瘤(DLBCL)临床病理特征及预后的影响。方法:对2013 - 2016年诊断的100例DLBCL新生患者进行福尔马林固定石蜡包埋组织块的回顾性研究。PD-L1表达通过改良的联合阳性评分(CPS)来定义,并审查他们的医疗记录,以收集他们的临床、实验室和放射学数据、治疗和结果。结果:纳入的患者年龄在23 ~ 85岁之间,采用利妥昔单抗-环磷酰胺、阿霉素、昂科因、强的松(R-CHOP)治疗;49%为男性;85%的病例出现在Ann Arbor III、IV期;33%的患者HCV血清阳性,87%的患者IPI为中高。所有纳入的病例均使用改良的CPS表达PD-L1。结论:本研究提示,DLBCL中PD-L1的高表达与侵袭性临床病理特征和R-CHOP反应降低有关。PD-L1表达水平可作为DLBCL DFS的独立预测因子。有必要进行更多的研究,以规范分界值和评分方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.50
自引率
0.00%
发文量
46
审稿时长
11 weeks
期刊介绍: As the official publication of the National Cancer Institute, Cairo University, the Journal of the Egyptian National Cancer Institute (JENCI) is an open access peer-reviewed journal that publishes on the latest innovations in oncology and thereby, providing academics and clinicians a leading research platform. JENCI welcomes submissions pertaining to all fields of basic, applied and clinical cancer research. Main topics of interest include: local and systemic anticancer therapy (with specific interest on applied cancer research from developing countries); experimental oncology; early cancer detection; randomized trials (including negatives ones); and key emerging fields of personalized medicine, such as molecular pathology, bioinformatics, and biotechnologies.
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