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CD155作为急性髓系白血病的预后和预测生物标志物

CD155 as a prognostic and predictive biomarker in acute myeloid leukemia.

作者信息

Abdalla Ashraf Zeidan, Khallaf Salah Mabrouk, Zahran Asmaa Mohammed, Rayan Nehal Adel, Elzaher Ahmed Refaat Abd

机构信息

Medical Oncology Department, Egypt Cancer Institute, Assiut University, Assiut, 71515, Egypt.

Clinical Pathology Department, Egypt Cancer Institute, Assiut University, Assiut, 71515, Egypt.

出版信息

Discov Oncol. 2025 May 24;16(1):902. doi: 10.1007/s12672-025-02665-2.

Abstract

BACKGROUND

Acute myeloid leukemia (AML) is a heterogeneous hematological malignancy with different molecular and genetic alterations. CD155 is expressed on myeloid cells and serves as a recognition molecule for natural killer (NK) cells to induce cytotoxicity. This study aimed to assess the prognostic and predictive value of CD155 in patients with AML.

METHODS

We studied the expression of CD155 via flow cytometry in 93 AML patients at initial diagnosis at the Medical Oncology Department, South Egypt Cancer Institute (SECI), Egypt.

RESULTS

Flow cytometry revealed that a mean fluorescence intensity ratio (MFIR) ≥2.68 was associated with high CD155 expression. This criterion was met in 62 patients (66.7%). High expression was associated with a worse composite complete remission (CRc) rate than low expression (29.0 vs. 54.8%; P = 0.015). High CD155 expression had significantly shorter relapse-free survival (RFS), with a median of 1.68 (95% CI 0.92-2.43) months (P = 0.015), and overall survival (OS), with a median of 1.68 (95% CI 0.74-2.88) months (P = 0.041).

CONCLUSIONS

High expression of CD155 in adult patients with AML is associated with a lower CRc, shorter RFS, and OS. It could be included within the predictive and prognostic panels.

摘要

背景

急性髓系白血病(AML)是一种具有不同分子和基因改变的异质性血液系统恶性肿瘤。CD155在髓系细胞上表达,作为自然杀伤(NK)细胞诱导细胞毒性的识别分子。本研究旨在评估CD155在AML患者中的预后和预测价值。

方法

我们通过流式细胞术研究了埃及南埃及癌症研究所(SECI)医学肿瘤学部门93例初诊AML患者中CD155的表达。

结果

流式细胞术显示平均荧光强度比值(MFIR)≥2.68与CD155高表达相关。62例患者(66.7%)符合该标准。高表达组的复合完全缓解(CRc)率低于低表达组(29.0%对54.8%;P = 0.015)。CD155高表达组的无复发生存期(RFS)显著缩短,中位生存期为1.68(95%CI 0.92 - 2.43)个月(P = 0.015),总生存期(OS)中位生存期为1.68(95%CI 0.74 - 2.88)个月(P = 0.041)。

结论

成年AML患者中CD155的高表达与较低的CRc、较短的RFS和OS相关。它可纳入预测和预后指标中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/808e/12103457/95dfabf9a966/12672_2025_2665_Fig1_HTML.jpg

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