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高预处理 C 反应蛋白与白蛋白比值预示弥漫性大 B 细胞淋巴瘤预后不良。

High level of pre-treatment C-reactive protein to albumin ratio predicts inferior prognosis in diffuse large B-cell lymphoma.

机构信息

Center for Hematologic Malignancy, National Cancer Center, 323 Ilsan-ro, Ilsandong-gu, Goyang, Geyonggi, 410-769, Republic of Korea.

Yonsei University College of Medicine, Seoul, Republic of Korea.

出版信息

Sci Rep. 2021 Jan 29;11(1):2674. doi: 10.1038/s41598-021-82087-6.

Abstract

The C-reactive protein-to-albumin ratio (CAR) has not been assessed in diffuse large B cell lymphoma (DLBCL, the most common non-Hodgkin lymphoma). This retrospective study evaluated the prognostic value of CAR in 186 DLBCL patients. A CAR value of 0.158 was selected as the most discriminative cut-off for identifying patients with high CAR values (73/141 patients, 51.8%). During a median follow-up of 32.5 months, the high CAR group had significantly poorer complete response to induction therapy (64.4% vs. 92.6%; p < 0.001), 3-year overall survival (OS) (68.3% vs. 96.2%; p < 0.0001), and 3-year progression-free survival (PFS) (53.5% vs. 88.0%; p < 0.0001). After adjusting for the International Prognostic Index components, a high CAR value independently predicted poor OS (HR: 6.02, 95% CI 1.19-30.38; p = 0.030) and PFS (HR: 3.62, 95% CI 1.40-9.36; p = 0.008). In an independent validation cohort (n = 50), patients with CAR > 0.158 also showed worse 3-year OS (47.9% vs. 87.2%, p = 0.0035) and 3-year PFS (36.1% vs. 82.1%, p = 0.0011). A high CAR remained significantly associated with poor outcomes for > 60-year-old patients (OS: p = 0.0038, PFS: p = 0.0015) and younger patients (OS: p = 0.0041, PFS: p = 0.0044). Among older patients, a high CAR value also predicted non-relapse mortality (p = 0.035). Therefore, the CAR might complement the International Prognostic Index in DLBCL cases.

摘要

C 反应蛋白与白蛋白比值(CAR)尚未在弥漫性大 B 细胞淋巴瘤(DLBCL,最常见的非霍奇金淋巴瘤)中进行评估。本回顾性研究评估了 CAR 在 186 例 DLBCL 患者中的预后价值。选择 CAR 值 0.158 作为区分高 CAR 值患者的最具判别性截止值(73/141 例患者,51.8%)。在中位随访 32.5 个月期间,高 CAR 组诱导治疗完全缓解率显著较低(64.4%比 92.6%;p<0.001),3 年总生存率(OS)(68.3%比 96.2%;p<0.0001)和 3 年无进展生存率(PFS)(53.5%比 88.0%;p<0.0001)。在校正国际预后指数成分后,高 CAR 值独立预测 OS 不良(HR:6.02,95%CI 1.19-30.38;p=0.030)和 PFS 不良(HR:3.62,95%CI 1.40-9.36;p=0.008)。在独立验证队列(n=50)中,CAR>0.158 的患者 3 年 OS 也较差(47.9%比 87.2%,p=0.0035)和 3 年 PFS(36.1%比 82.1%,p=0.0011)。高 CAR 与>60 岁患者(OS:p=0.0038,PFS:p=0.0015)和年轻患者(OS:p=0.0041,PFS:p=0.0044)的不良预后显著相关。在老年患者中,高 CAR 值也预测非复发死亡率(p=0.035)。因此,CAR 可能在 DLBCL 病例中补充国际预后指数。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b168/7846592/918e0c9cab32/41598_2021_82087_Fig1_HTML.jpg

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