CVAI、LAP和SMI与DLBCL患者免疫化疗后血液学毒性风险的关联:一项回顾性研究

IF 3.4 3区 医学 Q2 HEMATOLOGY
Therapeutic Advances in Hematology Pub Date : 2025-01-30 eCollection Date: 2025-01-01 DOI:10.1177/20406207251314631
Caifeng Liao, Hurong Lai, Yansong Tu, Ling He, Chuyang Lin, Huaijun Tu, Jian Li
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引用次数: 0

摘要

背景:弥漫性大b细胞淋巴瘤(DLBCL)患者免疫化疗后不良事件的发生经常影响化疗进程,导致患者生活质量和生存期进一步下降。目的:本研究的主要目的是探讨初诊断时中国脏器脂肪指数(CVAI)、脂质积累产物(LAP)指数和骨骼肌质量指数(SMI)与DLBCL患者免疫化疗后血液学毒性风险之间的关系。设计:回顾性、单中心研究。方法:结合患者临床资料计算CVAI、LAP、SMI。该研究纳入213例患者,其中117例(55%)患者在免疫化疗后出现3-4级血液学毒性。根据CVAI, LAP和SMI的四分位数将参与者分为四组(Q1, Q2, Q3, Q4)。结果:在完全调整模型中,与CVAI和LAP最低组相比,CVAI和LAP最高组的3-4级血液毒性风险降低了75.1% (OR: 0.249, 95% CI: 0.102-0.606, p = 0.002)和77.3% (OR: 0.227, 95% CI: 0.095-0.542, p = 0.001)。对于SMI,在未调整模型中,与最低SMI组相比,最高SMI组发生3-4级血液毒性的风险降低了62.9%。多变量调整限制三次样条曲线和亚群相互作用分析进一步证实了这些发现的稳健性。结论:初诊时CVAI、LAP、SMI较高的DLBCL患者化疗后发生严重血液学毒性的风险较低。因此,初始诊断时的CVAI、LAP和SMI是预测DLBCL患者免疫化疗后严重血液学毒性的可靠有效的生物标志物。试验注册:这是一项回顾性研究,没有在ClinicalTrials.gov上注册。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association of CVAI, LAP and SMI with risk of haematological toxicity after immunochemotherapy in patients with DLBCL: a retrospective study.

Background: The occurrence of adverse events after immunochemotherapy in patients with diffuse large B-cell lymphoma (DLBCL) frequently affects the course of chemotherapy, leading to a further decline in quality of life and survival.

Objectives: The primary objective of this study was to investigate the association between Chinese visceral adiposity index (CVAI), lipid accumulation product (LAP) index and skeletal muscle mass index (SMI) at initial diagnosis and the risk of haematological toxicity following immunochemotherapy in patients with DLBCL.

Design: Retrospective, single-centre study.

Methods: CVAI, LAP and SMI were calculated by combining clinical data of the patients. This study included 213 patients, of whom 117 (55%) patients experienced grades 3-4 haematological toxicity after immunochemotherapy. Participants were divided into four groups (Q1, Q2, Q3, Q4) based on the quartiles of CVAI, LAP and SMI.

Results: In the fully adjusted model, the risk of grades 3-4 haematological toxicity in group with the highest CVAI and LAP was reduced by 75.1% (OR: 0.249, 95% CI: 0.102-0.606, p = 0.002) and by 77.3% (OR: 0.227, 95% CI: 0.095-0.542, p = 0.001) compared to the group with the lowest CVAI and LAP. For SMI, the risk of grades 3-4 haematological toxicities in the group with the highest SMI was reduced by 62.9% compared with the lowest SMI group in the unadjusted model. The multivariable-adjusted restricted cubic spline curves and subgroup interaction analyses further confirmed the robustness of these findings.

Conclusion: The results indicate that DLBCL patients with relatively high CVAI, LAP and SMI at initial diagnosis have a lower risk of severe haematological toxicity following chemotherapy. Therefore, CVAI, LAP and SMI at initial diagnosis are reliable and effective biomarkers for predicting severe haematological toxicity after immunochemotherapy in DLBCL patients.

Trial registration: This is a retrospective study, and no registration on ClinicalTrials.gov.

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来源期刊
CiteScore
4.30
自引率
0.00%
发文量
54
审稿时长
7 weeks
期刊介绍: Therapeutic Advances in Hematology delivers the highest quality peer-reviewed articles, reviews, and scholarly comment on pioneering efforts and innovative studies across all areas of hematology. The journal has a strong clinical and pharmacological focus and is aimed at clinicians and researchers in hematology, providing a forum in print and online for publishing the highest quality articles in this area.
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