Impact of Obesity on Patients with Diffuse Large B-Cell Lymphoma Receiving CAR T-Cell Therapy.

IF 2.5 3区 医学 Q3 ONCOLOGY
Oncology Pub Date : 2025-06-13 DOI:10.1159/000545933
Jia Yi Tan, Yong Hao Yeo, Hermon Kha Kin Wong, Shatha Elemian, Marwa Mir, Qi Xuan Ang, Arya Mariam Roy, Daniel Ezekwudo, Hamid S Shaaban
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引用次数: 0

Abstract

Obesity has been associated with poorer outcomes in conventional cancer therapies. However, its impact on Chimeric Antigen Receptor (CAR) T-cell therapy for patients with diffuse large B-cell lymphoma (DLBCL) remains unclear. This study aims to evaluate how obesity affects in-hospital outcomes and adverse effects in patients with DLBCL receiving CAR-T therapy. Using the National Readmission Database (NRD), we included adults aged ≥18 with DLBCL who received CAR-T therapy between 2018 and 2020. We compared in-hospital outcomes and adverse effects between patients with and without obesity. Propensity score matching (caliper of 0.2, 1:1 ratio) was performed to ensure similar baseline characteristics between the groups. We adjusted the following confounding variables: age, comorbidities such as cardiovascular diseases including hypertension, coronary artery disease, congestive heart disease, and valvular heart disease, diabetes mellitus, hyperlipidemia, cerebrovascular accident, obstructive sleep apnea, liver disease, pulmonary disease, chronic kidney disease, obesity, anemia, and social factors including smoking, alcohol use, and illicit drug use. Data analysis was conducted using R studio software. A total of 1,874 patients with DLBCL who received CAR-T therapy were included in the study. Of these, 171 had obesity (9.1%, 59.5 ± 12.1 years of age, 41.5% female) and 1,703 did not (90.9%, 61.9 ±12.4 years of age, 35.9% female). After propensity score matching, there were 160 patients with obesity (50.0%, 59.7 ± 12.2 years of age, 41.9% female) and 160 patients without obesity (50.0%, 58.6 ± 13.0 years of age, 41.3% female). Patients with obesity had significantly higher rates of early mortality (10.6% vs. 4.4%, p = 0.03) and non-home discharge (18.8% vs. 8.1%, p = 0.01) compared to those without obesity. There were no significant differences in 30-day readmission (18.1% vs. 21.3%, p = 0.48). In terms of in-hospital complications, the rates of acute kidney injury (20.0% vs. 23.1%, p = 0.50), cardiac complications (4.4% vs. 3.8%, p = 0.78), leukopenia (41.3% vs. 44.4%, p = 0.57), neurotoxicity (10.6% vs. 8.1%, p = 0.44), pulmonary embolism (1.3% vs. 0.0%, p = 0.16), and infection (44.4% vs. 43.8%, p = 0.91) were comparable between the two groups. Patients with DLBCL and concomitant obesity receiving CAR-T therapy experienced higher rates of early mortality and non-home discharge compared to non-obese patients. These findings underscore the need for tailored management strategies to improve outcomes for this patient population.

肥胖对接受CAR - t细胞治疗的弥漫大b细胞淋巴瘤患者的影响
在传统的癌症治疗中,肥胖与较差的治疗效果有关。然而,其对弥漫大b细胞淋巴瘤(DLBCL)患者CAR - t细胞治疗的影响尚不清楚。本研究旨在评估肥胖如何影响接受CAR-T治疗的DLBCL患者的住院预后和不良反应。使用国家再入院数据库(NRD),我们纳入了2018年至2020年间接受CAR-T治疗的年龄≥18岁的DLBCL患者。我们比较了肥胖症患者和非肥胖症患者的住院结果和不良反应。进行倾向评分匹配(卡尺为0.2,1:1比例)以确保组间相似的基线特征。我们调整了以下混杂变量:年龄、合并症,如心血管疾病,包括高血压、冠状动脉疾病、充血性心脏病和瓣膜性心脏病、糖尿病、高脂血症、脑血管意外、阻塞性睡眠呼吸暂停、肝病、肺病、慢性肾病、肥胖、贫血,以及吸烟、饮酒和非法使用药物等社会因素。使用R studio软件进行数据分析。该研究共纳入了1874名接受CAR-T治疗的DLBCL患者。其中肥胖171例(9.1%,59.5±12.1岁,女性41.5%),无肥胖1703例(90.9%,61.9±12.4岁,女性35.9%)。倾向评分匹配后,肥胖患者160例(50.0%,59.7±12.2岁,女性41.9%),无肥胖患者160例(50.0%,58.6±13.0岁,女性41.3%)。肥胖患者的早期死亡率(10.6%比4.4%,p = 0.03)和非家庭出院率(18.8%比8.1%,p = 0.01)明显高于非肥胖患者。30天再入院率无显著差异(18.1% vs. 21.3%, p = 0.48)。在院内并发症方面,两组急性肾损伤(20.0%比23.1%,p = 0.50)、心脏并发症(4.4%比3.8%,p = 0.78)、白细胞减少(41.3%比44.4%,p = 0.57)、神经毒性(10.6%比8.1%,p = 0.44)、肺栓塞(1.3%比0.0%,p = 0.16)和感染(44.4%比43.8%,p = 0.91)的发生率具有可比性。与非肥胖患者相比,接受CAR-T治疗的DLBCL合并肥胖患者的早期死亡率和非家庭出院率更高。这些发现强调需要量身定制的管理策略来改善这一患者群体的预后。
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
Oncology
Oncology 医学-肿瘤学
CiteScore
6.00
自引率
2.90%
发文量
76
审稿时长
6-12 weeks
期刊介绍: Although laboratory and clinical cancer research need to be closely linked, observations at the basic level often remain removed from medical applications. This journal works to accelerate the translation of experimental results into the clinic, and back again into the laboratory for further investigation. The fundamental purpose of this effort is to advance clinically-relevant knowledge of cancer, and improve the outcome of prevention, diagnosis and treatment of malignant disease. The journal publishes significant clinical studies from cancer programs around the world, along with important translational laboratory findings, mini-reviews (invited and submitted) and in-depth discussions of evolving and controversial topics in the oncology arena. A unique feature of the journal is a new section which focuses on rapid peer-review and subsequent publication of short reports of phase 1 and phase 2 clinical cancer trials, with a goal of insuring that high-quality clinical cancer research quickly enters the public domain, regardless of the trial’s ultimate conclusions regarding efficacy or toxicity.
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