{"title":"免疫化疗弥漫性大b细胞淋巴瘤患者严重感染的发生率及危险因素","authors":"Haiqiu Zhao, Rong Su, Jie Luo, Lin Liu","doi":"10.1007/s00277-025-06296-z","DOIUrl":null,"url":null,"abstract":"<div><p>To determine the incidence and risk factors of severe infection (SI) in patients with diffuse large B-cell lymphoma (DLBCL) receiving rituximab–chemotherapy (R–C). This retrospective study was conducted at a tertiary care center in China. Patients with newly diagnosed DLBCL who were treated with R–C between January 1, 2022, and July 1, 2023, at our center were included in this study. SI was defined as an infection resulting in hospitalization. COVID-19 infections were excluded from the study. Patients were categorized as having SI or not by analyzing clinical data, comparing the characteristics of the two groups, and exploring the independent risk factors for SI using multivariate logistic analyses. A total of 300 patients were enrolled in this study, with a male-to-female ratio of 1:1.03 and a median age of 62 years (range: 20–88 years). A total of 117 patients (39.0%) developed SIs, with most (86.3%) occurring within six months of the first treatment. One-third of the infections were identified as opportunistic. Advanced stage disease (OR 2.814, 95% CI 1.603–4.939, <i>P</i> < 0.001), smoking history (OR 9.379, 95% CI 3.901–22.547, <i>P</i> < 0.001), concomitant autoimmune diseases (OR 3.730, 95% CI 1.349–10.311, <i>P</i> = 0.011), dexamethasone equivalent dose <b>≥</b> 15 mg/d (OR 2.436, 95% CI 1.213–4.894, <i>P</i> = 0.012) and prophylactic treatment with granulocyte-stimulating factors (OR 0.319, 95% CI 0.178–0.574, <i>P</i> < 0.001) were independently associated with the development of SI in DLBCL patients receiving R–C. Infection is a relatively common complication following R–C treatment in patients with DLBCL. Independent risk factors for SI were identified, which may aid clinicians in developing individualized infection prevention and treatment strategies.</p></div>","PeriodicalId":8068,"journal":{"name":"Annals of Hematology","volume":"104 5","pages":"2869 - 2879"},"PeriodicalIF":2.4000,"publicationDate":"2025-04-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12141122/pdf/","citationCount":"0","resultStr":"{\"title\":\"Incidence and risk factors of severe infections in diffuse large B-cell lymphoma patients undergoing immunochemotherapy\",\"authors\":\"Haiqiu Zhao, Rong Su, Jie Luo, Lin Liu\",\"doi\":\"10.1007/s00277-025-06296-z\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>To determine the incidence and risk factors of severe infection (SI) in patients with diffuse large B-cell lymphoma (DLBCL) receiving rituximab–chemotherapy (R–C). This retrospective study was conducted at a tertiary care center in China. Patients with newly diagnosed DLBCL who were treated with R–C between January 1, 2022, and July 1, 2023, at our center were included in this study. SI was defined as an infection resulting in hospitalization. COVID-19 infections were excluded from the study. Patients were categorized as having SI or not by analyzing clinical data, comparing the characteristics of the two groups, and exploring the independent risk factors for SI using multivariate logistic analyses. A total of 300 patients were enrolled in this study, with a male-to-female ratio of 1:1.03 and a median age of 62 years (range: 20–88 years). A total of 117 patients (39.0%) developed SIs, with most (86.3%) occurring within six months of the first treatment. One-third of the infections were identified as opportunistic. Advanced stage disease (OR 2.814, 95% CI 1.603–4.939, <i>P</i> < 0.001), smoking history (OR 9.379, 95% CI 3.901–22.547, <i>P</i> < 0.001), concomitant autoimmune diseases (OR 3.730, 95% CI 1.349–10.311, <i>P</i> = 0.011), dexamethasone equivalent dose <b>≥</b> 15 mg/d (OR 2.436, 95% CI 1.213–4.894, <i>P</i> = 0.012) and prophylactic treatment with granulocyte-stimulating factors (OR 0.319, 95% CI 0.178–0.574, <i>P</i> < 0.001) were independently associated with the development of SI in DLBCL patients receiving R–C. Infection is a relatively common complication following R–C treatment in patients with DLBCL. Independent risk factors for SI were identified, which may aid clinicians in developing individualized infection prevention and treatment strategies.</p></div>\",\"PeriodicalId\":8068,\"journal\":{\"name\":\"Annals of Hematology\",\"volume\":\"104 5\",\"pages\":\"2869 - 2879\"},\"PeriodicalIF\":2.4000,\"publicationDate\":\"2025-04-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12141122/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Annals of Hematology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s00277-025-06296-z\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"HEMATOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annals of Hematology","FirstCategoryId":"3","ListUrlMain":"https://link.springer.com/article/10.1007/s00277-025-06296-z","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"HEMATOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
目的:确定接受利妥昔单抗化疗(R-C)的弥漫大B细胞淋巴瘤(DLBCL)患者严重感染(SI)的发生率和风险因素。这项回顾性研究在中国的一家三级医疗中心进行。本研究纳入了2022年1月1日至2023年7月1日期间在本中心接受利妥昔单抗化疗的新诊断DLBCL患者。SI定义为导致住院的感染。研究中不包括 COVID-19 感染。通过分析临床数据,比较两组患者的特征,并使用多变量逻辑分析探究 SI 的独立风险因素,将患者分为有 SI 和无 SI 两类。本研究共招募了 300 名患者,男女比例为 1:1.03,中位年龄为 62 岁(范围:20-88 岁)。共有 117 名患者(39.0%)发生了 SI,其中大部分(86.3%)发生在首次治疗后的六个月内。三分之一的感染被确定为机会性感染。晚期疾病(OR 2.814,95% CI 1.603-4.939,P
Incidence and risk factors of severe infections in diffuse large B-cell lymphoma patients undergoing immunochemotherapy
To determine the incidence and risk factors of severe infection (SI) in patients with diffuse large B-cell lymphoma (DLBCL) receiving rituximab–chemotherapy (R–C). This retrospective study was conducted at a tertiary care center in China. Patients with newly diagnosed DLBCL who were treated with R–C between January 1, 2022, and July 1, 2023, at our center were included in this study. SI was defined as an infection resulting in hospitalization. COVID-19 infections were excluded from the study. Patients were categorized as having SI or not by analyzing clinical data, comparing the characteristics of the two groups, and exploring the independent risk factors for SI using multivariate logistic analyses. A total of 300 patients were enrolled in this study, with a male-to-female ratio of 1:1.03 and a median age of 62 years (range: 20–88 years). A total of 117 patients (39.0%) developed SIs, with most (86.3%) occurring within six months of the first treatment. One-third of the infections were identified as opportunistic. Advanced stage disease (OR 2.814, 95% CI 1.603–4.939, P < 0.001), smoking history (OR 9.379, 95% CI 3.901–22.547, P < 0.001), concomitant autoimmune diseases (OR 3.730, 95% CI 1.349–10.311, P = 0.011), dexamethasone equivalent dose ≥ 15 mg/d (OR 2.436, 95% CI 1.213–4.894, P = 0.012) and prophylactic treatment with granulocyte-stimulating factors (OR 0.319, 95% CI 0.178–0.574, P < 0.001) were independently associated with the development of SI in DLBCL patients receiving R–C. Infection is a relatively common complication following R–C treatment in patients with DLBCL. Independent risk factors for SI were identified, which may aid clinicians in developing individualized infection prevention and treatment strategies.
期刊介绍:
Annals of Hematology covers the whole spectrum of clinical and experimental hematology, hemostaseology, blood transfusion, and related aspects of medical oncology, including diagnosis and treatment of leukemias, lymphatic neoplasias and solid tumors, and transplantation of hematopoietic stem cells. Coverage includes general aspects of oncology, molecular biology and immunology as pertinent to problems of human blood disease. The journal is associated with the German Society for Hematology and Medical Oncology, and the Austrian Society for Hematology and Oncology.