Jing Wang, Dongming Zhou, Chenglan Lv, Min Zhou, Rongfu Zhou, Yuan Wan
{"title":"Primary diffuse large B-cell lymphoma in the era of targeted therapies: incidence, second primary malignancy and prognosis.","authors":"Jing Wang, Dongming Zhou, Chenglan Lv, Min Zhou, Rongfu Zhou, Yuan Wan","doi":"10.1080/17474086.2026.2680141","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>To comprehensively illustrate the status of primary diffuse large B-cell lymphoma (DLBCL) in the era of targeted therapies.</p><p><strong>Research design and methods: </strong>Data from patients who were newly diagnosed with primary DLBCL from 2000 to 2021 in SEER 17 Registry Database were analyzed. The incidence and occurrence of second primary malignancies (SPM) and the prognosis of DLBCL were identified.</p><p><strong>Results: </strong>A total of 106,501 DLBCL patients were included. The median age at diagnosis was 66.0 years, and the disease was more prevalent in male and white patients. The age-standardized incidence rate in 2021 was 5.6 per 100,000, showing a significant decrease (average annual percent change of -0.43%) from 2002 to 2021. The risk of developing any SPM among DLBCL survivors was approximately 30% higher than that in the general population (95% confidence interval (CI): 1.28-1.33, <i>p</i> < 0.05). Significant risk factors for SPMs included the male sex (hazard ratio (HR) = 1.21, 95% CI: 1.16-1.27) and a diagnosis after 2009 (HR = 1.25, 95% CI: 1.20-1.31).</p><p><strong>Conclusions: </strong>The incidence of DLBCL has slightly decreased, whereas the risk of SPM has increased. The prognosis has improved, likely because of targeted therapies. Further investigation is warranted to refine treatment strategies and reduce the SPM risk.</p>","PeriodicalId":12325,"journal":{"name":"Expert Review of Hematology","volume":" ","pages":"957-965"},"PeriodicalIF":2.8000,"publicationDate":"2026-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Expert Review of Hematology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/17474086.2026.2680141","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/5/29 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"HEMATOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Background: To comprehensively illustrate the status of primary diffuse large B-cell lymphoma (DLBCL) in the era of targeted therapies.
Research design and methods: Data from patients who were newly diagnosed with primary DLBCL from 2000 to 2021 in SEER 17 Registry Database were analyzed. The incidence and occurrence of second primary malignancies (SPM) and the prognosis of DLBCL were identified.
Results: A total of 106,501 DLBCL patients were included. The median age at diagnosis was 66.0 years, and the disease was more prevalent in male and white patients. The age-standardized incidence rate in 2021 was 5.6 per 100,000, showing a significant decrease (average annual percent change of -0.43%) from 2002 to 2021. The risk of developing any SPM among DLBCL survivors was approximately 30% higher than that in the general population (95% confidence interval (CI): 1.28-1.33, p < 0.05). Significant risk factors for SPMs included the male sex (hazard ratio (HR) = 1.21, 95% CI: 1.16-1.27) and a diagnosis after 2009 (HR = 1.25, 95% CI: 1.20-1.31).
Conclusions: The incidence of DLBCL has slightly decreased, whereas the risk of SPM has increased. The prognosis has improved, likely because of targeted therapies. Further investigation is warranted to refine treatment strategies and reduce the SPM risk.
期刊介绍:
Advanced molecular research techniques have transformed hematology in recent years. With improved understanding of hematologic diseases, we now have the opportunity to research and evaluate new biological therapies, new drugs and drug combinations, new treatment schedules and novel approaches including stem cell transplantation. We can also expect proteomics, molecular genetics and biomarker research to facilitate new diagnostic approaches and the identification of appropriate therapies. Further advances in our knowledge regarding the formation and function of blood cells and blood-forming tissues should ensue, and it will be a major challenge for hematologists to adopt these new paradigms and develop integrated strategies to define the best possible patient care. Expert Review of Hematology (1747-4086) puts these advances in context and explores how they will translate directly into clinical practice.