Background: This study investigated the predictive value of β2-microglobulin (β2-MG) on the prognosis of diffuse large B-cell lymphoma (DLBCL) patients.
Methods: Patients with DLBCL diagnosed by pathologic biopsy were collected from January 2021 through December 2022, and a total of 98 patients were finally included. The 98 patients were grouped according to their prognosis, i.e., into the survival group (n = 69) and death group (n = 29). The critical value of β2-MG for survival in DLBCL patients was obtained by ROC curve. Kaplan Meier curve was plotted to analyze the relationship between β2-MG and the overall survival of DLBCL patients, and a one-way test was performed to examine the clinical data of the patients. Independent predictors affecting the prognosis of DLBCL patients were screened using unifactorial and multifactorial Cox regression analysis. R 4.2.1 software was used to refit the constructed column-line graph prediction model and internal validation.
Results: The critical value of β2-MG for survival in DLBCL patients was 3.285 µg/L, obtained by ROC curve. All patients were categorized into the following two groups: β2-MG ≤ 3.285 group (n = 75) and β2-MG > 3.285 group (n = 23). During the follow-up period, 9 endpoint events occurred in the β2-MG ≤ 3.285 group and 20 endpoint events occurred in the β2-MG > 3.285 group. The β2-MG ≤ 3.285 group had a higher overall survival rate than the β2-MG > 3.285 group. High levels of β2-MG, LDH, and CRP were independent prognostic influences affecting overall survival in DLBCL patients. β2-MG, LDH, and CRP were combined to construct the prognostic prediction model, and there was a better consistency between the predicted probability and the actual results.
Conclusions: Poor treatment prognosis of DLBCL patients is closely related to abnormally elevated levels of β2-MG. High levels of β2-MG, LDH, and CRP are independent risk factors for disease progression and prognostic survival in DLBCL patients.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.7754/Clin.Lab.2024.240907 | DOI Listing |
Front Immunol
March 2025
State Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, China.
Diffuse large B-cell lymphoma (DLBCL) and chronic lymphocytic leukemia (CLL) are subtypes of non-Hogkin lymphoma (NHL) that are generally distinct form one cases, but the transformation of one of these diseases into the other is possible. Some patients with CLL, for instance, have the potential to develop Richter transformation such that they are diagnosed with a rare, invasive DLBCL subtype. In this study, bioinformatics analyses of these two NHL subtypes were conducted, identifying key patterns of gene expression and then experimentally validating the results.
View Article and Find Full Text PDFOncol Lett
April 2025
Department of Thoracic Oncology and State Key Laboratory of Biotherapy, Cancer Center, West China Hospital, Sichuan University, Chengdu, Sichuan 610041, P.R. China.
Primary gingival diffuse large B-cell lymphoma (DLBCL) with muscle invasion is rare and accounts for ~0.5% of all reported cases of extranodal lymphoma. The present study describes the case of a 49-year-old man that initially presented at Yingshan County People's Hospital (Nanchong, China) in August 2017 with a chief complaint of tenderness and swelling of the jaw.
View Article and Find Full Text PDFRegen Ther
March 2025
Novartis Pharma K.K., Tokyo, Japan.
Background: Tisagenlecleucel, an autologous CD19-directed chimeric antigen receptor T-cell therapy, was approved in Japan, in March 2019 for patients with relapsed/refractory (r/r) B-cell acute lymphoblastic leukamia and r/r diffuse large B-cell lymphoma, and in August 2022 for patients with r/r follicular lymphoma. Post-approval, a key goal has been to upscale and continuously improve manufacturing and shipment success rates (MSR and SSR, respectively) in the commercial setting to meet the needs of patients worldwide, including in Japan. Herein, we report accrued experience from a 4-year journey of commercial tisagenlecleucel manufacturing process optimization for patients in Japan.
View Article and Find Full Text PDFAnn Hematol
March 2025
Department of Biological Sciences, Minnesota State University Mankato, Mankato, USA.
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!