The Endothelial Activation and Stress Index (EASIX) score is an independent prognostic factor in patients with diffuse large B-cell lymphomaopen access
- Authors
- Park, Sungwoo; Go, Se-Il; Lee, Gyeong-Won
- Issue Date
- 25-Jul-2022
- Publisher
- BMC
- Keywords
- Lymphoma; Large B-cell; Diffuse; Endothelial Activation and Stress Index; Prognosis; Drug-related side effects and adverse reactions
- Citation
- BMC CANCER, v.22, no.1
- Indexed
- SCIE
SCOPUS
- Journal Title
- BMC CANCER
- Volume
- 22
- Number
- 1
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/1032
- DOI
- 10.1186/s12885-022-09915-4
- ISSN
- 1471-2407
1471-2407
- Abstract
- Background The endothelial activation and stress index (EASIX) score has been reported to predict overall survival (OS) in hematological cancers. However, it has not been validated as a prognostic marker for diffuse large B-cell lymphoma (DLBCL) to date. Methods The records of 265 patients who presented with DLBCL in the Republic of Korea between January 07, 2004, and March 05, 2020 were retrospectively reviewed. For all included patients, EASIX scores were calculated using serum lactate dehydrogenase (LDH) and creatinine levels and the platelet count measured at diagnosis as follows: LDH (U/L) x creatinine (mg/dL)/platelet count (10(9)/L). Results The median age of the patients was 64 years. The optimal cutoff value of EASIX according to the receiver operating characteristic analysis for OS was 1.33. All the patients were treated with cyclophosphamide, doxorubicin, vincristine, and prednisone combined with rituximab. The 1-year OS and progression-free survival (PFS) rates were lower in the high-EASIX group than in the low EASIX group (63.8% vs. 84.4%, p < 0.001 and 54.0% vs. 79.6%, p < 0.001, respectively). A high EASIX was an independent poor prognostic factor for OS and PFS (hazard ratio, 1.606; 95% CI, 1.077-2.395; p = 0.020 and hazard ratio, 1.621; 95% CI, 1.066-2.464; p = 0.024, respectively). Conclusions EASIX is a readily available and cheaply obtainable parameter in clinical studies and shows considerable potential as a new prognostic marker for patients with newly diagnosed DLBCL.
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