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Outcomes in Refractory Diffuse Large B-Cell Lymphoma: Results from Two Prospective Korean Cohorts

Authors
Yi, JH | Jeong, SH  | Kim, SJ | Yoon, DH | Kang, HJ | Koh, Y | Kim, JS | Lee, WS | Yang, DH | Do, YR | Kim, MK | Yoo, KH | Choi, YS  | Yun, WJ | Park, Y | Jo, JC | Eom, HS | Kwak, JY | Shin, HJ | Park, BB | Yi, SY | Kwon, JH | Oh, SY | Kim, HJ | Sohn, BS | Won, JH | Hong, DS | Lee, HS | Lee, GW | Suh, C | Kim, WS
Citation
Cancer research and treatment, 55(1). : 325-333, 2023
Journal Title
Cancer research and treatment
ISSN
1598-29982005-9256
Abstract
Purpose: Diffuse large B-cell lymphoma (DLBCL) is the most common hematologic malignancy worldwide. Although substantial improvement has been achieved by the frontline rituximab-based chemoimmunotherapy, up to 40%–50% of patients will eventually have relapsed or refractory disease, whose prognosis is extremely dismal.
Materials and Methods: We have carried out two prospective cohort studies that include over 1,500 DLBCL patients treated with rituximab plus CHOP (#NCT01202448 and #NCT02474550). In the current report, we describe the outcomes of refractory DLBCL patients. Patients were defined to have refractory DLBCL if they met one of the followings, not achieving at least partial response after 4 or more cycles of R-CHOP; not achieving at least partial response after 2 or more cycles of salvage therapy; progressive disease within 12 months after autologous stem cell transplantation.
Results: Among 1,581 patients, a total of 260 patients met the criteria for the refractory disease after a median time to progression of 9.1 months. The objective response rate of salvage treatment was 26.4%, and the complete response rate was 9.6%. The median overall survival (OS) was 7.5 months (95% confidence interval, 6.4 to 8.6), and the 2-year survival rate was 22.1%±2.8%. The median OS for each refractory category was not significantly different (p=0.529).
Conclusion : In line with the previous studies, the outcomes of refractory DLBCL patients were extremely poor, which necessitates novel approaches for this population.
Keywords

MeSH

DOI
10.4143/crt.2022.008
PMID
35468269
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Hematology-Oncology
Ajou Authors
정, 성현  |  최, 윤석
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