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Maintenance regimen of GM‐CSF with rituximab and lenalidomide improves survival in high‐risk B‐cell lymphoma by modulating natural killer cells
BACKGROUND: The treatment of high‐risk B‐cell lymphoma (BCL) remains a challenge, especially in the elderly. METHODS: A total of 83 patients (median age 65 years), who have achieved a complete response after induction therapy, were divided into two groups: R(2) + GM‐CSF regimen (lenalidomide, rituxi...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10315792/ https://www.ncbi.nlm.nih.gov/pubmed/37081754 http://dx.doi.org/10.1002/cam4.5969 |
Sumario: | BACKGROUND: The treatment of high‐risk B‐cell lymphoma (BCL) remains a challenge, especially in the elderly. METHODS: A total of 83 patients (median age 65 years), who have achieved a complete response after induction therapy, were divided into two groups: R(2) + GM‐CSF regimen (lenalidomide, rituximab, granulocyte‐macrophage colony‐stimulating factor [GM‐CSF]) as maintenance therapy (n = 39) and observation (n = 44). The efficacy of the R(2) + GM‐CSF regimen as maintenance in patient with high‐risk BCL was analyzed and compared with observation. RESULTS: The number of natural killer cells in patients increased after R(2) + GM‐CSF regimen administration (0.131 × 10(9)/L vs. 0.061 × 10(9)/L, p = 0.0244). Patients receiving the R(2) + GM‐CSF regimen as maintenance therapy had longer remission (duration of response: 18.9 vs. 11.3 months, p = 0.001), and longer progression‐free survival (not reached (NR) vs. 31.7 months, p = 0.037), and overall survival (OS) (NR vs. NR, p = 0.015). The R(2) + GM‐CSF regimen was safe and well tolerated. High international prognostic index score (p = 0.012), and high tumor burden (p = 0.005) appeared to be independent prognostic factors for worse PFS. CONCLUSIONS: The maintenance therapy of R(2) + GM‐CSF regimen may improve survival in high‐risk BCL patients, which might be modulated by amplification of natural killer cells. The efficacy of the R(2) + GM‐CSF maintenance regimen has to be further validated in prospective random clinical trials. |
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