Predictive levels of vascular endothelial growth factor (VEGF), thymidine kinase 1 (TK1) with interleukin-6 (IL-6), plasma T cells, NK cells as well as B cells in treating diffuse large B-cell lymphoma receiving rituximab
- PMID: 40837360
- PMCID: PMC12363351
- DOI: 10.5937/jomb0-54911
Predictive levels of vascular endothelial growth factor (VEGF), thymidine kinase 1 (TK1) with interleukin-6 (IL-6), plasma T cells, NK cells as well as B cells in treating diffuse large B-cell lymphoma receiving rituximab
Abstract
Background: The aim was to explore the effect of rituximab in combination with chemotherapy in treating diffuse large B-cell lymphoma and levels of vascular endothelial growth factor (VEGF), thymidine kinase 1(TK1) with interleukin-6 (IL-6), plasma T cells, NK cells as well as B cells.
Methods: Eighty patients admitted to Lujiang County People's Hospital from January 2022 to January 2024 were included. The control group accepted cyclophosphamide, doxorubicin, vincristine, and prednisone chemotherapy regimens. The research group was treated with rituximab based on the control group. The clinical effects, vascular endothelial growth factor (VEGF), thymidine kinase 1 (TK1) and interleukin-6 (IL-6) levels, lymphocyte subsets index, quality of life and occurrence of adverse reactions were compared in both groups.
Results: The research group's total clinical effective rate was better than the control group's (P<0.05). After therapy, compared to the control group, vascular endothelial growth factor, thymidine kinase 1, and interleukin-6 levels in the research group presented lower (P<0.05), plasma T cells, natural killer cells along with B cells in the research group presented lower (P<0.05), and Quality of Life Core Questionnaire-Core 30 scores in the research group presented higher (P<0.05). There was no difference in adverse reactions between the two groups (P>0.05).
Conclusions: Rituximab combined with chemotherapy is effective in treating DLBCL patients, which can reduce serum-related factors promoting immune function and quality of life. Our study may provide compelling evidence for supporting the therapeutic regimen of rituximab combined with chemotherapy in DLBCL patients.
Uvod: Cilj je bio da se ispita efekat rituksimaba u kombinaciji sa hemoterapijom u lečenju difuznog velikog B-ćelijskog limfoma, kao i nivoa vaskularnog endotelnog faktora rasta (VEGF), timidinske kinaze 1 (TK1) sa inter leukinom-6 (IL-6), plazma T ćelijama, NK ćelijama i B ćelijama.
Metode: U istraživanje je bilo uključeno 80 pacijenata primljenih u Narodnu bolnicu okruga Lujiang od januara 2022. do januara 2024. Kontrolna grupa je primala hemoterapijski režim koji je uključivao ciklofosfamid, dokso-rubicin, vinkristin i prednizon. Grupa ispitanika je, pored terapije kontrolne grupe, bila lečena i rituksimabom. Upoređivani su klinički efekti, nivoi vaskularnog endotelnog faktora rasta (VEGF), timidinske kinaze 1 (TK1) i interleukina-6 (IL-6), indeks podgrupa limfocita, kvalitet života i učestalost neželjenih reakcija kod obe grupe.
Rezultati: Ukupna klinička efikasnost u grupi ispitanika je bila bolja nego u kontrolnoj grupi (P<0,05). Nakon terapije, u poređenju sa kontrolnom grupom, nivoi vaskularnog endotelnog faktora rasta, timidinske kinaze 1 i interleukina-6 u grupi ispitanika su bili niži (P<0,05). Nivoi plazma T ćelija, prirodnih ćelija ubica (NK ćelija) i B ćelija su takođe bili niži u grupi ispitanika (P<0,05). Rezultati upitnika o kvalitetu života (Core 30) su u grupi ispitanika bili viši (P<0,05). Nije bilo razlike u učestalosti neželjenih reakcija između dve grupe (P>0,05).
Zaključak: Rituksimab u kombinaciji sa hemoterapijom je efika san u lečenju pacijenata sa DLBCL, jer može da smanji se rumske faktore povezane sa imunitetom, da poboljša funkciju imunog sistema i kvalitet života. Naša studija može da pruži ubedljive dokaze koji govore u prilog terapijskog režima rituksimaba u kombinaciji sa hemoterapijom kod pacijenata sa DLBCL.
Keywords: chemotherapy; diffuse large B-cell lymphoma; lymphocyte subsets index; rituximab.
2025 Lihua Tian, Baoan Luo, Jun Tang, Jiagui Ye, published by CEON/CEES.
Conflict of interest statement
All the authors declare that they have no conflict of interest in this work.Conflict of Interest: The authors stated that they have no conflicts of interest regarding the publication of this article.
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