BEGEV as Salvage Therapy in Relapsed/Refractory Non-Hodgkin Lymphoma: Real-World Outcomes and Transplantation Feasibility
| dc.contributor.author | Candan, Ozlem | |
| dc.contributor.author | Buyukkurkcu, Basak | |
| dc.contributor.author | Karti, Sami | |
| dc.contributor.author | Uzay, Ant | |
| dc.date.accessioned | 2026-11-05T11:00:29Z | |
| dc.date.issued | 2026 | |
| dc.description.abstract | Background and Objectives: Relapsed/refractory non-Hodgkin lymphoma (R/R NHL) remains a major therapeutic challenge, particularly in patients with peripheral T-cell lymphomas (PTCL), who frequently exhibit poor responses to salvage therapy and inferior survival outcomes. Achieving adequate disease control before autologous stem cell transplantation (ASCT) is a critical determinant of long-term survival. The bendamustine, gemcitabine, vinorelbine, and prednisolone (BEGEV) regimen has demonstrated high efficacy and favorable tolerability in relapsed/refractory classical Hodgkin lymphoma; however, data regarding its role in NHL are extremely limited. Materials and Methods: We conducted a retrospective, single-center analysis of patients with R/R NHL who received the BEGEV regimen as salvage therapy. Clinical characteristics, response rates, transplantation outcomes, progression-free survival (PFS), overall survival (OS), and safety data were evaluated. Treatment responses were assessed according to standard radiologic response criteria. Survival analyses were performed using the Kaplan-Meier method. Results: A total of 68 patients with R/R NHL were included in the analysis. Diffuse large B-cell lymphoma (DLBCL) was the predominant histological subtype, accounting for 49 patients (72.1%). BEGEV was administered predominantly in later salvage settings. Response assessments were available for 56 patients. Among evaluable patients, the objective response rate (ORR) was 73.2%, whereas the ITT ORR was 60.3% (41/68). Following BEGEV therapy, 25 patients (36.8%) proceeded to autologous stem cell transplantation (ASCT), while 8 patients (11.8%) underwent allogeneic stem cell transplantation (allo-SCT). Exploratory analyses demonstrated longer overall survival (log-rank p = 0.012) and progression-free survival (log-rank p = 0.011) among patients who subsequently underwent transplantation; however, these findings should be interpreted with caution because of the retrospective study design and the potential for selection and immortal time biases. Median PFS and OS were 4 and 26 months, respectively. Adverse events were predominantly hematologic and generally manageable. Conclusions: BEGEV may represent a reasonable salvage regimen for selected patients with R/R NHL and may facilitate disease control allowing subsequent transplantation in selected patients, including selected PTCL patients. | |
| dc.description.issue | 8 | |
| dc.description.pages | 1502 | |
| dc.description.volume | 62 | |
| dc.identifier.doi | 10.3390/medicina62081502 | |
| dc.identifier.issn | 1010-660X | |
| dc.identifier.issn | 1648-9144 | |
| dc.identifier.uri | https://doi.org/10.3390/medicina62081502 | |
| dc.identifier.uri | https://openaccess.acibadem.edu.tr/handle/11443/10453 | |
| dc.identifier.wos | WOS:001859379900001 | |
| dc.language.iso | en | |
| dc.publisher | MDPI | |
| dc.relation.hasversion | 10.3390/medicina62081502 | |
| dc.relation.ispartof | MEDICINA-LITHUANIA | |
| dc.subject | relapsed/refractory non-Hodgkin lymphoma | |
| dc.subject | BEGEV | |
| dc.subject | salvage therapy | |
| dc.subject | stem cell transplantation | |
| dc.subject | peripheral T-cell lymphoma | |
| dc.subject | STEM-CELL TRANSPLANTATION | |
| dc.subject | PROGNOSTIC VALUE | |
| dc.subject | PHASE-II | |
| dc.subject | BENDAMUSTINE | |
| dc.subject | RITUXIMAB | |
| dc.subject | CHEMOTHERAPY | |
| dc.subject | GEMCITABINE | |
| dc.subject | SURVIVAL | |
| dc.subject | Medicine, General & Internal | |
| dc.subject | General & Internal Medicine | |
| dc.title | BEGEV as Salvage Therapy in Relapsed/Refractory Non-Hodgkin Lymphoma: Real-World Outcomes and Transplantation Feasibility | |
| dc.type | Article | |
| oaire.citation.edition | Science Citation Index Expanded (SCI-EXPANDED) | |
| oaire.citation.issue | 8 | |
| oaire.citation.volume | 62 | |
| person.identifier.rid | JXN-7884-2024 | |
| person.identifier.rid | KIV-9553-2024 |
