Bortezomib, thalidomide, and dexamethasone versus bortezomib, lenalidomide, and dexamethasone in transplant-eligible newly diagnosed multiple myeloma: a systemic review and meta-analysis
Background The current study aimed to compare treatment responses, the incidence of the need for auto-HSCT, and the occurrence of specific adverse events (AEs) between VTD and velcade, VRD induction regimens in patients with transplant-eligible newly diagnosed multiple myeloma (NDMM).Methods This sy...
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2025-12-01
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author | Yin-Che Wang Cheng-Hsien Lin Yu-Chen Su Chieh-Lin Jerry Teng |
author_facet | Yin-Che Wang Cheng-Hsien Lin Yu-Chen Su Chieh-Lin Jerry Teng |
author_sort | Yin-Che Wang |
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description | Background The current study aimed to compare treatment responses, the incidence of the need for auto-HSCT, and the occurrence of specific adverse events (AEs) between VTD and velcade, VRD induction regimens in patients with transplant-eligible newly diagnosed multiple myeloma (NDMM).Methods This systematic review and meta-analysis included 15 studies: six evaluating the VTD regimen and nine evaluating the VRD one. The primary endpoints were response rates after induction therapy and the incidence of a need for autologous hematopoietic stem cell transplantion (auto-HSCT) between the groups. We also examined the occurrence of grade 3 or 4 hematological, infection, and thrombotic AEs in both groups.Results The VTD group showed an overall response rate (ORR) of 93%, while the VRD group had an ORR of 86%. The very good partial response (VGPR) rates were 61% in the VTD group and 60% in the VRD one. The auto-HSCT rate was higher in the VTD group, averaging 93% compared to 70% in the VRD one. The incidence of grade 3 or 4 hematological AEs was 31% for VTD and 33% for VRD. The rates of grade 3 or 4 infection-related AEs were 9% in the VTD group and 14% in the VRD one. The incidence of grade 3 or 4 thrombotic AEs was 4% for VTD and 3% for VRD.Conclusions With comparable safety profiles, VTD and VRD induction therapies are similarly effective for transplant-eligible NDMM, showing similar ORRs and VGPR rates. |
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language | English |
publishDate | 2025-12-01 |
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spelling | doaj-art-71b5547625d048a8b0554b05dd0ec5b92025-02-06T17:17:59ZengTaylor & Francis GroupHematology1607-84542025-12-0130110.1080/16078454.2025.2462249Bortezomib, thalidomide, and dexamethasone versus bortezomib, lenalidomide, and dexamethasone in transplant-eligible newly diagnosed multiple myeloma: a systemic review and meta-analysisYin-Che Wang0Cheng-Hsien Lin1Yu-Chen Su2Chieh-Lin Jerry Teng3Division of Hematology/Medical Oncology, Department of Medicine, Taichung Veterans General Hospital, Taichung, TaiwanDivision of Hematology/Medical Oncology, Department of Medicine, Taichung Veterans General Hospital, Taichung, TaiwanDivision of Hematology/Medical Oncology, Department of Medicine, Taichung Veterans General Hospital, Taichung, TaiwanDivision of Hematology/Medical Oncology, Department of Medicine, Taichung Veterans General Hospital, Taichung, TaiwanBackground The current study aimed to compare treatment responses, the incidence of the need for auto-HSCT, and the occurrence of specific adverse events (AEs) between VTD and velcade, VRD induction regimens in patients with transplant-eligible newly diagnosed multiple myeloma (NDMM).Methods This systematic review and meta-analysis included 15 studies: six evaluating the VTD regimen and nine evaluating the VRD one. The primary endpoints were response rates after induction therapy and the incidence of a need for autologous hematopoietic stem cell transplantion (auto-HSCT) between the groups. We also examined the occurrence of grade 3 or 4 hematological, infection, and thrombotic AEs in both groups.Results The VTD group showed an overall response rate (ORR) of 93%, while the VRD group had an ORR of 86%. The very good partial response (VGPR) rates were 61% in the VTD group and 60% in the VRD one. The auto-HSCT rate was higher in the VTD group, averaging 93% compared to 70% in the VRD one. The incidence of grade 3 or 4 hematological AEs was 31% for VTD and 33% for VRD. The rates of grade 3 or 4 infection-related AEs were 9% in the VTD group and 14% in the VRD one. The incidence of grade 3 or 4 thrombotic AEs was 4% for VTD and 3% for VRD.Conclusions With comparable safety profiles, VTD and VRD induction therapies are similarly effective for transplant-eligible NDMM, showing similar ORRs and VGPR rates.https://www.tandfonline.com/doi/10.1080/16078454.2025.2462249VTDVRDresponse rateprogression-free survivaladverse events |
spellingShingle | Yin-Che Wang Cheng-Hsien Lin Yu-Chen Su Chieh-Lin Jerry Teng Bortezomib, thalidomide, and dexamethasone versus bortezomib, lenalidomide, and dexamethasone in transplant-eligible newly diagnosed multiple myeloma: a systemic review and meta-analysis Hematology VTD VRD response rate progression-free survival adverse events |
title | Bortezomib, thalidomide, and dexamethasone versus bortezomib, lenalidomide, and dexamethasone in transplant-eligible newly diagnosed multiple myeloma: a systemic review and meta-analysis |
title_full | Bortezomib, thalidomide, and dexamethasone versus bortezomib, lenalidomide, and dexamethasone in transplant-eligible newly diagnosed multiple myeloma: a systemic review and meta-analysis |
title_fullStr | Bortezomib, thalidomide, and dexamethasone versus bortezomib, lenalidomide, and dexamethasone in transplant-eligible newly diagnosed multiple myeloma: a systemic review and meta-analysis |
title_full_unstemmed | Bortezomib, thalidomide, and dexamethasone versus bortezomib, lenalidomide, and dexamethasone in transplant-eligible newly diagnosed multiple myeloma: a systemic review and meta-analysis |
title_short | Bortezomib, thalidomide, and dexamethasone versus bortezomib, lenalidomide, and dexamethasone in transplant-eligible newly diagnosed multiple myeloma: a systemic review and meta-analysis |
title_sort | bortezomib thalidomide and dexamethasone versus bortezomib lenalidomide and dexamethasone in transplant eligible newly diagnosed multiple myeloma a systemic review and meta analysis |
topic | VTD VRD response rate progression-free survival adverse events |
url | https://www.tandfonline.com/doi/10.1080/16078454.2025.2462249 |
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