Autologous stem-cell collection following VTD or VRD induction therapy in multiple myeloma: a single-center experience

被引:12
作者
Laurent, Vanille [1 ]
Fronteau, Clementine [1 ]
Antier, Chloe [2 ]
Dupuis, Pascale [3 ]
Tessoulin, Benoit [2 ,4 ]
Gastinne, Thomas [2 ]
Mahe, Beatrice [2 ]
Blin, Nicolas [2 ]
Dubruille, Viviane [2 ]
Lok, Anne [2 ]
Chevallier, Patrice [2 ,4 ]
Guillaume, Thierry [2 ]
Garnier, Alice [2 ]
Peterlin, Pierre [2 ]
Le Bourgeois, Amandine [2 ]
Vantyghem, Sophie [2 ,4 ]
Tiab, Mourad [5 ]
Godmer, Pascal [6 ]
Sadot, Sophie [7 ]
Loirat, Marion [8 ]
Trebouet, Adrien [9 ]
Cormier, Nicolas [1 ]
Le Gouill, Steven [2 ,4 ,10 ,11 ,12 ]
Moreau, Philippe [2 ,4 ,10 ,11 ,12 ]
Touzeau, Cyrille [2 ,4 ,10 ,11 ,12 ]
机构
[1] Hop Hotel Dieu, Pharm Clin Oncol, Nantes, France
[2] Hop Hotel Dieu, Serv Hematol Clin, Nantes, France
[3] Etab Francais Sang, Nantes, France
[4] Univ Nantes, Fac Med, Nantes, France
[5] Ctr Hosp Dept, Serv Hematol Clin, La Roche Sur Yon, France
[6] Ctr Hosp, Serv Hematol Clin, Vannes, France
[7] Hop Prive Le Confluent, Nantes, France
[8] Ctr Hosp, Serv Hematol Clin, St Nazaire, France
[9] Ctr Hosp, Serv Hematol Clin, Lorient, France
[10] Univ Nantes, CNRS, INSERM, CRCINA, Nantes, France
[11] ILIAD, Site Rech Integree Canc SIRIC, Nantes, France
[12] Univ Nantes, Nantes, France
关键词
G-CSF; DOSE CYCLOPHOSPHAMIDE; MOBILIZATION; TRANSPLANTATION; LENALIDOMIDE; PLERIXAFOR; DEXAMETHASONE; BORTEZOMIB; SUPERIOR; IMPACT;
D O I
10.1038/s41409-020-01033-8
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Triplet-drug regimen bortezomib-thalidomide-dexamethasone (VTD) and bortezomib-lenalidomide-dexamethasone (VRD) are considered as standard of care induction prior autologous stem-cell transplantation (ASCT) in myeloma. In addition to improve response rate, induction therapy should preserve an adequate stem-cell collection. In the present retrospective study, we analyzed stem-cell collection in 325 newly diagnosed myeloma patients who received either VTD or VRD induction before ASCT. Stem-cell mobilization consisted of intravenous cyclophosphamide plus G-CSF. Plerixafor was administered preemptively to rescue mobilization. In comparison with VTD, VRD induction was associated with a more frequent use of plerixafor (19.3% versus 5.4%,p = 0.004) and with an increased number of apheresis to reach adequate collection (>2 apheresis required in 42.3% versus 30.2%,p = 0.05). Moreover, more patients experienced collection failure in the VRD group (6% versus 1.8%,p = 0.004). The median number of CD34-positive cells (x10(6)/kg) was lower in the VRD group: 8.5 versus 9.3 (p = 0.05) in the VTD group. The vast majority of patients underwent ASCT (93% versus 98%, in VRD and VTD group, respectively). These data highlight the need of optimal stem-cell collection strategy, especially in the context of tandem transplantation and incorporation of anti-CD38 monoclonal antibody into induction.
引用
收藏
页码:395 / 399
页数:5
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