Sequential response-driven bortezomib-based therapy followed by autologous stem cell transplant in AL amyloidosis

被引:22
作者
Basset, Marco [1 ,2 ]
Milani, Paolo [1 ,2 ]
Nuvolone, Mario [1 ,2 ]
Benigna, Francesca [1 ,2 ]
Rodigari, Lara [1 ,2 ]
Foli, Andrea [1 ,2 ]
Merlini, Giampaolo [1 ,2 ]
Palladini, Giovanni [1 ,2 ]
机构
[1] Univ Pavia, Amyloidosis Res & Treatment Ctr, Fdn Ist Ricovero & Cura Carattere Sci Policlin Sa, Pavia, Italy
[2] Univ Pavia, Dept Mol Med, Pavia, Italy
关键词
LIGHT-CHAIN AMYLOIDOSIS; HIGH-DOSE MELPHALAN; INDUCTION THERAPY; DARATUMUMAB; SURVIVAL;
D O I
10.1182/bloodadvances.2020002219
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Autologous stem cell transplant (ASCT) is highly effective in selected patients with light chain (AL) amyloidosis. Bortezomib, preceding or following ASCT, improves responses. Satisfactory responses, including at least a partial response, very good partial response (VGPR) with organ response, or complete response, can be observed after induction therapy alone. We report 139 patients treated upfront with cyclophosphamide/bortezomib/dexamethasone (CyBorD), followed by ASCT only if response was unsatisfactory. Only 1 treatment-related death was observed. After CyBorD, hematologic response (HR) rate was 68% (VGPR or better, 51%), with 45% satisfactory responses. Transplant was performed in 55 (40%) subjects and resulted in an 80% HR rate (65% >= VGPR). Five-year survival was 86% and 84% in patients treated with ASCT or CyBorD alone, respectively (P = .438). Also, 6- and 12-month landmark analyses did not show differences in survival. Duration of response was not different in the 2 groups (60 vs 49 months; P = .670). Twenty-one (15%) patients with an unsatisfactory response to CyBorD could not undergo ASCT because of ineligibility or refusal; instead, they received rescue chemotherapy, with HR in 38% of cases and 51% 5-year survival. This sequential response-driven approach, offering ASCT to patients who do not attain satisfactory response to upfront CyBorD, is very safe and effective in AL amyloidosis.
引用
收藏
页码:4175 / 4179
页数:5
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