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序贯反应驱动的基于硼替佐米的疗法,随后在AL淀粉样变性中进行自体干细胞移植。

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

作者信息

Basset Marco, Milani Paolo, Nuvolone Mario, Benigna Francesca, Rodigari Lara, Foli Andrea, Merlini Giampaolo, Palladini Giovanni

机构信息

Amyloidosis Research and Treatment Center, Fondazione Istituto di Ricovero e Cura a Carattere Scientifico Policlinico San Matteo and Department of Molecular Medicine, University of Pavia, Pavia, Italy.

出版信息

Blood Adv. 2020 Sep 8;4(17):4175-4179. doi: 10.1182/bloodadvances.2020002219.

Abstract

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.

摘要

自体干细胞移植(ASCT)对某些轻链(AL)淀粉样变性患者非常有效。在ASCT之前或之后使用硼替佐米可改善反应。仅诱导治疗后即可观察到满意的反应,包括至少部分反应、伴有器官反应的非常好的部分反应(VGPR)或完全反应。我们报告了139例 upfront接受环磷酰胺/硼替佐米/地塞米松(CyBorD)治疗的患者,仅在反应不满意时才进行ASCT。仅观察到1例与治疗相关的死亡。CyBorD治疗后,血液学反应(HR)率为68%(VGPR或更好为51%),45%为满意反应。55例(40%)受试者接受了移植,HR率为80%(65%≥VGPR)。单独接受ASCT或CyBorD治疗的患者5年生存率分别为86%和84%(P = 0.438)。此外,6个月和12个月的标志性分析未显示生存率有差异。两组的反应持续时间无差异(60对49个月;P = 0.670)。21例(15%)对CyBorD反应不满意的患者因不符合条件或拒绝而无法接受ASCT;相反,他们接受了挽救性化疗,38%的病例有血液学反应,5年生存率为51%。这种序贯反应驱动的方法,为对 upfront CyBorD未获得满意反应的患者提供ASCT,在AL淀粉样变性中非常安全有效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bba/7479942/11ff84955f07/advancesADV2020002219absf1.jpg

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