Successful treatment of renal light chain (AL) amyloidosis with bortezomib and dexamethasone (VD)

B. Huang , J. Li , X. Xu , D. Zheng , Z. Zhou , J. Liu
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引用次数: 8

Abstract

Objective

To assess the efficacy and tolerability of bortezomib with dexamethasone for patients with renal light chain (AL) amyloidosis.

Methods

Twelve newly diagnosed patients with renal AL amyloidosis were treated with a combination of bortezomib (1.3 mg/m2/d iv, d1, 4, 8, 11) and dexamethasone (20 mg/d iv drip, d1–4).

Results

Median follow-up time was 22.5 months (range, 2.1–53.6). Ten patients were evaluable. Five out of 10 (50%) patients achieved complete hematologic responses (CHR), and totally 8/10 (80%) achieved hematologic responses (HR). Median time to hematologic response was 1 month. All patients who received HR had no hematologic progression during follow-up period. Five patients (50%) had kidney responses and the other 5 patients (50%) were stable. Median time to kidney response was 3 months. No patients presented renal progression during follow-up. One patient achieved PR after 4 cycles of VD and then received autologous peripheral blood stem cell transplantation. Two out of 10 evaluable patients without hematologic response had died with median overall survival of 8.2 months. Eight of them who had HR were alive with median follow-up time of 28.5 months. Infection (6/12) and fatigue (5/12) were the most frequent side effects. Three patients developed herpes zoster and had to discontinue therapy.

Conclusions

VD produces rapid, deep and durable hematological responses and renal responses in the majority of patients with newly diagnosed renal AL. It is well tolerated. This treatment may be a good option as first-line treatment for renal AL amyloidosis patients.

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硼替佐米联合地塞米松成功治疗肾轻链淀粉样变性
目的评价硼替佐米联合地塞米松治疗肾轻链淀粉样变性的疗效和耐受性。方法采用硼替佐米(1.3 mg/m2/d iv, d1, 4, 8, 11)和地塞米松(20 mg/d iv滴注,d1 - 4)联合治疗12例新诊断的肾AL淀粉样变患者。结果中位随访时间为22.5个月(范围2.1 ~ 53.6个月)。10例患者可评估。10例患者中有5例(50%)达到完全血液学反应(CHR), 8/10例(80%)达到血液学反应(HR)。血液反应的中位时间为1个月。所有接受HR治疗的患者在随访期间均无血液学进展。5例患者(50%)出现肾脏反应,另外5例患者(50%)病情稳定。中位肾脏反应时间为3个月。随访期间无患者出现肾脏疾病进展。1例患者在VD 4个周期后达到PR,并接受自体外周血干细胞移植。10例可评估的无血液学反应的患者中有2例死亡,中位总生存期为8.2个月。8例HR患者存活,中位随访时间为28.5个月。感染(6/12)和疲劳(5/12)是最常见的副作用。三名患者出现带状疱疹,不得不停止治疗。结论svd在大多数新诊断的肾性AL患者中产生快速、深入、持久的血液学反应和肾反应,耐受性良好。这种治疗可能是肾AL淀粉样变患者的一线治疗的一个很好的选择。
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来源期刊
Pathologie-biologie
Pathologie-biologie 医学-病理学
自引率
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0
审稿时长
6-12 weeks
期刊最新文献
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