B. Huang , J. Li , X. Xu , D. Zheng , Z. Zhou , J. Liu
{"title":"Successful treatment of renal light chain (AL) amyloidosis with bortezomib and dexamethasone (VD)","authors":"B. Huang , J. Li , X. Xu , D. Zheng , Z. Zhou , J. Liu","doi":"10.1016/j.patbio.2014.10.001","DOIUrl":null,"url":null,"abstract":"<div><h3>Objective</h3><p>To assess the efficacy and tolerability of bortezomib with dexamethasone for patients with renal light chain (AL) amyloidosis.</p></div><div><h3>Methods</h3><p>Twelve newly diagnosed patients with renal AL amyloidosis were treated with a combination of bortezomib (1.3<!--> <!-->mg/m<sup>2</sup>/d iv, d1, 4, 8, 11) and dexamethasone (20<!--> <!-->mg/d iv drip, d1–4).</p></div><div><h3>Results</h3><p>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.</p></div><div><h3>Conclusions</h3><p>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.</p></div>","PeriodicalId":19743,"journal":{"name":"Pathologie-biologie","volume":"63 1","pages":"Pages 17-20"},"PeriodicalIF":0.0000,"publicationDate":"2015-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.patbio.2014.10.001","citationCount":"8","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pathologie-biologie","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S036981141400145X","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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.