Induction therapy with bortezomib and dexamethasone followed by autologous stem cell transplantation versus autologous stem cell transplantation alone in the treatment of renal AL amyloidosis: a randomized controlled trial

被引:64
作者
Huang, Xianghua [1 ]
Wang, Qingwen [1 ]
Chen, Wencui [1 ]
Zeng, Caihong [1 ]
Chen, Zhaohong [1 ]
Gong, Dehua [1 ]
Zhang, Haitao [1 ]
Liu, Zhihong [1 ]
机构
[1] Nanjing Univ, Jinling Hosp, Sch Med, Res Inst Nephrol, Nanjing 210002, Jiangsu, Peoples R China
关键词
AL amyloidosis; Bortezomib; Autologous stem cell transplantation; LIGHT-CHAIN AMYLOIDOSIS; HIGH-DOSE MELPHALAN; PRIMARY SYSTEMIC AMYLOIDOSIS; RELAPSED MULTIPLE-MYELOMA; TWICE-WEEKLY BORTEZOMIB; HEMATOLOGIC RESPONSE; SURVIVAL; CYCLOPHOSPHAMIDE; CHEMOTHERAPY; COMBINATION;
D O I
10.1186/1741-7015-12-2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Although the use of bortezomib alone and in combination with steroids has shown efficacy in AL amyloidosis, its role in combination with high-dose melphalan and autologous stem cell transplantation (HDM/SCT) is unknown. In this study, we evaluated bortezomib in combination with dexamethasone (BD) for induction chemotherapy prior to HDM/SCT. Methods: This was a single-center, prospective, randomized controlled trial comparing induction therapy consisting of two BD cycles followed by HDM/SCT (BD + HDM/SCT) with HDM/SCT alone in the treatment of patients with newly diagnosed AL amyloidosis. The hematological and organ responses of the patients were assessed every three months post HDM/SCT. Results: Fifty-six patients newly diagnosed with renal (100%), cardiac (57.1%), liver (7.1%), or nervous system (8.9%) AL amyloidosis were enrolled in this study; 28 patients were assigned to each arm. Two patients died within 100 days of HDM/SCT (3.6% treatment-related mortality). The overall hematologic response rates in the BD + HDM/SCT arm and HDM/SCT arm at three, six and twelve months were 78.5% versus 50%, 82.1% versus 53.5% and 85.7% versus 53.5%, respectively. In the BD + HDM/SCT arm, 15 (53.5%) patients achieved a hematologic response after BD and before HDM/SCT. An intention-to-treat analysis revealed a higher rate of complete remission in the BD + HDM/SCT arm at both 12 and 24 months (67.9% and 70%, respectively) than with the HDM/SCT-only therapy (35.7% and 35%, respectively, P = 0.03). After a median follow-up of 28 months, the survival rates at 24 months post-treatment start were 95.0% in the BD + HDM/SCT group and 69.4% in the HDM/SCT alone group (P = 0.03). Conclusions: Our preliminary data suggest that the outcome of treating AL amyloidosis with BD induction and HDM/SCT was superior to the outcome of the HDM/SCT treatment alone.
引用
收藏
页数:10
相关论文
共 44 条
[1]   Consensus guidelines for the conduct and reporting of clinical trials in systemic light-chain amyloidosis [J].
Comenzo, R. L. ;
Reece, D. ;
Palladini, G. ;
Seldin, D. ;
Sanchorawala, V. ;
Landau, H. ;
Falk, R. ;
Wells, K. ;
Solomon, A. ;
Wechalekar, A. ;
Zonder, J. ;
Dispenzieri, A. ;
Gertz, M. ;
Streicher, H. ;
Skinner, M. ;
Kyle, R. A. ;
Merlini, G. .
LEUKEMIA, 2012, 26 (11) :2317-2325
[2]   Amyloidosis [J].
Comenzo R.L. .
Current Treatment Options in Oncology, 2006, 7 (3) :225-236
[3]   Autologous stem cell transplantation for primary systemic amyloidosis [J].
Comenzo, RL ;
Gertz, MA .
BLOOD, 2002, 99 (12) :4276-4282
[4]   Dose-intensive melphalan with blood stem cell support for the treatment of AL amyloidosis: One-year follow-up in five patients [J].
Comenzo, RL ;
Vosburgh, E ;
Simms, RW ;
Bergethon, P ;
Sarnacki, D ;
Finn, K ;
Dubrey, S ;
Faller, DV ;
Wright, DG ;
Falk, RH ;
Skinner, M .
BLOOD, 1996, 88 (07) :2801-2806
[5]   Serum cardiac troponins and N-terminal pro-brain natriuretic peptide: A staging system for primary systemic amyloidosis [J].
Dispenzieri, A ;
Gertz, MA ;
Kyle, RA ;
Lacy, MQ ;
Burritt, MF ;
Therneau, TM ;
Greipp, PR ;
Witzig, TE ;
Lust, JA ;
Rajkumar, SV ;
Fonseca, R ;
Zeldenrust, SR ;
McGregor, CGA ;
Jaffe, AS .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (18) :3751-3757
[6]   Definition of organ involvement and treatment response in immunoglobulin light chain amyloidosis (AL): A consensus opinion from the 10th International Symposium on Amyloid and Amyloidosis [J].
Gertz, MA ;
Comenzo, R ;
Falk, RH ;
Fermand, JP ;
Hazenberg, BP ;
Hawkins, PN ;
Merlini, G ;
Moreau, P ;
Ronco, P ;
Sanchorawala, V ;
Sezer, O ;
Solomon, A ;
Grateau, G .
AMERICAN JOURNAL OF HEMATOLOGY, 2005, 79 (04) :319-328
[7]   Myeloablative chemotherapy with stem cell rescue for the treatment of primary systemic amyloidosis: a status report [J].
Gertz, MA ;
Lacy, MQ ;
Dispenzieri, A .
BONE MARROW TRANSPLANTATION, 2000, 25 (05) :465-470
[8]   Prospective randomized trial of melphalan and prednisone versus vincristine, carmustine, melphalan, cyclophosphamide, and prednisone in the treatment of primary systemic amyloidosis [J].
Gertz, MA ;
Lacy, MQ ;
Lust, JA ;
Greipp, PR ;
Witzig, TE ;
Kyle, RA .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (01) :262-267
[9]   Effect of hematologic response on outcome of patients undergoing transplantation for primary amyloidosis: importance of achieving a complete response [J].
Gertz, Morie A. ;
Lacy, Martha Q. ;
Dispenzieri, Angela ;
Hayman, Suzanne R. ;
Kumar, Shaji K. ;
Leung, Nelson ;
Gastineau, Dennis A. .
HAEMATOLOGICA, 2007, 92 (10) :1415-1418
[10]   Immunoglobulin light chain amyloidosis: 2013 update on diagnosis, prognosis, and treatment [J].
Gertz, Morie A. .
AMERICAN JOURNAL OF HEMATOLOGY, 2013, 88 (05) :417-425