4.3 Article

The role of induction therapy before autologous stem cell transplantation in low disease burden AL amyloidosis patients

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TAYLOR & FRANCIS LTD
DOI: 10.1080/13506129.2020.1835635

关键词

AL amyloidosis; stem cell transplantation; induction; prognosis; bortezomib

资金

  1. Key Research and Development Plan Project of Jiangsu Province - Social Development Projects [BE2017721]
  2. Jiangsu Natural Science Foundation Youth Fund Project [BK20170625]
  3. National Key Research and Development Program 'Stem Cell and Transformation Research' [2017YFA0104500]

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Induction therapy with bortezomib may benefit AL amyloidosis patients with low disease burden eligible for ASCT, showing significantly improved efficacy and survival rates compared to other induction therapies or no induction therapy.
Background Induction therapy is recommended before autologous stem cell transplantation (ASCT) for AL amyloidosis patients with high disease burden [bone marrow plasma cells (BMPCs) > 10%], but the role of induction therapy before ASCT in patients with low disease burden (BMPCs <= 10%) is still unknown. Methods A total of 227 patients with AL amyloidosis were included in this study. Among 227 patients, 124 patients received bortezomib-based induction prior to ASCT and were defined as group A, 35 patients received other chemotherapeutic induction and were defined as group B, and the other 68 patients without induction were defined as group C. We compared the differences of efficacy and prognosis between the three groups. Results The haematological overall response rates (ORR) of groups A, B and C were 91%, 67% and 75%, respectively. The complete response rates (CR) of groups A, B and C were 50%, 25% and 20%, respectively. Both the ORR and CR rates of group A were significantly higher than those of groups B and C. The renal response rates of groups A, B and C were 64%, 46% and 47%, respectively. The cardiac response rates of groups A, B and C were 74%, 45% and 40%, respectively. The renal and cardiac responses rates of group A were also significantly higher than those of the other two groups. After a median follow-up of 44 months, the median OS was not reached. The 5-year estimated overall survival (OS) rates of groups A, B and C were 81%, 57% and 67%, respectively. The median progression-free survival (PFS) was 83 months for all patients. The 5-year estimated PFS rates of groups A, B and C were 61%, 38% and 49%, respectively. Both the OS and PFS of group A were higher than those of both group B and group C. On multivariate analysis, baseline dFLC > 50 mg/L was associated with worse survival, but induction with bortezomib was associated with better survival. Conclusion Our study demonstrated that low disease burden AL patients who are eligible for ASCT may benefit from bortezomib-based induction therapy.

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