High-dose chemotherapy and autologous stem cell transplantation for primary central nervous system lymphoma: a multi-centre retrospective analysis from the United Kingdom

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作者
S Kassam
E Chernucha
A O’Neill
C Hemmaway
T Cummins
S Montoto
A Lennard
G Adams
K Linton
P McKay
D Davies
C Rowntree
S Easdale
T A Eyre
R Marcus
K Cwynarski
C P Fox
机构
[1] King’s College Hospital,Department of Haematology
[2] Nottingham University Hospitals NHS Trust,Department of Haematology
[3] University College Hospital,Department of Haematology
[4] Barking,Department of Haematology
[5] Havering and Redbridge University Hospitals,Department of Haematology
[6] University Hospital Southampton,Department of Haematology
[7] Barts Health NHS Trust,Department of Haematology
[8] Freeman Hospital,Department of Haematology
[9] Hammersmith Hospital,Department of Haematology
[10] The Christie NHS Foundation Trust,Department of Haematology
[11] Beatson West of Scotland Cancer Centre,Department of Haematology
[12] University Hospital of Wales,Department of Haematology
[13] The Royal Marsden Hospital,Department of Haematology
[14] Churchill Hospital,undefined
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摘要
The prognosis of patients with primary central nervous system lymphoma (PCNSL) has improved in recent years. This has partly been achieved by remission induction protocols incorporating high-dose methotrexate (HD-MTX) and rituximab. Given the high rates of relapse, consolidation therapy is usually considered in first response. Whole brain radiotherapy may prolong PFS but appears to confer no long-term survival advantage and is associated with significant neurocognitive dysfunction. Attempts to improve efficacy and reduce neurotoxicity of consolidation therapy have included thiotepa-based high-dose chemotherapy and autologous stem cell transplant (HDC-ASCT). This multi-centre, retrospective study reports the outcome of 70 patients undergoing HDC-ASCT for PCNSL in the United Kingdom. The median age at diagnosis was 56 years and all patients received HD-MTX-containing induction regimens. All patients underwent HDC-ASCT in first response. The rate of complete response increased from 50% before HDC-ASCT to 77% following HDC-ASCT. Treatment-related mortality was 6%. At a median follow-up of 12 months from HDC-ASCT, the estimated 1- and 2-year PFS rates were 71.5% and overall survival 86.4% and 83.3%, respectively. These data are comparable to published studies of HDC-ASCT for PCNSL, supporting its feasibility and efficacy.
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页码:1268 / 1272
页数:4
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