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

被引:0
|
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
来源
关键词
D O I
暂无
中图分类号
学科分类号
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.
引用
收藏
页码:1268 / 1272
页数:4
相关论文
共 50 条
  • [11] High-dose chemotherapy and autologous stem cell transplantation is feasible and effective for patients with human immunodeficiency virus and primary central nervous system lymphoma
    O'Neill, A. T.
    Mikesch, K.
    Fritsch, K.
    Kasenda, B.
    Banerjee, L.
    Burns, F.
    Zakout, G.
    Johnston, R.
    Illerhaus, G.
    Cwynarski, K.
    BRITISH JOURNAL OF HAEMATOLOGY, 2015, 169 : 94 - 95
  • [12] High-Dose Chemotherapy Followed By Autologous Stem Cell Transplantation As a Salvage Treatment in Patients with Relapsed or Refractory Primary Central Nervous System Lymphoma
    Hyung, Jaewon
    Hong, Jung Yong
    Yoon, Dok Hyun
    Kim, Shin
    Park, Jung Sun
    Park, Chan-Sik
    Lee, Sang Wook
    Ryu, Jin-Sook
    Huh, Jooryung
    Suh, Cheolwon
    BLOOD, 2018, 132
  • [13] Parkinsonism as a late presentation of lymphomatosis cerebri following high-dose chemotherapy with autologous stem cell transplantation for primary central nervous system lymphoma
    Sarah Merrill
    David J. Mauler
    Kent R. Richter
    Aditya Raghunathan
    Jose F. Leis
    Maciej M. Mrugala
    Journal of Neurology, 2020, 267 : 2239 - 2244
  • [14] Parkinsonism as a late presentation of lymphomatosis cerebri following high-dose chemotherapy with autologous stem cell transplantation for primary central nervous system lymphoma
    Merrill, Sarah
    Mauler, David J.
    Richter, Kent R.
    Raghunathan, Aditya
    Leis, Jose F.
    Mrugala, Maciej M.
    JOURNAL OF NEUROLOGY, 2020, 267 (08) : 2239 - 2244
  • [15] High-dose chemotherapy and autologous stem cell transplantation for secondary central nervous system lymphoma: many are called, but few are chosen
    Abramson, Jeremy S.
    HAEMATOLOGICA, 2013, 98 (05) : 662 - 664
  • [16] High-Dose Chemotherapy With Thiotepa, Busulfan, and Cyclophosphamide and Autologous Stem Cell Transplantation for Patients With Primary Central Nervous System Lymphoma in First Complete Remission
    DeFilipp, Zachariah
    Li, Shuli
    El-Jawahri, Areej
    Armand, Philippe
    Nayak, Lakshmi
    Wang, Nancy
    Batchelor, Tracy T.
    Chen, Yi-Bin
    CANCER, 2017, 123 (16) : 3073 - 3079
  • [17] High-Dose Chemotherapy With Thiotepa, Busulfan, and Cyclophosphamide and Autologous Stem Cell Transplantation for Pediatric Primary Central Nervous System Lymphoma in First Complete Remission
    Rajagopal, Revathi
    Miles, Gordon C. P.
    Kotecha, Rishi S.
    CANCER, 2017, 123 (14) : 2781 - 2782
  • [18] High-Dose Chemotherapy and Autologous Stem Cell Transplantation for Primary Central Nervous System Lymphoma (PCNSL) in First Complete Remission (CR1)
    DeFilipp, Zachariah
    Li, Shuli
    El-Jawahri, Areej R.
    Armand, Philippe
    Nayak, Lakshmi
    Batchelor, Tracy
    Chen, Yi-Bin
    BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2017, 23 (03) : S64 - S65
  • [19] High-dose chemotherapy with autologous stem cell transplantation in adults with recurrent embryonal tumors of the central nervous system
    Gill, Paula
    Litzow, Mark
    Buckner, Jan
    Arndt, Carola
    Moynihan, Timothy
    Christianson, Teresa
    Ansell, Stephen
    Galanis, Evanthia
    CANCER, 2008, 112 (08) : 1805 - 1811
  • [20] High-dose thiotepa-based chemotherapy with autologous stem cell support in elderly patients with primary central nervous system lymphoma: a European retrospective study
    E Schorb
    C P Fox
    K Fritsch
    L Isbell
    A Neubauer
    A Tzalavras
    R Witherall
    S Choquet
    O Kuittinen
    D De-Silva
    K Cwynarski
    C Houillier
    K Hoang-Xuan
    V Touitou
    N Cassoux
    J-P Marolleau
    J Tamburini
    R Houot
    V Delwail
    G Illerhaus
    C Soussain
    B Kasenda
    Bone Marrow Transplantation, 2017, 52 : 1113 - 1119