Autologous hematopoietic stem cell transplantation suppresses Gd-enhanced MRI activity in MS

被引:138
作者
Mancardi, GL
Saccardi, R
Filippi, M
Gualandi, F
Murialdo, A
Inglese, M
Marrosu, MG
Meucci, G
Massacesi, L
Lugaresi, A
Pagliai, F
Sormani, MP
Sardanelli, F
Marmont, A
机构
[1] Univ Genoa, Dept Neurol Sci & Vis, I-16132 Genoa, Italy
[2] Univ Gabriele dAnnunzio, Dept Oncol & Neurosci, Chieti, Italy
[3] Univ Pisa, Dept Neurosci, Pisa, Italy
[4] Univ Cagliari, Dept Neurosci, Cagliari, Italy
[5] Univ Milan, Osped San Raffaele, Inst Sci, Dept Neurosci,Neuroimaging Res Unit, I-20127 Milan, Italy
[6] Univ Florence, Dept Neurol & Psychiat Sci, Florence, Italy
[7] Careggi Hosp, Bone Marrow Transplantat Unit, Florence, Italy
[8] Inst Biomed, Dept Radiol, Genoa, Italy
关键词
D O I
10.1212/WNL.57.1.62
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Autologous hematopoietic stem cell transplantation (ASCT) has been recently utilized with encouraging results in patients with poorly controlled MS. Objective: To determine in severe cases of MS the effect of ASCT on gadolinium (Gd)-enhanced MRI and to obtain information on clinical course and safety. Methods: In a cooperative study, 10 patients with rapidly evolving secondary progressive MS were transplanted, after BEAM conditioning regimen (carmustine, etoposide, cytosine-arabinoside, and melphalan), with unmanipulated autologous peripheral blood SC mobilized with high-dose cyclophosphamide (CY; 4 g/m(2)) and granulocyte-colony-stimulating factor. Triple-dose Gd-enhanced scans were performed monthly for a pretreatment period of 3 months and compared with serial monthly Gd-enhanced MRT for the following 6 months and then once every 3 months. Results: The median follow-up is now 15 months (range 4 to 30 months). The number of Gd-enhancing lesions decreased immediately after mobilization with CY and finally dropped to zero in all cases after the conditioning regimen. The number of new T2-weighted positive lesions paralleled data obtained for Gd-enhanced MRI. Clinically, patients improved slightly or remained stable. Conclusion: These results demonstrate that the therapeutic sequence CY-BEAM-ASCT has the capacity to completely suppress MR-enhancing activity, an effect that is sustained with time. The final impact of this procedure on disease course remains to be established.
引用
收藏
页码:62 / 68
页数:7
相关论文
共 30 条
[1]   Improving interobserver variation in reporting gadolinium-enhanced MRI lesions in multiple sclerosis [J].
Barkhof, F ;
Filippi, M ;
van Waesberghe, JH ;
Molyneux, P ;
Rovaris, M ;
Nijeholt, GLA ;
Tubridy, N ;
Miller, DH ;
Yousry, TA ;
Radue, EW ;
Adèr, HJ .
NEUROLOGY, 1997, 49 (06) :1682-1688
[2]   The treatment of chronic progressive multiple sclerosis with cladribine [J].
Beutler, E ;
Sipe, JC ;
Romine, JS ;
Koziol, JA ;
McMillan, R ;
Zyroff, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (04) :1716-1720
[3]   Inflammatory central nervous system demyelination: Correlation of magnetic resonance imaging findings with lesion pathology [J].
Bruck, W ;
Bitsch, A ;
Kolenda, H ;
Bruck, Y ;
Stiefel, M ;
Lassmann, H .
ANNALS OF NEUROLOGY, 1997, 42 (05) :783-793
[4]  
BURT R, 2000, HEMATOPOIETIC STEM C, P203
[5]   Treatment of autoimmune disease by intense immunosuppressive conditioning and autologous hematopoietic stem cell transplantation [J].
Burt, RK ;
Traynor, AE ;
Pope, R ;
Schroeder, J ;
Cohen, B ;
Karlin, KH ;
Lobeck, L ;
Goolsby, C ;
Rowlings, P ;
Davis, FA ;
Stefoski, D ;
Terry, C ;
Keever-Taylor, C ;
Rosen, S ;
Vesole, D ;
Fishman, M ;
Brush, M ;
Mujias, S ;
Villa, M ;
Burns, WH .
BLOOD, 1998, 92 (10) :3505-3514
[6]   Therapeutic effect of mitoxantrone combined with methylprednisolone in multiple sclerosis: A randomised multicentre study of active disease using MRI and clinical criteria [J].
Edan, G ;
Miller, D ;
Clanet, M ;
Confavreux, C ;
LyonCaen, O ;
Lubetzki, C ;
Brochet, B ;
Berry, I ;
Rolland, Y ;
Froment, JC ;
Dousset, V ;
Cabanis, E ;
IbaZizen, MT ;
Gandon, JM ;
Lai, HM ;
Moseley, I ;
Sabouraud, O .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1997, 62 (02) :112-118
[7]   Peripheral blood stem cell transplantation in the treatment of progressive multiple sclerosis: first results of a pilot study [J].
Fassas, A ;
Anagnostopoulos, A ;
Kazis, A ;
Kapinas, K ;
Sakellari, I ;
Kimiskidis, V ;
Tsompanakou, A .
BONE MARROW TRANSPLANTATION, 1997, 20 (08) :631-638
[8]   Autologous stem cell transplantation in progressive multiple sclerosis - An interim analysis of efficacy [J].
Fassas, A ;
Anagnostopoulos, A ;
Kazis, A ;
Kapinas, K ;
Sakellari, I ;
Kimiskidis, V ;
Smias, C ;
Eleftheriadis, N ;
Tsimourtou, V .
JOURNAL OF CLINICAL IMMUNOLOGY, 2000, 20 (01) :24-30
[9]   Axonal damage in acute multiple sclerosis lesions [J].
Ferguson, B ;
Matyszak, MK ;
Esiri, MM ;
Perry, VH .
BRAIN, 1997, 120 :393-399
[10]   A multi-centre longitudinal study comparing the sensitivity of monthly MRI after standard and triple dose gadolinium-DTPA for monitoring disease activity in multiple sclerosis -: Implications for phase II clinical trials [J].
Filippi, M ;
Rovaris, M ;
Capra, R ;
Gasperini, C ;
Yousry, TA ;
Sormani, MP ;
Prandini, F ;
Horsfield, MA ;
Martinelli, V ;
Bastianello, S ;
Kühne, I ;
Pozzilli, C ;
Comi, G .
BRAIN, 1998, 121 :2011-2020