Immunologic recovery following autologous stem-cell transplantation with pre- and posttransplantation rituximab for low-grade or mantle cell lymphoma

被引:13
作者
Kasamon, Y. L. [1 ]
Jones, R. J. [1 ]
Brodsky, R. A. [1 ]
Fuchs, E. J. [1 ]
Matsui, W. [1 ]
Luznik, L. [1 ]
Powell, J. D. [1 ]
Blackford, A. L. [1 ]
Goodrich, A. [1 ]
Gocke, C. D. [1 ]
Abrams, R. A. [1 ]
Ambinder, R. F. [1 ]
Flinn, I. W. [1 ]
机构
[1] Sidney Kimmel Comprehens Canc Ctr Johns Hopkins, Baltimore, MD 21231 USA
基金
美国国家卫生研究院;
关键词
immune reconstitution; lymphoma; rituximab; transplantation; PROGRESSION-FREE SURVIVAL; NON-HODGKINS-LYMPHOMA; BONE-MARROW-TRANSPLANTATION; RELAPSED FOLLICULAR LYMPHOMA; DOSE SEQUENTIAL CHEMOTHERAPY; RANDOMIZED-TRIAL; PHASE-II; R-HDS; REMISSION; THERAPY;
D O I
10.1093/annonc/mdp484
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Rituximab may improve transplant outcomes but may delay immunologic recovery. Patients and methods: Seventy-seven patients with low-grade or mantle cell lymphoma received autologous stem-cell transplantation (ASCT) on a phase II study. Rituximab 375 mg/m(2) was administered 3 days before mobilization-dose cyclophosphamide, then weekly for four doses after count recovery from ASCT. Immune reconstitution was assessed. Results: Sixty percent of transplants occurred in first remission. Actuarial event-free survival (EFS) and overall survival (OS) were 60% and 73%, respectively, at 5 years, with 7.2-year median follow-up for OS in surviving patients. Median EFS was 8.3 years. Older age and transformed lymphomas were independently associated with inferior EFS, whereas day 60 lymphocyte counts did not predict EFS or late infections. Early and late transplant-related mortality was 1% and 8%, with secondary leukemia in two patients. B-cell counts recovered by 1-2 years; however, the median IgG level remained low at 2 years. Late-onset idiopathic neutropenia, generally inconsequential, was noted in 43%. Conclusion: ASCT with rituximab can produce durable remissions on follow-up out to 10 years. Major infections do not appear to be significantly increased or to be predicted by immune monitoring.
引用
收藏
页码:1203 / 1210
页数:8
相关论文
共 30 条
[1]  
[Anonymous], 1996, J COMPUT GRAPH STAT
[2]   Hematopoietic retroviral gene marking in patients with follicular non-Hodgkin's lymphoma [J].
Bachier, CR ;
Giles, RE ;
Ellerson, D ;
Hanania, EG ;
Garcia-Sanchez, F ;
Andreeff, M ;
Cabanillas, F ;
Champlin, R ;
Choudhury, R ;
Berenson, R ;
Heimfeld, S ;
Deisseroth, AB .
LEUKEMIA & LYMPHOMA, 1999, 32 (3-4) :279-288
[3]   Rituximab consolidation after high-dose chemotherapy and autologous blood stem cell transplantation in follicular and mantle cell lymphoma:: a prospective, multicenter phase II study [J].
Brugger, W ;
Hirsch, J ;
Grünebach, F ;
Repp, R ;
Brossart, P ;
Vogel, W ;
Kopp, HG ;
Manz, MG ;
Bitzer, M ;
Schlimok, G ;
Kaufmann, M ;
Ganser, A ;
Fehnle, K ;
Gramatzki, M ;
Kanzl, L .
ANNALS OF ONCOLOGY, 2004, 15 (11) :1691-1698
[4]   Granulocyte-macrophage colony-stimulating factor potentiates rituximab in patients with relapsed follicular lymphoma:: Results of a phase II study [J].
Cartron, Guillaume ;
Zhao-Yang, Lu ;
Baudard, Marion ;
Kanouni, Tarik ;
Rouille, Valerie ;
Quittet, Philippe ;
Klein, Bernard ;
Rossi, Jean-Francois .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (16) :2725-2731
[5]   Long-term follow-up of indolent lymphoma patients treated with high-dose sequential chemotherapy and autografting: Evidence that durable molecular and clinical remission frequently can be attained only in follicular subtypes [J].
Corradini, P ;
Ladetto, M ;
Zallio, F ;
Astolfi, M ;
Rizzo, E ;
Sametti, S ;
Cuttica, A ;
Rosato, R ;
Farina, L ;
Boccadoro, M ;
Benedetti, F ;
Pileri, A ;
Tarella, C .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (08) :1460-1468
[6]   Early consolidation by myeloablative radiochemotherapy followed by autologous stem cell transplantation in first remission significantly prolongs progression-free survival in mantle-cell lymphoma: results of a prospective randomized trial of the European MCL Network [J].
Dreyling, M ;
Lenz, G ;
Hoster, E ;
Van Hoof, A ;
Gisselbrecht, C ;
Schmits, R ;
Metzner, B ;
Truemper, L ;
Reiser, M ;
Steinhauer, H ;
Boiron, JM ;
Boogaerts, MA ;
Aldaoud, A ;
Silingardi, V ;
Kluin-Nelemans, HC ;
Hasford, J ;
Parwaresch, R ;
Unterhalt, M ;
Hiddemann, W .
BLOOD, 2005, 105 (07) :2677-2684
[7]   Immunotherapy with rituximab during peripheral blood stem cell transplantation for non-Hodgkin's lymphoma [J].
Flinn, IW ;
O'Donnell, PV ;
Goodrich, A ;
Vogelsang, G ;
Abrams, R ;
Noga, S ;
Marcellus, D ;
Borowitz, M ;
Jones, R ;
Ambinder, RF .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2000, 6 (06) :628-632
[8]   Rituximab in vivo purging is safe and effective in combination with CD34-positive selected autologous stem cell transplantation for salvage therapy in B-NHL [J].
Flohr, T ;
Hess, G ;
Kolbe, K ;
Gamm, H ;
Nolte, H ;
Stanislawski, T ;
Huber, C ;
Derigs, HG .
BONE MARROW TRANSPLANTATION, 2002, 29 (09) :769-775
[9]  
Friedberg J W, 1999, Biol Blood Marrow Transplant, V5, P262, DOI 10.1053/bbmt.1999.v5.pm10465106
[10]   Long-term progression-free survival of mantle cell lymphoma after intensive front-line immunochemotherapy with in vivo-purged stem cell rescue:: a nonrandomized phase 2 multicenter study by the Nordic Lymphoma Group [J].
Geisler, Christian H. ;
Kolstad, Arne ;
Laurell, Anna ;
Andersen, Niels S. ;
Pedersen, Lone B. ;
Jerkeman, Mats ;
Eriksson, Mikael ;
Nordstrom, Marie ;
Kimby, Eva ;
Boesen, Anne Marie ;
Kuittinen, Outi ;
Lauritzsen, Grete F. ;
Nilsson-Ehle, Herman ;
Ralfkiaer, Elisabeth ;
Akerman, Mans ;
Ehinger, Mats ;
Sundstrom, Christer ;
Langholm, Ruth ;
Delabie, Jan ;
Karjalainen-Lindsberg, Marja-Liisa ;
Brown, Peter ;
Elonen, Erkki .
BLOOD, 2008, 112 (07) :2687-2693