Stem Cell Transplantation for Follicular Lymphoma Relapsed/Refractory After Prior Rituximab

被引:54
作者
Evens, Andrew M. [1 ]
Vanderplas, Ann [2 ]
LaCasce, Ann S. [3 ]
Crosby, Allison L. [3 ]
Nademanee, Auayporn P. [4 ]
Kaminski, Mark S. [5 ]
Abel, Gregory A. [3 ]
Millenson, Michael [6 ]
Czuczman, Myron S. [7 ]
Rodriguez, Maria A. [8 ]
Niland, Joyce [2 ]
Zelenetz, Andrew D. [9 ]
Gordon, Leo I. [10 ]
Friedberg, Jonathan W. [11 ]
机构
[1] Tufts Univ, Sch Med, Div Hematol Oncol, Boston, MA 02111 USA
[2] City Hope Natl Med Ctr, Dept Biostat, Duarte, CA 91010 USA
[3] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[4] City Hope Natl Med Ctr, Dept Stem Cell Transplant, Duarte, CA 91010 USA
[5] Univ Michigan, Ctr Canc, Ann Arbor, MI 48109 USA
[6] Fox Chase Canc Ctr, Philadelphia, PA 19111 USA
[7] Roswell Pk Canc Inst, Buffalo, NY 14263 USA
[8] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA
[9] Mem Sloan Kettering Canc Ctr, New York, NY 10021 USA
[10] Northwestern Univ, Div Hematol Oncol, Chicago, IL 60611 USA
[11] Univ Rochester, Div Hematol Oncol, James P Wilmot Canc Ctr, Rochester, NY USA
关键词
follicular lymphoma; prognostication; autologous transplantation; allogeneic transplantation; survival; rituximab; non-Hodgkin lymphoma; stem cell transplantation; HIGH-DOSE THERAPY; BONE-MARROW-TRANSPLANTATION; NON-HODGKINS-LYMPHOMA; PRETRANSPLANTATION TREATMENT; SURVIVAL; REMISSION; IMPROVES; OUTCOMES; RELAPSE; IMPACT;
D O I
10.1002/cncr.28243
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUNDStem cell transplant (SCT)-related outcomes and prognostication for relapsed/refractory follicular lymphoma (FL) are not well-defined in the post-rituximab era. METHODSThrough the National Comprehensive Cancer Network (NCCN) lymphoma outcomes study, 184 patients with relapsed/refractory FL who underwent autologous SCT (autoSCT) or allogenic SCT (alloSCT) following disease relapse after prior rituximab-based therapy were examined. RESULTSPatients who underwent autoSCT (N=136) were older compared with patients who underwent alloSCT (N=48) (54 versus 51 years, respectively, P=.01) and more frequently had grade 3 FL (35% versus 8%, respectively, P=.006). Patients who underwent alloSCT received more prior therapies (4 versus 3, respectively, P<.0001) and more often had resistant disease at SCT (19% versus 6%, respectively, P=.008). Cumulative 100-day nonrelapse mortality (NRM) for autoSCT and alloSCT were 1% and 6%, respectively (P<.0001), whereas 3-year NRM rates were 3% versus 24%, respectively (P<.0001). For autoSCT and alloSCT, cumulative rates of relapse, progression, and/or transformation were 32% versus 16%, respectively (P=.03), whereas 3-year overall survival rates were 87% versus 61% (P<.0001); there were no differences in failure-free survival. AlloSCT was associated with increased risk of death on multivariate analysis (hazard ratio=2.77, 95% confidence interval=1.46-5.26, P=.002). This finding persisted on propensity scoring/matching. Multivariate analysis for autoSCT patients identified age>60 years and>3 prior therapies as adverse factors. Furthermore, a survival model was created for the autoSCT cohort based on number of factors present (0, 1, 2); 3-year failure-free survival was 72%, 47%, and 20%, respectively (P=.0003), and 3-year overall survival was 96%, 82%, and 62%, respectively (P<.0001). CONCLUSIONSAutoSCT remains an effective therapy for patients with FL. For alloSCT, continued strategies to reduce NRM are needed. Cancer 2013;119:3662-3671. (c) 2013 American Cancer Society.
引用
收藏
页码:3662 / 3671
页数:10
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