Maintenance rituximab following induction chemoimmunotherapy may prolong progression-free survival in mantle cell lymphoma: a pilot study from the Wisconsin Oncology Network

被引:80
作者
Kahl, B. S.
Longo, W. L.
Eickhoff, J. C.
Zehnder, J.
Jones, C.
Blank, J.
McFarland, T.
Bottner, W.
Rezazedeh, H.
Werndli, J.
Bailey, H. H.
机构
[1] Univ Wisconsin, Dept Med, Madison, WI USA
[2] Univ Wisconsin, Dept Stat & Bioinformat, Madison, WI USA
[3] Stanford Univ, Dept Pathol, Palo Alto, CA 94304 USA
[4] Green Bay Oncol, Green Bay, WI USA
[5] UW Hlth Hematol Oncol, Madison, WI USA
[6] Gundersen Lutheran Med Ctr, La Crosse, WI USA
[7] Aspirus Canc Ctr, Wausau, WI USA
关键词
mantle cell lymphoma; chemotherapy; biologic therapy;
D O I
10.1093/annonc/mdl127
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: There is no standard first line treatment for mantle cell lymphoma. Patients and methods: This was a multicenter phase II pilot study of rituximab and modified hyper-fractionated cyclophosphamide, vincristine doxorubicin, dexamethasone (modified R-hyperCVAD) administered every 28 days for four to six cycles followed by rituximab maintenance therapy consisting of four weekly doses every 6 months for 2 years. Unlike traditional hyperCVAD regimens, no methotrexate or cytarabine was administered. Results: Of 22 patients, the overall response rate was 77% and the complete response rate was 64%. With a median follow-up time of 37 months in surviving patients, the median PFS was 37 months and the median OS was not reached. The achievement of a molecular remission did not correlate with improved outcome. The major toxicity was expected myelosuppression. Two patients died during induction treatment. There were no major adverse effects during maintenance therapy. Conclusion: In a multicenter trial, modified R-hyperCVAD was tolerable and effective induction therapy for untreated MCL. Maintenance rituximab appeared to prolong PFS without increasing toxicity.
引用
收藏
页码:1418 / 1423
页数:6
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