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Clinical Trial
. 2015 Nov 20;33(33):3903-10.
doi: 10.1200/JCO.2015.61.1236. Epub 2015 Aug 17.

High Doses of Antimetabolites Followed by High-Dose Sequential Chemoimmunotherapy and Autologous Stem-Cell Transplantation in Patients With Systemic B-Cell Lymphoma and Secondary CNS Involvement: Final Results of a Multicenter Phase II Trial

Affiliations
Clinical Trial

High Doses of Antimetabolites Followed by High-Dose Sequential Chemoimmunotherapy and Autologous Stem-Cell Transplantation in Patients With Systemic B-Cell Lymphoma and Secondary CNS Involvement: Final Results of a Multicenter Phase II Trial

Andrés J M Ferreri et al. J Clin Oncol. .

Abstract

Purpose: Treatment of secondary CNS dissemination in patients with aggressive lymphomas remains an important, unmet clinical need. Herein, we report the final results of a multicenter phase II trial addressing a new treatment for secondary CNS lymphoma based on encouraging experiences with high doses of antimetabolites in primary CNS lymphoma and with rituximab plus high-dose sequential chemoimmunotherapy (R-HDS) in relapsed aggressive lymphoma.

Patients and methods: HIV-negative patients with aggressive B-cell lymphoma and secondary CNS involvement at diagnosis or relapse, age 18 to 70 years, and Eastern Cooperative Oncology Group performance status ≤ 3 were enrolled and treated with high-doses of methotrexate and cytarabine, followed by R-HDS (cyclophosphamide, cytarabine, and etoposide) supported by autologous stem-cell transplantation (ASCT). Treatment included eight doses of rituximab and four doses of intrathecal liposomal cytarabine. The primary end point was 2-year event-free survival; the planned accrual was 38 patients.

Results: Thirty-eight patients were enrolled; CNS disease was detected at presentation in 16 patients. Toxicity was usually hematologic and manageable, with grade 4 febrile neutropenia in 3% of delivered courses and grade 4 nonhematologic toxicity in 2% of delivered courses. Four patients died because of toxicity. Autologous stem cells were successfully collected in 24 (89%) of 27 patients (median, 10 × 10(6)/kg); 20 patients underwent ASCT. Complete response was achieved in 24 patients (complete response rate, 63%; 95% CI, 48% to 78%). At a median follow-up of 48 months, 17 patients remained relapse free, with a 2-year event-free survival rate of 50% ± 8%. At 5 years, 16 patients were alive, with a 5-year overall survival rate of 41% ± 8% for the whole series and 68% ± 11% for patients who received transplantation. Systemic (extra-CNS) and/or meningeal disease did not affect outcome.

Conclusion: The combination of high doses of antimetabolites, R-HDS, and ASCT is feasible and effective in patients age 18 to 70 years old with secondary CNS lymphoma, and we propose it as a new standard therapeutic option.

Trial registration: ClinicalTrials.gov NCT00801216.

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Comment in

  • Advances in the Treatment of Secondary CNS Lymphoma.
    Schmitz N, Wu HS. Schmitz N, et al. J Clin Oncol. 2015 Nov 20;33(33):3851-3. doi: 10.1200/JCO.2015.63.1143. Epub 2015 Aug 17. J Clin Oncol. 2015. PMID: 26282665 No abstract available.
  • Therapy for Secondary CNS Involvement in Malignant Lymphomas: No Standard Yet!
    Korfel A, Chamberlain M, Neuwelt E, Thiel E, Doolittle N, Schlegel U, Dreyling M, Rubenstein J, Fischer L, Björkholm M, Martus P, Weller M, Glantz M. Korfel A, et al. J Clin Oncol. 2016 May 20;34(15):1829-30. doi: 10.1200/JCO.2015.65.0879. Epub 2016 Mar 21. J Clin Oncol. 2016. PMID: 27001566 Free PMC article. No abstract available.
  • Reply to A. Korfel et al.
    Ferreri AJ, Tarella C, Ciceri F. Ferreri AJ, et al. J Clin Oncol. 2016 May 20;34(15):1830-1. doi: 10.1200/JCO.2016.66.4722. Epub 2016 Mar 21. J Clin Oncol. 2016. PMID: 27001567 No abstract available.
  • Reply to A. Korfel et al.
    Schmitz N, Nickelsen M. Schmitz N, et al. J Clin Oncol. 2016 May 20;34(15):1831-2. doi: 10.1200/JCO.2016.66.4730. Epub 2016 Mar 21. J Clin Oncol. 2016. PMID: 27001575 No abstract available.

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