Intensive Chemotherapy Followed by Hematopoietic Stem-Cell Rescue for Refractory and Recurrent Primary CNS and Intraocular Lymphoma: Société Française de Greffe de Moëlle Osseuse-Thérapie Cellulaire

Author:

Soussain Carole1,Hoang-Xuan Khê1,Taillandier Luc1,Fourme Emmanuelle1,Choquet Sylvain1,Witz Francis1,Casasnovas Olivier1,Dupriez Brigitte1,Souleau Bertrand1,Taksin Anne-Laure1,Gisselbrecht Christian1,Jaccard Arnaud1,Omuro Antonio1,Sanson Marc1,Janvier Maud1,Kolb Brigitte1,Zini Jean-Marc1,Leblond Véronique1

Affiliation:

1. From the Department of Hematology; Biostatistics Unit, Centre René Huguenin, Saint-Cloud; Departments of Neurology and Hematology, Hôpital Pitié-Salpétrière; Department of Hematology, Hôpital Lariboisière, Paris; Departments of Neurology and Hematology, Centre Hospitalier Universitaire (CHU), Nancy; Department of Hematology, CHU Dijon; Department of Hematology, CH Lens; Department of Hematology, Hôpital Militaire, Percy; Department of Hematology, Hôpital de Versailles, Versailles; Department of...

Abstract

Purpose The prognosis of relapsing primary CNS lymphoma (PCNSL) is poor. We report the results of a prospective multicenter trial of intensive chemotherapy followed by autologous hematopoietic stem-cell rescue (IC + HCR) in immunocompetent adult patients with PCNSL or intraocular lymphoma (IOL) after failure of high-dose methotrexate-based treatment. Patients and Methods Salvage treatment consisted of two cycles of high-dose cytarabine and etoposide (CYVE). Intensive chemotherapy combined thiotepa, busulfan, and cyclophosphamide. Forty-three patients (median age, 52 years; range, 23 to 65 years) were included, with relapse (n = 22), refractory disease (n = 17), or a partial response to first-line treatment (n = 4). The response to CYVE was not assessable in three cases because of treatment-related death. Twenty patients (47%) were chemosensitive to CYVE: 15 of them proceeded to IC + HCR. IC + HCR was also administered to 12 patients who did not respond to CYVE. All but one of the 27 patients who underwent IC + HCR entered complete remission. Results With a median follow-up of 36 months, the median overall survival was 18.3 months in the overall population, and 58.6 months among patients who completed IC + HCR. The respective median progression-free survival (PFS) times after IC + HCR were 11.6 and 41.1 months. The 2-year overall survival probability was 45% in the whole population and 69% among the 27 patients who received IC + HCR. The 2-year PFS probability was 43% among all the patients and 58% in the IC + HCR subpopulation. Conclusion IC + HCR is an effective treatment for refractory and recurrent PCNSL.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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