H Ghesquières1, C Ferlay2, C Sebban3, D Perol2, A Bosly4, O Casasnovas5, O Reman6, B Coiffier7, H Tilly8, P Morel9, E Van den Neste10, P Colin11, C Haioun12, P Biron3, J-Y Blay3. 1. Department of Hematology. Electronic address: ghesquie@lyon.fnclcc.fr. 2. Biostatistics Unit, Centre Léon Bérard, Université de Lyon, Lyon. 3. Department of Hematology. 4. Department of Hematology, UCL Mont Godine, Yvoir, Belgium. 5. Department of Hematology, Centre Hospitalier Universitaire, Dijon. 6. Department of Hematology, Centre Hospitalier, Caen. 7. Department of Clinical Hematology, Centre Hospitalier Lyon-Sud, Pierre Benite. 8. Department of Hematology, Centre Henri Becquerel, Rouen. 9. Department of Hematology, Hôpital Schaffner, Lens, France. 10. Department of Clinical Hematology, UCL St Luc, Bruxelles, Belgium. 11. Department of Hematology, Clinique Courlancy, Reims. 12. Department of Hematology, CHU Henri Mondor, Créteil, France.
Abstract
BACKGROUND: This prospective multicentric phase II study aimed to confirm the results of the C5R protocol of high-dose methotrexate (MTX)-based chemotherapy (CT) for immunocompetent primary central nervous system lymphoma. PATIENTS AND METHODS: A total of 99 patients received age-adapted CT (C5R protocol) followed by radiotherapy. Patients younger than 61 years (group 1, n = 45) received the full C5R with MTX, doxorubicin, vincristine, cyclophosphamide, and cytarabine. Patients aged 61-70 years (group 2, n = 36) received reduced doses. Patients older than 70 years (group 3, n = 18) received four courses of MTX, cyclophosphamide, and etoposide. RESULTS: Median age was 63 years and 51% of patients had performance status of more than one. Seventeen patients died of toxicity during CT. Complete response was achieved in 56%, 53%, and 28% of patients in groups 1, 2, and 3, respectively. With a median follow-up of 83 months, the 5-year progression-free survival was 31%, 28%, and 11% and the 5-year overall survival 42%, 31%, and 17% for groups 1, 2, and 3, respectively. Leukoencephalopathy occurred in 32% of assessable patients, in both group 1 and groups 2-3. CONCLUSION: The C5R protocol was feasible in the multicentric setting with favorable long-term survival in patients younger than 60 years. Despite dose adaptation, results in older patients were disappointing.
BACKGROUND: This prospective multicentric phase II study aimed to confirm the results of the C5R protocol of high-dose methotrexate (MTX)-based chemotherapy (CT) for immunocompetent primary central nervous system lymphoma. PATIENTS AND METHODS: A total of 99 patients received age-adapted CT (C5R protocol) followed by radiotherapy. Patients younger than 61 years (group 1, n = 45) received the full C5R with MTX, doxorubicin, vincristine, cyclophosphamide, and cytarabine. Patients aged 61-70 years (group 2, n = 36) received reduced doses. Patients older than 70 years (group 3, n = 18) received four courses of MTX, cyclophosphamide, and etoposide. RESULTS: Median age was 63 years and 51% of patients had performance status of more than one. Seventeen patients died of toxicity during CT. Complete response was achieved in 56%, 53%, and 28% of patients in groups 1, 2, and 3, respectively. With a median follow-up of 83 months, the 5-year progression-free survival was 31%, 28%, and 11% and the 5-year overall survival 42%, 31%, and 17% for groups 1, 2, and 3, respectively. Leukoencephalopathy occurred in 32% of assessable patients, in both group 1 and groups 2-3. CONCLUSION: The C5R protocol was feasible in the multicentric setting with favorable long-term survival in patients younger than 60 years. Despite dose adaptation, results in older patients were disappointing.
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