Your browser doesn't support javascript.
loading
R-hyper-CVAD versus R-CHOP/cytarabine with high-dose therapy and autologous haematopoietic stem cell support in fit patients with mantle cell lymphoma: 20 years of single-center experience.
Widmer, Fabienne; Balabanov, Stefan; Soldini, Davide; Samaras, Panagiotis; Gerber, Bernhard; Manz, Markus G; Goede, Jeroen S.
Afiliação
  • Widmer F; Division of Haematology, University Hospital and University of Zurich, Zurich, Switzerland.
  • Balabanov S; Division of Haematology, University Hospital and University of Zurich, Zurich, Switzerland.
  • Soldini D; Institute for Surgical Pathology, University Hospital and University of Zurich, Zurich, Switzerland.
  • Samaras P; Division of Oncology, University Hospital and University of Zurich, Zurich, Switzerland.
  • Gerber B; Division of Haematology, University Hospital and University of Zurich, Zurich, Switzerland.
  • Manz MG; Division of Haematology, Oncology Institute of Southern Switzerland, Bellinzona, Switzerland.
  • Goede JS; Division of Haematology, University Hospital and University of Zurich, Zurich, Switzerland.
Ann Hematol ; 97(2): 277-287, 2018 Feb.
Article em En | MEDLINE | ID: mdl-29147847
ABSTRACT
Standard of care for untreated mantle cell lymphoma (MCL) is still debated. At the University Hospital Zurich, advanced MCL in physically fit patients is treated either with rituximab plus cyclophosphamide, doxorubicin, vincristine and prednisone induction followed by consolidating high-dose chemotherapy and autologous stem cell support (R-CHOP/HD-ASCT), or with rituximab plus fractionated cyclophosphamide, vincristine, doxorubicin and dexamethasone alternating with high-dose methotrexate-cytarabine (R-hyper-CVAD/MTX-AraC) without consolidating HD-ASCT upon physicians' and patients' choice. We retrospectively analysed the outcome and therapy tolerance in patients with MCL treated with R-CHOP/HD-ASCT or R-hyper-CVAD/MTX-AraC at the University Hospital Zurich between January 1996 and January 2016. Forty-three patients were included; 29 patients received R-CHOP/HD-ASCT and 14 patients R-hyper-CVAD/MTX-AraC. Mean age at diagnosis was 54.4 years (range 38-68 years). Thirty-five patients (81.4%) completed the entire first-line therapy (n = 24 in the R-CHOP/HD-ASCT group, n = 11 in the R-hyper-CVAD group). Of those, all patients responded and 97% achieved a complete remission (CR). With a mean follow-up of 5.7 years 10-year progression-free survival (PFS) for all patients was 32% and overall survival (OS) was 76%, with no difference between the two therapy groups. Complication-induced hospitalisation rate, haematological toxicity and economic burden were significantly higher in the R-hyper-CVAD therapy group. In contrast, quality of life and global health state were better in the R-hyper-CVAD therapy group. Both first-line therapies showed similar outcome with a median OS longer than 10 years. Due to significantly lower haematological toxicity and lower economic burden, we recommend R-CHOP/HD-ASCT as first-line therapy in fit adult patients with advanced MCL.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Transplante de Células-Tronco Hematopoéticas / Linfoma de Célula do Manto / Citarabina / Hospitalização Tipo de estudo: Observational_studies / Risk_factors_studies Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Transplante de Células-Tronco Hematopoéticas / Linfoma de Célula do Manto / Citarabina / Hospitalização Tipo de estudo: Observational_studies / Risk_factors_studies Idioma: En Ano de publicação: 2018 Tipo de documento: Article