TY - JOUR
T1 - Nordic MCL2 trial update
T2 - six-year follow-up after intensive immunochemotherapy for untreated mantle cell lymphoma followed by BEAM or BEAC + autologous stem-cell support: still very long survival but late relapses do occur
AU - Geisler, Christian H
AU - Kolstad, Arne
AU - Laurell, Anna
AU - Jerkeman, Mats
AU - Räty, Riikka
AU - Andersen, Niels S
AU - Pedersen, Lone B
AU - Eriksson, Mikael
AU - Nordström, Marie
AU - Kimby, Eva
AU - Bentzen, Hans
AU - Kuittinen, Outi
AU - Lauritzsen, Grete F
AU - Nilsson-Ehle, Herman
AU - Ralfkiaer, Elisabeth
AU - Ehinger, Mats
AU - Sundström, Christer
AU - Delabie, Jan
AU - Karjalainen-Lindsberg, Marja-Liisa
AU - Brown, Peter
AU - Elonen, Erkki
AU - Nordic Lymphoma Group
N1 - © 2012 Blackwell Publishing Ltd.
PY - 2012
Y1 - 2012
N2 - Mantle cell lymphoma (MCL) is a heterogenic non-Hodgkin lymphoma entity, with a median survival of about 5 years. In 2008 we reported the early - based on the median observation time of 4 years - results of the Nordic Lymphoma Group MCL2 study of frontline intensive induction immunochemotherapy and autologous stem cell transplantation (ASCT), with more than 60% event-free survival at 5 years, and no subsequent relapses reported. Here we present an update after a median observation time of 6·5 years. The overall results are still excellent, with median overall survival and response duration longer than 10 years, and a median event-free survival of 7·4 years. However, six patients have now progressed later than 5 years after end of treatment. The international MCL Prognostic Index (MIPI) and Ki-67-expression were the only independent prognostic factors. Subdivided by the MIPI-Biological Index (MIPI + Ki-67, MIPI-B), more than 70% of patients with low-intermediate MIPI-B were alive at 10 years, but only 23% of the patients with high MIPI-B. These results, although highly encouraging regarding the majority of the patients, underline the need of a risk-adapted treatment strategy for MCL. The study was registered at www.isrctn.org as ISRCTN 87866680.
AB - Mantle cell lymphoma (MCL) is a heterogenic non-Hodgkin lymphoma entity, with a median survival of about 5 years. In 2008 we reported the early - based on the median observation time of 4 years - results of the Nordic Lymphoma Group MCL2 study of frontline intensive induction immunochemotherapy and autologous stem cell transplantation (ASCT), with more than 60% event-free survival at 5 years, and no subsequent relapses reported. Here we present an update after a median observation time of 6·5 years. The overall results are still excellent, with median overall survival and response duration longer than 10 years, and a median event-free survival of 7·4 years. However, six patients have now progressed later than 5 years after end of treatment. The international MCL Prognostic Index (MIPI) and Ki-67-expression were the only independent prognostic factors. Subdivided by the MIPI-Biological Index (MIPI + Ki-67, MIPI-B), more than 70% of patients with low-intermediate MIPI-B were alive at 10 years, but only 23% of the patients with high MIPI-B. These results, although highly encouraging regarding the majority of the patients, underline the need of a risk-adapted treatment strategy for MCL. The study was registered at www.isrctn.org as ISRCTN 87866680.
KW - Aged
KW - Antibodies, Monoclonal, Murine-Derived
KW - Antineoplastic Combined Chemotherapy Protocols
KW - Carmustine
KW - Cyclophosphamide
KW - Cytarabine
KW - Disease-Free Survival
KW - Etoposide
KW - Female
KW - Hematopoietic Stem Cell Transplantation
KW - Humans
KW - Immunotherapy
KW - Lymphoma, Mantle-Cell
KW - Male
KW - Melphalan
KW - Middle Aged
KW - Podophyllotoxin
KW - Prognosis
KW - Recurrence
KW - Survival Rate
KW - Transplantation, Autologous
U2 - 10.1111/j.1365-2141.2012.09174.x
DO - 10.1111/j.1365-2141.2012.09174.x
M3 - Journal article
C2 - 22640180
SN - 0007-1048
VL - 158
SP - 355
EP - 362
JO - British Journal of Haematology
JF - British Journal of Haematology
IS - 3
ER -