TY - JOUR
T1 - Management of mantle cell lymphoma
T2 - Key challenges and next steps
AU - Williams, Michael
AU - Dreyling, Martin
AU - Winter, Jane
AU - Muneer, Sabeeha
AU - Leonard, John
N1 - Funding Information:
Michael E. Williams has served on the Board of Directors for the Lymphoma Research Foundation and the European Mantle Cell Lymphoma Network; has received research funding from Celgene Corporation, Cephalon, Inc., Genentech, Inc., and Novartis Pharmaceuticals Corporation; and has served as a consultant or been on an advisory/research panel for Celgene Corporation. Martin Dreyling has received research funding from and served as a consultant or been on an advisory/research panel for Celgene Corporation, Mundipharma International Limited, Pfizer Inc./Wyeth Pharmaceuticals, and Roche Pharmaceuticals; and has received honoraria from Bayer Pharmaceuticals Corporation, Mundipharma International Limited, Pfizer Inc./Wyeth Pharmaceuticals, and Roche Pharmaceuticals. Jane N. Winter has received research funding from Angen, Ambit Biosciences, Bristol-Myers Squibb Company, Chroma Therapeutics, Genentech, Inc., Millennium Pharmaceuticals, Inc., Novartis Pharmaceuticals Corporation, Pfizer Inc., and Seattle Genetics, Inc.; has served as a consultant or been on an advisory/research panel for Antisoma plc, Caremark, LLC, Eisai Inc., the Federal Drug Administration, Hana Biosciences, Inc., and Novartis Pharmaceuticals Corporation; and has recieved honoraria from the American Society of Hematology, Bristol-Myers Squibb Company, the Institute for Medical Education and Research, and Physicians' Education Resource. John P. Leonard has served as a consultant or been on an advisory/research panel for Biogen Idec, Calistoga Pharmaceuticals, Inc., Celgene Corporation, Cell Therapeutics, Inc., Cephalon, Inc., EMD Serono, Inc., Facet Biotech Corporation, GlaxoSmithKline, Johnson & Johnson Services, Inc., Millennium Pharmaceuticals Corporation, Novartis Pharmaceuticals Corporation, and sanofi-aventis U.S.
PY - 2010/10
Y1 - 2010/10
N2 - Mantle cell lymphoma (MCL) is regarded as an aggressive lymphoid malignancy that exhibits varied clinical behavior and prognoses, reflecting the biologic heterogeneity of the disease. In most cases, patients with MCL achieve a shorter median survival compared with more common B-cell lymphomas, such as follicular lymphoma, and are less likely to achieve a durable response with chemotherapy. Currently, there is no defined standard of care for patients with MCL. Rituximab-containing immunochemotherapy strategies are commonly used, but the addition of rituximab to conventional induction chemotherapy has produced suboptimal responses that are relatively short-lived and have not resulted in a survival advantage. Further intensification of the chemotherapy component, including autologous stem cell transplantation, has increased response and survival rates but has not proven to be curative while being associated with higher toxicity. Clearly, there is a need for developing novel agents and strategies that will improve clinical outcomes for patients with MCL. Targeted therapies and new cytotoxic agents are showing great promise and may have a role in maintenance and/or initial therapy. This summary highlights current challenges in the management of MCL, and outlines expert perspectives, key questions, and future directions. For the third consecutive year, a panel of global experts in MCL assembled to deliberate on topical issues in MCL including advances in pathobiology, strategies for risk-adapted therapy, front-line treatment options, consolidation approaches, and novel therapeutic strategies. The proceedings of this workshop, held December 3, 2009 in New Orleans, LA, are summarized here. It must be emphasized that this synopsis is not meant to serve as an exhaustive review of MCL biology and management, but is a distillation of the expert discussions, highlighting key questions and future directions identified.
AB - Mantle cell lymphoma (MCL) is regarded as an aggressive lymphoid malignancy that exhibits varied clinical behavior and prognoses, reflecting the biologic heterogeneity of the disease. In most cases, patients with MCL achieve a shorter median survival compared with more common B-cell lymphomas, such as follicular lymphoma, and are less likely to achieve a durable response with chemotherapy. Currently, there is no defined standard of care for patients with MCL. Rituximab-containing immunochemotherapy strategies are commonly used, but the addition of rituximab to conventional induction chemotherapy has produced suboptimal responses that are relatively short-lived and have not resulted in a survival advantage. Further intensification of the chemotherapy component, including autologous stem cell transplantation, has increased response and survival rates but has not proven to be curative while being associated with higher toxicity. Clearly, there is a need for developing novel agents and strategies that will improve clinical outcomes for patients with MCL. Targeted therapies and new cytotoxic agents are showing great promise and may have a role in maintenance and/or initial therapy. This summary highlights current challenges in the management of MCL, and outlines expert perspectives, key questions, and future directions. For the third consecutive year, a panel of global experts in MCL assembled to deliberate on topical issues in MCL including advances in pathobiology, strategies for risk-adapted therapy, front-line treatment options, consolidation approaches, and novel therapeutic strategies. The proceedings of this workshop, held December 3, 2009 in New Orleans, LA, are summarized here. It must be emphasized that this synopsis is not meant to serve as an exhaustive review of MCL biology and management, but is a distillation of the expert discussions, highlighting key questions and future directions identified.
KW - Bendamustine
KW - HyperCVAD
KW - Lenalidomide
KW - MIPI
KW - R-CHOP
KW - Rituxumab
KW - Temsirolimus
KW - Transplantation
UR - http://www.scopus.com/inward/record.url?scp=79952279698&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=79952279698&partnerID=8YFLogxK
U2 - 10.3816/CLML.2010.n.066
DO - 10.3816/CLML.2010.n.066
M3 - Review article
C2 - 21030346
AN - SCOPUS:79952279698
SN - 2152-2669
VL - 10
SP - 336
EP - 346
JO - Clinical Lymphoma
JF - Clinical Lymphoma
IS - 5
ER -