Survival Outcomes of Younger Patients With Mantle Cell Lymphoma Treated in the Rituximab Era
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- James N. Gerson
- Fox Chase Cancer Center, Philadelphia, PA
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- Elizabeth Handorf
- Fox Chase Cancer Center, Philadelphia, PA
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- Diego Villa
- BC Cancer, Vancouver, British Columbia, Canada
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- Alina S. Gerrie
- BC Cancer, Vancouver, British Columbia, Canada
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- Parv Chapani
- BC Cancer, Vancouver, British Columbia, Canada
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- Shaoying Li
- MD Anderson Cancer Center, Houston, TX
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- L. Jeffrey Medeiros
- MD Anderson Cancer Center, Houston, TX
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- Michael I. Wang
- MD Anderson Cancer Center, Houston, TX
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- Jonathon B. Cohen
- Emory University, Atlanta, GA
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- Oscar Calzada
- Emory University, Atlanta, GA
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- Michael C. Churnetski
- Emory University, Atlanta, GA
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- Brian T. Hill
- Cleveland Clinic Foundation, Cleveland, OH
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- Yazeed Sawalha
- Cleveland Clinic Foundation, Cleveland, OH
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- Francisco J. Hernandez-Ilizaliturri
- Roswell Park Cancer Institute, Buffalo, NY
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- Shalin Kothari
- Roswell Park Cancer Institute, Buffalo, NY
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- Julie M. Vose
- University of Nebraska Cancer Center, Omaha, NE
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- Martin A. Bast
- University of Nebraska Cancer Center, Omaha, NE
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- Timothy S. Fenske
- Medical College of Wisconsin, Milwaukee, WI
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- Swapna Narayana Rao Gari
- Medical College of Wisconsin, Milwaukee, WI
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- Kami J. Maddocks
- Ohio State University; Columbus, OH
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- David Bond
- Ohio State University; Columbus, OH
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- Veronika Bachanova
- University of Minnesota, Minneapolis, MN
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- Bhaskar Kolla
- University of Minnesota, Minneapolis, MN
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- Julio Chavez
- Moffitt Cancer Center, Tampa, FL
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- Bijal Shah
- Moffitt Cancer Center, Tampa, FL
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- Frederick Lansigan
- Dartmouth-Hitchcock Medical Center, Lebanon, NH
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- Timothy F. Burns
- Dartmouth-Hitchcock Medical Center, Lebanon, NH
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- Alexandra M. Donovan
- Dartmouth-Hitchcock Medical Center, Lebanon, NH
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- Nina Wagner-Johnston
- Johns Hopkins University, Baltimore, MD
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- Marcus Messmer
- Johns Hopkins University, Baltimore, MD
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- Amitkumar Mehta
- University of Alabama Cancer Center, Birmingham, AL
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- Jennifer K. Anderson
- University of Alabama Cancer Center, Birmingham, AL
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- Nishitha Reddy
- Vanderbilt Ingram Cancer Center, Nashville, TN
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- Alexandra E. Kovach
- Vanderbilt Ingram Cancer Center, Nashville, TN
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- Daniel J. Landsburg
- University of Pennsylvania, Philadelphia, PA
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- Martha Glenn
- Huntsman Cancer Institute, Salt Lake City, UT
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- David J. Inwards
- Mayo Clinic, Rochester, MN
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- Reem Karmali
- Northwestern University, Evanston, IL
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- Jason B. Kaplan
- Northwestern University, Evanston, IL
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- Paolo F. Caimi
- Case Western Reserve University, Cleveland, OH
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- Saurabh Rajguru
- University of Wisconsin, Madison, WI
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- Andrew Evens
- Tufts University, Boston, MA
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- Andreas Klein
- Tufts University, Boston, MA
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- Elvira Umyarova
- University of Vermont, Burlington, VT
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- Bhargavi Pulluri
- University of Vermont, Burlington, VT
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- Jennifer E. Amengual
- Columbia University, New York, NY
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- Jennifer K. Lue
- Columbia University, New York, NY
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- Catherine Diefenbach
- New York University, New York, NY
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- Richard I. Fisher
- Fox Chase Cancer Center, Philadelphia, PA
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- Stefan K. Barta
- Fox Chase Cancer Center, Philadelphia, PA
Description
<jats:sec><jats:title>PURPOSE</jats:title><jats:p> Mantle cell lymphoma (MCL) is a B-cell lymphoma characterized by cyclin D1 expression. Autologous hematopoietic cell transplantation (AHCT) consolidation after induction chemotherapy is often used for eligible patients; however, the benefit remains uncertain in the rituximab era. Herein we retrospectively assessed the impact of AHCT consolidation on survival in a large cohort of transplantation-eligible patients age 65 years or younger. </jats:p></jats:sec><jats:sec><jats:title>PATIENTS AND METHODS</jats:title><jats:p> We retrospectively studied transplantation-eligible adults age 65 years or younger with newly diagnosed MCL treated between 2000 and 2015. The primary objective was to assess for improved progression-free survival (PFS) with AHCT consolidation and secondarily to assess for improved overall survival (OS). Cox multivariable regression analysis and propensity score–weighted (PSW) analysis were performed. </jats:p></jats:sec><jats:sec><jats:title>RESULTS</jats:title><jats:p> Data were collected from 25 medical centers for 1,254 patients; 1,029 met inclusion criteria. Median follow-up for the cohort was 76 months. Median PFS and OS were 62 and 139 months, respectively. On unadjusted analysis, AHCT was associated with improved PFS (75 v 44 months with v without AHCT, respectively; P < .01) and OS (147 v 115 months with v without AHCT, respectively; P < .05). On multivariable regression analysis, AHCT was associated with improved PFS (hazard ratio [HR], 0.54; 95% CI, 0.44 to 0.66; P < .01) and a trend toward improved OS (HR, 0.77; 95% CI, 0.59 to 1.01; P = .06). After PSW analysis, AHCT remained associated with improved PFS (HR, 0.70; 95% CI, 0.59 to 0.84; P < .05) but not improved OS (HR, 0.87; 95% CI, 0.69 to 1.1; P = .2). </jats:p></jats:sec><jats:sec><jats:title>CONCLUSION</jats:title><jats:p> In this large cohort of younger, transplantation-eligible patients with MCL, AHCT consolidation after induction was associated with significantly improved PFS but not OS after PSW analysis. Within the limitations of a retrospective analysis, our findings suggest that in younger, fit patients, AHCT consolidation may improve PFS. </jats:p></jats:sec>
Journal
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- Journal of Clinical Oncology
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Journal of Clinical Oncology 37 (6), 471-480, 2019-02-20
American Society of Clinical Oncology (ASCO)
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Details 詳細情報について
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- CRID
- 1360861291468462464
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- ISSN
- 15277755
- 0732183X
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- Data Source
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- Crossref