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Outcomes of patients with limited-stage aggressive large B-cell lymphoma with high-risk cytogenetics.
Torka, Pallawi; Kothari, Shalin K; Sundaram, Suchitra; Li, Shaoying; Medeiros, L Jeffrey; Ayers, Emily C; Landsburg, Daniel J; Bond, David A; Maddocks, Kami J; Giri, Anshu; Hess, Brian; Pham, Luu Q; Advani, Ranjana; Liu, Yang; Barta, Stefan Klaus; Vose, Julie M; Churnetski, Michael C; Cohen, Jonathon B; Burkart, Madelyn; Karmali, Reem; Zurko, Joanna; Mehta, Amitkumar; Olszewski, Adam J; Lee, Sarah; Hill, Brian T; Burns, Timothy F; Lansigan, Frederick; Rabinovich, Emma; Peace, David; Groman, Adrienne; Attwood, Kristopher; Hernandez-Ilizaliturri, Francisco J.
Afiliación
  • Torka P; Roswell Park Comprehensive Cancer Center, Buffalo, NY.
  • Kothari SK; Department of Medicine, Yale University, New Haven, CT.
  • Sundaram S; Roswell Park Comprehensive Cancer Center, Buffalo, NY.
  • Li S; The University of Texas MD Anderson Cancer Center, Houston, TX.
  • Medeiros LJ; The University of Texas MD Anderson Cancer Center, Houston, TX.
  • Ayers EC; Abramson Cancer Center, University of Pennsylvania, Philadelphia, PA.
  • Landsburg DJ; Abramson Cancer Center, University of Pennsylvania, Philadelphia, PA.
  • Bond DA; The Ohio State University Cancer Center, Columbus, OH.
  • Maddocks KJ; The Ohio State University Cancer Center, Columbus, OH.
  • Giri A; Division of Hematology and Oncology, Medical University of South Carolina, Charleston, SC.
  • Hess B; Division of Hematology and Oncology, Medical University of South Carolina, Charleston, SC.
  • Pham LQ; Lymphoma Division, Stanford University, Stanford, CA.
  • Advani R; Lymphoma Division, Stanford University, Stanford, CA.
  • Liu Y; Fox Chase Cancer Center, Philadelphia, PA.
  • Barta SK; Fox Chase Cancer Center, Philadelphia, PA.
  • Vose JM; University of Nebraska Medical Center, Omaha, NE.
  • Churnetski MC; Winship Cancer Institute, Emory University, Atlanta, GA.
  • Cohen JB; Winship Cancer Institute, Emory University, Atlanta, GA.
  • Burkart M; Feinberg School of Medicine, Northwestern University, Chicago, IL.
  • Karmali R; Feinberg School of Medicine, Northwestern University, Chicago, IL.
  • Zurko J; Division of Hematology and Oncology, University of Alabama at Birmingham, Birmingham, AL.
  • Mehta A; Division of Hematology and Oncology, University of Alabama at Birmingham, Birmingham, AL.
  • Olszewski AJ; Department of Medicine, Alpert Medical School, Brown University, Providence, RI.
  • Lee S; Taussig Cancer Institute, Cleveland Clinic Foundation, Cleveland, OH.
  • Hill BT; Taussig Cancer Institute, Cleveland Clinic Foundation, Cleveland, OH.
  • Burns TF; Dartmouth-Hitchcock Medical Center, Lebanon, NH; and.
  • Lansigan F; Dartmouth-Hitchcock Medical Center, Lebanon, NH; and.
  • Rabinovich E; Division of Hematology & Oncology, University of Illinois at Chicago, Chicago, IL.
  • Peace D; Division of Hematology & Oncology, University of Illinois at Chicago, Chicago, IL.
  • Groman A; Roswell Park Comprehensive Cancer Center, Buffalo, NY.
  • Attwood K; Roswell Park Comprehensive Cancer Center, Buffalo, NY.
  • Hernandez-Ilizaliturri FJ; Roswell Park Comprehensive Cancer Center, Buffalo, NY.
Blood Adv ; 4(2): 253-262, 2020 01 28.
Article en En | MEDLINE | ID: mdl-31945157
ABSTRACT
There is a paucity of data regarding outcomes and response to standard therapy in patients with limited-stage (LS) agressive B-cell lymphoma (LS-ABCL) who harbor MYC rearrangement (MYC-R) with or without BCL2 and/or BCL6 rearrangements. We conducted a multicenter retrospective study of MYC-R LS-ABCL patients who received either rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP), or more intensive immunochemotherapy (IIC) plus or minus consolidative involved-field radiation therapy (IFRT). One hundred four patients from 15 academic centers were included. Forty four patients (42%) received R-CHOP, of whom 52% had IFRT. Sixty patients (58%) received IIC, of whom 40% had IFRT. Overall response rate was 91% (84% complete response [CR]; 7% partial response). Patients with double-hit lymphoma (DHL; n = 40) had a lower CR rate compared with patients with MYC-R only (75% vs 98%; P = .003). CR rate was higher in the IFRT vs no-IFRT group (98% vs 72%; P < .001). Median follow-up was 3.2 years; 2-year progression-free survival (PFS) and overal survival (OS) were 78% and 86% for the entire cohort, and 74% and 81% for the DHL patients, respectively. PFS and OS were similar across treatment groups (IFRT vs no IFRT, R-CHOP vs IIC) in the entire cohort and in DHL patients. Our data provide a historical benchmark for MYC-R LS-ABCL and LS-DHL patients and show that outcomes for this population may be better than previously recognized. There was no benefit of using IIC over R-CHOP in patients with MYC-R LS-ABCL and LS-DHL.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Linfoma de Células B Grandes Difuso / Citogenética Tipo de estudio: Clinical_trials / Etiology_studies / Observational_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Aged80 / Humans / Middle aged Idioma: En Revista: Blood Adv Año: 2020 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Linfoma de Células B Grandes Difuso / Citogenética Tipo de estudio: Clinical_trials / Etiology_studies / Observational_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Aged80 / Humans / Middle aged Idioma: En Revista: Blood Adv Año: 2020 Tipo del documento: Article