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Impact of initial chemotherapy regimen on outcomes for patients with double-expressor lymphoma: A multi-center analysis.
D'Angelo, Christopher R; Hanel, Walter; Chen, Yi; Yu, Menggang; Yang, David; Guo, Ling; Karmali, Reem; Burkart, Madelyn; Ciccosanti, Colleen; David, Kevin; Risch, Zachary; Murga-Zamalloa, Carlos; Devata, Sumana; Wilcox, Ryan; Savani, Malvi; Courville, Elizabeth L; Bachanova, Veronika; Rabinovich, Emma; Peace, David; Osman, Fauzia; Epperla, Narendranath; Kenkre, Vaishalee P.
Afiliação
  • D'Angelo CR; Fred and Pamela Buffett Cancer Center, University of Nebraska Medical Center, Omaha, Nebraska, USA.
  • Hanel W; Department of Internal Medicine, Division of Hematology/Oncology, The Ohio State University Hospital, Columbus, Ohio, USA.
  • Chen Y; Department of Biostatistics and Medical Informatics, University of Wisconsin-Madison, Madison, Wisconsin, USA.
  • Yu M; Department of Biostatistics and Medical Informatics, University of Wisconsin-Madison, Madison, Wisconsin, USA.
  • Yang D; Department of Pathology, University of Wisconsin Carbone Cancer Center Madison, Wisconsin, USA.
  • Guo L; The James Cancer Hospital and Solove Research Institute, The Ohio State University, Columbus, Ohio, USA.
  • Karmali R; Robert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.
  • Burkart M; Robert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.
  • Ciccosanti C; Department of Internal Medicine, Rutgers Robert Wood Johnson Medical School, New Brunswick, New Jersey, USA.
  • David K; Division of Hematology/Oncology, Rutgers Cancer Institute of New Jersey, New Brunswick, New Jersey, USA.
  • Risch Z; The James Cancer Hospital and Solove Research Institute, The Ohio State University, Columbus, Ohio, USA.
  • Murga-Zamalloa C; Department of Pathology, University of Illinois at Chicago, Chicago, Illinois, USA.
  • Devata S; Department of Pathology, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
  • Wilcox R; Department of Internal Medicine, Division of Hematology/Oncology, University of Michigan, Ann Arbor, Michigan, USA.
  • Savani M; Division of Hematology and Oncology, Department of Medicine, University of Arizona Cancer Center, Tucson, Arizona, USA.
  • Courville EL; Department of Pathology, University of Virginia, Charlottesville, Virginia, USA.
  • Bachanova V; Department of Internal Medicine, Division of Hematology/Oncology, University of Minnesota, Minneapolis, Minnesota, USA.
  • Rabinovich E; Department of Pathology, University of Illinois at Chicago, Chicago, Illinois, USA.
  • Peace D; Department of Pathology, University of Illinois at Chicago, Chicago, Illinois, USA.
  • Osman F; Department of Biostatistics and Medical Informatics, University of Wisconsin-Madison, Madison, Wisconsin, USA.
  • Epperla N; The James Cancer Hospital and Solove Research Institute, The Ohio State University, Columbus, Ohio, USA.
  • Kenkre VP; Department of Pathology, University of Wisconsin Carbone Cancer Center Madison, Wisconsin, USA.
Hematol Oncol ; 39(4): 473-482, 2021 Oct.
Article em En | MEDLINE | ID: mdl-34347909
ABSTRACT
Diffuse large B-cell lymphoma featuring overexpression of MYC and B-Cell Lymphoma 2 (double expressor lymphoma, DEL) is associated with poor outcomes. Existing evidence suggesting improved outcomes for DEL with the use of more intensive regimens than R-CHOP is restricted to younger patients and based on limited evidence from low patient numbers. We retrospectively evaluated the impact of intensive frontline regimens versus R-CHOP in a multicenter analysis across 7 academic medical centers in the United States. We collected 90 cases of DEL, 46 out of 90 patients (51%) received R-CHOP and 44/90 (49%) received an intensive regimen, which was predominantly DA-EPOCH-R. Treatment cohorts were evenly balanced for demographics and disease characteristics, though the intensive group had a higher lactate dehydrogenase (LDH, 326 vs. 230 U/L p = 0.06) and presence of B-symptoms (50% vs. 22%, p = 0.01) compared to the R-CHOP cohort. There was no difference in PFS (median 53 vs. 38 months, p = 0.49) or overall survival (67 vs. not reached months, p = 0.14) between the R-CHOP and intensive therapy cohorts, respectively. On multivariate analysis, intensive therapy was associated with a hazard ratio of 2.35 (95% CI 0.74-7.41), though this was not statistically significant. Additionally, a subgroup analysis of intermediate high-risk lymphoma defined by IPI ≥3 did not identify a difference in survival outcomes between regimens. We conclude that in our multi-center cohort there is no evidence supporting the use of intensive regimens over R-CHOP, suggesting that R-CHOP remains the standard of care for treating DEL.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Linfoma Difuso de Grandes Células B Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Linfoma Difuso de Grandes Células B Idioma: En Ano de publicação: 2021 Tipo de documento: Article