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Impact of induction regimen and stem cell transplantation on outcomes in double-hit lymphoma: a multicenter retrospective analysis.
Petrich, Adam M; Gandhi, Mitul; Jovanovic, Borko; Castillo, Jorge J; Rajguru, Saurabh; Yang, David T; Shah, Khushboo A; Whyman, Jeremy D; Lansigan, Frederick; Hernandez-Ilizaliturri, Francisco J; Lee, Lisa X; Barta, Stefan K; Melinamani, Shruthi; Karmali, Reem; Adeimy, Camille; Smith, Scott; Dalal, Neil; Nabhan, Chadi; Peace, David; Vose, Julie; Evens, Andrew M; Shah, Namrata; Fenske, Timothy S; Zelenetz, Andrew D; Landsburg, Daniel J; Howlett, Christina; Mato, Anthony; Jaglal, Michael; Chavez, Julio C; Tsai, Judy P; Reddy, Nishitha; Li, Shaoying; Handler, Caitlin; Flowers, Christopher R; Cohen, Jonathon B; Blum, Kristie A; Song, Kevin; Sun, Haowei Linda; Press, Oliver; Cassaday, Ryan; Jaso, Jesse; Medeiros, L Jeffrey; Sohani, Aliyah R; Abramson, Jeremy S.
  • Petrich AM; Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, IL;
  • Gandhi M; Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, IL;
  • Jovanovic B; Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, IL;
  • Castillo JJ; Division of Hematologic Malignancies, Dana-Farber Cancer Institute, Boston, MA;
  • Rajguru S; Division of Hematology/Oncology and.
  • Yang DT; Department of Pathology and Laboratory Medicine, University of Wisconsin, Madison, WI;
  • Shah KA; Hematology/Oncology, Dartmouth-Hitchcock Medical Center, Lebanon, NH;
  • Whyman JD; Hematology/Oncology, Dartmouth-Hitchcock Medical Center, Lebanon, NH;
  • Lansigan F; Hematology/Oncology, Dartmouth-Hitchcock Medical Center, Lebanon, NH;
  • Hernandez-Ilizaliturri FJ; Departments of Immunology and Medicine, Roswell Park Cancer Institute, Buffalo, NY;
  • Lee LX; Department of Oncology, Albert-Einstein Cancer Center-Montefiore Medical Center, Bronx, NY;
  • Barta SK; Department of Oncology, Albert-Einstein Cancer Center-Montefiore Medical Center, Bronx, NY;
  • Melinamani S; Hematology & Oncology, Rush University Medical Center, Chicago, IL;
  • Karmali R; Hematology & Oncology, Rush University Medical Center, Chicago, IL;
  • Adeimy C; Cardinal Bernardin Cancer Center, Loyola University Medical Center, Maywood, IL;
  • Smith S; Cardinal Bernardin Cancer Center, Loyola University Medical Center, Maywood, IL;
  • Dalal N; Division of Hematology/Oncology, Advocate Lutheran General Hospital, Park Ridge, IL;
  • Nabhan C; Section of Hematology and Oncology, Department of Medicine, The University of Chicago, Chicago, IL;
  • Peace D; Department of Medicine, Section of Hematology-Oncology, University of Illinois at Chicago, Chicago, IL;
  • Vose J; Hematology/Oncology, University of Nebraska Medical Center, Omaha, NE;
  • Evens AM; Division of Hematology/Oncology, Tufts Medical Center and Tufts University School of Medicine, Boston, MA;
  • Shah N; Division of Hematology & Oncology, Medical College of Wisconsin, Milwaukee, WI;
  • Fenske TS; Division of Hematology & Oncology, Medical College of Wisconsin, Milwaukee, WI;
  • Zelenetz AD; Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, NY;
  • Landsburg DJ; Division of Hematology/Oncology, Hospital of the University of Pennsylvania, Philadelphia, PA;
  • Howlett C; Division of Hematology/Oncology, Hackensack University Medical Center, Hackensack, NJ; Ernest Mario School of Pharmacy, Rutgers, The State University of New Jersey, Piscataway, NJ;
  • Mato A; Division of Hematology/Oncology, Hospital of the University of Pennsylvania, Philadelphia, PA; Division of Hematology/Oncology, Hackensack University Medical Center, Hackensack, NJ;
  • Jaglal M; Department of Malignant Hematology, Moffitt Cancer Center, Tampa, FL;
  • Chavez JC; Department of Malignant Hematology, Moffitt Cancer Center, Tampa, FL;
  • Tsai JP; Division of Hematology/Oncology and.
  • Reddy N; Division of Hematology/Oncology and.
  • Li S; Department of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, TN;
  • Handler C; Department of Hematology and Medical Oncology, Winship Cancer Institute of Emory University, Atlanta, GA;
  • Flowers CR; Department of Hematology and Medical Oncology, Winship Cancer Institute of Emory University, Atlanta, GA;
  • Cohen JB; Department of Hematology and Medical Oncology, Winship Cancer Institute of Emory University, Atlanta, GA; Division of Hematology, The Ohio State University-James Comprehensive Cancer Center, Columbus, OH;
  • Blum KA; Division of Hematology, The Ohio State University-James Comprehensive Cancer Center, Columbus, OH;
  • Song K; Leukemia/BMT Program of British Columbia, British Columbia Cancer Agency, Vancouver, BC, Canada;
  • Sun HL; Leukemia/BMT Program of British Columbia, British Columbia Cancer Agency, Vancouver, BC, Canada;
  • Press O; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA;
  • Cassaday R; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA;
  • Jaso J; Department of Pathology, MD Anderson Cancer Center, Houston, TX; and.
  • Medeiros LJ; Department of Pathology, MD Anderson Cancer Center, Houston, TX; and.
  • Sohani AR; Department of Pathology and.
  • Abramson JS; Center for Lymphoma, Massachusetts General Hospital Cancer Center, Boston, MA.
Blood ; 124(15): 2354-61, 2014 Oct 09.
Article en En | MEDLINE | ID: mdl-25161267
ABSTRACT
Patients with double-hit lymphoma (DHL), which is characterized by rearrangements of MYC and either BCL2 or BCL6, face poor prognoses. We conducted a retrospective multicenter study of the impact of baseline clinical factors, induction therapy, and stem cell transplant (SCT) on the outcomes of 311 patients with previously untreated DHL. At median follow-up of 23 months, the median progression-free survival (PFS) and overall survival (OS) rates among all patients were 10.9 and 21.9 months, respectively. Forty percent of patients remain disease-free and 49% remain alive at 2 years. Intensive induction was associated with improved PFS, but not OS, and SCT was not associated with improved OS among patients achieving first complete remission (P = .14). By multivariate analysis, advanced stage, central nervous system involvement, leukocytosis, and LDH >3 times the upper limit of normal were associated with higher risk of death. Correcting for these, intensive induction was associated with improved OS. We developed a novel risk score for DHL, which divides patients into high-, intermediate-, and low-risk groups. In conclusion, a subset of DHL patients may be cured, and some patients may benefit from intensive induction. Further investigations into the roles of SCT and novel agents are needed.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Trasplante de Células Madre / Linfoma Tipo de estudio: Observational_studies / Prognostic_studies Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Año: 2014 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Trasplante de Células Madre / Linfoma Tipo de estudio: Observational_studies / Prognostic_studies Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Año: 2014 Tipo del documento: Article