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Maintenance versus Induction Therapy Choice on Outcomes after Autologous Transplantation for Multiple Myeloma.
Cornell, Robert F; D'Souza, Anita; Kassim, Adetola A; Costa, Luciano J; Innis-Shelton, Racquel D; Zhang, Mei-Jie; Huang, Jiaxing; Abidi, Muneer; Aiello, Jack; Akpek, Gorgun; Bashey, Asad; Bashir, Qaiser; Cerny, Jan; Comenzo, Raymond; Diaz, Miguel Angel; Freytes, César; Gale, Robert Peter; Ganguly, Siddhartha; Hamadani, Mehdi; Hashmi, Shahrukh; Holmberg, Leona; Hossain, Nasheed; Kamble, Rammurti T; Kharfan-Dabaja, Mohamed; Kindwall-Keller, Tamila; Kyle, Robert; Kumar, Shaji; Lazarus, Hillard; Lee, Cindy; Maiolino, Angelo; Marks, David I; Meehan, Kenneth; Mikhael, Joe; Nath, Rajneesh; Nishihori, Taiga; Olsson, Richard F; Ramanathan, Muthalagu; Saad, Ayman; Seo, Sachiko; Usmani, Saad; Vesole, David; Vij, Ravi; Vogl, Dan; Wirk, Baldeep M; Yared, Jean; Krishnan, Amrita; Mark, Tomer; Nieto, Yago; Hari, Parameswaran.
Afiliação
  • Cornell RF; Division of Hematology/Oncology Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
  • D'Souza A; Center for International Blood and Marrow Transplant Research (CIBMTR), Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin. Electronic address: andsouza@mcw.edu.
  • Kassim AA; Division of Hematology/Oncology Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
  • Costa LJ; Division of Hematology/Oncology, Department of Medicine, University of Alabama at Birmingham, Birmingham, Alabama.
  • Innis-Shelton RD; Division of Hematology/Oncology, Department of Medicine, University of Alabama at Birmingham, Birmingham, Alabama.
  • Zhang MJ; Center for International Blood and Marrow Transplant Research (CIBMTR), Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin; Division of Biostatistics, Institute for Health and Society, Medical College of Wisconsin, Milwaukee, Wisconsin.
  • Huang J; Center for International Blood and Marrow Transplant Research (CIBMTR), Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.
  • Abidi M; Division of BMT, Department of Oncology, Karmanos Cancer Institute, Wayne State University, Detroit, Michigan.
  • Aiello J; Patient, San Jose, California.
  • Akpek G; Stem Cell Transplantation and Cell Therapy, Department of Internal Medicine, Rush University Medical Center, Chicago, Illinois.
  • Bashey A; Blood and Marrow Transplant Program at Northside Hospital, Atlanta, Georgia.
  • Bashir Q; Department of Stem Cell Transplantation, Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Cerny J; Division of Hematology and Oncology, Department of Medicine, UMass Memorial Medical Center, Worchester, Massachusetts.
  • Comenzo R; Tufts Medical Center, Boston, Massachusetts.
  • Diaz MA; Department of Hematology/Oncology, Hospital Infantil Universitario Nino Jesus, Madrid, Spain.
  • Freytes C; South Texas Veterans Health Care System and University of Texas Health Science Center San Antonio, San Antonio, Texas.
  • Gale RP; Hematology Research Centre, Division of Experimental Medicine, Department of Medicine, Imperial College London, London, United Kingdom.
  • Ganguly S; Blood and Marrow Transplantation, Division of Hematology and Oncology, University of Kansas Medical Center, Kansas City, Kansas.
  • Hamadani M; Center for International Blood and Marrow Transplant Research (CIBMTR), Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.
  • Hashmi S; Mayo Clinic Rochester, Rochester, Minnesota.
  • Holmberg L; Fred Hutchinson Cancer Research Center, Seattle, Washington.
  • Hossain N; Fox Chase Cancer Center, Philadelphia, Pennsylvania.
  • Kamble RT; Division of Hematology and Oncology, Center for Cell and Gene Therapy, Baylor College of Medicine, Houston, Texas.
  • Kharfan-Dabaja M; Department of Blood and Marrow Transplantation, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.
  • Kindwall-Keller T; Division of Hematology/Oncology, University of Virginia Health System, Charlottesville, Virginia.
  • Kyle R; Mayo Clinic Rochester, Rochester, Minnesota.
  • Kumar S; Mayo Clinic Rochester, Rochester, Minnesota.
  • Lazarus H; Seidman Cancer Center, University Hospitals Case Medical Center, Cleveland, Ohio.
  • Lee C; Royal Adelaide Hospital, Adelaide, South Australia, Australia.
  • Maiolino A; Hospital Universitbrio Clementinio Fraga Filho, Universidade Federal do Rio de Janerio, Rio de Janerio, Brazil.
  • Marks DI; Adult Bone Marrow Transplant, University Hospitals Bristol NHS Trust, Bristol, United Kingdom.
  • Meehan K; Dartmouth Hitchcock Medical Center, Lebanon, New Hampshire.
  • Mikhael J; Mayo Clinic Arizona and Phoenix Children's Hospital, Phoenix, Arizona.
  • Nath R; Division of Hematology and Oncology, Department of Medicine, UMass Memorial Medical Center, Worchester, Massachusetts.
  • Nishihori T; Department of Blood and Marrow Transplantation, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.
  • Olsson RF; Division of Therapeutic Immunology, Department of Laboratory Medicine, Karolinksa Institutet, Stockholm, Sweden; Centre for Clinical Research Sormland, Uppsala University, Uppsala, Sweden.
  • Ramanathan M; Division of Hematology and Oncology, Department of Medicine, UMass Memorial Medical Center, Worchester, Massachusetts.
  • Saad A; Division of Hematology/Oncology, Department of Medicine, University of Alabama at Birmingham, Birmingham, Alabama.
  • Seo S; National Cancer Research Center, East Hospital, Chiba, Japan.
  • Usmani S; Department of Hematology v Medical Oncology, Levine Cancer Institute, Carolinas HealthCare System, Charlotte, North Carolina.
  • Vesole D; John Theurer Cancer Center at Hackensack UMC, Hackensack, New Jersey.
  • Vij R; Divison of Hematology and Oncology, Washington University School of Medicine, St. Louis, Missouri.
  • Vogl D; Abramson Cancer Center, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Wirk BM; Division of Bone Marrow Transplant, Seattle Cancer Care Alliance, Seattle, Washington.
  • Yared J; Blood & Marrow Transplantation Program, Division of Hematology/Oncology, Department of Medicine, Greenebaum Cancer Center, University of Maryland, Baltimore, Maryland.
  • Krishnan A; City of Hope National Medical Center, Duarte, California.
  • Mark T; Department of Medicine, Weill Cornell Medical College, New York, New York.
  • Nieto Y; Department of Stem Cell Transplantation, Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Hari P; Center for International Blood and Marrow Transplant Research (CIBMTR), Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.
Biol Blood Marrow Transplant ; 23(2): 269-277, 2017 Feb.
Article em En | MEDLINE | ID: mdl-27864161
ABSTRACT
Bortezomib (V), lenalidomide (R), cyclophosphamide (C), and dexamethasone (D) are components of the most commonly used modern doublet (RD, VD) or triplet (VRD, CVD) initial induction regimens before autologous hematopoietic cell transplantation (AHCT) for multiple myeloma (MM) in the United States. In this study we evaluated 693 patients receiving "upfront" AHCT after initial induction therapy with modern doublet or triplet regimens using data reported to the Center for International Blood and Marrow Transplant Research from 2008 to 2013. Analysis was limited to those receiving a single AHCT after 1 line of induction therapy within 12 months from treatment initiation for MM. In multivariate analysis, progression-free survival (PFS) and overall survival were similar irrespective of induction regimen. However, high-risk cytogenetics and nonreceipt of post-transplant maintenance/consolidation therapy were associated with higher risk of relapse. Patients receiving post-transplant therapy had significantly improved 3-year PFS versus no post-transplant therapy (55% versus 39%, P = .0001). This benefit was most evident in patients not achieving at least a complete response post-AHCT (P = .005). In patients receiving upfront AHCT, the choice of induction regimen (doublet or triplet therapies) appears to be of lower impact than use of post-transplant therapy.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Transplante de Células-Tronco Hematopoéticas / Mieloma Múltiplo Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Biol Blood Marrow Transplant Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Transplante de Células-Tronco Hematopoéticas / Mieloma Múltiplo Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Biol Blood Marrow Transplant Ano de publicação: 2017 Tipo de documento: Article