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Contribution of chemotherapy mobilization to disease control in multiple myeloma treated with autologous hematopoietic cell transplantation.
Uy, G L; Costa, L J; Hari, P N; Zhang, M-J; Huang, J-X; Anderson, K C; Bredeson, C N; Callander, N S; Cornell, R F; Perez, M A D; Dispenzieri, A; Freytes, C O; Gale, R P; Garfall, A; Gertz, M A; Gibson, J; Hamadani, M; Lazarus, H M; Kalaycio, M E; Kamble, R T; Kharfan-Dabaja, M A; Krishnan, A Y; Kumar, S K; Kyle, R A; Landau, H J; Lee, C H; Maiolino, A; Marks, D I; Mark, T M; Munker, R; Nishihori, T; Olsson, R F; Ramanathan, M; Rodriguez, T E; Saad, A A; Savani, B N; Schiller, G J; Schouten, H C; Schriber, J R; Scott, E; Seo, S; Sharma, M; Ganguly, S; Stadtmauer, E A; Tay, J; To, L B; Vesole, D H; Vogl, D T; Wagner, J L; Wirk, B.
Affiliation
  • Uy GL; Department of Medicine, Washington University School of Medicine, St Louis, MO, USA.
  • Costa LJ; Division of Hematology/Oncology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL, USA.
  • Hari PN; Center for International Blood and Marrow Transplant Research (CIBMTR), Department of Medicine, Medical College of Wisconsin, Milwaukee, WI, USA.
  • Zhang MJ; Center for International Blood and Marrow Transplant Research (CIBMTR), Department of Medicine, Medical College of Wisconsin, Milwaukee, WI, USA.
  • Huang JX; Division of Biostatistics, Institute for Health and Society, Medical College of Wisconsin, Milwaukee, WI, USA.
  • Anderson KC; Center for International Blood and Marrow Transplant Research (CIBMTR), Department of Medicine, Medical College of Wisconsin, Milwaukee, WI, USA.
  • Bredeson CN; Hematologic Oncology Treatment Center, Dana-Farber Cancer Institute, Boston, MA, USA.
  • Callander NS; The Ottawa Hospital Blood and Marrow Transplant Program and the Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
  • Cornell RF; University of Wisconsin Carbone Cancer Center, Madison, WI, USA.
  • Perez MA; Division of Hematology/Oncology, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
  • Dispenzieri A; Servicio de Oncohematologia, Hospital Infantil Universitario Nino Jesus, Madrid, Spain.
  • Freytes CO; Department of Hematology, Mayo Clinic, Rochester, MN, USA.
  • Gale RP; South Texas Veterans Health Care System and University of Texas Health Science Center San Antonio, San Antonio, TX, USA.
  • Garfall A; Hematology Research Centre, Division of Experimental Medicine, Department of Medicine, Imperial College London, London, UK.
  • Gertz MA; Division of Hematology/Oncology, Perelman Center for Advanced Medicine, Abramson Cancer Center, University of Pennsylvania, Philadelphia, PA, USA.
  • Gibson J; Department of Hematology, Mayo Clinic, Rochester, MN, USA.
  • Hamadani M; Haematology Department, Royal Prince Alfred Hospital Institute of Haematology, Camperdown, New South Wales, Australia.
  • Lazarus HM; Center for International Blood and Marrow Transplant Research (CIBMTR), Department of Medicine, Medical College of Wisconsin, Milwaukee, WI, USA.
  • Kalaycio ME; Seidman Cancer Center, University Hospitals Case Medical Center, Cleveland, OH, USA.
  • Kamble RT; Hematologic Oncology and Blood Disorders, Cleveland Clinic, Cleveland, OH, USA.
  • Kharfan-Dabaja MA; Division of Hematology and Oncology, Center for Cell and Gene Therapy, Baylor College of Medicine, Houston, TX, USA.
  • Krishnan AY; Department of Blood and Marrow Transplantation, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.
  • Kumar SK; Department of Hematology/Oncology, City of Hope National Medical Center, Duarte, CA, USA.
  • Kyle RA; Department of Hematology, Mayo Clinic, Rochester, MN, USA.
  • Landau HJ; Department of Hematology, Mayo Clinic, Rochester, MN, USA.
  • Lee CH; Bone Marrow Transplant Service, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Maiolino A; Haematology and Bone Marrow Transplant Unit, Royal Adelaide Hospital/SA Pathology, Adelaide, South Australia, Australia.
  • Marks DI; Hospital Universitário Clementinio Fraga Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
  • Mark TM; Pediatric Bone Marrow Transplant, University Hospitals Bristol NHS Trust, Bristol, UK.
  • Munker R; Department of Medicine, New York Presbyterian Hospital at Cornell, New York, NY, USA.
  • Nishihori T; Section of Hematology/Oncology, Department of Internal Medicine, Louisiana State University Health Shreveport, Shreveport, LA, USA.
  • Olsson RF; Department of Blood and Marrow Transplantation, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.
  • Ramanathan M; Division of Therapeutic Immunology, Department of Laboratory Medicine, Karolinska Institutet, Stockholm, Sweden.
  • Rodriguez TE; Centre for Clinical Research Sörmland, Uppsala University, Uppsala, Sweden.
  • Saad AA; Division of Hematology and Oncology, Department of Medicine, UMass Memorial Medical Center, Worcester, MA, USA.
  • Savani BN; Bone Marrow Transplant Program, Loyola University Medical Center, Chicago, IL, USA.
  • Schiller GJ; Division of Hematology/Oncology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL, USA.
  • Schouten HC; Division of Hematology/Oncology, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
  • Schriber JR; Bone Marrow Transplant Program, UCLA Center for Health Sciences, Los Angeles, CA, USA.
  • Scott E; Department of Hematology, Academische Ziekenhuis, Maastricht, The Netherlands.
  • Seo S; Cancer Transplant Institute, Virginia G. Piper Cancer Center, Scottsdale, AZ, USA.
  • Sharma M; Arizona Oncology, Scottsdale, AZ, USA.
  • Ganguly S; Center for Hematologic Malignancies, Oregon Health and Science University, Portland, OR, USA.
  • Stadtmauer EA; Department of Vaccine and Infectious Disease, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
  • Tay J; Department of Hematology/Oncology, Thomas Jefferson University, Philadelphia, PA, USA.
  • To LB; Blood and Marrow Transplantation, Division of Hematology and Oncology, University of Kansas Medical Center, Kansas City, KS, USA.
  • Vesole DH; Division of Hematology/Oncology, Perelman Center for Advanced Medicine, Abramson Cancer Center, University of Pennsylvania, Philadelphia, PA, USA.
  • Vogl DT; Department of Medicine, University of Ottawa, Ottawa, Ontario, Canada.
  • Wagner JL; Haematology and Bone Marrow Transplant Unit, Royal Adelaide Hospital/SA Pathology, Adelaide, South Australia, Australia.
  • Wirk B; Hackensack University Medical Center, Hackensack, NJ, USA.
Bone Marrow Transplant ; 50(12): 1513-8, 2015 Dec.
Article in En | MEDLINE | ID: mdl-26301967
ABSTRACT
In patients with multiple myeloma (MM) undergoing autologous hematopoietic cell transplantation (auto-HCT), peripheral blood progenitor cells may be collected following mobilization with growth factor alone (GF) or cytotoxic chemotherapy plus GF (CC+GF). It is uncertain whether the method of mobilization affects post-transplant outcomes. We compared these mobilization strategies in a retrospective analysis of 968 patients with MM from the Center for International Blood and Marrow Transplant Research database who received an auto-HCT in the US and Canada between 2007 and 2012. The kinetics of neutrophil engraftment (⩾0.5 × 10(9)/L) was similar between groups (13 vs 13 days, P=0.69) while platelet engraftment (⩾20 × 10(9)/L) was slightly faster with CC+GF (19 vs 18 days, P=0.006). Adjusted 3-year PFS was 43% (95% confidence interval (CI) 38-48) in GF and 40% (95% CI 35-45) in CC+GF, P=0.33. Adjusted 3-year OS was 82% (95% CI 78-86) vs 80% (95% CI 75-84), P=0.43 and adjusted 5-year OS was 62% (95% CI 54-68) vs 60% (95% CI 52-67), P=0.76, for GF and CC+GF, respectively. We conclude that MM patients undergoing auto-HCT have similar outcomes irrespective of the method of mobilization and found no evidence that the addition of chemotherapy to mobilization contributes to disease control.
Subject(s)

Full text: 1 Collection: 01-internacional Health context: 1_ASSA2030 / 2_ODS3 Database: MEDLINE Main subject: Hematopoietic Stem Cell Transplantation / Hematopoietic Stem Cell Mobilization / Multiple Myeloma Type of study: Clinical_trials / Observational_studies Limits: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Bone Marrow Transplant Year: 2015 Document type: Article

Full text: 1 Collection: 01-internacional Health context: 1_ASSA2030 / 2_ODS3 Database: MEDLINE Main subject: Hematopoietic Stem Cell Transplantation / Hematopoietic Stem Cell Mobilization / Multiple Myeloma Type of study: Clinical_trials / Observational_studies Limits: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Bone Marrow Transplant Year: 2015 Document type: Article