Evidence map›Paper›PMID 24184335›Full record

ArticleBiology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation2014

Effect of postremission therapy before reduced-intensity conditioning allogeneic transplantation for acute myeloid leukemia in first complete remission.

Erica D Warlick, Kristjan Paulson, Ruta Brazauskas, Xiaobo Zhong, Alan M Miller, Bruce M Camitta, Biju George, Bipin N Savani, Celalettin Ustun, David I Marks and 30 more

Open access · hybridAbstract read
In one paragraph

Article in Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.1field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 34 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

40 authors at 20 institutions in 8 countries.

Erica D WarlickDivision of Hematology, Oncology, and Transplantation, Department of Medicine, University of Minnesota, Minneapolis, Minnesota. Electronic address: ewarlick@umn.edu.
Kristjan PaulsonDepartment of Hematology, University of Manitoba, Winnipeg, Manitoba, Canada.
Ruta BrazauskasCenter for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, Wisconsin.
Xiaobo ZhongCenter for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, Wisconsin.
Alan M MillerDepartment of Oncology, Baylor University Medical Center, Dallas, Texas.
Bruce M CamittaDepartment of Pediatrics, Midwest Center for Cancer and Blood Disorders, Medical College of Wisconsin and Children's Hospital of Wisconsin, Milwaukee, Wisconsin.
Biju GeorgeDepartment of Hematology, Christian Medical College Hospital, Vellore, India.
Bipin N SavaniDepartment of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
Celalettin UstunDivision of Hematology, Oncology, and Transplantation, Department of Medicine, University of Minnesota, Minneapolis, Minnesota.
David I MarksBristol Adult BMT Unit, Bristol Children's Hospital, Bristol, United Kingdom.
Edmund K WallerBone Marrow and Stem Cell Transplant Center, Emory University Hospital, Atlanta, Georgia.
Frédéric BaronUniversitaire de Liege, Centre Hospitalier Universitaire - Sart-Tilman, Liege, Belgium.
César O FreytesDepartment of Hematopoietic Stem Cell Transplant Program, South Texas Veterans Health Care System and University of Texas Health Science Center San Antonio, San Antonio, Texas.
Gérard SocieService d'Hematologie, Hopital Saint Louis, Paris, France.
Gorgun AkpekSCTCT Program, Banner MD Anderson Cancer Center, Gilbert, Arizona.
Harry C SchoutenDivision of Hematology, Academische Ziekenhuis Maastricht, Maastricht, Netherlands.
Hillard M LazarusSeidman Cancer Center, University Hospitals Case Medical Center, Cleveland, Ohio.
Edwin M HorwitzChildren's Hospital of Philadelphia, Philadelphia, Pennsylvania.
John KorethDepartment of Medical Oncology, Dana Farber Cancer Institute, Boston, Massachusetts.
Jean-Yves CahnDepartment of Hematology, University Hospital, Grenoble, France.
Martin BornhauserMedizinische Klinik und Poliklinik I, Universitatsklinikum Carl Gustav Carus, Dresden, Germany.
Matthew SeftelDepartment of Hematology, University of Manitoba, Winnipeg, Manitoba, Canada.
Mitchell S CairoDepartment of Pediatric Hematology, Oncology and Stem Cell Transplantation, Maria Fareri Children's Hospital, New York Medical College, Valhalla, New York.
Mary J LaughlinHematopoietic Cell Transplantation Program, University of Virginia, Charlottesville, Virginia.
Mitchell SabloffDivision of Hematology, Department of Medicine, University of Ottawa and The Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
Olle RingdénCentre for Allogeneic Stem Cell Transplantation, Karolinska University Hospital, Stockholm, Sweden.
Robert Peter GaleSection of Hematology, Division of Experimental Medicine, Department of Medicine, Imperial College, London, United Kingdom.
Rammurti T KambleCenter for Cell and Gene Therapy, Baylor College of Medicine, Houston, Texas.
Ravi VijWashington University School of Medicine, St. Louis, Missouri.
Usama GergisWeill Cornell Medical College, New York, New York.
Vikram MathewsDepartment of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
Wael SaberCenter for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, Wisconsin.
Yi-Bin ChenDepartment of BMT, Massachusetts General Hospital, Boston, Massachusetts.
Jane L LiesveldDepartment of Hematology/Oncology, Strong Memorial Hospital, University of Rochester Medical Center, Rochester, New York.
Corey S CutlerDepartment of Medical Oncology, Dana Farber Cancer Institute, Boston, Massachusetts.
Armin GhobadiDepartment of Stem Cell Transplantation and Cellular Therapy, MD Anderson Cancer Center, Houston, Texas.
Geoffrey L UySection of Hematology, Division of Experimental Medicine, Department of Medicine, Imperial College, London, United Kingdom.
Mary EapenCenter for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, Wisconsin.
Daniel J WeisdorfDivision of Hematology, Oncology, and Transplantation, Department of Medicine, University of Minnesota, Minneapolis, Minnesota.
Mark R LitzowDepartment of Hematology and Internal Medicine, Mayo Clinic Rochester, Rochester, Minnesota.
Medical College of Wisconsin · USUniversity of Minnesota · USDana-Farber Cancer Institute · USImperial College London · GBThe University of Texas MD Anderson Cancer Center · USUniversity of Manitoba · CAVanderbilt University Medical Center · USBaylor College of Medicine · USBaylor University Medical Center · USBristol Royal Hospital for Children · GBCentre Hospitalier Universitaire de Liège · BEChildren's Hospital of Philadelphia · USChristian Medical College · INCornell University · USEmory University Hospital · USHôpital Saint-Louis · FRKarolinska University Hospital · SEKlinik und Poliklinik für Psychotherapie und Psychosomatik · DEMassachusetts General Hospital · USMayo Clinic · US

Funding

Data Resource for Analyzing Blood &Marrow TransplantsU24CA076518 · NCI · MEDICAL COLLEGE OF WISCONSIN · PI Amy M Moskop, Bronwen Shaw · 1998 to 2026
$105.2M
Easy-to-read Informed Consent for HCT Clinical TrialsU10HL069294 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI HOROWITZ, MARY MARESCA · 2011 to 2016
$43.8M
Washington University Institute of Clinical and Translational SciencesUL1TR000448 · NCATS · WASHINGTON UNIVERSITY · PI EVANOFF, BRADLEY A · 2012 to 2016
$41.4M
RESEARCH TRAINING IN HEMATOLOGYT32HL007899 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI Jane Ellen Churpek · 1998 to 2026
$8.2M
NCATS NIH HHS UL1 TR000448NCI NIH HHS U24 CA076518NHLBI NIH HHS T32 HL007899NHLBI NIH HHS U10 HL069294
6 · The paper itself

Abstract

The impact of pretransplant (hematopoietic cell transplantation [HCT]) cytarabine consolidation therapy on post-HCT outcomes has yet to be evaluated after reduced-intensity or nonmyeloablative conditioning. We analyzed 604 adults with acute myeloid leukemia in first complete remission (CR1) reported to the Center for International Blood and Marrow Transplant Research who received a reduced-intensity or nonmyeloablative conditioning HCT from an HLA-identical sibling, HLA-matched unrelated donor, or umbilical cord blood donor from 2000 to 2010. We compared transplant outcomes based on exposure to cytarabine postremission consolidation. Three-year survival rates were 36% (95% confidence interval [CI], 29% to 43%) in the no consolidation arm and 42% (95% CI, 37% to 47%) in the cytarabine consolidation arm (P = .16). Disease-free survival was 34% (95% CI, 27% to 41%) and 41% (95% CI, 35% to 46%; P = .15), respectively. Three-year cumulative incidences of relapse were 37% (95% CI, 30% to 44%) and 38% (95% CI, 33% to 43%), respectively (P = .80). Multivariate regression confirmed no effect of consolidation on relapse, disease-free survival, and survival. Before reduced-intensity or nonmyeloablative conditioning HCT, these data suggest pre-HCT consolidation cytarabine does not significantly alter outcomes and support prompt transition to transplant as soon as morphologic CR1 is attained. If HCT is delayed while identifying a donor, our data suggest that consolidation does not increase transplant treatment-related mortality and is reasonable if required.

Indexed as

AdolescentAdultAgedCohort StudiesFemaleHematopoietic Stem Cell TransplantationHumansLeukemia, Myeloid, AcuteMaleMiddle AgedRemission InductionRisk FactorsSurvival AnalysisTransplantation ConditioningTransplantation, HomologousYoung AdultAMLCytarabine consolidationRIC

Identifiers

PMID24184335
PMCPMC3924751
OpenAlexW2110335058

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.