Evidence map›Paper›PMID 27315441›Full record

ArticleCancer2016

Does FLT3 mutation impact survival after hematopoietic stem cell transplantation for acute myeloid leukemia? A Center for International Blood and Marrow Transplant Research (CIBMTR) analysis.

Abhinav Deol, Salyka Sengsayadeth, Kwang Woo Ahn, Hai-Lin Wang, Mahmoud Aljurf, Joseph Harry Antin, Minoo Battiwalla, Martin Bornhauser, Jean-Yves Cahn, Bruce Camitta and 34 more

Abstract read
In one paragraph

Article in Cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

34 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Gilteritinib as Post-Transplant Maintenance for AML With Internal Tandem Duplication Mutation ofJournal of clinical oncology : official journal of the American Society of Clinical Oncology · 2024
    Trial
  4. Trial
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Clinical Outcomes and Treatment Patterns in Adults With FLT3-ITDTransplantation and cellular therapy · 2024
    Observational
  11. Article
  12. Review
  13. FLT3-targeted treatment for acute myeloid leukemia.International journal of hematology · 2022
    Review
  14. Article
  15. Review
  16. Review
  17. Review
  18. Review
  19. Article
  20. Current Approaches to Transplantation for FLT3-ITD AML.Current hematologic malignancy reports · 2020
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

44 authors.

Abhinav Deol *Department of Oncology, Karmanos Cancer Institute, Wayne State University, Detroit, MI.
Salyka Sengsayadeth *Vanderbilt University Medical Center, Nashville, TN.
Kwang Woo AhnCIBMTR, Department of Medicine, Medical College of Wisconsin, Milwaukee, WI.
Hai-Lin WangCIBMTR, Department of Medicine, Medical College of Wisconsin, Milwaukee, WI.
Mahmoud AljurfDepartment of Oncology, King Faisal Specialist Hospital Center & Research, Riydah, Saudi Arabia.
Joseph Harry AntinCenter for Hematologic Oncology, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
Minoo BattiwallaHematology Branch, National Heart Lung and Blood Institute, Bethesda, MD.
Martin BornhauserUniversitatsklinikum Carl Gustav Carus, Dresden, Germany.
Jean-Yves CahnDepartment of Hematology, University Hospital, Grenoble, France.
Bruce CamittaMidwest Center for Cancer and Blood Disorders, Medical College of Wisconsin and Children's Hospital of Wisconsin, Milwaukee, WI.
Yi-Bin ChenDivision of Hematology/Oncology, Massachusetts General Hospital, Boston, MA.
Corey S CutlerCenter for Hematologic Oncology, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
Robert Peter GaleHematology Research Centre, Division of Experimental Medicine, Department of Medicine, Imperial College London, London, United Kingdom.
Siddhartha GangulyBlood and Marrow Transplantation, Division of Hematology and Oncology, University of Kansas Medical Center, Kansas City, KS.
Mehdi HamadaniCIBMTR, Department of Medicine, Medical College of Wisconsin, Milwaukee, WI.
Yoshihiro InamotoDivision of Hematopoietic Stem Cell Transplantation, National Cancer Center Hospital, Tokyo, Japan.
Madan JagasiaVanderbilt University Medical Center, Nashville, TN.
Rammurti KambleDivision of Hematology and Oncology, Center for Cell and Gene Therapy, Baylor College of Medicine, Houston, TX.
John KorethCenter for Hematologic Oncology, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
Hillard M LazarusSeidman Cancer Center, University Hospitals Case Medical Center, Cleveland, OH.
Jane LiesveldDepartment of Medicine, University of Rochester Medical Center, Rochester, NY.
Mark R LitzowDivision of Hematology and Transplant Center, Mayo Clinic Rochester.
David I MarksPediatric Bone Marrow Transplant, University Hospitals Bristol NHS Trust, Bristol, United Kingdom.
Taiga NishihoriDepartment of Blood and Marrow Transplantation, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL.
Richard F OlssonDivision of Therapeutic Immunology, Department of Laboratory Medicine, Karolinska Institutet, Stockholm, Sweden.
Ran ReshefBlood and Marrow Transplantation Program and Columbia Center for Translational Immunology, Columbia University Medical Center, New York, NY.
Jacob M RoweDepartment of Hematology, Shaare Zedek Medical Center, Jerusalem, Israel.
Ayman A SaadDivision of Hematology/Oncology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL.
Mitchell SabloffDivision of Hematology, Department of Medicine, University of Ottawa and Ottawa Hospital Research institute, Ottawa, Canada.
Harry C SchoutenDepartment of Hematology, Academische Ziekenhuis, Maastricht, Netherlands.
Thomas C SheaDivision of Hematology and Oncology, Department of Medicine, University of North Carolina Health Care, Chapel Hill, NC.
Robert J SoifferCenter for Hematologic Oncology, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
Geoffrey L UyDivsion of Onocology, Washington University School of Medicine, St. Louis, MO.
Edmond K WallerDepartment of Hematology and Medical Oncology, Winship Cancer Insitute, Emory University, Atlanta, GA.
Peter H WiernikOur Lady of Mercy Medical Center, Bronx, NY.
Baldeep WirkDivision of Bone Marrow Transplant, Seattle Cancer Care Alliance, Seattle, WA.
Ann E WoolfreyFred Hutchinson Cancer Research Center, Seattle, WA.
Donald BunjesDepartment of Internal Medicine III, Universitatsklinkum Ulm, Ulm, Germany.
Steven DevineDepartment of Internal Medicine, The Ohio State University Comprehensive Cancer Center- James, Columbus, OH.
Marcos de LimaDepartment of Medicine, Seidman Cancer Center, University Hospitals Case Medical Center, Cleveland, OH.
Brenda M SandmaierDivision of Medical Oncology, University of Washington and Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
Dan WeisdorfCIBMTR, NMDP/ Be The Match, Minneapolis, MN.
Hanna Jean KhouryDepartment of Hematology and Medical Oncology, Winship Cancer Insitute, Emory University, Atlanta, GA.
Wael SaberCIBMTR, Department of Medicine, Medical College of Wisconsin, Milwaukee, WI.

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
NCI NIH HHS U24 CA076518NHLBI NIH HHS U10 HL069294
6 · The paper itself

Abstract

backgroundPatients with FMS like tyrosine kinase 3 (FLT3)-mutated acute myeloid leukemia (AML) have a poor prognosis and are referred for early allogeneic hematopoietic stem cell transplantation (HCT).

methodsData from the Center for International Blood and Marrow Transplant Research (CIBMTR) were used to evaluate 511 adult patients with de novo AML who underwent HCT during 2008 through 2011 to determine whether FLT3 mutations had an impact on HCT outcomes.

resultsIn total, 158 patients (31%) had FLT3 mutations. Univariate and multivariate analyses revealed an increased risk of relapse at 3 years in the FLT3 mutated group compared with the wild-type (WT) group (38% [95% confidence interval (CI), 30%-45%] vs 28% [95% CI, 24%-33%]; P = .04; relative risk, 1.60 [95% CI, 1.15-2.22]; P = .0048). However, FLT3 mutation status was not significantly associated with nonrelapse mortality, leukemia-free survival, or overall survival. Although more patients in the FLT3 mutated group died from relapsed primary disease compared with those in the WT group (60% vs 46%), the 3-year overall survival rate was comparable for the 2 groups (mutated group: 49%; 95% CI, 40%-57%; WT group: 55%, 95% CI, 50%-60%; P = .20).

conclusionsThe current data indicate that FLT3 mutation status did not adversely impact overall survival after HCT, and about 50% of patients with this mutation who underwent HCT were long-term survivors. Cancer 2016;122:3005-3014. © 2016 American Cancer Society.

Indexed as

SurvivorsAdolescentAdultAllograftsFemalefms-Like Tyrosine Kinase 3Follow-Up StudiesHematopoietic Stem Cell TransplantationHumansLeukemia, Myeloid, AcuteMaleMiddle AgedMutationNeoplasm StagingPrognosisSurvival RateFLT3 protein, humanfms-Like Tyrosine Kinase 31 moreacute myeloid leukemiaallogeneic stem cell transplantationFMS-like tyrosine kinase 3 (FLT3)

Identifiers

PMID27315441
PMCPMC5030151

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