Evidence map›Paper›PMID 25983043›Full record

Trial reportBiology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation2015

Impact of Pretransplantation (18)F-fluorodeoxy Glucose-Positron Emission Tomography Status on Outcomes after Allogeneic Hematopoietic Cell Transplantation for Non-Hodgkin Lymphoma.

Veronika Bachanova, Linda J Burns, Kwang Woo Ahn, Ginna G Laport, Görgün Akpek, Mohamed A Kharfan-Dabaja, Taiga Nishihori, Edward Agura, Philippe Armand, Samantha M Jaglowski and 29 more

Open access · hybridAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
4.9field-weighted citation impact, top 5% 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

19 citing papers in PubMed, 39 citations in OpenAlex.

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  14. Emerging Diagnostic and Therapeutic Strategies for Tauopathies.Current neurology and neuroscience reports · 2017
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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

39 authors at 20 institutions in 7 countries.

Veronika BachanovaBlood and Marrow Transplant Program, University of Minnesota Medical Center, Minneapolis, Minnesota. Electronic address: bach0173@umn.edu.
Linda J BurnsHealth Services Research, National Marrow Donor Program/Be The Match, Minneapolis, Minnesota.
Kwang Woo AhnCenter for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin; Division of Biostatistics, Institute for Health and Society, Medical College of Wisconsin, Milwaukee, Wisconsin.
Ginna G LaportDivision of Bone Marrow Transplant, Stanford Hospital and Clinics, Stanford, California.
Görgün AkpekStem Cell Transplantation and Cellular Therapy Program, Banner MD Anderson Cancer Center, Gilbert, Arizona.
Mohamed A Kharfan-DabajaDepartment of Blood and Marrow Transplantation, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.
Taiga NishihoriDepartment of Blood and Marrow Transplantation, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.
Edward AguraBlood and Marrow Transplant Services, Baylor University Medical Center, Dallas, Texas.
Philippe ArmandDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Samantha M JaglowskiDivision of Hematology, The Ohio State University Medical Center, Columbus, Ohio.
Mitchell S CairoDepartment of Pediatrics, New York Medical College, Valhalla, New York.
Amanda F CashenDepartment of BMT/Oncology, Barnes Jewish Hospital, St. Louis, Missouri.
Jonathon B CohenDepartment of Hematology and Medical Oncology, Winship Cancer Institute, Emory University School of Medicine, Atlanta, Georgia.
Anita D'SouzaCenter for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.
César O FreytesSouth Texas Veterans Health Care System and University of Texas Health Science Center San Antonio, San Antonio, Texas.
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, Kansas.
Nilanjan GhoshDepartment of Hematologic Oncology and Blood Disorders, Levine Cancer Institute, Carolinas Healthcare System, Charlotte, North Carolina.
Leona A HolmbergClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
David J InwardsDivision of Hematology, Mayo Clinic, Rochester, Minnesota.
Abraham S KanateOsborn Hematopoietic Malignancy and Transplantation Program, West Virginia University, Morgantown, West Virginia.
Hillard M LazarusSeidman Cancer Center, University Hospitals Case Medical Center, Cleveland, Ohio.
Adriana K MaloneTisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, New York.
Reinhold MunkerSection of Hematology/Oncology, Department of Internal Medicine, Louisiana State University Health Shreveport, Shreveport, Louisiana.
Alberto MussettiS.C. Ematologia e Trapianto Midollo Osseo, Fondazione IRCCS Instituto Nazionale dei Tumori, Milan, Italy; Università degli Studi di Milano, Milan, Italy.
Maxim NorkinDivision of Hematology/Oncology, University Florida College of Medicine, Gainesville, Florida.
Tim D PrestidgeBlood and Cancer Centre, Starship Children's Hospital, Auckland, New Zealand.
Jacob M RoweDepartment of Hematology, Shaare Zedek Medical Center, Jerusalem, Israel.
Prakash SatwaniDivision of Pediatric Hematology, Oncology, and Stem Cell Transplantation, Department of Pediatrics, Columbia University Medical Center, New York, New York.
Tanya SiddiqiDepartment of Hematology Oncology, City of Hope National Medical Center, Duarte, California.
Patrick J StiffDepartment of Hematology/Oncology, Loyola University Medical Center, Chicago, Illinois.
Basem M WilliamSeidman Cancer Center, University Hospitals Case Medical Center, Cleveland, Ohio.
Baldeep WirkDivision of Bone Marrow Transplant, Seattle Cancer Care Alliance, Seattle, Washington.
David G MaloneyClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Sonali M SmithSection of Hematology/Oncology, The University of Chicago, Chicago, Illinois.
Anna M SuredaServei d'Hematologia, Institut Català d'Oncologia, Hospital Duran i Reynals, Barcelona, Spain; Secretary, European Group for Blood and Marrow Transplantation.
Jeanette CarrerasCenter for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.
Mehdi HamadaniCenter for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.
Center for International Blood and Marrow Transplant Research Lymphoma Working Committee
Medical College of Wisconsin · USFred Hutch Cancer Center · USMoffitt Cancer Center · USBarnes-Jewish Hospital · USBaylor University Medical Center · USCarolinas Healthcare System · USCity Of Hope National Medical Center · USColumbia University Irving Medical Center · USDana-Farber Cancer Institute · USEmory University · USFlorida College · USIcahn School of Medicine at Mount Sinai · USImperial College London · GBInstitut Català d'Oncologia · ESLouisiana State University · USLoyola University Medical Center · USMayo Clinic · USNational Marrow Donor Program · USNew York Medical College · USSeattle Cancer Care Alliance · 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
Transgenic Mouse FacilityP30CA033572 · NCI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI STANLEY R. HAMILTON · 1985 to 2026
$86.3M
PB vs. BMU01HL069294 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI HOROWITZ, MARY MARESCA · 2001 to 2010
$63.3M
Easy-to-read Informed Consent for HCT Clinical TrialsU10HL069294 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI HOROWITZ, MARY MARESCA · 2011 to 2016
$43.8M
University of Minnesota Clinical and Translational Science Institute (UMN CTSI)UL1TR000114 · NCATS · UNIVERSITY OF MINNESOTA · PI BLAZAR, BRUCE R · 2012 to 2015
$35.0M
University of Minnesota Clinical and Translational Science Institute (UMN CTSI)KL2TR000113 · NCATS · UNIVERSITY OF MINNESOTA · PI BLAZAR, BRUCE R · 2012 to 2015
$5.4M
NCATS NIH HHS KL2 TR000113NCATS NIH HHS UL1 TR000114NCI NIH HHS P30 CA033572NCI NIH HHS U24 CA076518NCI NIH HHS U24-CA076518NHLBI NIH HHS 5U10HL069294NHLBI NIH HHS U01 HL069294NHLBI NIH HHS U10 HL069294PHS HHS HHSH250201200016C
6 · The paper itself

Abstract

Assessment with (18)F-fluorodeoxy glucose (FDG)-positron emission tomography (PET) before hematopoietic cell transplantation (HCT) for lymphoma may be prognostic for outcomes. Patients with chemotherapy-sensitive non-Hodgkin lymphoma (NHL) undergoing allogeneic HCT reported to the Center of International Blood and Marrow Transplantation Registry between 2007 and 2012 were included. Pre-HCT PET status (positive versus negative) was determined by the reporting transplantation centers. We analyzed 336 patients; median age was 55 years and 60% were males. Follicular lymphoma (n = 104) was more common than large cell (n = 85), mantle cell (n = 69), and mature natural killer or T cell lymphoma (n = 78); two thirds of the cohort received reduced-intensity conditioning; one half had unrelated donor grafts. Patients underwent PET scanning a median of 1 month (range, .07 to 2.83 months) before HCT; 159 were PET positive and 177 were PET negative. At 3 years, relapse/progression, progression-free survival (PFS), and overall survival (OS) in PET-positive versus PET-negative groups were 40% versus 26%; P = .007; 43% versus 47%; P = .47; and 58% versus 60%; P = .73, respectively. On multivariate analysis, a positive pretransplantation PET was associated with an increased risk of relapse/progression (risk ratio [RR], 1.86; P = .001) but was not associated with increased mortality (RR, 1.29, 95% confidence interval [CI], .96 to 1.7; P = .08), therapy failure (RR, 1.32; 95% CI, .95 to 1.84; P = .10), or nonrelapse mortality (RR, .75; 95% CI, .48 to 1.18; P = .22). PET status conferred no influence on graft-versus-host disease. A positive PET scan before HCT is associated with increased relapse risk but should not be interpreted as a barrier to a successful allograft. PET status does not appear to predict survival after allogeneic HCT for NHL.

Indexed as

Hematopoietic Stem Cell TransplantationPositron-Emission TomographyAdolescentAdultAgedAllograftsDisease-Free SurvivalFemaleFluorodeoxyglucose F18HumansLymphoma, Non-HodgkinMaleMiddle AgedRadiographySurvival RateFluorodeoxyglucose F18Allogeneic transplantationNon-Hodgkin lymphomaPositron emission tomography

Identifiers

PMID25983043
PMCPMC4558181
OpenAlexW1503923315

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Registered trials

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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.