Evidence map›Paper›PMID 26501769›Full record

ArticleBone marrow transplantation2016

Influence of pre-existing invasive aspergillosis on allo-HSCT outcome: a retrospective EBMT analysis by the Infectious Diseases and Acute Leukemia Working Parties.

O Penack, G Tridello, J Hoek, G Socié, D Blaise, J Passweg, P Chevallier, C Craddock, N Milpied, H Veelken and 10 more

Open access · bronzeAbstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Bone marrow transplantation, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

8 citing papers in PubMed, 27 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Review
  6. JMM case reports · 2018
    Article
  7. Article
  8. Invasive aspergillosis before HCT: safe to proceed?Bone marrow transplantation · 2016
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 17 institutions in 9 countries.

O PenackDepartment of Hematology, Oncology and Tumorimmunology, Charité University Medicine Berlin, Campus Virchow Klinikum, Allogeneic Stem Cell Transplantation Service, Berlin, Germany.
G TridelloDepartment of Paediatric Hematology and Oncology, Policlinico GB Rossi, Verona, Italy.
J HoekEBMT Data Office, Leiden, The Netherlands.
G SociéService d'Hématologie Greffe, Hopital St Louis, Paris, France.
D BlaiseUnité de Transplantation et de Thérapie Cellulaire, Institut Paoli Calmettes, Marseille, France.
J PasswegDepartment of Hematology, University Hospital, Basel, Switzerland.
P ChevallierDepartment of Hematology, CHU Nantes, Nantes, France.
C CraddockBMT Unit, Queen Elizabeth Hospital, Birmingham, UK.
N MilpiedHématologie Clinique et thérapie cellulaire, CHU Bordeaux, Pessac, France.
H VeelkenDepartment of Hematology, Leiden University Hospital, Leiden, The Netherlands.
J MaertensDepartment of Hematology, University Hospital Gasthuisberg, Leuven, Belgium.
P LjungmanDepartment of Hematology, Karolinska University Hospital, Stockholm, Sweden.ORCID http://orcid.org/0000-0002-8281-3245
J CornelissenDepartment of Hematology, Erasmus MC-Daniel den Hoed Cancer Centre, Rotterdam, The Netherlands.
A Thiebaut-BertrandClinique d'hématologie, Hopital A Michallon, Grenoble, France.
B LioureDepartment of Onco-Hematology, Nouvel Hopital Civil, Strasbourg, France.
M MichalletDepartment of Hematology, Centre Hospitalier Lyon Sud, Lyon, France.
S IacobelliCentro Interdipartimentale di Biostatistica e Bioinformatica, Università Tor Vergata, Rome, Italy.
A NaglerDivision of Hematology and Bone Marrow Transplantation, Chaim Sheba Medical Center, Tel Aviv University, Tel-Hashomer, Israel.
M MohtyService d'Hématologie Clinique et de Thérapie Cellulaire, Hospital Saint Antoine, Paris, France.
S CesaroDepartment of Paediatric Hematology and Oncology, Policlinico GB Rossi, Verona, Italy.
Charité - Universitätsmedizin Berlin · DEErasmus MC Cancer Institute · NLEuropean Society for Blood and Marrow Transplantation · NLHôpital Albert Michallon · FRHôpital Civil, Strasbourg · FRHôpital Lyon Sud · FRHôpital Saint-Louis · FRInstitut Paoli-Calmettes · FRKarolinska University Hospital · SELaboratoire de Thermique et Energie de Nantes · FRLeiden University · NLQueen Elizabeth Hospital Birmingham · GBSorbonne Université · FRTel Aviv University · ILUniversitair Ziekenhuis Leuven · BEUniversity Hospital of Basel · CHUniversity of Rome Tor Vergata · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Historically, invasive aspergillosis (IA) has been a major barrier for allogeneic hematopoietic stem cell transplantation (allo-HSCT). The influence of invasive IA on long-term survival and on transplant-related complications has not been investigated in a larger patient cohort under current conditions. Our aim was to analyze the long-term outcome of patients undergoing allo-HSCT with a history of prior IA. We used European Society for Blood and Marrow Transplantation database data of first allo-HSCTs performed between 2005 and 2010 in patients with acute leukemia. One thousand one hundred and fifty patients with data on IA before allo-HSCT were included in the analysis. The median follow-up time was 52.1 months. We found no significant impact of IA on major transplant outcome variables such as overall survival, relapse-free survival, non-relapse mortality, cumulative incidence of acute GvHD grade II-IV, chronic GvHD, pulmonary complications and leukemia relapse. However, we found a trend toward lower overall survival (P=0.078, hazard ratio (HR) (95% confidence interval (CI)): 1.16 (0.98, 1.36)) and higher non-relapse mortality (P=0.150, HR (95% CI): 1.19 (0.94, 1.50)) in allo-HSCT recipients with pre-existing IA. Our data suggest that a history of IA should not generally be a contraindication when considering the performance of allo-HSCT in patients with acute leukemia.

Indexed as

AspergillosisHematopoietic Stem Cell TransplantationLeukemiaAcute DiseaseAdolescentAdultAgedAllograftsChildChild, PreschoolChronic DiseaseDisease-Free SurvivalFemaleGraft vs Host DiseaseHumansInfant

Identifiers

PMID26501769
OpenAlexW1862348505

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.