Evidence map›Paper›PMID 26626557›Full record

ReviewCurrent opinion in pediatrics2016

Evolving hematopoietic stem cell transplantation strategies in severe aplastic anemia.

Andrew C Dietz, Giovanna Lucchini, Sujith Samarasinghe, Michael A Pulsipher

Abstract readReview
In one paragraph

Review in Current opinion in pediatrics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.7field-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

9 citing papers in PubMed, 18 citations in OpenAlex.

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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

4 authors at 3 institutions in 2 countries.

Andrew C DietzaChildren's Hospital Los Angeles, University of Southern California Keck School of Medicine, Los Angeles, California, USA bDepartment of Paediatric Bone Marrow Transplant cDepartment of Paediatric Haematology, Great Ormond Street Hospital, London, UK *Andrew C. Dietz and Giovanna Lucchini contributed equally to the writing of this article.
Giovanna Lucchini
Sujith Samarasinghe
Michael A Pulsipher
Children's Hospital of Los Angeles · USUniversity College London · GBUniversity of Southern California · US

Funding

RDSafe: A Multi-Institutional Study of HSC Donor Safety and Quality LifeR01HL085707 · NHLBI · UNIVERSITY OF UTAH · PI PULSIPHER, MICHAEL A, SWITZER, GALEN E. · 2009 to 2013
$3.1M
Pediatric Blood and Marrow Transplant ConsortiumU01HL069254 · NHLBI · NATIONAL CHILDHOOD CANCER FOUNDATION · PI PULSIPHER, MICHAEL A · 2001 to 2010
$2.0M
Late Effects after Pediatric HSCT: State of the Science, Future DirectionsR13CA159788 · NCI · NATIONAL CHILDHOOD CANCER FOUNDATION · PI BAKER, KEVIN S, PULSIPHER, MICHAEL A · 2011 to 2011
$13k
PBMTC-ASPHO 2014: NEW FRONTIERS IN PEDIATRIC STEM CELL TRANSPLANTATIONR13HL127918 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI NEMECEK, ENEIDA R, PULSIPHER, MICHAEL A · 2015 to 2015
$5k
NCI NIH HHS R13 CA159788NHLBI NIH HHS 2U01HL069254NHLBI NIH HHS R01 HL085707NHLBI NIH HHS R13 HL127918NHLBI NIH HHS U01 HL069254
6 · The paper itself

Abstract

purpose of reviewSignificant improvements in unrelated donor hematopoietic stem cell transplantation (HSCT) in recent years have solidified its therapeutic role in severe aplastic anemia (SAA) and led to the evolution of treatment algorithms, particularly for children. RECENT

findingsAdvances in understanding the genetics of inherited bone marrow failure syndromes (IBMFS) have allowed more confidence in accurately diagnosing SAA and avoiding treatments that could be dangerous and ineffective in individuals with IBMFS, which can be diagnosed in 10-20% of children presenting with a picture of SAA. Additionally long-term survival after matched sibling donor and matched unrelated donor HSCT now exceed 90% in children. Late effects after HSCT for SAA are minimal with current strategies, and compare favorably to late effects after upfront immunosuppressive therapy, except for patients with chronic graft versus host disease. SUMMARY: Careful assessment for signs or symptoms of IBMFS, along with genetic screening for these disorders, is of major importance. Matched sibling donor HSCT is already considered the standard of care for upfront therapy and some groups are evaluating matched unrelated donor HSCT as primary therapy. Ongoing studies will continue to challenge treatment algorithms and may lead to an even more expanded role for HSCT in SAA.

Indexed as

AlgorithmsAnemia, AplasticHematopoietic Stem Cell TransplantationHistocompatibilityHumansTissue DonorsTransplantation Conditioning

Identifiers

PMID26626557
PMCPMC4725196
OpenAlexW2415467107

What OpenQuestion holds

Textmetadata
LicenceTDM
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.