Evidence map›Paper›PMID 27607445›Full record

ReviewCurrent opinion in hematology2016

Hematopoietic stem cell transplantation for acquired aplastic anemia.

George E Georges, Rainer Storb

Abstract readReview
In one paragraph

Review in Current opinion in hematology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Insensitive to PTH of CD8International journal of medical sciences · 2020
    Article
  8. Article
  9. Article
  10. Article
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

2 authors.

George E GeorgesaClinical Research Division, Fred Hutchinson Cancer Research Center bDepartment of Medicine, University of Washington, Seattle, Washington, USA.
Rainer Storb

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Marian Esvelt · 1985 to 2026
$296.4M
Project 3: Gene Therapy for Correction of Blood DisordersP01HL122173 · NHLBI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI KIEM, HANS-PETER · 2015 to 2019
$12.9M
Improving Engraftment of Hematopoietic Stem Cell Gene TherapyR01HL125183 · NHLBI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI GEORGES, GEORGE EARL · 2015 to 2017
$2.4M
Improving Engraftment of Hematopoietic Stem Cell Gene TherapyR56HL125183 · NHLBI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI GEORGES, GEORGE EARL · 2014 to 2014
$837k
NCI NIH HHS P30 CA015704NHLBI NIH HHS P01 HL122173NHLBI NIH HHS R01 HL125183NHLBI NIH HHS R56 HL125183
6 · The paper itself

Abstract

purpose of reviewThere has been a steady improvement in outcomes with allogeneic bone marrow transplantation (BMT) for severe aplastic anemia (SAA), because of progress in optimization of the conditioning regimens, donor hematopoietic cell source, and supportive care. Here, we review recently published data that highlight the improvements and current issues in the treatment of SAA. RECENT

findingsApproximately one-third of aplastic anemia patients treated with immune suppressive therapy (IST) have acquired mutations in myeloid cancer candidate genes. Because of the greater probability for eventual failure of IST, human leukocyte antigen (HLA)-matched sibling donor BMT is the first-line of treatment for SAA. HLA-matched unrelated donor (URD) BMT is generally recommended for patients who have failed IST. However, in younger patients for whom a 10/10-HLA-allele matched URD can be rapidly identified, there is a strong rationale to proceed with URD BMT as first-line therapy. HLA-haploidentical BMT using posttransplant cyclophosphamide conditioning regimens is now a reasonable second-line treatment for patients who failed IST. SUMMARY: Improved outcomes have led to an increased first-line role of BMT for treatment of SAA. The optimal cell source from an HLA-matched donor is bone marrow. Additional studies are needed to determine the optimal conditioning regimen for HLA-haploidentical donors.

Indexed as

Hematopoietic Stem Cell TransplantationAnemia, AplasticBone Marrow TransplantationChromosome AberrationsGenetic Predisposition to DiseaseHematopoiesisHLA AntigensHumansImmunosuppressive AgentsMutationPeptidesSiblingsTissue DonorsTransplantation ConditioningTransplantation, HomologousTreatment OutcomeHLA AntigensImmunosuppressive AgentsPeptidesthrombopoietin mimetic peptide

Identifiers

PMID27607445
PMCPMC5125541

What OpenQuestion holds

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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.