Evidence map›Paper›PMID 25580823›Full record

ArticleAmerican journal of hematology2015

Pediatric aplastic anemia and refractory cytopenia: A retrospective analysis assessing outcomes and histomorphologic predictors.

Craig M Forester, Sarah E Sartain, Dongjing Guo, Marian H Harris, Olga K Weinberg, Mark D Fleming, Wendy B London, David A Williams, Inga Hofmann

Open access · hybridAbstract read
In one paragraph

Article in American journal of hematology, 2015. 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
3.2field-weighted citation impact, top 8% 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, 28 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

9 authors at 4 institutions in 1 country.

Craig M ForesterDepartment of Pediatrics, Boston Children's Hospital, Boston, Massachusetts.
Sarah E Sartain
Dongjing Guo
Marian H Harris
Olga K Weinberg
Mark D Fleming
Wendy B London
David A Williams
Inga Hofmann
Boston Children's Museum · USHarvard University · USBoston Children's Hospital · USDana-Farber Cancer Institute · US

Funding

Research Training in Childhood CancerT32CA128583 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Eric Alejandro Sweet-Cordero · 2007 to 2026
$6.0M
The role of Hedgehog in hematopoiesis and leukemogenesisK08CA140723 · NCI · BOSTON CHILDREN'S HOSPITAL · PI HOFMANN ZHANG, INGA · 2010 to 2014
$684k
Molecular Genetic Investigation of Pediatric Myelodysplastic SyndromeR24DK094746 · NIDDK · BOSTON CHILDREN'S HOSPITAL · PI EBERT, BENJAMIN LEVINE, FLEMING, MARK D · 2012 to 2012
$539k
NCI NIH HHS 1K08CA140723NCI NIH HHS K08 CA140723NCI NIH HHS T32 CA128583NIDDK NIH HHS 1R24 DK 094746-01NIDDK NIH HHS R24 DK094746
6 · The paper itself

Abstract

Pediatric acquired aplastic anemia (AA) is a bone marrow disorder that is difficult to distinguish from inherited bone marrow failure syndromes and hypocellular refractory cytopenia of childhood (RCC). Historically, patients with hypocellular RCC have been given the diagnosis of AA. To assess the clinical and histologic distinction between RCC and AA, we performed a retrospective analysis of 149 patients previously diagnosed with AA between 1976 and 2010. We evaluated event free survival (EFS), overall survival (OS), response rates to immunosuppressive therapy, treatment-related toxicities and clonal evolution. The 5-year EFS and OS were 50.8% ± 5.5% and 73.1% ± 4.7%, respectively. Patients with very severe AA had worse OS compared to patients with severe and moderately severe AA. Seventy-two patients had diagnostic pathology specimens available for review. Three pediatric hematopathologists reviewed and reclassified these specimens as AA, RCC or Other based on 2008 WHO Criteria. The concordance between pathologists in the diagnosis of AA or RCC was modest. RCC was associated with a trend toward improved OS and EFS and was not prognostic of immunosuppression therapy treatment failure. There was a low rate of clonal evolution exclusively associated with moderately severe AA. Our findings indicate that a diagnosis of RCC is difficult to establish with certainty and does not predict outcomes, calling into question the reproducibility and clinical significance of the RCC classification and warranting further studies.

Indexed as

Anemia, AplasticBone MarrowChildClonal EvolutionDiagnosis, DifferentialFemaleHumansImmunosuppressive AgentsMaleMedical RecordsMyelodysplastic SyndromesPredictive Value of TestsRetrospective StudiesSurvival AnalysisTreatment OutcomeImmunosuppressive Agents

Identifiers

PMID25580823
PMCPMC4384448
OpenAlexW1568156520

What OpenQuestion holds

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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.