Evidence map›Paper›PMID 25369606›Full record

Trial reportBlood transfusion = Trasfusione del sangue2015

Angiopoietins in haematopoietic stem cell mobilisation in patients with haematological malignancies.

Anna Szmigielska-Kaplon, Anna Krawczynska, Magdalena Czemerska, Agnieszka Pluta, Barbara Cebula-Obrzut, Katarzyna Szmigielska, Konrad Stępka, Piotr Smolewski, Tadeusz Robak, Agnieszka Wierzbowska

Abstract readClinical Trial
In one paragraph

Trial report in Blood transfusion = Trasfusione del sangue, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
4.6field-weighted citation impact, top 7% 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

2 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. 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

10 authors at 1 institution in 1 country.

Anna Szmigielska-KaplonDepartment of Haematology, Medical University of Lodz, Lodz, Poland.
Anna KrawczynskaDepartment of Haematology, Medical University of Lodz, Lodz, Poland.
Magdalena CzemerskaDepartment of Haematology, Medical University of Lodz, Lodz, Poland.
Agnieszka PlutaDepartment of Haematology, Medical University of Lodz, Lodz, Poland.
Barbara Cebula-ObrzutDepartment of Experimental Haematology, Medical University of Lodz, Lodz, Poland.
Katarzyna SzmigielskaDepartment of Sports Medicine, Medical University of Lodz, Lodz, Poland.
Konrad StępkaDepartment of Haematology, Medical University of Lodz, Lodz, Poland.
Piotr SmolewskiDepartment of Experimental Haematology, Medical University of Lodz, Lodz, Poland.
Tadeusz RobakDepartment of Haematology, Medical University of Lodz, Lodz, Poland.
Agnieszka WierzbowskaDepartment of Haematology, Medical University of Lodz, Lodz, Poland.
Medical University of Lodz · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe bone marrow niche contains different types of cells including osteoblasts and endothelial progenitors, all of which interact and take part in the process of mobilisation. The aim of our study was to evaluate the levels of cytokines (osteopontin and angiopoietins 1 and 2) active in the bone marrow niche during the mobilisation of haematopoietic stem cells for autologous transplantation. MATERIALS AND

methodsForty-eight patients (24 females, 24 males), median age 56.5 years, entered the study. The group consisted of patients with multiple myeloma (n=34), lymphoma (n=13) and acute myeloid leukaemia (n=1). Blood samples were collected before chemotherapy and on the day of the first apheresis. Cytokines were evaluated by enzyme-linked immunosorbent assays. Additionally, circulating endothelial cells were assessed by flow cytometry.

resultsThe median concentration of angiopoietin 1 at the time of apheresis was lower than that at baseline (2.7 vs 7.8 ng/mL, p<0.001). In contrast, the median level of angiopoietin 2 increased during the mobilisation procedure (3.6 vs 2.8 ng/mL, p=0.001). The patients were divided according to the number of days of granulocyte colony-stimulating factor treatment before the first apheresis into "early" (<median=11 days) and "late" (>median) mobilisers. The group of "early mobilisers" had higher baseline angiopoietin 1 levels (median=11.6 ng/mL) than those of the "late mobilisers" (median=6.0 ng/mL, p=0.05). An adverse correlation was observed between duration of granulocyte colony-stimulating factor treatment and baseline angiopoietin 1 level. Baseline angiopoietin 1 levels correlated with numbers of circulating endothelial cells. Low angiopoietin 2 level increased the chance of poor mobilisation.

conclusionsThe angiogenic processes can influence the timing of mobilisation. Angiopoietins 1 and 2 need further evaluation in the context of mobilisation.

Indexed as

Hematopoietic Stem Cell MobilizationAdultAgedAngiopoietin-1Angiopoietin-2AutograftsFemaleHematologic NeoplasmsHematopoietic Stem Cell TransplantationHumansMaleMiddle AgedOsteopontinAngiopoietin-1Angiopoietin-2ANGPT1 protein, humanANGPT2 protein, humanOsteopontin

Identifiers

PMID25369606
PMCPMC4317096
OpenAlexW32184212

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.