Evidence map›Paper›PMID 26629153›Full record

ArticleInternational journal of clinical and experimental medicine2015

Not all anti-T lymphocyte globulin preparations are suitable for use in aplastic anemia: significantly inferior results with jurkat cell-reactive anti-T lymphocyte globulin in clinical practice.

Eliacik Eylem, Buyukasik Yahya, Bektas Ozlen, Malkan Umit, Gunes Gursel, Isik Ayse, Demiroglu Haluk, Aksu Salih, Goker Hakan, Sayinalp Nilgun and 2 more

Abstract read
In one paragraph

Article in International journal of clinical and experimental medicine, 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
0.4field-weighted citation impact, top 32% 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, 6 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

12 authors at 1 institution in 1 country.

Eliacik EylemDepartment of Internal Medicine, Hacettepe University Medical School, Division of Hematology Ankara, Turkey.
Buyukasik YahyaDepartment of Internal Medicine, Hacettepe University Medical School, Division of Hematology Ankara, Turkey.
Bektas OzlenDepartment of Internal Medicine, Hacettepe University Medical School, Division of Hematology Ankara, Turkey.
Malkan UmitDepartment of Internal Medicine, Hacettepe University Medical School, Division of Hematology Ankara, Turkey.
Gunes GurselDepartment of Internal Medicine, Hacettepe University Medical School, Division of Hematology Ankara, Turkey.
Isik AyseDepartment of Internal Medicine, Hacettepe University Medical School, Division of Hematology Ankara, Turkey.
Demiroglu HalukDepartment of Internal Medicine, Hacettepe University Medical School, Division of Hematology Ankara, Turkey.
Aksu SalihDepartment of Internal Medicine, Hacettepe University Medical School, Division of Hematology Ankara, Turkey.
Goker HakanDepartment of Internal Medicine, Hacettepe University Medical School, Division of Hematology Ankara, Turkey.
Sayinalp NilgunDepartment of Internal Medicine, Hacettepe University Medical School, Division of Hematology Ankara, Turkey.
Haznedaroğlu IbrahimDepartment of Internal Medicine, Hacettepe University Medical School, Division of Hematology Ankara, Turkey.
Ozcebe OsmanDepartment of Internal Medicine, Hacettepe University Medical School, Division of Hematology Ankara, Turkey.
Hacettepe University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundImmunosuppressive therapy (IST) with anti-T lymphocyte globulin (ATG) plus cyclosporine (CSA) is standard therapy in patients with non-severe aplastic anemia (AA) in need of treatment and severe aplastic anemia (SAA) who do not have an available HLA-matched donor. The aim of this study was to analyze patients submitted to different ATG preparations as first-line treatment. PATIENTS AND

methodsWe retrospectively analyzed adult aplastic anemia (AA) patients who received ATG as first-line treatment between 1999 and 2013 to compare hematologic response and survival.

resultsDuring the time period mentioned 4 different ATG preparations had been used in 38 AA patients (34 severe, 4 non-severe). Responses were better with Lymphoglobulin (6 complete response 1 partial response, 0 refractory disease and 2 death within 3 months after ATG, i.e. during induction), Thymoglobulin (3, 1, 4 and 1, respectively) or ATGAM (1, 2, 1 and 1) compared to the ATG-Fresenius (ATG-F) group (3, 0, 6 and 6) (P = .07). Statistically significant inferior results with ATG-Fresenius (3 complete or partial responses, 6 refractoriness and 6 induction deaths) were evident when other preparations are lumped together (14 complete or partial responses, 5 refractoriness and 4 induction mortalities) (P = .045). Estimated 1 year survival rates were 52.5% versus 76.9%, respectively (P = .13).

conclusionsThese data support the notion that not all ATG preparations are suitable for use in AA.

Indexed as

anti-T lymphocyte globulinAplastic anemiaimmunosuppressive treatment

Identifiers

PMID26629153
PMCPMC4659041
OpenAlexW2413395092

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.