Evidence map›Paper›PMID 28849374›Full record

ArticleInternational journal of hematology2017

Toxicological effects of fludarabine and treosulfan conditioning before allogeneic stem-cell transplantation.

Mats Remberger, Johan Törlen, Ibrahim El Serafi, Karin Garming-Legert, Andreas Björklund, Per Ljungman, Mikael Sundin, Moustapha Hassan, Jonas Mattsson

Abstract read
PubMed Publisher
In one paragraph

Article in International journal of hematology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-weighted citation impact, top 24% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. In Vitro Study of the Enzymatic and Nonenzymatic Conjugation of Treosulfan with Glutathione.European journal of drug metabolism and pharmacokinetics · 2019
    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

9 authors at 2 institutions in 1 country.

Mats RembergerCenter for Allogeneic Stem Cell Transplantation Unit, Karolinska University Hospital, SE-141 86, Stockholm, Sweden. mats.remberger@ki.se.ORCID http://orcid.org/0000-0003-0520-4312
Johan TörlenCenter for Allogeneic Stem Cell Transplantation Unit, Karolinska University Hospital, SE-141 86, Stockholm, Sweden.
Ibrahim El SerafiExperimental Cancer Medicine, Department of Laboratory Medicine, Karolinska Institutet, Stockholm, Sweden.
Karin Garming-LegertDivision of Oral and Maxillofacial Surgery, Department of Dental Medicine, Karolinska Institute, Huddinge, Stockholm, Sweden.
Andreas BjörklundDepartment of Hematology, Karolinska University Hospital, Stockholm, Sweden.
Per LjungmanCenter for Allogeneic Stem Cell Transplantation Unit, Karolinska University Hospital, SE-141 86, Stockholm, Sweden.
Mikael SundinBlood Disorders, Immunodeficiency and Stem Cell Transplantation, Astrid Lindgren Children's Hospital, Karolinska University Hospital, Stockholm, Sweden.
Moustapha HassanExperimental Cancer Medicine, Department of Laboratory Medicine, Karolinska Institutet, Stockholm, Sweden.
Jonas MattssonCenter for Allogeneic Stem Cell Transplantation Unit, Karolinska University Hospital, SE-141 86, Stockholm, Sweden.
Karolinska University Hospital · SEKarolinska Institutet · SE

Funding

Marianne and Marcus Wallenbergs Foundation 2013-0117Stockholm County Council 20140451Swedish childrens cancer foundation PR2013-0022Sweish cancer society CF2014-2016
6 · The paper itself

Abstract

We studied early potential treosulfan-related toxicity in 118 patients treated with treosulfan-based conditioning before allogeneic hematopoietic stem-cell transplantation. Most patients (n = 93) had a hematological malignancy. In 80 cases, a HLA-A, -B and -DR matched unrelated donor was used, while 33 patients had a HLA-identical sibling donor, and five received an HLA-A, -B or -DR allele mismatched, unrelated donor. Levels of AST, ALT, and bilirubin were significantly increased 1 week after HSCT compared to before HSCT. However, only a few patients had transaminase levels >2 to 3 × the upper normal level. All patients became neutropenic; 61% were already so at the time of graft infusion. Nearly all patients engrafted, except for three who died very early. Non-relapse mortality was 7.5% at 100 days and 11.9% at 1 year after HSCT. Veno-occlusive disease of the liver occurred in one patient and hemorrhagic cystitis in two patients. This study shows that early regimen-related toxicity after HSCT was low despite similar marrow toxicities compared to myeloablative regimens.

Indexed as

CystitisHematopoietic Stem Cell TransplantationHemorrhageVascular DiseasesAdolescentAdultAgedAllograftsBusulfanChildChild, PreschoolFemaleHumansInfantMaleMiddle AgedBusulfanfludarabinetreosulfanVidarabineConditioningHSCTToxicityTreosulfan

Identifiers

PMID28849374
OpenAlexW2746112460

What OpenQuestion holds

Textmetadata
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.