Evidence map›Paper›PMID 28699225›Full record

Trial reportAmerican journal of hematology2017

Intensive consolidation with G-CSF support: Tolerability, safety, reduced hospitalization, and efficacy in acute myeloid leukemia patients ≥60 years.

Wolfgang R Sperr, Susanne Herndlhofer, Karoline Gleixner, Michael Girschikofsky, Ansgar Weltermann, Sigrid Machherndl-Spandl, Thamer Sliwa, Rainer Poehnl, Veronika Buxhofer-Ausch, Karin Strecker and 6 more

Open access · bronzeAbstract readClinical Trial, Phase IVMulticenter Study
In one paragraph

Trial report in American journal of hematology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 27% 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

4 citing papers in PubMed, 10 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
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

16 authors at 6 institutions in 1 country.

Wolfgang R SperrDepartment of Internal Medicine I, Division of Hematology and Hemostaseology, Medical University of Vienna, Wien, Austria.ORCID http://orcid.org/0000-0003-3288-8027
Susanne HerndlhoferDepartment of Internal Medicine I, Division of Hematology and Hemostaseology, Medical University of Vienna, Wien, Austria.
Karoline GleixnerDepartment of Internal Medicine I, Division of Hematology and Hemostaseology, Medical University of Vienna, Wien, Austria.
Michael Girschikofsky1st Medical Department, Hospital of the Elisabethinen Linz, Linz, Austria.
Ansgar Weltermann1st Medical Department, Hospital of the Elisabethinen Linz, Linz, Austria.
Sigrid Machherndl-Spandl1st Medical Department, Hospital of the Elisabethinen Linz, Linz, Austria.
Thamer Sliwa5th Medical Department, Krankenhaus Hietzing, Wien, Austria.
Rainer Poehnl3rd Medical Department, Kaiser-Franz-Josef-Spital, Wien, Austria.
Veronika Buxhofer-Ausch1st Medical Department, Hospital of the Elisabethinen Linz, Linz, Austria.
Karin Strecker2nd Medical Department, Donauspital, Wien, Austria.
Gregor HoermannDepartment of Laboratory Medicine, Medical University of Vienna, Wien, Austria.
Paul KnoeblDepartment of Internal Medicine I, Division of Hematology and Hemostaseology, Medical University of Vienna, Wien, Austria.
Ulrich JaegerDepartment of Internal Medicine I, Division of Hematology and Hemostaseology, Medical University of Vienna, Wien, Austria.
Klaus Geissler5th Medical Department, Krankenhaus Hietzing, Wien, Austria.
Michael KundiInstitute of Environmental Health, Medical University of Vienna, Wien, Austria.
Peter ValentDepartment of Internal Medicine I, Division of Hematology and Hemostaseology, Medical University of Vienna, Wien, Austria.
Medical University of Vienna · ATKrankenhaus der Elisabethinen · ATDonauspital · ATKlinik Hietzing · ATLudwig Boltzmann Institute for Cardiovascular Research · ATKaiser-Franz-Josef-Spital · AT

Funding

Austrian Science Fund FWF F 4704
6 · The paper itself

Abstract

The aim of this study was to evaluate the efficacy and feasibility of intensified consolidation therapy employing fludarabine and ARA-C in cycle 1 and intermediate-dose ARA-C (IDAC) in cycles 2 through 4, in elderly acute myeloid leukemia (AML) patients and to analyze the effects of pegfilgrastim on the duration of neutropenia, overall toxicity, and hospitalization-time during consolidation in these patients. Thirty nine elderly patients with de novo AML (median age 69.9 years) who achieved complete remission (CR) after induction-chemotherapy were analyzed. To examine the effect of pegfilgrastim on neutropenia and hospitalization, we compared cycles 2 and 4 where pegfilgrastim was given routinely from day 6 (IDAC-P) with cycle 3 where pegfilgrastim was only administered in case of severe infections and/or prolonged neutropenia. All four planned cycles were administered in 23/39 patients (59.0%); 5/39 patients (12.8%) received 3 cycles, 3/39 (7.7%) 2 cycles, and 8/39 (20.5%) one consolidation-cycle. The median duration of severe neutropenia was 7 days in cycle 2 (IDAC-P), 11.5 days in cycle 3 (IDAC), and 7.5 days in cycle 4 (IDAC-P) (P < .05). Median overall survival was 1.1 years and differed significantly between patients aged <75 and ≥75 years (P < .05). The probability to be alive after 5 years was 32%. Together, intensified consolidation can be administered in AML patients ≥60, and those who are <75 may benefit from this therapy. Routine administration of pegfilgrastim during consolidation shortens the time of neutropenia and hospitalization in these patients.

Indexed as

AgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsConsolidation ChemotherapyCytarabineDisease-Free SurvivalDrug Administration ScheduleFeasibility StudiesFilgrastimGranulocyte Colony-Stimulating FactorHospitalizationHumansLeukemia, Myeloid, AcuteMiddle AgedNeutropeniaPolyethylene GlycolsCytarabineFilgrastimfludarabineGranulocyte Colony-Stimulating FactorpegfilgrastimPolyethylene GlycolsRecombinant ProteinsVidarabine

Identifiers

PMID28699225
PMCPMC7115890
OpenAlexW2734477894

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.