Evidence map›Paper›PMID 28548643›Full record

Trial reportBlood cancer journal2017

Condensed versus standard schedule of high-dose cytarabine consolidation therapy with pegfilgrastim growth factor support in acute myeloid leukemia.

S Jaramillo, A Benner, J Krauter, H Martin, T Kindler, M Bentz, H R Salih, G Held, C-H Köhne, K Götze and 23 more

Open access · goldAbstract readComparative StudyMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Blood cancer journal, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

30 citing papers in PubMed, 57 citations in OpenAlex.

  1. Gemtuzumab Ozogamicin inJournal of clinical oncology : official journal of the American Society of Clinical Oncology · 2020
    Trial
  2. Trial
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  4. Trial
  5. Trial
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Real-world treatment outcomes from a retrospective cohort of patients with acute myeloid leukemia from an urban safety net hospital.Journal of oncology pharmacy practice : official publication of the International Society of Oncology Pharmacy Practitioners · 2025
    Article
  13. Efficacy of delayed pegfilgrastim administration following consolidation therapy with high-dose cytarabine (HiDAC) in acute myeloid leukemia (AML) patients.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2024
    Article
  14. Review
  15. AML consolidation therapy: timing matters.Journal of cancer research and clinical oncology · 2023
    Article
  16. Digital twins in oncology.Journal of cancer research and clinical oncology · 2023
    Article
  17. Article
  18. Article
  19. Review
  20. Outcomes of HIDAC 18 g Versus IDAC 9 g in Consolidation Therapy of Acute Myeloid Leukemia: A Retrospective Study.Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion · 2022
    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

33 authors at 20 institutions in 2 countries.

S JaramilloDepartment of Internal Medicine III, University Hospital of Ulm, Ulm, Germany.
A BennerDivision of Biostatistics, German Cancer Research Center, Heidelberg, Germany.
J KrauterDepartment of Oncology and Hematology, Klinikum Braunschweig, Braunschweig, Germany.
H MartinDepartment of Internal Medicine II, University Hospital, Frankfurt, Germany.
T KindlerDepartment of Medicine III, Johannes Gutenberg-University Mainz, Mainz, Germany.
M BentzDepartment of Internal Medicine III, Städtisches Klinikum Karlsruhe, Karlsruhe, Germany.
H R SalihDepartment of Hematology and Oncology, Eberhard-Karls University, Tübingen, Germany.
G HeldDepartment of Internal Medicine I, University Hospital of Saarland, Homburg, Germany.
C-H KöhneDepartment of Oncology and Hematology, Klinikum Oldenburg, Oldenburg, Germany.
K GötzeDepartment of Internal Medicine III, Technical University of Munich, Munich, Germany.
M LübbertDepartment of Hematology and Oncology, University Hospital of Freiburg, Freiburg, Germany.
A KündgenDepartment of Hematology, Oncology and Clinical Immunology, Heinrich-Heine-University, Düsseldorf, Germany.
P BrossartDepartment of Internal Medicine III, University Hospital of Bonn, Bonn, Germany.
M WattadDepartment of Hematology, Oncology and Stem Cell Transplantation, Klinikum Essen Süd, Essen, Germany.
H SalwenderDepartment of Hematology and Oncology, Asklepios Klinik Altona, Hamburg, Germany.
B HertensteinDepartment of Internal Medicine I, Klinikum Bremen Mitte, Bremen, Germany.
D NachbaurDepartment of Internal Medicine V, University Hospital Innsbruck, Innsbruck, Austria.
G WulfDepartment of Hematology and Oncology, University Hospital of Göttingen, Göttingen, Germany.
H-A HorstDepartment of Internal Medicine II, University Hospital Schleswig-Holstein, Kiel, Germany.
H KirchenDepartment of Internal Medicine I, Krankenhaus der Barmherzigen Brüder, Trier, Germany.
W FiedlerDepartment of Internal Medicine II, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
A RaghavacharDepartment of Internal Medicine I, Helios Universitätsklinikum Wuppertal, Wuppertal, Germany.
G RussDepartment of Internal Medicine III, University of Salzburg, Salzburg, Austria.
S KremersDepartment of Hematology/Oncology, Caritas Krankenhaus Lebach, Lebach, Germany.
E KollerDepartment of Internal Medicine III, Hanuschkrankenhaus, Wien, Austria.
V RundeDepartment of Hematology/Oncology, Wilhelm-Anton Hospital Goch, Goch, Germany.
G HeilDepartment of Internal Medicine V, Klinikum Lüdenscheid, Lüdenscheid, Germany.
D WeberDepartment of Internal Medicine III, University Hospital of Ulm, Ulm, Germany.
G GöhringInstitute of Human Genetics, Hannover Medical School, Hannover Germany.
K DöhnerDepartment of Internal Medicine III, University Hospital of Ulm, Ulm, Germany.
A GanserDepartment of Hematology, Hemostasis, Oncology and Stem Cell Transplantation, Hannover Medical School, Hannover, Germany.
H DöhnerDepartment of Internal Medicine III, University Hospital of Ulm, Ulm, Germany.
R F SchlenkDepartment of Internal Medicine III, University Hospital of Ulm, Ulm, Germany.
University Hospital Ulm · DEMedizinische Hochschule Hannover · DEAsklepios Klinik Altona · DECaritas-Krankenhaus St. Josef · DEHanusch Hospital · ATHeidelberg University · DEHeinrich Heine University Düsseldorf · DEHelios Universitätsklinikum Wuppertal · DEJohannes Gutenberg University Mainz · DEKlinikum Braunschweig · DEKlinikum Bremen-Mitte · DEKlinikum Lüdenscheid · DEKlinikum Oldenburg · DEKrankenhaus der Barmherzigen Brüder Trier · DENational Center for Tumor Diseases · DESaarland University · DEStädtisches Klinikum Karlsruhe · DETechnical University of Munich · DEUniversitätsmedizin Göttingen · DEUniversity Hospital Bonn · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this cohort study was to compare a condensed schedule of consolidation therapy with high-dose cytarabine on days 1, 2 and 3 (HDAC-123) with the HDAC schedule given on days 1, 3 and 5 (HDAC-135) as well as to evaluate the prophylactic use of pegfilgrastim after chemotherapy in younger patients with acute myeloid leukemia in first complete remission. One hundred and seventy-six patients were treated with HDAC-135 and 392 patients with HDAC-123 with prophylactic pegfilgrastim at days 10 and 8, respectively, in the AMLSG 07-04 and the German AML Intergroup protocol. Time from start to chemotherapy until hematologic recovery with white blood cells >1.0 G/l and neutrophils >0.5 G/l was in median 4 days shorter in patients receiving HDAC-123 compared with HDAC-135 (P<0.0001, each), and further reduced by 2 days (P<0.0001) by pegfilgrastim. Rates of infections were reduced by HDAC-123 (P<0.0001) and pegfilgrastim (P=0.002). Days in hospital and platelet transfusions were significantly reduced by HDAC-123 compared with HDAC-135. Survival was neither affected by HDAC-123 versus HDAC-135 nor by pegfilgrastim. In conclusion, consolidation therapy with HDAC-123 leads to faster hematologic recovery and less infections, platelet transfusions as well as days in hospital without affecting survival.

Indexed as

Leukemia, Myeloid, AcutePlatelet TransfusionAdolescentAdultAntineoplastic Combined Chemotherapy ProtocolsConsolidation ChemotherapyCytarabineDaunorubicinDisease-Free SurvivalFemaleFilgrastimHumansLength of StayMaleMiddle AgedPolyethylene GlycolsCytarabineDaunorubicinFilgrastimpegfilgrastimPolyethylene Glycols

Identifiers

PMID28548643
PMCPMC5518888
OpenAlexW2617245268

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.