Evidence map›Paper›PMID 27798749›Full record

Trial reportBreast cancer research and treatment2017

A randomized phase III study evaluating pegylated liposomal doxorubicin versus capecitabine as first-line therapy for metastatic breast cancer: results of the PELICAN study.

Nadia Harbeck, Steffen Saupe, Elke Jäger, Marcus Schmidt, Rolf Kreienberg, Lothar Müller, Burkhard Joerg Otremba, Dirk Waldenmaier, Julia Dorn, Mathias Warm and 11 more

Open access · hybridAbstract readClinical Trial, Phase IIIMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Breast cancer research and treatment, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 2 pooled it
1.9field-weighted citation impact, top 12% 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

24 citing papers in PubMed, 2 syntheses or guidelines pooled it, 49 citations in OpenAlex.

  1. Guideline
  2. Pooled it
  3. Trial
  4. Pegylated liposomal doxorubicin (DuomeisuBreast cancer research and treatment · 2023
    Trial
  5. Trial
  6. Trial
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Cost-Effectiveness of Pharmacologic Treatment Options for Women With Endocrine-Refractory or Triple-Negative Metastatic Breast Cancer.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2023
    Article
  17. Review
  18. Article
  19. Article
  20. 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

21 authors at 13 institutions in 2 countries.

Nadia HarbeckBreast Center, Department of Obstetrics and Gynecology and CCC of LMU, University of Munich, Munich, Germany. nadia.harbeck@med.uni-muenchen.de.
Steffen SaupeDepartment of Obstetrics and Gynecology, Technical University of Munich, Munich, Germany.
Elke JägerOncology and Hematology, Krankenhaus Nordwest, Frankfurt, Germany.
Marcus SchmidtDepartment of Obstetrics and Gynecology, Johannes Gutenberg University, Mainz, Germany.
Rolf KreienbergUniversitätsfrauenklinik, Ulm, Germany.
Lothar MüllerOnkologische Schwerpunktpraxis, Leer, Germany.
Burkhard Joerg OtrembaOnkologische Praxis Oldenburg, Oldenburg, Germany.
Dirk WaldenmaierMSD Sharp & Dohme, Haar, Germany.
Julia DornDepartment of Obstetrics and Gynecology, Technical University of Munich, Munich, Germany.
Mathias WarmBrustzentrum, Krankenhaus Köln-Holweide, Cologne, Germany.
Michael ScholzTrium Analysis Online GmbH, Munich, Germany.
Michael UntchHelios Klinikum Berlin-Buch, Berlin, Germany.
Maike de WitVivantes Klinikum Neukoelln, Berlin, Germany.
Jana BarinoffDr.-Horst-Schmidt-Kliniken Wiesbaden, Wiesbaden, Germany.
Hans-Joachim LückDr.-Horst-Schmidt-Kliniken Wiesbaden, Wiesbaden, Germany.
Philipp HarterKliniken Essen-Mitte, Essen, Germany.
Doris AugustinKlinikum des Landkreises Deggendorf, Deggendorf, Germany.
Paul HarnettCrown Princess Mary Cancer Centre Westmead, Sydney, Australia.
Matthias W BeckmannDepartment of Gynecology and Obstetrics, Comprehensive Cancer Center Erlangen-EMN, University Hospital Erlangen, Erlangen, Germany.
Salah-Eddin Al-BatranOncology and Hematology, Krankenhaus Nordwest, Frankfurt, Germany.
PELICAN Investigators
Helios Dr. Horst Schmidt Kliniken Wiesbaden · DEJohannes Gutenberg University Mainz · DEKrankenhaus Köln-Holweide · DEKrankenhaus Nordwest · DEMSD (Germany) · DEPraxis für Hämatologie und Onkologie · DEUniversitätsklinikum Erlangen · DEBreast Center · CHDeggendorf Institute of Technology · DEHelios Hospital Berlin-Buch · DEKliniken Essen-Mitte · DELudwig-Maximilians-Universität München · DEVivantes Klinikum · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe PELICAN trial evaluates for the first time efficacy and safety of pegylated liposomal doxorubicin (PLD) versus capecitabine as first-line treatment of metastatic breast cancer (MBC).

methodsThis randomized, phase III, open-label, multicenter trial enrolled first-line MBC patients who were ineligible for endocrine or trastuzumab therapy. Cumulative adjuvant anthracyclines of 360 mg/m

results210 patients were randomized (n = 105, PLD and n = 105, capecitabine). Adjuvant anthracyclines were given to 37 % (PLD) and 36 % (capecitabine) of patients. No significant difference was observed in TTP [HR = 1.21 (95 % confidence interval, 0.838-1.750)]. Median TTP was 6.0 months for both PLD and capecitabine. Comparing patients with or without prior anthracyclines, no significant difference in TTP was observed in the PLD arm (log-rank P = 0.64). For PLD versus capecitabine, respectively, overall survival (median, 23.3 months vs. 26.8 months) and time-to-treatment failure (median, 4.6 months vs. 3.7 months) were not statistically significantly different. Compared to PLD, patients on capecitabine experienced more serious adverse events (P = 0.015) and more cardiac events among patients who had prior anthracycline exposure (18 vs. 8 %; P = 0.31).

conclusionBoth PLD and capecitabine are effective first-line agents for MBC.

Indexed as

AdultAgedAged, 80 and overAntimetabolites, AntineoplasticBreast NeoplasmsCapecitabineDisease ProgressionDoxorubicinFemaleHumansMiddle AgedNeoplasm MetastasisNeoplasm StagingPolyethylene GlycolsQuality of LifeRisk FactorsAntimetabolites, AntineoplasticCapecitabineDoxorubicinliposomal doxorubicinPolyethylene GlycolsCapecitabineMetastatic breast cancerPegylated liposomal doxorubicinPELICAN

Identifiers

PMID27798749
PMCPMC5222915
OpenAlexW2546350357

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.