Evidence map›Paper›PMID 31227025›Full record

Observational studyBMC cancer2019

Influence of patient and tumor characteristics on therapy persistence with letrozole in postmenopausal women with advanced breast cancer: results of the prospective observational EvAluate-TM study.

Markus Wallwiener, Naiba Nabieva, Manuel Feisst, Tanja Fehm, Johann de Waal, Mahdi Rezai, Bernd Baier, Gerold Baake, Hans-Christian Kolberg, Martin Guggenberger and 41 more

Open access · goldAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in BMC cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-weighted citation impact, top 23% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
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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

51 authors at 20 institutions in 2 countries.

Markus WallwienerDepartment of Gynecology, University of Tübingen, Tübingen, Germany.
Naiba NabievaDepartment of Gynecology, University Hospital Erlangen, Friedrich-Alexander University Erlangen-Nuremberg, Comprehensive Cancer Center Erlangen-EMN, Universitätsstrasse 21-23, 91054, Erlangen, Germany.
Manuel FeisstInstitute of Medical Biometry and Informatics, University of Heidelberg, Heidelberg, Germany.
Tanja FehmDepartment of Gynecology, Heinrich Heine University of Dusseldorf, Dusseldorf, Germany.
Johann de WaalDepartment of Gynecology, Dachau Clinic, Dachau, Germany.
Mahdi RezaiLuisen-Hospital Dusseldorf, Dusseldorf, Germany.
Bernd BaierDepartment of Gynecology, Dachau Clinic, Dachau, Germany.
Gerold BaakeOncological Medical Practice Pinneberg, Pinneberg, Germany.
Hans-Christian KolbergMarien-Hospital Bottrop, Bottrop, Germany.
Martin GuggenbergerTuttlingen Clinic, Tuttlingen, Germany.
Mathias WarmBreast center, Department of Gynecology, University Hospital Cologne, Cologne, Germany.
Nadia HarbeckBreast center, Department of Gynecology, University Hospital Cologne, Cologne, Germany.
Rachel WuerstleinBreast center, Department of Gynecology, University Hospital Cologne, Cologne, Germany.
Jörg-Uwe DeukerVinzenz-Hospital Hanover GmbH, Hanover, Germany.
Peter DallDepartment of Gynecology, Lüneburg Clinic, Lüneburg, Germany.
Barbara RichterElbland Clinics, Meissen-Radebeul, Germany.
Grischa WachsmannCounty hospital Böblingen, Böblingen, Germany.
Cosima BruckerDepartment of Gynecology and Obstetrics, Paracelsus Medical University, Nuremberg, Germany.
Jan Willem SiebersDepartment of Gynecology of the St. Josef's Clinic Offenburg, Offenburg, Germany.
Milos PopovicDepartment of Gynecology, Bayreuth clinic GmbH, CCC ER-EMN, Bayreuth, Germany.
Thomas KuhnBrustzentrum am Diakonie Klinikum Stuttgart, Stuttgart, Germany.
Christopher WolfMedical Center ULM, Ulm, Germany.
Hans-Walter VollertMedical Campus Bodensee, Klinikum Friedrichshafen, Friedrichshafen, Germany.
Georg-Peter BreitbachDepartment of Gynecology, Neunkirchen Clinic, Neunkirchen, Germany.
Wolfgang JanniDepartment of Gynecology, University Hospital Ulm, Ulm, Germany.
Robert LandthalerGynecological Medical Practice of the County Hospital Krumbach, Krumbach, Germany.
Andreas KohlsEvangelic County Hospital Ludwigsfelde-Teltow, Ludwigsfelde-Teltow, Germany.
Daniela RezekMarien-Hospital Wesel, Wesel, Germany.
Thomas NoesseltDepartment of Gynecology of the Sana hospital Hameln, Hameln, Germany.
Gunnar FischerMittweida Hospital gGmbH, Mittweida, Germany.
Stephan HenschenJohanniter Hospital Genthin Stendal gGmbH, Hansestadt Stendal, Germany.
Thomas PraetzCaritas-Hospital Bad Mergentheim, Bad Mergentheim, Germany.
Volker HeylAsklepios Paulinen Clinic Wiesbaden, Wiesbaden, Germany.
Thorsten KühnDepartment of Gynecology, Esslingen Clinics a.N, Esslingen, Germany.
Thomas KraussDepartment of Gynecology Passau, Passau, Germany.
Christoph ThomssenDepartment of Gynecology, Martin-Luther-University Halle-Wittenberg, Halle-Wittenberg, Germany.
Andre HohnStädtisches Krankenhaus Kiel GmbH, Kiel, Germany.
Hans TeschOncology Bethanien Frankfurt, Frankfurt, Germany.
Christoph MundhenkeDepartment of Gynecology, University Hospital Schleswig-Holstein Campus Kiel, Kiel, Germany.
Alexander HeinDepartment of Gynecology, University Hospital Erlangen, Friedrich-Alexander University Erlangen-Nuremberg, Comprehensive Cancer Center Erlangen-EMN, Universitätsstrasse 21-23, 91054, Erlangen, Germany.
Claudia RauhDepartment of Gynecology, University Hospital Erlangen, Friedrich-Alexander University Erlangen-Nuremberg, Comprehensive Cancer Center Erlangen-EMN, Universitätsstrasse 21-23, 91054, Erlangen, Germany.
Christian M BayerDepartment of Gynecology, University Hospital Erlangen, Friedrich-Alexander University Erlangen-Nuremberg, Comprehensive Cancer Center Erlangen-EMN, Universitätsstrasse 21-23, 91054, Erlangen, Germany.
Katja SchmidtNovartis Pharma GmbH Nuremberg, Nuremberg, Germany.
Erik BellevilleClin-Sol GmbH Würzburg, Würzburg, Germany.
Sara Y BruckerDepartment of Gynecology, University of Tübingen, Tübingen, Germany.
Peyman HadjiDepartment of Gynecology, Nordwest Hospital, Frankfurt, Germany.
Matthias W BeckmannDepartment of Gynecology, University Hospital Erlangen, Friedrich-Alexander University Erlangen-Nuremberg, Comprehensive Cancer Center Erlangen-EMN, Universitätsstrasse 21-23, 91054, Erlangen, Germany.
Diethelm WallwienerDepartment of Gynecology, University of Tübingen, Tübingen, Germany.
Sherko KümmelBreast center, Essen Mitte Clinics, Evang. Huyssens-Stiftung/Knappschaft GmbH, Essen, Germany.
Andreas HartkopfDepartment of Gynecology, University of Tübingen, Tübingen, Germany.
Peter A FaschingDepartment of Gynecology, University Hospital Erlangen, Friedrich-Alexander University Erlangen-Nuremberg, Comprehensive Cancer Center Erlangen-EMN, Universitätsstrasse 21-23, 91054, Erlangen, Germany. Peter.Fasching@uk-erlangen.de.ORCID http://orcid.org/0000-0003-4885-8471
Universitätsklinikum Erlangen · DEUniversity of Tübingen · DEHeidelberg University · DEHelios Amper-Klinikum Dachau · DEKlinikum Esslingen · DEMünchen Klinik · DEAsklepios · DEBayreuth Medical Center · DECardiovascular Center Bethanien · DECaritas-Krankenhaus Bad Mergentheim · DEDie Johanniter · DEHeinrich Heine University Düsseldorf · DEHewlett-Packard (Germany) · DEHochschule Mittweida · DEKliniken Essen-Mitte · DEKlinikum Lüneburg · DEKrankenhaus Nordwest · DELuisenkrankenhaus · DEMarienhospital Bottrop · DEMarien Hospital Wesel · DE

Funding

Novartis Pharma not applicable
6 · The paper itself

Abstract

backgroundTreatment of postmenopausal, hormone receptor-positive metastatic breast cancer (MBC) patients varies despite clear therapy guidelines, favoring endocrine treatment (ET). Aim of this study was to analyze persistence of palliative aromatase inhibitor (AI) monotherapy in MBC patients.

methodsEvAluate-TM is a prospective, multicenter, noninterventional study to evaluate treatment with letrozole in postmenopausal women with hormone receptor-positive breast cancer. To assess therapy persistence, defined as the time from therapy start to the end of the therapy (TTEOT), two pre-specified study visits took place after 6 and 12 months. Competing risk survival analyses were performed to identify patient and tumor characteristics that predict TTEOT.

resultsOut of 200 patients, 66 patients terminated treatment prematurely, 26 (13%) of them due to causes other than disease progression. Persistence rate for reasons other than progression at 12 months was 77.7%. Persistence was lower in patients who reported any adverse event (AE) in the first 30 days of ET (89.5% with no AE and 56% with AE). Furthermore, patients had a lower persistence if they reported compliance problems in the past before letrozole treatment.

conclusionsDespite suffering from a life-threatening disease, AEs of an AI will result in a relevant number of treatment terminations that are not related to progression. Some subgroups of patients have very low persistence rates. Especially with regard to novel endocrine combination therapies, these data imply that some groups of patients will need special attention to guide them through the therapy process.

trial registrationClinical Trials Number: CFEM345DDE19.

Indexed as

Patient CompliancePostmenopauseAgedAromatase InhibitorsBreast NeoplasmsFemaleFollow-Up StudiesHumansKaplan-Meier EstimateLetrozoleMiddle AgedPatient DropoutsProspective StudiesTreatment OutcomeTreatment RefusalAromatase InhibitorsLetrozoleAdvanced/metastatic breast cancerAromatase inhibitorComplianceEndocrine treatment/therapyPalliative/metastatic treatmentPersistence

Identifiers

PMID31227025
PMCPMC6588890
OpenAlexW2951091741

What OpenQuestion holds

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LicenceCC BY
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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.