Evidence map›Paper›PMID 29230665›Full record

Trial reportBreast cancer research and treatment2018

Relevant factors for the optimal duration of extended endocrine therapy in early breast cancer.

Erik J Blok, Judith R Kroep, Elma Meershoek-Klein Kranenbarg, Marjolijn Duijm-de Carpentier, Hein Putter, Gerrit-Jan Liefers, Johan W R Nortier, Emiel J Th Rutgers, Caroline M Seynaeve, Cornelis J H van de Velde and 1 more

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

Trial report in Breast cancer research and treatment, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
1.1field-weighted citation impact, top 18% 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

0 citing papers in PubMed, 8 citations in OpenAlex.

No citing paper in PubMed yet.

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

11 authors at 2 institutions in 1 country.

Erik J BlokDepartment of Surgery, Leiden University Medical Center, 2300 RC, Leiden, The Netherlands.
Judith R KroepDepartment of Medical Oncology, Leiden University Medical Center, P.O. Box 9600, Leiden, The Netherlands.
Elma Meershoek-Klein KranenbargDepartment of Surgery, Leiden University Medical Center, 2300 RC, Leiden, The Netherlands.
Marjolijn Duijm-de CarpentierDepartment of Surgery, Leiden University Medical Center, 2300 RC, Leiden, The Netherlands.
Hein PutterDepartment of Medical Statistics, Leiden University Medical Center, Leiden, The Netherlands.
Gerrit-Jan LiefersDepartment of Surgery, Leiden University Medical Center, 2300 RC, Leiden, The Netherlands.
Johan W R NortierDepartment of Medical Oncology, Leiden University Medical Center, P.O. Box 9600, Leiden, The Netherlands.
Emiel J Th RutgersDepartment of Surgery, Netherlands Cancer Institute, Amsterdam, The Netherlands.
Caroline M SeynaeveDepartment of Medical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
Cornelis J H van de VeldeDepartment of Surgery, Leiden University Medical Center, 2300 RC, Leiden, The Netherlands. c.j.h.van_de_velde@lumc.nl.
IDEAL Study Group
Leiden University Medical Center · NLThe Netherlands Cancer Institute · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeFor postmenopausal patients with hormone receptor-positive early breast cancer, the optimal subgroup and duration of extended endocrine therapy is not clear yet. The aim of this study using the IDEAL patient cohort was to identify a subgroup for which longer (5 years) extended therapy is beneficial over shorter (2.5 years) extended endocrine therapy.

methodsIn the IDEAL trial, 1824 patients who completed 5 years of adjuvant endocrine therapy (either 5 years of tamoxifen (12%), 5 years of an AI (29%), or a sequential strategy of both (59%)) were randomized between either 2.5 or 5 years of extended letrozole. For each prior therapy subgroup, the value of longer therapy was assessed for both node-negative and node-positive patients using Kaplan Meier and Cox regression survival analyses.

resultsIn node-positive patients, there was a significant benefit of 5 years (over 2.5 years) of extended therapy (disease-free survival (DFS) HR 0.67, p = 0.03, 95% CI 0.47-0.96). This effect was only observed in patients who were treated initially with a sequential scheme (DFS HR 0.60, p = 0.03, 95% CI 0.38-0.95). In all other subgroups, there was no significant benefit of longer extended therapy. Similar results were found in patients who were randomized for their initial adjuvant therapy in the TEAM trial (DFS HR 0.37, p = 0.07, 95% CI 0.13-1.06), although this additional analysis was underpowered for definite conclusions.

conclusionsThis study suggests that node-positive patients could benefit from longer extended endocrine therapy, although this effect appears isolated to patients treated with sequential endocrine therapy during the first 5 years and needs validation and long-term follow-up.

Indexed as

AgedAntineoplastic Agents, HormonalAromatase InhibitorsBreast NeoplasmsChemotherapy, AdjuvantDisease-Free SurvivalFemaleFollow-Up StudiesHumansKaplan-Meier EstimateLymphatic MetastasisMiddle AgedNetherlandsPostmenopauseReceptors, EstrogenTime FactorsAntineoplastic Agents, HormonalAromatase InhibitorsReceptors, EstrogenAdjuvantExtendedIDEALLetrozolePostmenopausalSubgroup

Identifiers

PMID29230665
PMCPMC5838141
OpenAlexW2774842578

What OpenQuestion holds

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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.