Evidence map›Paper›PMID 33939116›Full record

ArticleBreast cancer (Tokyo, Japan)2021

Evaluation of the ability of the Clinical Treatment Score at 5 years (CTS5) compared to other risk stratification methods to predict the response to an extended endocrine therapy in breast cancer patients.

Andrea Villasco, Francesca Accomasso, Marta D'Alonzo, Francesca Agnelli, Piero Sismondi, Nicoletta Biglia

Open access · hybridAbstract readEvaluation Study
In one paragraph

Article in Breast cancer (Tokyo, Japan), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
0.4field-weighted citation impact, top 47% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Pooled it
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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

6 authors at 2 institutions in 1 country.

Andrea VillascoAcademic Division of Gynecology and Obstetrics, Mauriziano Umberto I Hospital, University of Turin, Via Magellano 1, 10128, Turin, Italy. andrea.villasco@unito.it.ORCID http://orcid.org/0000-0002-9841-7722
Francesca AccomassoAcademic Division of Gynecology and Obstetrics, Mauriziano Umberto I Hospital, University of Turin, Via Magellano 1, 10128, Turin, Italy.
Marta D'AlonzoAcademic Division of Gynecology and Obstetrics, Mauriziano Umberto I Hospital, University of Turin, Via Magellano 1, 10128, Turin, Italy.
Francesca AgnelliSchool of Medicine, University of Turin, Turin, Italy.
Piero SismondiAcademic Division of Gynecology and Obstetrics, Mauriziano Umberto I Hospital, University of Turin, Via Magellano 1, 10128, Turin, Italy.
Nicoletta BigliaAcademic Division of Gynecology and Obstetrics, Mauriziano Umberto I Hospital, University of Turin, Via Magellano 1, 10128, Turin, Italy.
University of Turin · ITCTO Hospital · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeExtension of adjuvant endocrine therapy (ET) reduces the risk of recurrence in women diagnosed with ER-positive breast cancers, but a significant benefit is unlikely to happen to all individual patients. This study is aimed at evaluating the ability of different clinical late distant recurrence (LDR) risk stratification methods and in particular the clinical treatment score at 5 years (CTS5) to predict the response to extended adjuvant ET.

methods783 patients diagnosed with ER+ BC between 1988 and 2014 at Umberto I Hospital of Turin, of which 180 received an extended adjuvant ET, were retrospectively selected. They were stratified according to pT, pN, disease stage, tumor grade, Ki67 level, progesterone receptor status and CTS5. The primary endpoint was LDR rate. LDR rates according to ET duration were confronted in each subgroup.

resultThe median duration of extended ET was 7 years (6-10). Median follow-up from diagnosis was 9 years (6-26). Retrospective risk stratification according to tumor size, nodal status, disease stage, tumor grade, Ki67 level, and progesterone receptor status did not appear to be able to predict the response to extended ET. In the CTS5 high-risk subgroup instead, the risk of developing an LDR was significantly lower in the patients who underwent extended ET compared to standard ET (HR 0.37, 95% CI 0.15-0.91), while no significant benefit was demonstrated for low and intermediate-risk patients.

conclusionsRisk stratification according to CTS5 appeared to be predictive of the response to extended endocrine therapy in our population of real-life pre and postmenopausal patients.

Indexed as

AdultAgedAged, 80 and overAntineoplastic Agents, HormonalBreast NeoplasmsFemaleFollow-Up StudiesHumansMiddle AgedNeoplasm Recurrence, LocalRetrospective StudiesRisk AssessmentTamoxifenAntineoplastic Agents, HormonalTamoxifenBreast cancerCTS5Estrogen receptor-positiveExtended endocrine therapyLate distant recurrence

Identifiers

PMID33939116
PMCPMC8354987
OpenAlexW3158739802

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.