Evidence map›Paper›PMID 33810205›Full record

ReviewCancers2021

Endocrine-Based Treatments in Clinically-Relevant Subgroups of Hormone Receptor-Positive/HER2-Negative Metastatic Breast Cancer: Systematic Review and Meta-Analysis.

Francesco Schettini, Mario Giuliano, Fabiola Giudici, Benedetta Conte, Pietro De Placido, Sergio Venturini, Carla Rognoni, Angelo Di Leo, Mariavittoria Locci, Guy Jerusalem and 11 more

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 3 pooled it
3.7field-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

19 citing papers in PubMed, 3 syntheses or guidelines pooled it, 32 citations in OpenAlex.

  1. Pooled it
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  13. Budget impact analysis of breast cancer medications: a systematic review.Journal of pharmaceutical policy and practice · 2022
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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

21 authors at 14 institutions in 4 countries.

Francesco SchettiniDepartment of Clinical Medicine and Surgery, University of Naples "Federico II", 80131 Naples, Italy.ORCID 0000-0001-6561-1919
Mario GiulianoDepartment of Clinical Medicine and Surgery, University of Naples "Federico II", 80131 Naples, Italy.
Fabiola GiudiciUnit of Biostatistics, Department of Cardiac, Thoracic, Vascular Sciences and Public Health, University of Padova, 35122 Padova, Italy.ORCID 0000-0002-4160-3479
Benedetta ConteTranslational Genomics and Targeted Therapies in Solid Tumors, IDIBAPS, 08036 Barcelona, Spain.
Pietro De PlacidoDepartment of Clinical Medicine and Surgery, University of Naples "Federico II", 80131 Naples, Italy.
Sergio VenturiniDepartment of Management, University of Turin, 10124 Turin, Italy.
Carla RognoniCentre for Research on Health and Social Care Management (CERGAS), SDA Bocconi School of Management, 20136 Milan, Italy.ORCID 0000-0002-6330-0591
Angelo Di Leo"Sandro Pitigliani" Medical Oncology Department, Hospital of Prato, 59100 Prato, Italy.
Mariavittoria LocciDepartment of Neuroscience, Reproductive Medicine and Odontostomatological Sciences, University of Naples Federico II, 80131 Naples, Italy.
Guy JerusalemMedical Oncology Department, Centre Hospitalier Universitaire de Liège and Liège University, 4000 Liège, Belgium.ORCID 0000-0002-8845-0043
Lucia Del MastroBreast Unit, IRCCS Ospedale Policlinico San Martino, 16132 Genoa, Italy.ORCID 0000-0002-9546-5841
Fabio PuglisiDepartment of Medicine, University of Udine, 33100 Udine, Italy.ORCID 0000-0003-0573-4938
PierFranco ConteDepartment of Surgery, Oncology and Gastroenterology, University of Padova, 35122 Padova, Italy.ORCID 0000-0002-5210-5344
Michelino De LaurentiisBreast Oncology Unit, INT-Fondazione "G. Pascale", 80131 Naples, Italy.ORCID 0000-0001-9009-1572
Lajos PusztaiDepartment of Medicine, Yale University School of Medicine, New Haven, CT 06510, USA.ORCID 0000-0001-9632-6686
Mothaffar F RimawiDan L Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, TX 77030, USA.ORCID 0000-0002-4284-5656
Rachel SchiffDan L Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, TX 77030, USA.
Grazia ArpinoDepartment of Clinical Medicine and Surgery, University of Naples "Federico II", 80131 Naples, Italy.
Sabino De PlacidoDepartment of Clinical Medicine and Surgery, University of Naples "Federico II", 80131 Naples, Italy.
Aleix PratTranslational Genomics and Targeted Therapies in Solid Tumors, IDIBAPS, 08036 Barcelona, Spain.ORCID 0000-0003-2377-540X
Daniele GeneraliDepartment of Medical, Surgery and Health Sciences, University of Trieste, 34127 Trieste, Italy.ORCID 0000-0001-6002-1530
University of Naples Federico II · ITBaylor College of Medicine · USOspedale Policlinico San Martino · ITUniversity of Padua · ITBocconi University · ITCentre Hospitalier Universitaire de Liège · BEHospital Clínic de Barcelona · ESHospital of Prato · ITIstituto Nazionale Tumori IRCCS "Fondazione G. Pascale" · ITSolti · ESUniversity of Trieste · ITUniversity of Turin · ITUniversity of Udine · ITYale University · US

Funding

European Society for Medical Oncology ESMO Fellowship 2020 - TranslationalItalian Ministry of University and Research (MIUR) 2017EKMFTN_006
6 · The paper itself

Abstract

A precise assessment of the efficacy of first-/second-line endocrine therapies (ET) ± target therapies (TT) in clinically-relevant subgroups of hormone receptor-positive (HR+)/HER2-negative metastatic breast cancer (MBC) has not yet been conducted. To improve our current knowledge and support clinical decision-making, we thus conducted a systematic literature search to identify all first-/second-line phase II/III randomized clinical trials (RCT) of currently approved or most promising ET ± TT. Then, we performed a meta-analysis to assess progression-free (PFS) and/or overall survival (OS) benefit in several clinically-relevant prespecified subgroups. Thirty-five RCT were included (17,595 patients). Pooled results show significant reductions in the risk of relapse or death of 26-41% and 12-27%, respectively, depending on the clinical subgroup. Combination strategies proved to be more effective than single-agent ET (PFS hazard ratio (HR) range for combinations: 0.60-0.65 vs. HR range for single agent ET: 0.59-1.37; OS HR range for combinations: 0.74-0.87 vs. HR range for single agent ET: 0.68-0.98), with CDK4/6-inhibitors(i) + ET being the most effective regimen. Single agent ET showed comparable efficacy with ET+TT combinations in non-visceral (

Indexed as

endocrine therapyhormone receptormeta-analysismetastatic breast cancersystematic review

Identifiers

PMID33810205
PMCPMC8004645
OpenAlexW3136518379

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.