Evidence map›Paper›PMID 34554372›Full record

Trial reportBreast cancer research and treatment2021

Lack of cross-resistance between non-steroidal and steroidal aromatase inhibitors in breast cancer patients: the potential role of the adipokine leptin.

Nazli Bahrami, Shakila Jabeen, Andliena Tahiri, Torill Sauer, Hilde Presterud Ødegård, Stephanie Beate Geisler, Berit Gravdehaug, Laurens Cornelus Reitsma, Knut Selsås, Vessela Kristensen and 1 more

Open access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Breast cancer research and treatment, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
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  8. Review
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 3 institutions in 1 country.

Nazli Bahrami *Department of Oncology, Akershus University Hospital, Lørenskog, Norway.
Shakila Jabeen *Department of Clinical Molecular Biology (EPIGEN), Akershus University Hospital, Lørenskog, Norway.
Andliena TahiriDepartment of Clinical Molecular Biology (EPIGEN), Akershus University Hospital, Lørenskog, Norway.
Torill SauerDepartment of Pathology, Akershus University Hospital, Lørenskog, Norway.
Hilde Presterud ØdegårdDepartment of Oncology, Akershus University Hospital, Lørenskog, Norway.
Stephanie Beate GeislerDepartment of Oncology, Akershus University Hospital, Lørenskog, Norway.
Berit GravdehaugDepartment of Breast and Endocrine Surgery, Akershus University Hospital, Lørenskog, Norway.
Laurens Cornelus ReitsmaDepartment of Breast and Endocrine Surgery, Akershus University Hospital, Lørenskog, Norway.
Knut SelsåsDepartment of Breast and Endocrine Surgery, Akershus University Hospital, Lørenskog, Norway.
Vessela KristensenDepartment of Clinical Molecular Biology (EPIGEN), Akershus University Hospital, Lørenskog, Norway.
Jürgen GeislerDepartment of Oncology, Akershus University Hospital, Lørenskog, Norway. juergen.geisler@medisin.uio.no.ORCID http://orcid.org/0000-0001-6239-3856
Akershus University Hospital · NOOslo University Hospital · NOUniversity of Oslo · NO

Funding

Helse Sør-Øst RHF 2017033
6 · The paper itself

Abstract

purposeThe aromatase inactivator exemestane may cause clinical disease stabilization following progression on non-steroidal aromatase inhibitors like letrozole in patients with metastatic breast cancer, indicating that additional therapeutic effects, not necessarily related to estrogen-suppression, may be involved in this well-known "lack of cross-resistance".

methodsPostmenopausal women with ER positive, HER-2 negative, locally advanced breast cancer were enrolled in the NEOLETEXE-trial and randomized to sequential treatment starting with either letrozole (2.5 mg o.d.) or exemestane (25 mg o.d.) followed by the alternative aromatase inhibitor. Serum levels of 54 cytokines, including 12 adipokines were assessed using Luminex xMAP technology (multiple ELISA).

resultsSerum levels of leptin were significantly decreased during treatment with exemestane (p < 0.001), regardless whether exemestane was given as first or second neoadjuvant therapy. In contrast, letrozole caused a non-significant increase in serum leptin levels in vivo.

conclusionsOur findings suggest an additional and direct effect of exemestane on CYP-19 (aromatase) synthesis presumably due to effects on the CYP19 promoter use that is not present during therapy with the non-steroidal aromatase inhibitor letrozole. Our findings provide new insights into the influence of clinically important aromatase inhibitors on cytokine levels in vivo that contribute to the understanding of the clinically observed lack of cross-resistance between non-steroidal and steroidal aromatase inhibitors in breast cancer patients.

trial registrationRegistered on March 23rd 2015 in the National trial database of Norway (Registration number: REK-SØ-84-2015).

Indexed as

Aromatase InhibitorsBreast NeoplasmsAdipokinesAndrostadienesFemaleHumansLeptinLetrozoleNitrilesAdipokinesAndrostadienesAromatase InhibitorsLeptinLetrozoleNitrilesAdipokineAromatase inhibitorBreast cancerExemestaneLeptinLetrozole

Identifiers

PMID34554372
PMCPMC8558290
OpenAlexW3200983152

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.