Evidence map›Paper›PMID 37395895›Full record

ArticleClinical and experimental medicine2023

Association of serum cortisol and cortisone levels and risk of recurrence after endocrine treatment in breast cancer.

Feng Wang, Guro F Giskeødegård, Sissel Skarra, Monica J Engstrøm, Lars Hagen, Jürgen Geisler, Tomi S Mikkola, Matti J Tikkanen, Julia Debik, Randi J Reidunsdatter and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Clinical and experimental medicine, 2023. 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
2.1field-weighted citation impact, top 12% 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.

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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

11 authors at 5 institutions in 2 countries.

Feng WangDepartment of Circulation and Medical Imaging, Norwegian University of Science and Technology, NTNU, Trondheim, Norway. feng.wang@ntnu.no.
Guro F GiskeødegårdDepartment of Breast and Endocrine Surgery, St. Olavs Hospital, Trondheim University Hospital, Trondheim, Norway.
Sissel SkarraDepartment of Circulation and Medical Imaging, Norwegian University of Science and Technology, NTNU, Trondheim, Norway.
Monica J EngstrømDepartment of Breast and Endocrine Surgery, St. Olavs Hospital, Trondheim University Hospital, Trondheim, Norway.
Lars HagenDeprtment of Clinical and Molecular Medicine, Norwegian University of Science and Technology, NTNU, Trondheim, Norway.
Jürgen GeislerDeparment of Oncology, Akershus University Hospital, Lørenskog, Norway.
Tomi S MikkolaDepartment of Gynecology, Helsinki University Hospital, Helsinki, Finland.
Matti J TikkanenFolkhälsan Research Center, University of Helsinki, Helsinki, Finland.
Julia DebikDepartment of Circulation and Medical Imaging, Norwegian University of Science and Technology, NTNU, Trondheim, Norway.
Randi J ReidunsdatterDepartment of Circulation and Medical Imaging, Norwegian University of Science and Technology, NTNU, Trondheim, Norway.
Tone F BathenDepartment of Circulation and Medical Imaging, Norwegian University of Science and Technology, NTNU, Trondheim, Norway. tone.f.bathen@ntnu.no.
Norwegian University of Science and Technology · NOSt Olav's University Hospital · NOHelsinki University Hospital · FIAkershus University Hospital · NOCentral Norway Regional Health Authority · NO

Funding

Kreftfondet at St. Olavs Hospital 2020/14-304/2020Norwegian National Network for Breast Cancer Research 2019NTNU ISB småforsk 2020 and 2021Stiftelsen Dam 2020/FO298770The Liaison Committee for Education, Research and Innovation in Central Norway 2020/3806-4 and 28346
6 · The paper itself

Abstract

Metabolic reprogramming in breast cancer involves changes in steroid hormone synthesis and metabolism. Alterations in estrogen levels in both breast tissue and blood may influence carcinogenesis, breast cancer growth, and response to therapy. Our aim was to examine whether serum steroid hormone concentrations could predict the risk of recurrence and treatment-related fatigue in patients with breast cancer. This study included 66 postmenopausal patients with estrogen receptor-positive breast cancer who underwent surgery, radiotherapy, and adjuvant endocrine treatment. Serum samples were collected at six different time points [before the start of radiotherapy (as baseline), immediately after radiotherapy, and then 3, 6, 12 months, and 7-12 years after radiotherapy]. Serum concentrations of eight steroid hormones (cortisol, cortisone, 17α-hydroxyprogesterone, 17β-estradiol, estrone, androstenedione, testosterone, and progesterone) were measured using a liquid chromatography-tandem mass spectrometry-based method. Breast cancer recurrence was defined as clinically proven relapse/metastatic breast cancer or breast cancer-related death. Fatigue was assessed with the QLQ-C30 questionnaire. Serum steroid hormone concentrations measured before and immediately after radiotherapy differed between relapse and relapse-free patients [(accuracy 68.1%, p  = 0.02, and 63.2%, p  = 0.03, respectively, partial least squares discriminant analysis (PLS-DA)]. Baseline cortisol levels were lower in patients who relapsed than in those who did not (p < 0.05). The Kaplan-Meier analysis showed that patients with high baseline concentrations of cortisol (≥ median) had a significantly lower risk of breast cancer recurrence than patients with low cortisol levels (<median) (p  = 0.02). During follow-up, there was a decrease in cortisol and cortisone concentrations in relapse-free patients, whereas these steroid hormones increased in patients who relapsed. In addition, steroid hormone concentrations immediately after radiotherapy were associated with treatment-related fatigue (accuracy of 62.7%, p  = 0.03, PLS-DA). However, baseline steroid hormone levels did not predict fatigue at 1 year or at 7-12 years. In conclusion, breast cancer patients with low baseline cortisol levels were more likely to experience recurrence. During follow-up, cortisol and cortisone levels decreased in relapse-free patients but increased in patients with recurrence. Thus, cortisol and cortisone may act as potential biomarkers indicating individual risk of recurrence.

Indexed as

Breast NeoplasmsCortisoneFemaleHumansHydrocortisoneNeoplasm Recurrence, LocalRecurrenceSteroidsCortisoneHydrocortisoneSteroidsBreast cancer recurrenceCortisolCortisoneFatigueSteroid hormones

Identifiers

PMID37395895
PMCPMC10618334
OpenAlexW4382919476

What OpenQuestion holds

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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.