Evidence map›Paper›PMID 41193536›Full record

ArticleScientific reports2025

First real-world evidence from the Emilia-Romagna region suggests tamoxifen protects breast cancer patients from COVID-19.

Sara Bravaccini, Fabio Nicolini, William Balzi, Irene Azzali, Luigi Pasini, Lucia Mazzotti, Anna Gaimari, Anna De Lucia, Matteo Zurlo, Roberta Maltoni and 10 more

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. Article
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

20 authors.

Sara Bravaccini *Department of Medicine and Surgery, University of Enna "Kore", 94100, Enna, Italy.
Fabio NicoliniAdvanced Cellular Therapies and Rare Tumors Unit, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Italy.
William BalziHealthcare Administration, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Italy.
Irene AzzaliUnit of Biostatistics and Clinical Trials, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Italy.
Luigi PasiniAdvanced Cellular Therapies and Rare Tumors Unit, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Italy.
Lucia MazzottiAdvanced Cellular Therapies and Rare Tumors Unit, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Italy.
Anna GaimariAdvanced Cellular Therapies and Rare Tumors Unit, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Italy.
Anna De LuciaAdvanced Cellular Therapies and Rare Tumors Unit, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Italy.
Matteo ZurloAdvanced Cellular Therapies and Rare Tumors Unit, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Italy.
Roberta MaltoniHealthcare Administration, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Italy.
Francesca PiriniBiosciences Laboratory, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Italy.
Michela CortesiBiosciences Laboratory, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Italy.
Michele ZanoniBiosciences Laboratory, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Italy.
Maria Maddalena TumedeiAdvanced Cellular Therapies and Rare Tumors Unit, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Italy.
Oriana NanniUnit of Biostatistics and Clinical Trials, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Italy.
Claudio CerchioneHematology Unit, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Italy.
Vittorio SambriUnit of Microbiology, The Great Romagna Area Hub Laboratory, Cesena, Italy.
Patricia Borges de SouzaAdvanced Cellular Therapies and Rare Tumors Unit, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Italy.
Giovanni MartinelliScientific Directorate, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Italy.
Massimiliano Mazza *Advanced Cellular Therapies and Rare Tumors Unit, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Italy. massimiliano.mazza@irst.emr.it.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

COVID-19 severity is uneven between genders. A role for sex hormones is possible and has been postulated. Considering this idea, we hypothesized hormonal therapies might influence the severity of COVID-19 in breast cancer (BC) patients. We mined the Emilia-Romagna region (Italy) registries to compare the rates of hospitalization and mortality by COVID-19 in 2020 amongst 22,987 BC patients treated with tamoxifen, aromatase inhibitors (AIs), fulvestrant, and anti-HER2 therapies (trastuzumab and pertuzumab) in 2020, the latter used as reference group. The hospitalization rate observed in 4719 tamoxifen-treated BC patients was the lowest (0.61%, OR, 0.38; 90% CI, 0.20-0.76; p = 0.03) among hormonal therapies. Importantly, only one COVID-19 fatality was observed in tamoxifen-treated BC patients, who showed a striking 0.02% COVID-19 death frequency as compared to 0.24% observed for the whole BC patients population. In addition, tamoxifen emerged in the sex and age adjusted analysis as the only agent significantly decreasing the standard mortality rate (SMR) by COVID-19 as compared to the regional population consisting of 2,296,559 female residents from the Emilia Romagna region in 2020. Our results show that BC patients are at increased risk of COVID-19 hospitalization and that COVID-19 mortality is hindered by SERM-based therapies like tamoxifen. These findings are relevant to choose adequate treatments in order to protect cancer patients from concomitant SARS-CoV-2 contagion and related symptoms and contribute to the idea that SERMs could be used as prophylactic agents and therapeutics to prevent the progression of severity of COVID-19.

Indexed as

Antineoplastic Agents, HormonalBreast NeoplasmsCOVID-19TamoxifenAdultAgedAged, 80 and overAromatase InhibitorsFemaleHospitalizationHumansItalyMaleMiddle AgedRegistriesSARS-CoV-2Antineoplastic Agents, HormonalAromatase InhibitorsTamoxifenAromatase inhibitorsBreast cancerCOVID-19 protectionCOVID-19 severityFulvestrantTamoxifen

Identifiers

PMID41193536
PMCPMC12589471

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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.