Evidence map›Paper›PMID 40658620›Full record

ArticleJournal of the National Cancer Institute2025

Aprepitant use during chemotherapy and association with survival in women with early breast cancer.

Edoardo Botteri, Sarah Hjorth, Fabio Conforti, Vincenzo Bagnardi, Bettina K Andreassen, Nathalie C Støer, Sameer Bhargava, Giske Ursin, Sara Gandini, Erica K Sloan and 1 more

Abstract read
In one paragraph

Article in Journal of the National Cancer Institute, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. 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

11 authors.

Edoardo BotteriDepartment of Research, Cancer Registry of Norway, Norwegian Institute of Public Health, Oslo, Norway.ORCID 0000-0002-9023-8068
Sarah HjorthDepartment of Research, Cancer Registry of Norway, Norwegian Institute of Public Health, Oslo, Norway.ORCID 0000-0003-2841-5868
Fabio ConfortiDepartment of Medical Oncology, Humanitas Gavazzeni, Bergamo, Italy.ORCID 0000-0002-6233-0502
Vincenzo BagnardiDepartment of Statistics and Quantitative Methods, University of Milan-Bicocca, Milan, Italy.
Bettina K AndreassenDepartment of Research, Cancer Registry of Norway, Norwegian Institute of Public Health, Oslo, Norway.ORCID 0000-0001-5087-2913
Nathalie C StøerDepartment of Research, Cancer Registry of Norway, Norwegian Institute of Public Health, Oslo, Norway.ORCID 0000-0001-8994-9332
Sameer BhargavaDepartment of Colorectal Cancer Screening, Cancer Registry of Norway, Norwegian Institute of Public Health, Oslo, Norway.ORCID 0000-0002-2770-584X
Giske UrsinCancer Registry of Norway, Norwegian Institute of Public Health, Oslo, Norway.ORCID 0000-0002-0835-9507
Sara GandiniDepartment of Experimental Oncology, European Institute of Oncology IRCCS, Milan, Italy.ORCID 0000-0002-1348-4548
Erica K SloanMonash Institute of Pharmaceutical Sciences, Monash University, Parkville, Victoria, Australia.ORCID 0000-0002-2355-1433
Aeson ChangMonash Institute of Pharmaceutical Sciences, Monash University, Parkville, Victoria, Australia.ORCID 0000-0003-0769-516X

Funding

Cancer Council Victoria Grants-In-AidHelse-Sør Øst 2019088Helse-Sør Øst 2021042Helse-Sør Øst 2022058National Health and Medical Research Council 2020851National Health and Medical Research Council 2038108Wellcome Trust 223187
6 · The paper itself

Abstract

backgroundPreclinical studies have shown that aprepitant, an antiemetic used to prevent chemotherapy-induced nausea and vomiting, slows mammary tumor growth and progression. Here, we evaluated the association between aprepitant and survival in a large cohort of women with early breast cancer.

methodsUsing linked nationwide registry data, we identified 13 811 women diagnosed with early breast cancer between 2008 and 2020 in Norway, who received chemotherapy and antiemetics. Women were followed for metastasis and death from 1 year after diagnosis until the end of 2021. To evaluate the association between aprepitant use and distant disease-free survival (DDFS) and breast cancer-specific survival (BCSS), we used Cox regression models, controlling for tumor and patient characteristics, chemotherapy regimens, and use of other antiemetics.

resultsDuring chemotherapy, 7047 (51%) women were supplied with aprepitant. Overall, aprepitant use was associated with better DDFS (HRDDFS = 0.89; 95% CI = 0.79 to 1.00) and BCSS (HRBCSS = 0.83; 95% CI = 0.71 to 0.97). The survival advantage was specific to women with non-luminal breast cancer (HRDDFS = 0.69; 95% CI = 0.56 to 0.83; HRBCSS = 0.64; 95% CI = 0.51 to 0.81) and was strongest in women with triple negative breast cancer (TNBC) (HRDDFS = 0.66; 95% CI = 0.53 to 0.83; HRBCSS = 0.61; 95% CI = 0.47 to 0.80). In women with non-luminal breast cancer, longer durations of aprepitant use were associated with increasingly favorable survival outcomes (DDFS: Ptrend = .002; BCSS: Ptrend = .016). Supply of other antiemetics of different drug classes was not associated with survival.

conclusionsAprepitant use during chemotherapy treatment was associated with better prognosis for women with non-luminal early breast cancer, in particular TNBC. Long-term clinical trials are required to confirm these findings.

Indexed as

AntiemeticsAntineoplastic Combined Chemotherapy ProtocolsAprepitantBreast NeoplasmsNauseaAdultAgedDisease-Free SurvivalFemaleHumansMiddle AgedNorwayRegistriesVomitingAntiemeticsAprepitant

Identifiers

PMID40658620
PMCPMC12597503

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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.