Evidence map›Paper›PMID 41796085›Full record

ArticleBritish journal of clinical pharmacology2026

Completion vs. early discontinuation of chemotherapy and the impact on 5-year all-cause mortality in women treated for early-stage breast cancer from 2015 to 2020: A cohort study using a target trial emulation approach.

Luke Steventon, Chengsheng Ju, Kenneth K C Man, Rebecca Roylance, Diego Ottaviani, Chiara Creed, Michal Sladkowski, Alec Wisner, Li Wei, Pinkie Chambers

Abstract read
In one paragraph

Article in British journal of clinical pharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

10 authors.

Luke SteventonUCL School of Pharmacy, London, UK.ORCID https://orcid.org/0009-0004-6759-4701
Chengsheng JuUCL School of Pharmacy, London, UK.
Kenneth K C ManUCL School of Pharmacy, London, UK.
Rebecca RoylanceUniversity College London Hospital NHS Foundation Trust, London, UK.
Diego OttavianiUniversity College London Hospital NHS Foundation Trust, London, UK.
Chiara CreedUniversity College London Hospital NHS Foundation Trust, London, UK.
Michal SladkowskiYork and Scarborough Teaching Hospitals NHS Foundation Trust, York, UK.
Alec WisnerCleveland Clinic, Cleveland, Ohio, USA.
Li WeiUCL School of Pharmacy, London, UK.
Pinkie ChambersUCL School of Pharmacy, London, UK.ORCID https://orcid.org/0000-0002-6669-9411

Funding

British Oncology Pharmacy Association (BOPA) BOPA_PRUK-2023-1-PC
6 · The paper itself

Abstract

aimChemotherapy is given for early-stage breast cancer; however, some patients discontinue before completing all planned cycles. This study investigated the impact of early chemotherapy discontinuation on treatment outcomes.

methodsThis retrospective cohort study used a target trial emulation framework to conduct a causal analysis of the all-cause mortality impact of completing a standard course of chemotherapy. Early-stage breast cancer patients treated with chemotherapy in England between 01/01/2014 and 31/12/2015 were identified from the National Disease Registration Service and Systemic Anti-Cancer Therapy datasets. Five-year OS was estimated for patients completing greater than or equal to six chemotherapy cycles relative to discontinuing chemotherapy early (less than six cycles), representing standard treatment during the study period. A clone-censor-weight approach was used to account for time-related bias and baseline confounding. Absolute risk and hazard ratios (HRs) were calculated.

resultsA total of 10 253 patients were included: 68% (n = 7014) received greater than or equal to six chemotherapy cycles, and 32% (n = 3239) received fewer than six cycles. Individuals completing greater than or equal to six cycles showed superior 5-year OS compared with discontinuation less than six cycles (absolute risk difference -1.6, 95% confidence interval [CI], -3.2, -0.1; HR 0.85, 95% CI 0.74, 0.98). Subgroup analyses showed OS benefit in patients diagnosed at stage 2 relative to Stage 3 (HR 0.82, 95% CI 0.69, 0.98), ER+/HER2+ histology (HR 0.46, 95% CI 0.24, 0.96) and Non-White ethnicity (HR 0.56, 95% CI 0.34, 0.91) when receiving six cycles.

conclusionPatients who completed greater than or equal to six cycles showed improved OS compared with those who discontinued before receiving six cycles. These findings support the identification and pre-emptive management of patients at high risk of discontinuing chemotherapy prematurely, to maximize treatment benefit.

Indexed as

Antineoplastic AgentsAntineoplastic Combined Chemotherapy ProtocolsBreast NeoplasmsAdultAgedCohort StudiesEnglandFemaleHumansMiddle AgedNeoplasm StagingRetrospective StudiesTime FactorsTreatment InterruptionTreatment OutcomeWithholding TreatmentAntineoplastic Agentsbreast cancerchemotherapysurvival outcomestreatment discontinuation

Identifiers

PMID41796085
PMCPMC13304275

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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.