Evidence map›Paper›PMID 42699083›Full record

ArticleESMO real world data and digital oncology2026

Treatment and survival of

N Ding, S M E Geurts, K E P E Hermans, I J H Vriens, R Visserman, L F S Kooreman, N A J B Peters, E M Heuts, J Verloop, A C Voogd and 1 more

Abstract read
In one paragraph

Article in ESMO real world data and digital oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

N DingDivision of Medical Oncology, Department of Internal Medicine, GROW Research Institute for Oncology and Reproduction, Maastricht University Medical Centre, Maastricht, the Netherlands.
S M E GeurtsDivision of Medical Oncology, Department of Internal Medicine, GROW Research Institute for Oncology and Reproduction, Maastricht University Medical Centre, Maastricht, the Netherlands.
K E P E HermansDivision of Medical Oncology, Department of Internal Medicine, GROW Research Institute for Oncology and Reproduction, Maastricht University Medical Centre, Maastricht, the Netherlands.
I J H VriensDivision of Medical Oncology, Department of Internal Medicine, GROW Research Institute for Oncology and Reproduction, Maastricht University Medical Centre, Maastricht, the Netherlands.
R VissermanDivision of Medical Oncology, Department of Internal Medicine, GROW Research Institute for Oncology and Reproduction, Maastricht University Medical Centre, Maastricht, the Netherlands.
L F S KooremanDepartment of Pathology, GROW Research Institute for Oncology and Reproduction, Maastricht University Medical Centre, Maastricht, the Netherlands.
N A J B PetersDepartment of Internal Medicine, Sint Jans Gasthuis Hospital, Weert, the Netherlands.
E M HeutsDepartment of Surgery, Maastricht University Medical Centre, Maastricht, the Netherlands.
J VerloopDepartment of Research and Development, Netherlands Comprehensive Cancer Organisation, Utrecht, the Netherlands.
A C VoogdDepartment of Epidemiology, Maastricht University, Maastricht, the Netherlands.
V C G Tjan-HeijnenDivision of Medical Oncology, Department of Internal Medicine, GROW Research Institute for Oncology and Reproduction, Maastricht University Medical Centre, Maastricht, the Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Human epidermal growth factor receptor 2 (HER2)-targeted therapy has improved survival in HER2-positive metastatic breast cancer (MBC). Real-world practice may differ across oncologic networks, even within countries with uniform treatment guidelines. We assessed regional variation in first-line treatment and overall survival (OS) among patients with Patients and methods: Data from the Netherlands Cancer Registry were analysed. The registry includes seven regions, anonymised as A-G. Crude regional proportions of first-line HER2-targeted therapy were described. Inverse probability of treatment weighting (IPTW) was applied, with region as the exposure. Risk ratios for receiving HER2-targeted therapy were estimated using IPTW-adjusted Poisson regression. OS was analysed using the Kaplan-Meier method and IPTW-adjusted Cox regression, additionally adjusting for baseline covariates and first-line treatment. Results: Among 2158 patients, use of first-line HER2-targeted therapy ranged from 70% (region F) to 88% (region C). After adjustment, no regional differences were observed ( Conclusions: No large regional differences in first-line HER2-targeted therapy were observed among

Indexed as

breast neoplasmsErbB-2health care disparitiesneoplasm metastasisreceptorsurvival

Identifiers

PMID42699083
PMCPMC13542605

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.