Evidence map›Paper›PMID 37178424›Full record

ArticleJournal of cancer research and clinical oncology2023

Characterization of clinicopathological features, treatment practices, and outcomes among Finnish advanced breast cancer patients in real-life clinical practice.

Krista Heinolainen, Silva Saarinen, Simona Vertuani, Antti Ellonen, Antti Karlsson, Meri Utriainen, Peter Carlqvist, Jami Mandelin, Barbro Holm

Open access · hybridAbstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2023. 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
0.5field-weighted citation impact, top 30% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  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

9 authors at 5 institutions in 2 countries.

Krista HeinolainenNovartis Finland Oy, Espoo, Finland.
Silva SaarinenNovartis Finland Oy, Espoo, Finland.
Simona VertuaniNovartis Sverige AB, Kista, Sweden.
Antti EllonenDepartment of Oncology, Turku University Central Hospital, Turku, Finland.
Antti KarlssonAuria Biobank and University of Turku, Turku, Finland.
Meri UtriainenComprehensive Cancer Center, Helsinki University Central Hospital, Helsinki, Finland.
Peter CarlqvistNordic Market Access, Stockholm, Sweden.
Jami MandelinFaron Pharmaceuticals, Turku, Finland.
Barbro HolmNovartis Sverige AB, Kista, Sweden. babbo.holm@gmail.com.ORCID http://orcid.org/0000-0002-2944-9464
Novartis (Sweden) · SEFaron Pharmaceutical (Finland) · FIHelsinki University Hospital · FITurku University Hospital · FIUniversity of Turku · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeIn recent years, several new targeted therapies have emerged for advanced breast cancer (aBC). However, real-life data specific to aBC and different breast cancer subtypes are scarce. This retrospective cohort study was designed to describe the distribution of aBC subtypes, incidence, treatment patterns, survival, and PIK3CA hotspot mutation frequency.

methodsThe study included all patients in the Hospital District of Southwest Finland diagnosed with aBC between 2004 and 2013 and with a sample available in Auria Biobank. In addition to registry-based data collection, 161 HR+/HER2- aBCs were screened for PIK3CA mutations.

resultsAltogether, 54.7% of the 444 patients included in the study had luminal B subtype. The smallest representations were in HR-/HER2+ (4.5%) and triple-negative (5.6%) subgroups. The percentage of aBC among all diagnosed breast cancers increased until 2010, after which it remained stable. The triple-negative cancers were associated with shorter median overall survival (5.5 months) compared to other subgroups (16.5-24.6 months). Most (84%) triple-negative cancers also metastasized during the first two years, whereas this was more evenly distributed over time in other subgroups. Of the HR+/HER2- tumors, 32.3% harbored a PIK3CA hotspot mutation. These patients, however, did not have inferior survival compared to patients with PIK3CA wild-type cancers.

conclusionThis study described real-world aBC subgroups and indicated that the clinical outcomes of subgroups vary. Although PIK3CA hotspot mutations did not lead to inferior survival, they are relevant as possible treatment targets. Overall, these data could be utilized to further evaluate the subgroup-specific medical needs in breast cancer.

Indexed as

Breast NeoplasmsClass I Phosphatidylinositol 3-KinasesErb-b2 Receptor Tyrosine KinasesFemaleFinlandHumansMutationRetrospective StudiesClass I Phosphatidylinositol 3-KinasesErb-b2 Receptor Tyrosine KinasesAdvanced breast cancerBreast cancer subtypesBreast cancer treatmentPIK3CA mutation screeningRetrospective register study

Identifiers

PMID37178424
PMCPMC10374819
OpenAlexW4376598523

What OpenQuestion holds

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LicenceCC BY
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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.