Evidence map›Paper›PMID 37866031›Full record

ArticleESMO open2023

A comparison of the efficacy of trastuzumab deruxtecan in advanced HER2-positive breast cancer: active brain metastasis versus progressive extracranial disease alone.

J Pearson, A Khan, T Bhogal, H Wong, A Law, S Mills, N Santamaria, J Bishop, J Cliff, D Errington and 10 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in ESMO open, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
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  3. Review
  4. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 2 institutions in 1 country.

J PearsonThe Clatterbridge Cancer Centre NHS Foundation Trust, Liverpool; Department of Molecular and Clinical Cancer Medicine, Institute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool.
A KhanThe Clatterbridge Cancer Centre NHS Foundation Trust, Liverpool.
T BhogalThe Clatterbridge Cancer Centre NHS Foundation Trust, Liverpool; Department of Molecular and Clinical Cancer Medicine, Institute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool.
H WongThe Clatterbridge Cancer Centre NHS Foundation Trust, Liverpool.
A LawThe Clatterbridge Cancer Centre NHS Foundation Trust, Liverpool.
S MillsThe Walton NHS Foundation Trust, Liverpool, UK.
N SantamariaThe Clatterbridge Cancer Centre NHS Foundation Trust, Liverpool.
J BishopThe Clatterbridge Cancer Centre NHS Foundation Trust, Liverpool.
J CliffThe Clatterbridge Cancer Centre NHS Foundation Trust, Liverpool.
D ErringtonThe Clatterbridge Cancer Centre NHS Foundation Trust, Liverpool.
A HallThe Clatterbridge Cancer Centre NHS Foundation Trust, Liverpool.
C HartThe Clatterbridge Cancer Centre NHS Foundation Trust, Liverpool.
Z MalikThe Clatterbridge Cancer Centre NHS Foundation Trust, Liverpool.
R SripadamThe Clatterbridge Cancer Centre NHS Foundation Trust, Liverpool.
H InnesThe Clatterbridge Cancer Centre NHS Foundation Trust, Liverpool.
H FlintThe Clatterbridge Cancer Centre NHS Foundation Trust, Liverpool.
G LangtonThe Clatterbridge Cancer Centre NHS Foundation Trust, Liverpool.
E AhmedThe Clatterbridge Cancer Centre NHS Foundation Trust, Liverpool.
R JacksonDepartment of Molecular and Clinical Cancer Medicine, Institute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool.
C PalmieriThe Clatterbridge Cancer Centre NHS Foundation Trust, Liverpool; Department of Molecular and Clinical Cancer Medicine, Institute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool. Electronic address: c.palmieri@liverpool.ac.uk.
Clatterbridge Cancer Centre NHS Foundation Trust · GBUniversity of Liverpool · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTrastuzumab deruxtecan (T-DXd) has demonstrated efficacy in patients with brain metastasis (BM), a group historically with poor outcomes. The prevalence of BMs in patients commencing T-DXd is currently unknown. No direct comparisons have been made of the activity of T-DXd in patients with active BM versus those with extracranial progression alone. This real-world study explored the prevalence of BMs in patients commencing T-DXd, the efficacy of T-DXd in active BM versus extracranial progression alone and the safety of T-DXd. PATIENTS AND

methodsPatients with human epidermal growth factor receptor 2-positive advanced breast cancer treated with T-DXd between June 2021 and February 2023 at our specialist cancer hospital were identified and notes reviewed. Clinicopathological information, prior treatment, the presence or absence of central nervous system (CNS) disease, outcomes and treatment-emergent adverse events (TEAEs) were recorded.

resultsTwenty-nine female patients, with a median age of 52 years (interquartile range 44-62 years), were identified; the prevalence of BM was 41%. Median number of lines of prior therapy was 2 (range 2-6). At a median follow-up of 13.8 months, median progression-free survival (PFS) for the overall population was 13.9 months [95% confidence interval (CI) 12.4 months-not estimable (NE)], 16.1 months (95% CI 15.1 months-NE) for active BMs and 12.4 months (95% CI 8.3 months-NE) for progressive extracranial disease alone. The 12-month overall survival (OS) rate was 74% (95% CI 59% to 95%) in the overall population, and 83% (95% CI 58% to 100%) and 66% (95% CI 45% to 96%) for active BMs and extracranial disease only, respectively. Most common TEAEs were fatigue, alopecia, and constipation. In nine patients (31%, including two deaths), pneumonitis occurred.

conclusionIn this real-world population, we demonstrate T-DXd to be effective in patients with active BMs and those with progressive extracranial disease alone. PFS and OS were numerically longer in those with active BMs. These data demonstrate that patients with active BM treated with T-DXd have at least comparable outcomes to those with extracranial disease alone. The high rate of pneumonitis warrants further consideration.

Indexed as

Brain NeoplasmsBreast NeoplasmsPneumoniaAdultCamptothecinFemaleHumansImmunoconjugatesMiddle AgedTrastuzumabCamptothecinImmunoconjugatesTrastuzumabtrastuzumab deruxtecanbrain metastasesbreast cancerHER2trastuzumab deruxtecan

Identifiers

PMID37866031
PMCPMC10774880
OpenAlexW4387835007

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.