Evidence map›Paper›PMID 38764581›Full record

ArticleFrontiers in oncology2024

Dynamic changes in tumor profiling reveal intra- and inter-tumoral heterogeneity focused on an uncharacterized HER2 mutation: a case report of a young breast cancer patient.

Dörthe Schaffrin-Nabe, Anke Josten-Nabe, Andrea Tannapfel, Waldemar Uhl, Marietta Garmer, Razelle Kurzrock, Timothy Crook, Sewanti Limaye, Stefan Schuster, Darshana Patil and 3 more

Abstract readCase Reports
In one paragraph

Article in Frontiers in oncology, 2024. 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. Review
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

13 authors.

Dörthe Schaffrin-NabePraxis für Hämatologie und Onkologie, Bochum, Germany.
Anke Josten-NabePraxis für Hämatologie und Onkologie, Bochum, Germany.
Andrea TannapfelPathologie Ruhr-Universität Bochum, Bochum, Germany.
Waldemar UhlAllgemein- und Viszeralchirurgie, St. Josef-Hospital, Bochum, Germany.
Marietta GarmerGarmer Radiologie, Bochum, Germany.
Razelle KurzrockMedical College of Winconsin (MCW) Cancer Center, Froedtert Hospital & Medical College of Wisconsin, Milwaukee, WI, United States.
Timothy CrookOncology Department, Cromwell Hospital, London, United Kingdom.
Sewanti LimayeMedical Oncology, Sir H.N. Reliance Foundation Hospital, Mumbai, India.
Stefan SchusterDatar Cancer Genetics Europe GmbH, Bayreuth, Germany.
Darshana PatilDatar Cancer Genetics, Bayreuth, India.
Merle SchaffrinPraxis für Hämatologie und Onkologie, Bochum, Germany.
Kefah MokbelLondon Breast Institute, Princess Grace Hospital, HCA Healthcare, London, United Kingdom.
Rudolf VoigtmannPraxis für Hämatologie und Onkologie, Bochum, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite multiple recent advances in systemic therapy for metastatic breast cancer, cases which display suboptimal response to guideline-driven treatment are frequently seen in the clinic. Effective options for such patients are limited, particularly in later line of therapy, and selection of optimal treatment options is essentially empirical and based largely on considerations of previous regimens received. Comprehensive cancer profiling includes detection of genetic alterations in tissue and circulating tumor DNA (ctDNA), immunohistochemistry (IHC) from re-biopsied metastatic disease, circulating tumor cells (CTCs), gene expression analysis and pharmacogenomics. The advent of this methodology and application to metastatic breast cancer, facilitates a more scientifically informed approach to identification of optimal systemic therapy approaches independent of the restrictions implied by clinical guidelines. Here we describe a case of metastatic breast cancer where consecutive comprehensive tumor profiling reveals ongoing tumor evolution, guiding the identification of novel effective therapeutic strategies.

Indexed as

extensive tumor profilingmetastatic breast cancerpersonalized therapyprecision oncologytreatment strategies

Identifiers

PMID38764581
PMCPMC11099277

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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.