Evidence map›Paper›PMID 41647594›Full record

ArticleESMO gastrointestinal oncology2024

High prevalence of NTRK fusions in sporadic dMMR/MSI mCRC RAS/RAF wild-type: an opportunity for a post-immune checkpoint inhibitors progression rescue strategy.

M Svrcek, A Cayre, T Samaille, R Colle, L Mas, P Bourgoin, E Guillerm, R Cohen, F Penault-Llorca, T André and 1 more

Abstract read
In one paragraph

Article in ESMO gastrointestinal oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Review
  2. Review
  3. Annals of medicine and surgery (2012) · 2026
    Article
  4. Review
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  7. Article
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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.

M SvrcekDepartment of Pathology, Sorbonne University, Saint-Antoine Hospital, AP-HP, Paris.
A CayreDepartment of Genetics, Functional Unit of Onco-Angiogenetics and Genomics of Solid Tumors, AP-HP, Sorbonne University, Pitié Salpêtrière Hospital, Paris.
T SamailleDepartment of Medical Oncology, Sorbonne University, Saint-Antoine Hospital, AP-HP, Paris.
R ColleDepartment of Medical Oncology, Sorbonne University, Saint-Antoine Hospital, AP-HP, Paris.
L MasDepartment of Medical Oncology, Sorbonne University, Saint-Antoine Hospital, AP-HP, Paris.
P BourgoinDepartment of Pathology, Sorbonne University, Saint-Antoine Hospital, AP-HP, Paris.
E GuillermSorbonne University, INSERM UMRS_938, Microsatellite Instability and Cancer, Saint-Antoine Research Center, Paris.
R CohenDepartment of Medical Oncology, Sorbonne University, Saint-Antoine Hospital, AP-HP, Paris.
F Penault-LlorcaDepartment of Pathology, Clermont Auvergne University, INSERM U1240, Centre Jean Perrin, Clermont-Ferrand, France.
T AndréDepartment of Medical Oncology, Sorbonne University, Saint-Antoine Hospital, AP-HP, Paris.
N Radosevic-RobinDepartment of Pathology, Clermont Auvergne University, INSERM U1240, Centre Jean Perrin, Clermont-Ferrand, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Currently, mismatch repair deficient/microsatellite instable (dMMR/MSI) status constitutes a validated predictive marker of response to immune checkpoint inhibitors (ICIs) in patients with metastatic colorectal cancer (mCRC). Unfortunately, some of these patients do not benefit from ICIs. Very limited therapeutic options for patients with dMMR/MSI mCRC after progression on ICI(s) exist. These patients show poor outcomes with conventional chemotherapy. Inhibitors of tropomyosin receptor kinase (TRK) have shown promising activity against neurotrophic tropomyosin receptor kinase ( Materials and methods: A total of 187 dMMR/MSI mCRC patients, including 120 immune ICI-treated, were screened for Results: Tumor samples of 10 (5.3%) patients harbored Conclusions: These results underline the importance of screening for

Indexed as

immune checkpoint inhibitorsmetastatic colorectal cancermismatch repair deficienttropomyosin receptor kinase

Identifiers

PMID41647594
PMCPMC12836570

What Socratic 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 Socratic graph.