Evidence map›Paper›PMID 41675805›Full record

ArticleAnnals of medicine and surgery (2012)2026

Taletrectinib as an emerging therapy for ROS1-positive non-small cell lung cancer: findings from TRUST phase 2 trials.

Hassan Khalid, Hafiz Muhammad Haris, Suleman Arshad, Taha Yahya, Fajar Nadeem, Yahya Samadi

Abstract readLetter
In one paragraph

Article in Annals of medicine and surgery (2012), 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

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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

6 authors.

Hassan KhalidShaikh Khalifa Bin Zayed Al-Nahyan Medical and Dental College, Lahore, Pakistan.
Hafiz Muhammad HarisKing Edward Medical University, Lahore, Pakistan.ORCID https://orcid.org/0009-0001-5574-0810
Suleman ArshadShaikh Khalifa Bin Zayed Al-Nahyan Medical and Dental College, Lahore, Pakistan.
Taha YahyaShaikh Khalifa Bin Zayed Al-Nahyan Medical and Dental College, Lahore, Pakistan.
Fajar NadeemRashid Latif Medical College, Lahore, Pakistan.
Yahya SamadiDepartment of Curative Medicine, Faculty of Medicine, Kateb University, Kabul, Afghanistan.ORCID https://orcid.org/0009-0005-4872-5603

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Non-small cell lung cancer (NSCLC) that is ROS1-positive is a rare but important molecular subtype of lung cancer that predominantly affects younger patients and non-smokers. This form of cancer presents a distinctive opportunity for targeted therapy, as it is driven by specific gene fusions. Nevertheless, the current treatments, although initially effective, frequently fail to meet expectations because of the emergence of resistance and the limited control over the spread of the disease to the brain. These challenges have been addressed by the development of taletrectinib, an advanced tyrosine kinase inhibitor. It has the potential to address mutations that render previous treatments less effective by precisely acting on both ROS1 and NTRK-driven pathways. According to preliminary clinical research, taletrectinib not only demonstrates significant effectiveness in resistant situations but also possesses characteristics that could improve protection against brain metastases. In ROS1-positive NSCLC patients, taletrectinib has been effective and well tolerated, as evidenced by early clinical trials, including those that are resistant to crizotinib. It demonstrates potential for disease control, as it has excellent oral absorption and is able to combat the spread of neurological disorders. Taletrectinib is emerging as a promising candidate for enhancing the outcomes of patients with ROS1-positive lung cancer as the treatment landscape for this disease continues to evolve.

Indexed as

brain metastasescentral nervous system penetrationG2032R mutationlung adenocarcinomanext-gen tyrosine kinase inhibitionNTRK fusiononcogenic fusion proteinsROS1-altered non-small cell lung cancertaletrectinib

Identifiers

PMID41675805
PMCPMC12889246

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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.