Evidence map›Paper›PMID 37492039›Full record

ReviewCureus2023

Consensus Recommendations for the Diagnosis, Biomarker Testing, and Clinical Management of Advanced or Metastatic Non-small Cell Lung Cancer With Mesenchymal-Epithelial Transition Exon 14 Skipping Mutations in the Middle East, Africa, and Russia.

Mervat Mahrous, Abdalla Omar Jebriel, Ahmed Allehebi, Amr Shafik, Fadi El Karak, Filippo Venturini, Hamed Alhusaini, Matthias Meergans, Mehmet Ali Nahit Sendur, Mohamed Ouda and 5 more

Open access · diamondAbstract readReview
In one paragraph

Review in Cureus, 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 29% 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. 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

15 authors at 12 institutions in 9 countries.

Mervat MahrousOncology, Minia University, Minia, EGY.
Abdalla Omar JebrielOncology, School of Medicine, Misurata University, Misurata, LBY.
Ahmed AllehebiOncology, King Faisal Specialist Hospital & Research Center, Jeddah, SAU.
Amr ShafikOncology, Faculty of Medicine, Ain Shams University, Cairo, EGY.
Fadi El KarakOncology, Saint Joseph University of Beirut, School of Medicine, Beirut, LBN.
Filippo VenturiniOncology, Merck Serono S.p.A., Rome, ITA.
Hamed AlhusainiOncology, King Faisal Specialist Hospital & Research Center, Riyadh, SAU.
Matthias MeergansOncology, Merck Serono Middle East FZ-Ltd., Dubai, ARE.
Mehmet Ali Nahit SendurOncology, Ankara Yıldırım Beyazıt University, Faculty of Medicine, Ankara, TUR.
Mohamed OudaOncology, Merck Serono Middle East FZ-Ltd., Dubai, ARE.
Muath Al-NassarOncology, Kuwait Cancer Control Center, Kuwait City, KWT.
Saadettin KilickapMedical Oncology, Istinye University, Faculty of Medicine, Ankara, TUR.
Saeed Al TurkiOncology, Anwa Labs, Riyadh, SAU.
Turki Al-FayeaOncology, King Fahad Medical City - Ministry of National Guard, Jeddah, SAU.
Yasser Abdel KaderOncology, Faculty of Medicine, Cairo University, Cairo, EGY.
Merck Serono (Italy) · ITKing Faisal Specialist Hospital & Research Centre · SAAin Shams University · EGAnkara University · TRCairo University · EGIstinye University · TRKing Saud bin Abdulaziz University for Health Sciences · SAKuwait Cancer Control Center · KWMisurata University · LYRiyadh Armed Forces Hospital · SASaint Joseph University · LBSystems, Applications & Products in Data Processing (United Kingdom) · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mesenchymal-epithelial transition exon 14 (METex14) skipping mutations occur in about 3%-4% of patients with non-small cell lung cancer (NSCLC). This is an aggressive subtype associated with poor prognosis. METex14 skipping is a potentially targetable mutation. Targeted therapy is a promising treatment modality for patients with advanced/metastatic METex14-mutant NSCLC. Performing systematic molecular testing to detect the driver mutation is essential for initiating targeted therapy. However, there is a lack of guidelines on molecular testing for assessing the eligibility of patients for targeted therapy. Therefore, a multidisciplinary panel consisting of experts from the Middle East, Africa, and Russia convened via a virtual advisory board meeting to provide their insights on various molecular testing techniques for the diagnosis of METex14 skipping mutation, management of patients with targeted therapies, and developing consensus recommendations for improving the processes. The expert panel emphasized performing molecular testing and liquid biopsy before treatment initiation and tissue re-biopsy for patients with failed molecular testing. Liquid biopsy was recommended as complementary to tissue biopsy for disease monitoring and prognosis. Selective MET inhibitors were recommended as the first and subsequent lines of therapy. These consensus recommendations will facilitate the management of METex14 skipping NSCLC in routine practice and warrant optimum outcomes for these patients.

Indexed as

chemotherapyimmunotherapyliquid biopsylung cancermet exon 14 skipping mutationmet tyrosine kinase inhibitorsnext-generation sequencingnon-small-cell lung canceroverall survivaltargeted therapy

Identifiers

PMID37492039
PMCPMC10365828
OpenAlexW4384524314

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.