Evidence map›Paper›PMID 41373672›Full record

ReviewInternational journal of molecular sciences2025

Advances in Targeted Therapy for Non-Small-Cell Lung Cancer: Current Progress and Future Directions.

Supriya Peshin, Ehab Takrori, Joseph H Yazji, Johum Haque, Adit Dharia, Mohammad Sajid Mithani, Fnu Anum, Ummul Asfeen, Jill Kristen Couch, Mabe Donovan and 1 more

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Biomimetic Scaffold-Based 3D Models for Decoding Cancer Biology and Advancing Therapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
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  6. Pharmacogenomics in oncology: mutation-targeted therapy and biomarker integration in non-small cell lung cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
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  8. 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.

Supriya PeshinDepartment of Internal Medicine, Norton Community Hospital, Norton, VA 24273, USA.ORCID 0000-0002-3895-9474
Ehab TakroriCollege of Medicine, Alfaisal University, Riyadh 11533, Saudi Arabia.ORCID 0009-0009-9062-9761
Joseph H YazjiHCA Florida Oak Hill Hospital, Brooksville, FL 34613, USA.
Johum HaqueDepartment of Internal Medicine, Norton Community Hospital, Norton, VA 24273, USA.
Adit DhariaHCA Florida Oak Hill Hospital, Brooksville, FL 34613, USA.
Mohammad Sajid MithaniCollege of Medicine, Alfaisal University, Riyadh 11533, Saudi Arabia.
Fnu AnumDepartment of Internal Medicine, Norton Community Hospital, Norton, VA 24273, USA.
Ummul AsfeenMD Anderson Cancer Center, 1515 Holcombe Blvd, Houston, TX 77030, USA.
Jill Kristen CouchDepartment of Internal Medicine, Norton Community Hospital, Norton, VA 24273, USA.
Mabe DonovanDepartment of Pulmonary Critical Care, Norton Community Hospital, Norton, VA 24273, USA.
Sakshi SingalDepartment of Hematology and Oncology, East Tennessee State University, Johnson City, TN 37614, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The advent of targeted therapies has significantly transformed the management of non-small-cell lung cancer (NSCLC), improving survival across all disease stages. Discoveries of both common and rare oncogenic drivers are advancing rapidly, posing a challenge for clinicians and researchers to remain up to date in this dynamic field. This review highlights the evolving landscape of therapeutic strategies for actionable mutations in lung cancer, with particular attention given to the latest developments in KRAS-targeted treatments including non-G12C mutations, pan-RAS inhibitors, and agents targeting RAS-GTP. We also examine the existing standards of care for NSCLC harboring EGFR and ALK alterations, as well as emerging therapies poised for clinical use. Additional discussion includes advancements in therapies directed at MET, HER2, RET, ROS1, and FGFR alterations-each representing promising targets in NSCLC. This review concludes by exploring the growing evidence surrounding TROP-2 as a novel therapeutic target, especially relevant in cases where previous targeted treatments have failed.

Indexed as

Antineoplastic AgentsCarcinoma, Non-Small-Cell LungLung NeoplasmsMolecular Targeted TherapyErbB ReceptorsHumansMutationProtein Kinase InhibitorsProto-Oncogene Proteins p21(ras)Antineoplastic AgentsErbB ReceptorsProtein Kinase InhibitorsProto-Oncogene Proteins p21(ras)ALKBRAF V600EEGFRHER2KRASMETnon-small cell lung cancerNSCLCNTRKRETtargeted therapiesTROP-2

Identifiers

PMID41373672
PMCPMC12692500

What OpenQuestion holds

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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.