Evidence map›Paper›PMID 41959903›Full record

ReviewFrontiers in oncology2026

Evolving treatment strategies for HER2-altered non-small-cell lung cancer: the rise of TKIs and ADCs.

Sevinc Balli, Tugba Basoglu, Mustafa Ozdogan

Abstract readReview
In one paragraph

Review in Frontiers in oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

3 authors.

Sevinc BalliDepartment of Medical Oncology, Samsun City Hospital, Samsun, Türkiye.
Tugba BasogluDepartment of Medical Oncology, Memorial Göztepe Cancer Center, Istanbul, Türkiye.
Mustafa OzdoganDepartment of Medical Oncology, Memorial Göztepe Cancer Center, Istanbul, Türkiye.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human epidermal growth factor receptor 2 (HER2) is an actionable oncogenic driver in a small subset of non-small cell lung cancer (NSCLC), occurring as gene mutations and less frequently as gene amplification or protein overexpression. Until recently, HER2-driven NSCLC lacked effective targeted treatments, and patients were managed with conventional chemotherapy and immunotherapy. However, the therapeutic landscape has rapidly evolved with the advent of novel HER2-directed antibody-drug conjugates (ADCs) and tyrosine kinase inhibitors (TKIs). Following the 2022 approval of the antibody-drug conjugate fam-trastuzumab deruxtecan (T-DXd), the therapeutic landscape of HER2-mutant NSCLC further expanded in 2025 with the regulatory approval of two highly selective oral HER2 tyrosine kinase inhibitors, zongertinib and sevabertinib. This review provides a comprehensive update on these emerging HER2-targeted therapies, including their clinical trial data, mechanisms of action, and comparative benefits over older pan-HER agents. We discuss the emerging therapeutic scope in HER2-"low" NSCLC, challenges with immunotherapy in HER2-driven tumors, and known resistance mechanisms to TKIs and ADCs. An evidence-based treatment algorithm is proposed, integrating new agents into current practice and addressing special considerations such as central nervous system (CNS) metastases. We also outline ongoing trials that may further shift first-line standards. In summary, recent breakthroughs in HER2-targeted TKIs and ADCs are transforming outcomes in this rare NSCLC subset, though optimizing sequencing, managing resistance, and improving patient selection through biomarker development remain priorities for future research.

Indexed as

antibody–drug conjugatebrain metastasesHER2-mutant NSCLCresistance mechanismstargeted therapytyrosine kinase inhibitor

Identifiers

PMID41959903
PMCPMC13056646

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.