Evidence map›Paper›PMID 41090369›Full record

ArticleCancer discovery2026

Sevabertinib, a Reversible HER2 Inhibitor with Activity in Lung Cancer.

Franziska Siegel, Stephan Siegel, Kristýna Kotýnková, Gizem Karsli Uzunbas, Daniel Korr, Haruna Tomono, Sawyer Andersen, Daniel Denney, Markus Berger, Volker K Schulze and 16 more

Abstract read
In one paragraph

Article in Cancer discovery, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Review
  2. Review
  3. Small-Molecule Drugs Approved by the FDA in 2025.Molecules (Basel, Switzerland) · 2026
    Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. HER2 Therapies in Non-Small Cell Lung Cancer (NSCLC).International journal of molecular sciences · 2026
    Review
  9. Review
  10. Article
  11. Review
  12. International journal of molecular sciences · 2026
    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

26 authors.

Franziska SiegelBayer AG, Pharmaceuticals, Research & Early Development Oncology, Berlin, Germany.ORCID 0009-0002-8685-2142
Stephan SiegelBayer AG, Pharmaceuticals, Research & Early Development Oncology, Berlin, Germany.ORCID 0000-0002-4913-1146
Kristýna KotýnkováCancer Program, Broad Institute of MIT and Harvard, Cambridge, Massachusetts.ORCID 0000-0003-2066-9505
Gizem Karsli UzunbasCancer Program, Broad Institute of MIT and Harvard, Cambridge, Massachusetts.ORCID 0009-0007-5868-2592
Daniel KorrNuvisan ICB GmbH, Berlin, Germany.ORCID 0000-0002-6250-6344
Haruna TomonoCancer Program, Broad Institute of MIT and Harvard, Cambridge, Massachusetts.ORCID 0009-0007-2371-8647
Sawyer AndersenCancer Program, Broad Institute of MIT and Harvard, Cambridge, Massachusetts.ORCID 0009-0009-1828-4818
Daniel DenneyCancer Program, Broad Institute of MIT and Harvard, Cambridge, Massachusetts.ORCID 0009-0000-0565-5426
Markus BergerBayer AG, Pharmaceuticals, Research & Early Development Oncology, Berlin, Germany.ORCID 0000-0001-6676-6090
Volker K SchulzeBayer AG, Pharmaceuticals, Research & Early Development Oncology, Berlin, Germany.ORCID 0000-0002-0158-1789
Timothy A LewisCenter for the Development of Therapeutics, Broad Institute of MIT and Harvard, Cambridge, Massachusetts.ORCID 0000-0001-9748-9575
Bethany KaplanCancer Program, Broad Institute of MIT and Harvard, Cambridge, Massachusetts.ORCID 0009-0002-8503-7533
Sven GolfierNuvisan ICB GmbH, Berlin, Germany.ORCID 0009-0005-6506-8182
Jérémie MortierBayer AG, Pharmaceuticals, Research & Early Development Oncology, Berlin, Germany.ORCID 0000-0001-8707-3867
Roman C HilligNuvisan ICB GmbH, Berlin, Germany.ORCID 0000-0001-6267-7250
Ulf BoemerNuvisan ICB GmbH, Berlin, Germany.ORCID 0009-0004-7147-039X
Kirstin PetersenBayer AG, Pharmaceuticals, Research & Early Development Oncology, Berlin, Germany.ORCID 0000-0002-4655-2914
Knut EisBayer AG, Pharmaceuticals, Research & Early Development Oncology, Berlin, Germany.ORCID 0000-0003-2881-8798
Sybil WilliamsBayer HealthCare Pharmaceuticals Inc., Research & Early Development Oncology, Cambridge, Massachusetts.ORCID 0009-0009-5779-3391
Dominik RüttingerBayer AG, Pharmaceuticals, Research & Early Development Oncology, Berlin, Germany.ORCID 0000-0003-4846-3955
Andrew D CherniackCancer Program, Broad Institute of MIT and Harvard, Cambridge, Massachusetts.ORCID 0000-0003-0470-0111
Herbert H LoongThe Chinese University of Hong Kong, Hong Kong SAR, China.ORCID 0000-0002-6607-1106
Koichi GotoNational Cancer Center Hospital East, Kashiwa, Japan.ORCID 0000-0002-3023-2510
Paolo GrassiBayer S.p.A., Milan, Italy.ORCID 0000-0002-5691-2768
Matthew MeyersonCancer Program, Broad Institute of MIT and Harvard, Cambridge, Massachusetts.ORCID 0000-0002-9133-8108
Heidi GreulichCancer Program, Broad Institute of MIT and Harvard, Cambridge, Massachusetts.ORCID 0000-0001-5571-9862

Funding

Inhibitor-sensitive and -resistant EGFR mutants from lung cancer and glioblastomaR01CA116020 · NCI · DANA-FARBER CANCER INST · PI ECK, MICHAEL J, MEYERSON, MATTHEW L. · 2006 to 2022
$5.1M
National Cancer Institute (NCI) R01CA116020NCI NIH HHS R01 CA116020
6 · The paper itself

Abstract

Exon 20 insertions of HER2, encoded by erb-b2 receptor tyrosine kinase 2 (ERBB2), and other activating HER2 mutations occur in 2% to 4% of lung adenocarcinomas, but there are only limited therapeutic options available for these patients. Sevabertinib (BAY 2927088) is a potent and reversible dual EGFR-HER2 inhibitor that is selective with respect to wild-type EGFR. In this study, we report the preclinical activity of sevabertinib in lung cancer models harboring alterations of HER2, including exon 20 insertions, point mutations, and amplification of wild-type ERBB2. We furthermore demonstrate the activity of sevabertinib in a cancer cell line dependent on a fusion of neuregulin-1, a ligand for the HER2 family member and heterodimerization partner, HER3. Finally, we report patient responses to sevabertinib from a phase 1/2 clinical trial, indicating potential benefit for patients with HER2-mutant lung cancer. SIGNIFICANCE: Additional therapeutic options are needed for patients with lung cancer with HER2 activating mutations, including exon 20 insertions. Sevabertinib shows activity against ERBB2-encoded HER2 exon 20 insertions in preclinical models of lung cancer, corroborated by early data from a phase 1/2 clinical trial.

Indexed as

Antineoplastic AgentsErb-b2 Receptor Tyrosine KinasesLung NeoplasmsProtein Kinase InhibitorsAnimalsCell Line, TumorFemaleHumansMiceXenograft Model Antitumor AssaysAntineoplastic AgentsERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesProtein Kinase Inhibitors

Identifiers

PMID41090369
PMCPMC12793832

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.