Evidence map›Paper›PMID 42836958›Full record

ReviewInnere Medizin (Heidelberg, Germany)2026

[Personalized drug therapy of metastatic lung cancer].

Sofia Stilianakis, Lea Ruge, Heather Scharpenseel, Malte Verheyen, Jürgen Wolf

Abstract readEnglish AbstractReview
PubMed Publisher
In one paragraph

Review in Innere Medizin (Heidelberg, Germany), 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

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

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

5 authors.

Sofia StilianakisFaculty of Medicine and University Hospital Cologne, Department I of Internal Medicine, Center for Integrated Oncology Aachen Bonn Cologne Duesseldorf, Lung Cancer Group Cologne (LCGC), University of Cologne, Kerpener Str. 62, 50937, Köln, Deutschland.
Lea RugeFaculty of Medicine and University Hospital Cologne, Department I of Internal Medicine, Center for Integrated Oncology Aachen Bonn Cologne Duesseldorf, Lung Cancer Group Cologne (LCGC), University of Cologne, Kerpener Str. 62, 50937, Köln, Deutschland.
Heather ScharpenseelFaculty of Medicine and University Hospital Cologne, Department I of Internal Medicine, Center for Integrated Oncology Aachen Bonn Cologne Duesseldorf, Lung Cancer Group Cologne (LCGC), University of Cologne, Kerpener Str. 62, 50937, Köln, Deutschland.
Malte VerheyenFaculty of Medicine and University Hospital Cologne, Department I of Internal Medicine, Center for Integrated Oncology Aachen Bonn Cologne Duesseldorf, Lung Cancer Group Cologne (LCGC), University of Cologne, Kerpener Str. 62, 50937, Köln, Deutschland.
Jürgen WolfFaculty of Medicine and University Hospital Cologne, Department I of Internal Medicine, Center for Integrated Oncology Aachen Bonn Cologne Duesseldorf, Lung Cancer Group Cologne (LCGC), University of Cologne, Kerpener Str. 62, 50937, Köln, Deutschland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In precision oncology, therapies are tailored to the tumor's individual molecular and immunological characteristics in order to maximize efficacy while minimizing side effects. This approach has recently led to a significant expansion of treatment options, particularly for non-small cell lung cancer (NSCLC). Traditionally, this refers to receptor inhibitors-mostly tyrosine kinase inhibitors-that inhibit receptors on the cell surface activated by oncogenic alterations (e.g., mutations, fusions). More recent approaches also include bispecific antibodies, antibody-drug conjugates (ADCs), and, in a broader sense, the selection of immunotherapies for specific molecular subgroups. Comprehensive immunohistochemical and molecular diagnostics are therefore crucial for selecting the optimal and personalized treatment strategy-both at initial diagnosis and following disease progression. Furthermore, new prospects are currently emerging in the treatment of small cell lung cancer (SCLC) through the development of bispecific T‑cell engagers. This article aims to provide an overview of the latest targeted treatment options for lung cancer, with a particular focus on NSCLC.

Indexed as

Lung cancer/driver mutationsLung cancer/resistance mechanismsMolecular targeted therapyNon-small cell lung cancerTyrosine kinase inhibitors

Identifiers

What Socratic holds

Textmetadata
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 Socratic graph.