ReviewInnere Medizin (Heidelberg, Germany)2026
[Personalized drug therapy of metastatic lung cancer].
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.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
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
Identifiers
42836958What Socratic holds
Registered trials
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.