Evidence map›Paper›PMID 30968324›Full record

ReviewCellular oncology (Dordrecht, Netherlands)2019

Notch pathway in small-cell lung cancer: from preclinical evidence to therapeutic challenges.

Alessandro Leonetti, Francesco Facchinetti, Roberta Minari, Alessio Cortellini, Christian D Rolfo, Elisa Giovannetti, Marcello Tiseo

Open access · greenAbstract readReview
In one paragraph

Review in Cellular oncology (Dordrecht, Netherlands), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
3.9field-weighted citation impact, top 5% of its field
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

48 citing papers in PubMed, 75 citations in OpenAlex.

  1. Review
  2. Article
  3. [Chinese Expert Consensus on Delta-like Ligand 3-T Cell Engager Therapy 
for SCLC].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2026
    Review
  4. Article
  5. Article
  6. Overexpression ofTranslational lung cancer research · 2025
    Article
  7. Review
  8. Review
  9. Decoding the NRF2-NOTCH Crosstalk in Lung Cancer-An Update.Antioxidants (Basel, Switzerland) · 2025
    Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. DLL3-targeted immunoPET and radioimmunotherapy ligands.American journal of nuclear medicine and molecular imaging · 2025
    Article
  16. Review
  17. Review
  18. Review
  19. Review
  20. Effects ofCancers · 2024
    Article
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

7 authors at 4 institutions in 4 countries.

Alessandro LeonettiMedical Oncology Unit, University Hospital of Parma, 43126, Parma, Italy. alessandroleonetti@hotmail.com.ORCID http://orcid.org/0000-0001-5415-6703
Francesco FacchinettiMedical Oncology Unit, University Hospital of Parma, 43126, Parma, Italy.
Roberta MinariMedical Oncology Unit, University Hospital of Parma, 43126, Parma, Italy.
Alessio CortelliniMedical Oncology, St. Salvatore Hospital, Department of Biotechnological and Applied Clinical Sciences, University of L'Aquila, 67100, L'Aquila, Italy.
Christian D RolfoUniversity of Maryland Greenebaum Comprehensive Cancer Center, Baltimore, MD, 21220, USA.
Elisa GiovannettiDepartment of Medical Oncology, VU University Medical Center, Amsterdam, 1081, HV, The Netherlands.
Marcello TiseoMedical Oncology Unit, University Hospital of Parma, 43126, Parma, Italy.
University of Parma · ITUniversity of L'Aquila · ITUniversity of Maryland, Baltimore · USUniversity of Pisa · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSmall-cell lung cancer (SCLC) is an aggressive disease with still limited therapeutic options. Despite being both a chemo- and radiation-sensitive malignancy, SCLC recurrence occurs in most cases and negatively impacts patients' prognosis. Over the last few years, a deeper understanding of SCLC molecular aberrations has led to the identification of Notch pathway deregulation as a crucial event in SCLC tumorigenesis, disease progression and chemoresistance. In particular, the delta-like protein 3 (DLL3), a Notch inhibitory ligand whose expression is directly related to the key neuroendocrine transcription factor ASCL1, was found to be expressed in ~85% of SCLCs, while it exhibits minimal to absent surface expression in normal lungs. DLL3 thus represents an appealing novel biomarker as well as a potential target in SCLC.

conclusionsThe first DLL3-targeted antibody-drug conjugate rovalpituzumab tesirine (Rova-T, SC16LD6.5) has shown promising results in terms of efficacy and safety for the management of extensive SCLC, supporting further studies on this novel therapeutic approach that combines specific SCLC targeting with the cell-killing ability of a pyrrolobenzodiazepine dimer. In the present review, we discuss currently available evidence on the biological role of Notch signaling in SCLC from early preclinical findings to current and future clinical implications.

Indexed as

Antibodies, Monoclonal, HumanizedBenzodiazepinonesHumansImmunoconjugatesIntracellular Signaling Peptides and ProteinsLungLung NeoplasmsMembrane ProteinsPrognosisReceptors, NotchSignal TransductionSmall Cell Lung CarcinomaAntibodies, Monoclonal, HumanizedBenzodiazepinonesDLL3 protein, humanImmunoconjugatesIntracellular Signaling Peptides and ProteinsMembrane ProteinsReceptors, Notchrovalpituzumab tesirineDLL3Notch pathwayRovalpituzumab tesirineSmall cell lung cancer (SCLC)

Identifiers

PMID30968324
PMCPMC12994342
OpenAlexW2937415626

What OpenQuestion 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 OpenQuestion graph.