Evidence map›Paper›PMID 32912860›Full record

ArticleESMO open2020

Induction of natural killer antibody-dependent cell cytotoxicity and of clinical activity of cetuximab plus avelumab in non-small cell lung cancer.

Morena Fasano, Carminia Maria Della Corte, Raimondo Di Liello, Giusi Barra, Francesca Sparano, Giuseppe Viscardi, Maria Lucia Iacovino, Fernando Paragliola, Vincenzo Famiglietti, Vincenza Ciaramella and 8 more

Open access · goldAbstract read
In one paragraph

Article in ESMO open, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.5field-weighted citation impact, top 9% 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

27 citing papers in PubMed, 46 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Review
  12. Identification of a novel ADCC-related gene signature for predicting the prognosis and therapy response in lung adenocarcinoma.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2024
    Article
  13. Article
  14. Article
  15. Article
  16. Immunotherapy in Anal Cancer.Current oncology (Toronto, Ont.) · 2023
    Review
  17. Article
  18. Mass Cytometry Reveals Classical Monocytes, NK Cells, and ICOS+ CD4+ T Cells Associated with Pembrolizumab Efficacy in Patients with Lung Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2022
    Article
  19. Article
  20. 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

18 authors at 4 institutions in 1 country.

Morena FasanoDepartment of Precision Medicine, University of Campania 'Luigi Vanvitelli', Napoli, Campania, Italy.
Carminia Maria Della CorteDepartment of Precision Medicine, University of Campania 'Luigi Vanvitelli', Napoli, Campania, Italy.
Raimondo Di LielloDepartment of Precision Medicine, University of Campania 'Luigi Vanvitelli', Napoli, Campania, Italy.
Giusi BarraDepartment of Precision Medicine, University of Campania 'Luigi Vanvitelli', Napoli, Campania, Italy.
Francesca SparanoDepartment of Precision Medicine, University of Campania 'Luigi Vanvitelli', Napoli, Campania, Italy.
Giuseppe ViscardiDepartment of Precision Medicine, University of Campania 'Luigi Vanvitelli', Napoli, Campania, Italy.
Maria Lucia IacovinoDepartment of Precision Medicine, University of Campania 'Luigi Vanvitelli', Napoli, Campania, Italy.
Fernando ParagliolaDepartment of Precision Medicine, University of Campania 'Luigi Vanvitelli', Napoli, Campania, Italy.
Vincenzo FamigliettiDepartment of Precision Medicine, University of Campania 'Luigi Vanvitelli', Napoli, Campania, Italy.
Vincenza CiaramellaDepartment of Precision Medicine, University of Campania 'Luigi Vanvitelli', Napoli, Campania, Italy.
Flora CimminoDepartment of Molecular Medicine and Biotechnologies, CEINGE Advanced Biotechnologies, Napoli, Campania, Italy.
Mario CapassoDepartment of Molecular Medicine and Biotechnologies, CEINGE Advanced Biotechnologies, Napoli, Campania, Italy.
Achille IolasconDepartment of Molecular Medicine and Biotechnologies, CEINGE Advanced Biotechnologies, Napoli, Campania, Italy.
Vincenzo SforzaDepartment of Thoracic Oncology, Istituto Nazionale Tumori IRCCS Fondazione Pascale, Napoli, Italy.
Alessandro MorabitoDepartment of Thoracic Oncology, Istituto Nazionale Tumori IRCCS Fondazione Pascale, Napoli, Italy.
Evaristo MaielloMedical Oncology and Immunotherapy Division, Istituto Toscano Tumori, Ospedale Casa Sollievo della Sofferenza, San Giovanni Rotondo, Italy.
Fortunato CiardielloDepartment of Precision Medicine, University of Campania 'Luigi Vanvitelli', Napoli, Campania, Italy.
Floriana MorgilloDepartment of Precision Medicine, University of Campania 'Luigi Vanvitelli', Napoli, Campania, Italy. Electronic address: floriana.morgillo@unicampania.it.
University of Campania "Luigi Vanvitelli" · ITCeinge Biotecnologie Avanzate (Italy) · ITIstituto Nazionale Tumori IRCCS "Fondazione G. Pascale" · ITCasa Sollievo della Sofferenza · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAntibody-dependent cell-mediated cytotoxicity (ADCC) may mediate antitumour activity of IgG1-isotype monoclonal antibody (mAb), suggesting as potential treatment combination of IgG1-mAbs, anti-epidermal growth factor receptor cetuximab and anti-programmed death-ligand-1 avelumab.

methodsWe evaluated ADCC induction in lung cancer cells by lactate dehydrogenase (LDH) release assay. Antitumour activity and safety of cetuximab plus avelumab were explored in a single-arm proof-of-concept study in pre-treated non-small cell lung cancer (NSCLC) patients (pt) (Cetuximab-AVElumab-lung, CAVE-Lung). Search for predictive biomarkers of response was done.

resultsAvelumab plus cetuximab induced ADCC in NSCLC cells in vitro in presence of natural killers (NK) from healthy donors (HD) or NSCLC pt, as effectors. Sixteen relapsed NSCLC pt were treated with avelumab plus cetuximab. Antitumour activity was observed in 6/16 pt, defined by progression free survival (PFS) ≥8 months, with 4 of them still on treatment at data lock time (range, 14-19 months). Of note, 3/6 responders had received as previous line anti-programmed death-1 therapy. In responders, clinical benefit was accompanied by significant increase in LDH release over baseline at the first radiological evaluation (8 weeks) (p=0.01) and by early skin toxicity; while in the 10 non-responders, that had PFS ≤5 months, LDH release tends to reduce. Baseline circulating DNA levels were higher in non-responders compared with responders and HD (p=0.026) and decrease in responders during therapy. Mutations in DNA damage responsive family genes were found in responders.

conclusionCetuximab and avelumab activates NSCLC pt NK cells. Ex vivo evaluation of ADCC, circulating DNA levels and early skin toxicity may predict response to cetuximab plus avelumab in NSCLC.EUDRACT 2017-004195-58.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsAntibodies, Monoclonal, HumanizedAntibody-Dependent Cell CytotoxicityCell Line, TumorCetuximabHumansImmunoglobulin GKiller Cells, NaturalAntibodies, Monoclonal, HumanizedavelumabCetuximabImmunoglobulin GADCCavelumabcetuximabNK cellsNSCLC

Identifiers

PMID32912860
PMCPMC7484864
OpenAlexW3085126468

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.