Evidence map›Paper›PMID 31138260›Full record

ArticleJournal of experimental & clinical cancer research : CR2019

Third generation EGFR inhibitor osimertinib combined with pemetrexed or cisplatin exerts long-lasting anti-tumor effect in EGFR-mutated pre-clinical models of NSCLC.

Silvia La Monica, Roberta Minari, Daniele Cretella, Lisa Flammini, Claudia Fumarola, Mara Bonelli, Andrea Cavazzoni, Graziana Digiacomo, Maricla Galetti, Denise Madeddu and 9 more

Abstract read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
–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

34 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Review
  4. Targeted therapy for stage IA non-small cell lung cancer withTranslational lung cancer research · 2026
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. EGFR-TKIs Induced DPP4 Drives Metabolic Reprogramming of Persister Cells in Lung Cancer.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. IL6 Mediates Suppression of T- and NK-cell Function in EMT-associated TKI-resistant EGFR-mutant NSCLC.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
    Article
  18. Article
  19. Review
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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

19 authors.

Silvia La MonicaDepartment of Medicine and Surgery, University of Parma, Parma, Italy.
Roberta MinariMedical Oncology Unit, University Hospital of Parma, Parma, Italy.
Daniele CretellaDepartment of Medicine and Surgery, University of Parma, Parma, Italy.
Lisa FlamminiFood and Drug Department, University of Parma, Parma, Italy.
Claudia FumarolaDepartment of Medicine and Surgery, University of Parma, Parma, Italy.
Mara BonelliDepartment of Medicine and Surgery, University of Parma, Parma, Italy.
Andrea CavazzoniDepartment of Medicine and Surgery, University of Parma, Parma, Italy.
Graziana DigiacomoDepartment of Medicine and Surgery, University of Parma, Parma, Italy.
Maricla GalettiItalian Workers' Compensation Authority (INAIL) Research Center, Parma, Italy.
Denise MadedduDepartment of Medicine and Surgery, University of Parma, Parma, Italy.
Angela FalcoDepartment of Medicine and Surgery, University of Parma, Parma, Italy.
Costanza Annamaria LagrastaDepartment of Medicine and Surgery, University of Parma, Parma, Italy.
Anna SquadrilliMedical Oncology Unit, University Hospital of Parma, Parma, Italy.
Elisabetta BarocelliFood and Drug Department, University of Parma, Parma, Italy.
Alessandro RomanelCentre for Integrative Biology (CIBIO), University of Trento, Trento, Italy.
Federico QuainiDepartment of Medicine and Surgery, University of Parma, Parma, Italy.
Pier Giorgio PetroniniDepartment of Medicine and Surgery, University of Parma, Parma, Italy.
Marcello TiseoDepartment of Medicine and Surgery, University of Parma, Parma, Italy. marcello.tiseo@unipr.it.
Roberta AlfieriDepartment of Medicine and Surgery, University of Parma, Parma, Italy. roberta.alfieri@unipr.it.ORCID http://orcid.org/0000-0003-0601-7244

Funding

Associazione Italiana Ricerca sul Cancro IG2017-20074
6 · The paper itself

Abstract

backgroundThe third generation Epidermal Growth Factor Receptor (EGFR) Tyrosine Kinase Inhibitor (TKI) osimertinib has been initially approved for T790M positive Non-Small Cell Lung Cancer (NSCLC) and more recently for first-line treatment of EGFR-mutant T790M negative NSCLC patients. Similarly to previous generation TKIs, despite the high response rate, disease progression eventually occurs and current clinical research is focused on novel strategies to delay the emergence of osimertinib resistance. In this study we investigated the combination of osimertinib with pemetrexed or cisplatin in EGFR-mutated NSCLC cell lines and xenografts.

methodsTumor growth was evaluated in a PC9T790M xenograft model and tissue composition was morphometrically determined. PC9, PC9T790M and HCC827 cell lines were employed to test the efficacy of osimertinib and chemotherapy combination in vitro. Cell viability and cell death were evaluated by MTT assay and fluorescence microscopy. Protein expression and gene status were analysed by Western blotting, fluorescence in situ hybridization analysis, next-generation sequencing and digital droplet PCR.

resultsIn xenograft models, osimertinib significantly inhibited tumor growth, however, as expected, in 50% of mice drug-resistance developed. A combination of osimertinib with pemetrexed or cisplatin prevented or at least delayed the onset of resistance. Interestingly, such combinations increased the fraction of fibrotic tissue and exerted a long-lasting activity after stopping therapy. In vitro studies demonstrated the stronger efficacy of the combination over the single treatments in inhibiting cell proliferation and inducing cell death in PC9T790M cells as well as in T790M negative PC9 and HCC827 cell lines, suggesting the potential role of this strategy also as first-line treatment. Finally, we demonstrated that osimertinib resistant clones, either derived from resistant tumors or generated in vitro, were less sensitive to pemetrexed prompting to use a chemotherapy regimen non-containing pemetrexed in patients after progression to osimertinib treatment.

conclusionsOur results identify a combination between osimertinib and pemetrexed or cisplatin potentially useful in the treatment of EGFR-mutated NSCLC patients, which might delay the appearance of osimertinib resistance with long-lasting effects.

Indexed as

AcrylamidesAniline CompoundsAnimalsCarcinoma, Non-Small-Cell LungCell Line, TumorCell ProliferationCell SurvivalCisplatinDrug Resistance, NeoplasmDrug SynergismErbB ReceptorsFemaleGene Expression Regulation, NeoplasticHumansIndolesLung NeoplasmsAcrylamidesAniline CompoundsCisplatinEGFR protein, humanErbB ReceptorsIndolesosimertinibPemetrexedPyrimidinesCisplatinEpidermal Growth Factor ReceptorNon-Small Cell Lung CancerOsimertinibPemetrexedResistance

Identifiers

PMID31138260
PMCPMC6537372

What OpenQuestion holds

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Registered trials

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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.