Evidence map›Paper›PMID 33542076›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2021

Optimized EGFR Blockade Strategies in

Simona Corso, Filippo Pietrantonio, Maria Apicella, Cristina Migliore, Daniela Conticelli, Annalisa Petrelli, Laura D'Errico, Stefania Durando, Daniel Moya-Rull, Sara E Bellomo and 32 more

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

15 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Curcumin for gastric cancer: Mechanism predictionWorld journal of gastrointestinal oncology · 2024
    Article
  8. Article
  9. Article
  10. Epidermal Growth Factor Receptor Inhibition in Epidermal Growth Factor Receptor-Amplified Gastroesophageal Cancer: Retrospective Global Experience.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2022
    Article
  11. Review
  12. EGFR Amplification in Metastatic Colorectal Cancer.Journal of the National Cancer Institute · 2021
    Article
  13. Review
  14. Back from the Brink: EGFR Inhibition in Gastroesophageal Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2021
    Article
  15. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

42 authors at 14 institutions in 4 countries.

Simona Corso *Department of Oncology, University of Torino, Candiolo, Torino, Italy. silvia.giordano@unito.it simona.corso@unito.it.ORCID 0000-0002-5069-1503
Filippo Pietrantonio *Department of Medical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.ORCID 0000-0002-8530-8420
Maria Apicella *Candiolo Cancer Institute, FPO-IRCCS, Candiolo, Torino, Italy.
Cristina Migliore *Department of Oncology, University of Torino, Candiolo, Torino, Italy.ORCID 0000-0003-3722-2814
Daniela ConticelliDepartment of Oncology, University of Torino, Candiolo, Torino, Italy.ORCID 0000-0003-4661-9776
Annalisa PetrelliCandiolo Cancer Institute, FPO-IRCCS, Candiolo, Torino, Italy.
Laura D'ErricoDepartment of Oncology, University of Torino, Candiolo, Torino, Italy.
Stefania DurandoCandiolo Cancer Institute, FPO-IRCCS, Candiolo, Torino, Italy.ORCID 0000-0002-9986-919X
Daniel Moya-RullCandiolo Cancer Institute, FPO-IRCCS, Candiolo, Torino, Italy.
Sara E BellomoCandiolo Cancer Institute, FPO-IRCCS, Candiolo, Torino, Italy.ORCID 0000-0001-5738-2351
Stefano UghettoDepartment of Oncology, University of Torino, Candiolo, Torino, Italy.
Maurizio DegiuliDepartment of Oncology, University of Torino, Orbassano, Torino, Italy.ORCID 0000-0002-9812-7020
Rossella ReddavidDepartment of Oncology, University of Torino, Orbassano, Torino, Italy.ORCID 0000-0003-0603-9953
Uberto FumagalliChirurgia Generale 2, Brescia, Italy.
Stefano De PascaleChirurgia Generale 2, Brescia, Italy.
Giovanni SgroiSurgical Oncology Unit, Department of Surgical Science, ASST Bergamo Ovest, Treviglio, Bergamo, Italy.ORCID 0000-0003-4956-124X
Emanuele RausaSurgical Oncology Unit, Department of Surgical Science, ASST Bergamo Ovest, Treviglio, Bergamo, Italy.ORCID 0000-0001-6780-1783
Gian Luca BaiocchiDepartment of Clinical and Experimental Sciences, Surgical Clinic, University of Brescia, Brescia, Italy.ORCID 0000-0003-2402-2178
Sarah MolfinoDepartment of Clinical and Experimental Sciences, Surgical Clinic, University of Brescia, Brescia, Italy.
Giovanni De ManzoniDepartment of Surgical Sciences, Dentistry, Gynecology and Pediatrics, Section of Surgery, University of Verona, Verona, Italy.
Maria BencivengaDepartment of Surgical Sciences, Dentistry, Gynecology and Pediatrics, Section of Surgery, University of Verona, Verona, Italy.
Salvatore SienaDepartment of Oncology and Hemato-Oncology, University of Milan, Milan, Italy.ORCID 0000-0002-2681-2846
Andrea Sartore-BianchiDepartment of Oncology and Hemato-Oncology, University of Milan, Milan, Italy.ORCID 0000-0003-0780-0409
Federica MoranoDepartment of Medical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.ORCID 0000-0002-5306-3596
Salvatore CoralloDepartment of Medical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.ORCID 0000-0002-6672-0233
Michele PrisciandaroDepartment of Medical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.ORCID 0000-0001-5596-469X
Maria Di BartolomeoDepartment of Medical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Annunziata GloghiniDepartment of Pathology and Laboratory Medicine, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.ORCID 0000-0002-7226-1942
Silvia MarsoniCandiolo Cancer Institute, FPO-IRCCS, Candiolo, Torino, Italy.ORCID 0000-0002-5361-7122
Antonino SottileCandiolo Cancer Institute, FPO-IRCCS, Candiolo, Torino, Italy.
Anna SapinoCandiolo Cancer Institute, FPO-IRCCS, Candiolo, Torino, Italy.ORCID 0000-0003-3542-9571
Caterina MarchiòCandiolo Cancer Institute, FPO-IRCCS, Candiolo, Torino, Italy.ORCID 0000-0003-2024-6131
Asa Dahle-SmithTayside Cancer Centre, Ninewells Hospital, Dundee, Scotland, United Kingdom.
Zosia MiedzybrodzkaUniversity of Aberdeen, Aberdeen, Scotland, United Kingdom.ORCID 0000-0003-2890-8136
Jessica LeeFoundation Medicine, Inc., Cambridge, Massachusetts.
Siraj M AliFoundation Medicine, Inc., Cambridge, Massachusetts.ORCID 0000-0001-7477-4023
Jeffrey S RossFoundation Medicine, Inc., Cambridge, Massachusetts.ORCID 0000-0001-8494-2596
Brian M AlexanderFoundation Medicine, Inc., Cambridge, Massachusetts.ORCID 0000-0003-3903-9175
Vincent A MillerFoundation Medicine, Inc., Cambridge, Massachusetts.
Russell PettyDivision of Molecular and Clinical Medicine, School of Medicine, University of Dundee, Dundee, Scotland, United Kingdom.
Alexa B SchrockFoundation Medicine, Inc., Cambridge, Massachusetts.
Silvia GiordanoDepartment of Oncology, University of Torino, Candiolo, Torino, Italy. silvia.giordano@unito.it simona.corso@unito.it.ORCID 0000-0003-1854-1086
Candiolo Cancer Institute · ITTorino e-district · ITFondazione IRCCS Istituto Nazionale dei Tumori · ITGlobalFoundries (United States) · USUniversity of Brescia · ITUniversity of Milan · IT5T Torino (Italy) · ITUniversity of Bergamo · ITUniversity of Turin · ITUniversity of Verona · ITNinewells Hospital · GBSUNY Upstate Medical University · USUniversity of Aberdeen · GBUniversity of Dundee · GB

Funding

Cancer Research UK 29637Chief Scientist Office ETM/116Chief Scientist Office TCS/19/18
6 · The paper itself

Abstract

purposeGastric and gastroesophageal adenocarcinomas represent the third leading cause of cancer mortality worldwide. Despite significant therapeutic improvement, the outcome of patients with advanced gastroesophageal adenocarcinoma is poor. Randomized clinical trials failed to show a significant survival benefit in molecularly unselected patients with advanced gastroesophageal adenocarcinoma treated with anti-EGFR agents. EXPERIMENTAL

designWe performed analyses on four cohorts: IRCC (570 patients), Foundation Medicine, Inc. (9,397 patients), COG (214 patients), and the Fondazione IRCCS Istituto Nazionale dei Tumori (206 patients). Preclinical trials were conducted in patient-derived xenografts (PDX).

resultsThe analysis of different gastroesophageal adenocarcinoma patient cohorts suggests that

conclusionsThis study underscores EGFR as a potential therapeutic target in gastric cancer and identifies the combination of an EGFR TKI and a mAb as an effective therapeutic approach. Finally, it recognizes mTOR pathway activation as a novel mechanism of primary resistance that can be overcome by the combination of EGFR and mTOR inhibitors.

Indexed as

AdenocarcinomaAnimalsAntibodies, MonoclonalCohort StudiesErbB ReceptorsEsophageal NeoplasmsHEK293 CellsHumansMiceMolecular Targeted TherapyProtein Kinase InhibitorsProtein-Tyrosine KinasesSignal TransductionStomach NeoplasmsTOR Serine-Threonine KinasesTumor Cells, CulturedAntibodies, MonoclonalEGFR protein, humanErbB ReceptorsMTOR protein, humanProtein Kinase InhibitorsProtein-Tyrosine KinasesTOR Serine-Threonine Kinases

Identifiers

PMID33542076
OpenAlexW3126578253

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.