Evidence map›Paper›PMID 32372141›Full record

ArticleGastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association2020

Glycolytic competence in gastric adenocarcinomas negatively impacts survival outcomes of patients treated with salvage paclitaxel-ramucirumab.

Annamaria Ruzzo, Francesco Graziano, Irene Bagaloni, Maria Di Bartolomeo, Michele Prisciandaro, Giuseppe Aprile, Elena Ongaro, Bruno Vincenzi, Giuseppe Perrone, Daniele Santini and 14 more

Open access · hybridAbstract readEvaluation Study
In one paragraph

Article in Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.7field-weighted citation impact, top 36% 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

11 citing papers in PubMed, 12 citations in OpenAlex.

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  6. Translational cancer research · 2022
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  9. [Progress in the clinical application and correlation between glucose transporter-1 andSheng wu yi xue gong cheng xue za zhi = Journal of biomedical engineering = Shengwu yixue gongchengxue zazhi · 2021
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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

24 authors at 10 institutions in 1 country.

Annamaria Ruzzo *Department of Biomolecular Sciences (DiSB), University of Urbino "Carlo Bo", Via Arco d'Augusto, 2, 61032, Fano, PU, Italy. annamaria.ruzzo@uniurb.it.ORCID http://orcid.org/0000-0003-2815-1890
Francesco Graziano *Department of Onco-Hematology, Division of Oncology, Azienda Ospedaliera "Ospedali Riuniti Marche Nord", 61122, Pesaro, Italy. francesco.graziano@ospedaliriunitimarchenord.it.
Irene BagaloniDepartment of Biomolecular Sciences (DiSB), University of Urbino "Carlo Bo", Via Arco d'Augusto, 2, 61032, Fano, PU, Italy.
Maria Di BartolomeoOncologia Medica GI Fondazione IRCCS Istituto Tumori Milano, Milan, Italy.
Michele PrisciandaroOncologia Medica GI Fondazione IRCCS Istituto Tumori Milano, Milan, Italy.
Giuseppe AprileDepartment of Medical Oncology, San Bortolo General Hospital, AULSS8 Berica, Vicenza, Italy.
Elena OngaroDepartment of Oncology, University and General Hospital, Udine, Italy.
Bruno VincenziUniversity Campus Bio-Medico, Rome, Italy.
Giuseppe PerroneUniversity Campus Bio-Medico, Rome, Italy.
Daniele SantiniUniversity Campus Bio-Medico, Rome, Italy.
Lorenzo FornaroAzienda Ospedaliero-Universitaria Pisana, Pisa, Italy.
Caterina VivaldiAzienda Ospedaliero-Universitaria Pisana, Pisa, Italy.
Gianluca TomaselloS. C. Oncologia, ASST Hospital of Cremona, Cremona, Italy.
Fotios LoupakisDepartment of Oncology, Veneto Institute of Oncology IOV - IRCCS, Padua, Italy.
Sara LonardiDepartment of Oncology, Veneto Institute of Oncology IOV - IRCCS, Padua, Italy.
Matteo FassanSurgical Pathology Unit, Department of Medicine (DIMED), University of Padua, Padua, Italy.
Michele ValmasoniClinica Chirurgica 3, Department of Surgical, Oncological and Gastroenterological Sciences (DISCOG), University of Padua, Padua, Italy.
Donatella SartiDepartment of Onco-Hematology, Division of Oncology, Azienda Ospedaliera "Ospedali Riuniti Marche Nord", 61122, Pesaro, Italy.
Paola LorenziniDepartment of Onco-Hematology, Division of Oncology, Azienda Ospedaliera "Ospedali Riuniti Marche Nord", 61122, Pesaro, Italy.
Vincenzo CatalanoDepartment of Onco-Hematology, Division of Oncology, Azienda Ospedaliera "Ospedali Riuniti Marche Nord", 61122, Pesaro, Italy.
Renato BisonniMedical Oncology Unit, Hospital of Fermo, Fermo, Italy.
Michela Del PreteMedical Oncology Unit, Hospital of Fermo, Fermo, Italy.
Guido CollinaArea vasta 5, Ospedale "C. e G. Mazzoni" Ascoli Piceno, Ascoli Piceno, Italy.
Mauro MagnaniDepartment of Biomolecular Sciences (DiSB), University of Urbino "Carlo Bo", Via Arco d'Augusto, 2, 61032, Fano, PU, Italy.
Ospedali Riuniti Marche Nord · ITUniversità Campus Bio-Medico · ITUniversity of Urbino · ITAzienda Ospedaliera Universitaria Pisana · ITFondazione IRCCS Istituto Nazionale dei Tumori · ITIstituto Oncologico Veneto · ITUniversity of Padua · ITIstituti Ospitalieri di Cremona · ITOspedale San Bortolo · ITUniversity of Udine · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionFor energy production, cancer cells maintain a high rate of glycolysis instead of oxidative phosphorylation converting glucose into lactic acid. This metabolic shift is useful to survive in unfavorable microenvironments. We investigated whether a positive glycolytic profile (PGP) in gastric adenocarcinomas may be associated with unfavorable outcomes under an anticancer systemic therapy, including the anti-angiogenic ramucirumab. MATERIALS AND

methodsNormal mucosa (NM) and primary tumor (PT) of 40 metastatic gastric adenocarcinomas patients who received second-line paclitaxel-ramucirumab (PR) were analyzed for mRNA expression of the following genes: HK-1, HK-2, PKM-2, LDH-A, and GLUT-1. Patients were categorized with PGP when at least a doubling of mRNA expression (PT vs. NM) in all glycolytic core enzymes (HK-1 or HK-2, PKM-2, LDH-A) was observed. PGP was also related to TP53 mutational status.

resultsMean LDH-A, HK-2, PKM-2 mRNA expression levels were significantly higher in PT compared with NM. 18 patients were classified as PGP, which was associated with significantly worse progression-free and overall survival times. No significant association was observed between PGP and clinical-pathologic features, including TP53 positive mutational status, in 28 samples.

conclusionsGlycolytic proficiency may negatively affect survival outcomes of metastatic gastric cancer patients treated with PR systemic therapy. TP53 mutational status alone does not seem to explain such a metabolic shift.

Indexed as

AdenocarcinomaAgedAntibodies, Monoclonal, HumanizedAntineoplastic Combined Chemotherapy ProtocolsFemaleGastric MucosaGlycolysisHumansMaleMutationPaclitaxelRamucirumabRetrospective StudiesRNA, MessengerSalvage TherapyStomach NeoplasmsAntibodies, Monoclonal, HumanizedPaclitaxelRamucirumabRNA, MessengerTumor Suppressor Protein p53AngiogenesisGlycolysisPaclitaxelRamucirumabWarburg effect

Identifiers

PMID32372141
PMCPMC7567716
OpenAlexW3021634683

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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.