Evidence map›Paper›PMID 31600989›Full record

ArticleCancers2019

KRAS Mutations Predict Response and Outcome in Advanced Lung Adenocarcinoma Patients Receiving First-Line Bevacizumab and Platinum-Based Chemotherapy.

Aron Kristof Ghimessy, Aron Gellert, Erzsebet Schlegl, Balazs Hegedus, Erzsebet Raso, Tamas Barbai, Jozsef Timar, Gyula Ostoros, Zsolt Megyesfalvi, Balazs Gieszer and 8 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.7field-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

25 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
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  6. Exploration of efficacy of different therapy regimens for advanced NSCLC patients with KRAS mutation in the first-line treatment.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2024
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  13. The Effect of the Kirsten Rat Sarcoma Viral Oncogene Homolog (Genetic testing and molecular biomarkers · 2022
    Article
  14. Direct TargetingCancers · 2022
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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

18 authors at 3 institutions in 3 countries.

Aron Kristof GhimessyDepartment of Thoracic Surgery, National Institute of Oncology-Semmelweis University, 1122 Budapest, Hungary. aronghimessy@gmail.com.
Aron GellertDepartment of Thoracic Surgery, National Institute of Oncology-Semmelweis University, 1122 Budapest, Hungary. werte02@gmail.com.
Erzsebet SchleglDepartment of Tumor Biology, National Koranyi Institute of Pulmonology-Semmelweis University, 1122 Budapest, Hungary. erschlegl@gmail.com.
Balazs HegedusDepartment of Thoracic Surgery, Ruhrlandklinik, University Duisburg-Essen, 45239 Essen, Germany. Balazs.Hegedues@rlk.uk-essen.de.
Erzsebet Rasond Department of Pathology, Semmelweis University, 1091 Budapest, Hungary. raso.erzsebet@med.semmelweis-univ.hu.
Tamas Barbaind Department of Pathology, Semmelweis University, 1091 Budapest, Hungary. tbarbai@gmail.com.
Jozsef Timarnd Department of Pathology, Semmelweis University, 1091 Budapest, Hungary. jtimar@gmail.com.
Gyula Ostorosth Department of Pulmonology, National Koranyi Institute of Pulmonology, 1122 Budapest, Hungary. drostorosgyula@gmail.com.
Zsolt MegyesfalviDepartment of Thoracic Surgery, National Institute of Oncology-Semmelweis University, 1122 Budapest, Hungary. megyesfalvi_2007@yahoo.com.
Balazs GieszerDepartment of Thoracic Surgery, National Institute of Oncology-Semmelweis University, 1122 Budapest, Hungary. dr.gieszer@gmail.com.
Judit MoldvayDepartment of Tumor Biology, National Koranyi Institute of Pulmonology-Semmelweis University, 1122 Budapest, Hungary. drmoldvay@hotmail.com.
Ferenc Renyi-VamosDepartment of Thoracic Surgery, National Institute of Oncology-Semmelweis University, 1122 Budapest, Hungary. drrenyivamosferenc@gmail.com.
Zoltan LohinaiDepartment of Tumor Biology, National Koranyi Institute of Pulmonology-Semmelweis University, 1122 Budapest, Hungary. lohinaiz@gmail.com.
Mir Alireza HodaDivision of Thoracic Surgery, Department of Surgery, Comprehensive Cancer Centre Vienna, Medical University Vienna, A-1090 Vienna, Austria. mir.hoda@meduniwien.ac.at.
Thomas KlikovitsDivision of Thoracic Surgery, Department of Surgery, Comprehensive Cancer Centre Vienna, Medical University Vienna, A-1090 Vienna, Austria. thomas.klikovits@meduniwien.ac.at.
Walter KlepetkoDivision of Thoracic Surgery, Department of Surgery, Comprehensive Cancer Centre Vienna, Medical University Vienna, A-1090 Vienna, Austria. walter.klepetko@meduniwien.ac.at.
Viktoria LaszloDepartment of Tumor Biology, National Koranyi Institute of Pulmonology-Semmelweis University, 1122 Budapest, Hungary. viktoria.laszlo@meduniwien.ac.at.
Balazs DomeDepartment of Thoracic Surgery, National Institute of Oncology-Semmelweis University, 1122 Budapest, Hungary. balazs.dome@meduniwien.ac.at.
Semmelweis University · HUComprehensive Cancer Center Vienna · ATOrszágos Korányi Tbc és Pulmonológiai Intézet · HU

Funding

Hungarian National Research, Development and Innovation Office KH130356, K109626, and SNN114490, BD; NVKP-16-1-2016-0020, JT; KH126753, OG
6 · The paper itself

Abstract

Bevacizumab, combined with platinum-based chemotherapy, has been widely used in the treatment of advanced-stage lung adenocarcinoma (LADC). Although KRAS (V-Ki-ras2 Kirsten rat sarcoma viral oncogene homolog) mutation is the most common genetic alteration in human LADC and its role in promoting angiogenesis has been well established, its prognostic and predictive role in the above setting remains unclear. The association between KRAS exon 2 mutational status and clinicopathological variables including progression-free survival and overall survival (PFS and OS, respectively) was retrospectively analyzed in 501 Caucasian stage IIIB-IV LADC patients receiving first-line platinum-based chemotherapy (CHT) with or without bevacizumab (BEV). EGFR (epidermal growth factor receptor)-mutant cases were excluded. Of 247 BEV/CHT and 254 CHT patients, 95 (38.5%) and 75 (29.5%) had mutations in KRAS, respectively. KRAS mutation was associated with smoking (

Indexed as

advanced-stage lung adenocarcinomabevacizumabKRAS mutationnon-small-cell lung cancerplatinum-based chemotherapy

Identifiers

PMID31600989
PMCPMC6827133
OpenAlexW2980109711

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.