Evidence map›Paper›PMID 30773851›Full record

ArticleCancer medicine2019

Retinoblastoma mutation predicts poor outcomes in advanced non small cell lung cancer.

Priyanka Bhateja, Michelle Chiu, Gary Wildey, Mary Beth Lipka, Pingfu Fu, Michael Chiu Lee Yang, Fatemeh Ardeshir-Larijani, Neelesh Sharma, Afshin Dowlati

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
3.3field-weighted citation impact, top 6% 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

44 citing papers in PubMed, 57 citations in OpenAlex.

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  12. Translational lung cancer research · 2024
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  14. An advanced NSCLC patient withTranslational lung cancer research · 2023
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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

9 authors at 4 institutions in 1 country.

Priyanka BhatejaDepartment of Hematology and Oncology, Case Western Reserve University, University Hospitals Seidman Cancer Center, Cleveland, Ohio.
Michelle ChiuSchool of Medicine, Case Western Reserve University, Cleveland, Ohio.
Gary WildeySchool of Medicine, Case Western Reserve University, Cleveland, Ohio.ORCID 0000-0001-7105-1313
Mary Beth LipkaDepartment of Hematology and Oncology, University Hospitals Seidman Cancer Center, Cleveland, Ohio.
Pingfu FuDepartment of Population and Quantitative Health Sciences, Case Western Reserve University, Cleveland, Ohio.
Michael Chiu Lee YangDepartment of Pathology, University Hospitals Cleveland Medical Center, Cleveland, Ohio.
Fatemeh Ardeshir-LarijaniDepartment of Internal Medicine, University Hospitals Cleveland Medical Center, Cleveland, Ohio.
Neelesh SharmaDepartment of Biomedical Research, Novartis Pharmaceuticals Corporation, East Hanover, New Jersey.
Afshin DowlatiDepartment of Hematology and Oncology, Case Western Reserve University, University Hospitals Seidman Cancer Center, Cleveland, Ohio.
Case Western Reserve University · USUniversity Hospitals Seidman Cancer Center · USUniversity Hospitals of Cleveland · USNovartis (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The retinoblastoma gene (RB1) encodes the retinoblastoma (RB) pocket protein that plays an important role in cell cycle progression. Here we determine the frequency and prognostic significance of RB1 mutation in non small cell lung cancer (NSCLC), restricting inclusion to Stage III and IV patients with linked genomic and clinical data. The primary outcome was median overall survival (OS). We identified RB1 mutation in 8.2% of NSCLC patients. The median OS for wild-type (wt) RB1 was 28.3 months vs 8.3 months for mutant RB1 (Hazard Ratio = 2.59, P = 0.002). Of special interest, RB1 mutation also correlated with lack of response to immunotherapy. Our study focused on RB1 mutation in locally advanced and advanced non small cell lung cancer to better facilitate comparisons with small cell lung cancer (SCLC). In our SCLC cohort, RB1 mutation was identified in 75% of patients and wt RB1 was associated with significantly shorter OS (P = 0.002). The different outcomes of RB1 mutation observed among lung cancer subtypes suggest a more complicated mechanism than simple regulation of cell cycle or response to chemotherapy.

Indexed as

MutationAdultAgedAntineoplastic Agents, ImmunologicalCarcinoma, Non-Small-Cell LungDiagnosis, DifferentialFemaleHumansLung NeoplasmsMaleMiddle AgedMutation RateNeoplasm StagingPrognosisRetinoblastoma Binding ProteinsSmall Cell Lung CarcinomaAntineoplastic Agents, ImmunologicalRB1 protein, humanRetinoblastoma Binding ProteinsUbiquitin-Protein Ligasesgenomicsimmunotherapynon small cell lung cancerresponseretinoblastomasmall cell lung cancer

Identifiers

PMID30773851
PMCPMC6488103
OpenAlexW2917631733

What OpenQuestion holds

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LicenceCC BY
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.