Evidence map›Paper›PMID 37358877›Full record

ArticleThe oncologist2023

Clinicogenomic factors and treatment patterns among patients with advanced non-small cell lung cancer with or without brain metastases in the United States.

Emily Nash Smyth, Jincy John, Ramon V Tiu, Melinda Dale Willard, Julie Kay Beyrer, Lee Bowman, Kristin M Sheffield, Yimei Han, Priscilla K Brastianos

Open access · goldAbstract read
In one paragraph

Article in The oncologist, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.8field-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

6 citing papers in PubMed, 7 citations in OpenAlex.

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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 2 institutions in 1 country.

Emily Nash SmythEli Lilly and Company, Value Evidence Outcomes - Research, Indianapolis, IN 46225, USA.
Jincy JohnEli Lilly and Company, Value Evidence Outcomes - Research, Indianapolis, IN 46225, USA.
Ramon V TiuEli Lilly and Company, Value Evidence Outcomes - Research, Indianapolis, IN 46225, USA.
Melinda Dale WillardEli Lilly and Company, Lilly Global Clinical Development, Indianapolis, IN 46225, USA.
Julie Kay BeyrerEli Lilly and Company, Value Evidence Outcomes - Research, Indianapolis, IN 46225, USA.
Lee BowmanEli Lilly and Company, Value Evidence Outcomes - Research, Indianapolis, IN 46225, USA.
Kristin M SheffieldEli Lilly and Company, Value Evidence Outcomes - Research, Indianapolis, IN 46225, USA.
Yimei HanEli Lilly and Company, Statistics RWE, Indianapolis, IN 46225, USA.
Priscilla K BrastianosDivisions of Hematology/Oncology and Neuro-Oncology, Massachusetts General Hospital, Boston, MA 02114, USA.
Eli Lilly (United States) · USMassachusetts General Hospital · US

Funding

Eli Lilly and Company
6 · The paper itself

Abstract

backgroundThis retrospective, real-world study evaluated the prevalence of brain metastases, clinicodemographic characteristics, systemic treatments, and factors associated with overall survival among patients with advanced non-small cell lung cancer (aNSCLC) in the US. We also described the genomic characterization of 180 brain metastatic specimens and frequency of clinically actionable genes. MATERIALS AND

methodsDe-identified electronic health records-derived data of adult patients diagnosed with aNSCLC between 2011 and 2017 were analyzed from a US-nationwide clinicogenomic database.

resultsOf 3257 adult patients with aNSCLC included in the study, approximately 31% (n = 1018) had brain metastases. Of these 1018 patients, 71% (n = 726) were diagnosed with brain metastases at initial NSCLC diagnosis; 57% (n = 583) of patients with brain metastases received systemic treatment. Platinum-based chemotherapy combinations were the most common first-line therapy; single-agent chemotherapies, epidermal growth factor receptor tyrosine kinase inhibitors, and platinum-based chemotherapy combinations were used in second line. Patients with brain metastases had a 1.56 times greater risk of death versus those with no brain metastases. In the brain metastatic specimens (n = 180), a high frequency of genomic alterations in the p53, MAPK, PI3K, mTOR, and cell-cycle associated pathways was observed.

conclusionThe frequency of brain metastases at initial clinical presentation and associated poor prognosis for patients in this cohort underscores the importance of early screening for brain metastasis in NSCLC. Genomic alterations frequently identified in this study emphasize the continued need for genomic research and investigation of targeted therapies in patients with brain metastases.

Indexed as

Brain NeoplasmsCarcinoma, Non-Small-Cell LungLung NeoplasmsAdultGenomicsHumansRetrospective StudiesUnited Statesadvanced NSCLCbrain metastasisgenomicssurvivaltreatment patterns

Identifiers

PMID37358877
PMCPMC10628559
OpenAlexW4382011169

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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.