Evidence map›Paper›PMID 37223888›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2023

The GENIE BPC NSCLC Cohort: A Real-World Repository Integrating Standardized Clinical and Genomic Data for 1,846 Patients with Non-Small Cell Lung Cancer.

Noura J Choudhury, Jessica A Lavery, Samantha Brown, Ino de Bruijn, Justin Jee, Thinh Ngoc Tran, Hira Rizvi, Kathryn C Arbour, Karissa Whiting, Ronglai Shen and 19 more

Open access · hybridAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
9.6field-weighted citation impact, top 2% 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

23 citing papers in PubMed, 35 citations in OpenAlex.

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  18. Article
  19. Representing mutations for predicting cancer drug response.Bioinformatics (Oxford, England) · 2024
    Article
  20. Article
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

29 authors at 7 institutions in 3 countries.

Noura J ChoudhuryDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0002-5980-4973
Jessica A LaveryDepartment of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0002-2746-5647
Samantha BrownDepartment of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0001-5352-974X
Ino de BruijnMarie-Josee and Henry R. Kravis Center for Molecular Oncology, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0001-5427-4750
Justin JeeDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0001-9783-0139
Thinh Ngoc TranMarie-Josee and Henry R. Kravis Center for Molecular Oncology, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0002-3428-2507
Hira RizviAstraZeneca, Cambridge, United Kingdom.ORCID 0000-0002-8007-096X
Kathryn C ArbourDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0001-5951-8427
Karissa WhitingDepartment of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0002-4683-1868
Ronglai ShenDepartment of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0001-9694-584X
Matthew HellmannAstraZeneca, Cambridge, United Kingdom.ORCID 0000-0002-2670-9777
Philippe L BedardCancer Clinical Research Unit, Princess Margaret Cancer Centre, Toronto, Ontario, Canada.ORCID 0000-0002-6771-2999
Celeste YuCancer Clinical Research Unit, Princess Margaret Cancer Centre, Toronto, Ontario, Canada.ORCID 0000-0002-8764-1091
Natasha LeighlCancer Clinical Research Unit, Princess Margaret Cancer Centre, Toronto, Ontario, Canada.ORCID 0000-0002-3249-4602
Michele LeNoue-NewtonDepartment of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, Tennessee.ORCID 0000-0003-3469-3784
Christine MicheelDepartment of Medicine, Vanderbilt Ingram Cancer Center, Nashville, Tennessee.ORCID 0000-0002-7744-9039
Jeremy L WarnerDepartment of Medicine, Vanderbilt Ingram Cancer Center, Nashville, Tennessee.ORCID 0000-0002-2851-7242
Michelle S GinsbergDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0003-0304-110X
Andrew PlodkowskiDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0002-3772-370X
Jeffrey GirshmanDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0003-0533-0423
Peter SawanDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0002-7757-899X
Shirin PillaiDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0009-0002-0699-0458
Shawn M SweeneyAmerican Association for Cancer Research, Philadelphia, Pennsylvania.ORCID 0000-0002-4269-6566
Kenneth L KehlDepartment of Medical Oncology, Division of Population Sciences, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0001-5339-9797
Katherine S PanageasDepartment of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0002-6591-604X
Nikolaus SchultzMarie-Josee and Henry R. Kravis Center for Molecular Oncology, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0002-0131-4904
Deborah SchragDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0002-4334-5717
Gregory J RielyDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0001-5357-4313
AACR GENIE BPC Core Team
Memorial Sloan Kettering Cancer Center · USPrincess Margaret Cancer Centre · CAAstraZeneca (United Kingdom) · GBVanderbilt University · USAmerican Association For Cancer Research · USDana-Farber Cancer Institute · USVanderbilt University Medical Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
The Vanderbilt Institute for Clinical and Translational Research (VICTR)UL1TR000445 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BERNARD, GORDON RAPHAEL · 2012 to 2016
$41.4M
NCATS NIH HHS UL1 TR000445NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

purposeWe describe the clinical and genomic landscape of the non-small cell lung cancer (NSCLC) cohort of the American Association for Cancer Research (AACR) Project Genomics Evidence Neoplasia Information Exchange (GENIE) Biopharma Collaborative (BPC). EXPERIMENTAL

designA total of 1,846 patients with NSCLC whose tumors were sequenced from 2014 to 2018 at four institutions participating in AACR GENIE were randomly chosen for curation using the PRISSMM data model. Progression-free survival (PFS) and overall survival (OS) were estimated for patients treated with standard therapies.

resultsIn this cohort, 44% of tumors harbored a targetable oncogenic alteration, with EGFR (20%), KRAS G12C (13%), and oncogenic fusions (ALK, RET, and ROS1; 5%) as the most frequent. Median OS (mOS) on first-line platinum-based therapy without immunotherapy was 17.4 months [95% confidence interval (CI), 14.9-19.5 months]. For second-line therapies, mOS was 9.2 months (95% CI, 7.5-11.3 months) for immune checkpoint inhibitors (ICI) and 6.4 months (95% CI, 5.1-8.1 months) for docetaxel ± ramucirumab. In a subset of patients treated with ICI in the second-line or later setting, median RECIST PFS (2.5 months; 95% CI, 2.2-2.8) and median real-world PFS based on imaging reports (2.2 months; 95% CI, 1.7-2.6) were similar. In exploratory analysis of the impact of tumor mutational burden (TMB) on survival on ICI treatment in the second-line or higher setting, TMB z-score harmonized across gene panels was associated with improved OS (univariable HR, 0.85; P = 0.03; n = 247 patients).

conclusionsThe GENIE BPC cohort provides comprehensive clinicogenomic data for patients with NSCLC, which can improve understanding of real-world patient outcomes.

Indexed as

Antineoplastic Agents, ImmunologicalCarcinoma, Non-Small-Cell LungLung NeoplasmsGenomicsHumansProtein-Tyrosine KinasesProto-Oncogene ProteinsAntineoplastic Agents, ImmunologicalProtein-Tyrosine KinasesProto-Oncogene Proteins

Identifiers

PMID37223888
PMCPMC10472103
OpenAlexW4377940137

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LicenceCC BY-NC-ND
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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.