Evidence map›Paper›PMID 33795256›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2021

Next-Generation Sequencing of 487 Esophageal Adenocarcinomas Reveals Independently Prognostic Genomic Driver Alterations and Pathways.

Smita Sihag, Samuel C Nussenzweig, Henry S Walch, Meier Hsu, Kay See Tan, Francisco Sanchez-Vega, Walid K Chatila, Sergio A De La Torre, Assem Patel, Yelena Y Janjigian and 11 more

Open access · bronzeAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
7.3field-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

15 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Esophageal cancer: from pathogenesis to precision therapies.Signal transduction and targeted therapy · 2026
    Review
  5. Article
  6. Article
  7. Review
  8. Article
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  10. Review
  11. Review
  12. Article
  13. The Role of the TP53 Pathway in Predicting Response to Neoadjuvant Therapy in Esophageal Adenocarcinoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2022
    Article
  14. Article
  15. Drivers of Esophageal Adenocarcinoma and Opportunities for Cancer Interception.Cellular and molecular gastroenterology and hepatology · 2021
    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

21 authors at 1 institution in 1 country.

Smita SihagThoracic Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, New York. sihags@mskcc.org.
Samuel C NussenzweigThoracic Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, New York.
Henry S WalchCenter for Molecular Oncology, Memorial Sloan Kettering Cancer Center, New York, New York.
Meier HsuDepartment of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York.
Kay See TanDepartment of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York.
Francisco Sanchez-VegaColorectal Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, New York.
Walid K ChatilaCenter for Molecular Oncology, Memorial Sloan Kettering Cancer Center, New York, New York.
Sergio A De La TorreThoracic Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0002-5213-2780
Assem PatelThoracic Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, New York.
Yelena Y JanjigianDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
Steven MaronDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
Geoffrey Y KuDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0002-0448-1038
Laura H TangDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Jaclyn HechtmanDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Pari M ShahDepartment of Gastroenterology, Memorial Sloan Kettering Cancer Center, New York, New York.
Abraham J WuDepartment of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0002-2597-7091
David R JonesThoracic Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, New York.
Daniela MolenaThoracic Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0003-1655-4473
David B SolitCenter for Molecular Oncology, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0002-6614-802X
Nikolaus SchultzCenter for Molecular Oncology, Memorial Sloan Kettering Cancer Center, New York, New York.
Michael F BergerCenter for Molecular Oncology, Memorial Sloan Kettering Cancer Center, New York, New York.
Memorial Sloan Kettering Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
MSK Paul Calabresi Career Development Award for Clinical OncologyK12CA184746 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI Omar Abdel-Wahab, Simon N. Powell · 2015 to 2026
$8.3M
BRMS1-mediated suppression of metastases in p53 mutant lung adenocarcinomaR01CA217169 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI JONES, DAVID R · 2018 to 2022
$2.5M
NCI NIH HHS K12 CA184746NCI NIH HHS P30 CA008748NCI NIH HHS R01 CA217169
6 · The paper itself

Abstract

purposeTo delineate recurrent oncogenic driver alterations and dysregulated pathways in esophageal adenocarcinoma and to assess their prognostic value. EXPERIMENTAL

designWe analyzed a large cohort of patients with lower esophageal and junctional adenocarcinoma, prospectively sequenced by MSK-IMPACT with high-quality clinical annotation. Patients were subdivided according to treatment intent, curative versus palliative, which closely mirrored clinical staging. Genomic features, alterations, and pathways were examined for association with overall survival using Cox proportional hazard models, adjusted for relevant clinicopathologic factors knowable at the time of diagnosis.

resultsAnalysis of 487 patients revealed 16 oncogenic driver alterations, mostly amplifications, present in ≥5% of patients. Patients in the palliative-intent cohort, compared with those in the curative-intent cohort, were more likely to have metastatic disease,

conclusionsOur study suggests that higher levels of genomic instability are associated with more advanced disease in esophageal adenocarcinoma. Furthermore,

Indexed as

AdenocarcinomaBiomarkers, TumorHigh-Throughput Nucleotide SequencingHumansMutationPrognosisBiomarkers, Tumor

Identifiers

PMID33795256
PMCPMC8228505
OpenAlexW3144563489

What OpenQuestion holds

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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.