Evidence map›Paper›PMID 35954353›Full record

ArticleCancers2022

Gastrointestinal Stromal Tumors (GIST): A Population-Based Study Using the SEER Database, including Management and Recent Advances in Targeted Therapy.

Jaffar Khan, Asad Ullah, Abdul Waheed, Nabin Raj Karki, Nawaraj Adhikari, Lakshmi Vemavarapu, Sami Belakhlef, Samy Malik Bendjemil, Siamak Mehdizadeh Seraj, Feroze Sidhwa and 8 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 2 pooled it
7.8field-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

40 citing papers in PubMed, 2 syntheses or guidelines pooled it, 50 citations in OpenAlex.

  1. Pooled it
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  15. CT of gastrointestinal stromal tumor.Radiology case reports · 2025
    Article
  16. Article
  17. Article
  18. International journal of molecular sciences · 2025
    Review
  19. Trends and outcomes for patients receiving neoadjuvant therapy for stage I to III gastric gastrointestinal stromal tumors.Journal of gastrointestinal surgery : official journal of the Society for Surgery of the Alimentary Tract · 2025
    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

18 authors at 9 institutions in 1 country.

Jaffar KhanDepartment of Pathology, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
Asad UllahDepartment of Pathology, Vanderbilt University Medical Center, Nashville, TN 37232, USA.ORCID 0000-0002-9435-9625
Abdul WaheedDepartment of Surgery, San Joaquin General Hospital, French Camp, CA 95231, USA.ORCID 0000-0002-9992-6051
Nabin Raj KarkiGeorgia Cancer Center, Department of Hematology Oncology, Medical College of Georgia, Augusta University, Augusta, GA 30912, USA.
Nawaraj AdhikariDepartment of Medicine, Bon Secours Memorial Regional Medical Center, Mechanicsville, VA 23116, USA.
Lakshmi VemavarapuDepartment of Pathology, Charlie Norwood Veterans Affairs Medical Center, Augusta, GA 30904, USA.
Sami BelakhlefDepartment of Pathology, Medical College of Georgia, Augusta University, Augusta, GA 30912, USA.
Samy Malik BendjemilDepartment of Surgery, San Joaquin General Hospital, French Camp, CA 95231, USA.
Siamak Mehdizadeh SerajDepartment of Surgery, San Joaquin General Hospital, French Camp, CA 95231, USA.
Feroze SidhwaDepartment of Surgery, San Joaquin General Hospital, French Camp, CA 95231, USA.
Intisar GhleilibDepartment of Pathology, Medical College of Georgia, Augusta University, Augusta, GA 30912, USA.
Shahin ForoutanDepartment of Surgery, San Joaquin General Hospital, French Camp, CA 95231, USA.
Andrew M BlakelyNational Cancer Institute (NCI), Bethesda, MD 20892, USA.ORCID 0000-0002-5013-3851
Jaydira Del RiveroNational Cancer Institute (NCI), Bethesda, MD 20892, USA.ORCID 0000-0001-9710-4030
Nagla Abdel KarimInova Schar Cancer Institute, Department of Medicine, University of Virginia, Fairfax, VA 22031, USA.ORCID 0000-0002-8913-793X
Eric VailMolecular Pathology Laboratory, Cedars-Sinai Medical Center, Los Angeles, CA 90048, USA.ORCID 0000-0002-6578-178X
Saleh HeneidiMolecular Pathology Laboratory, Cedars-Sinai Medical Center, Los Angeles, CA 90048, USA.
Hector MesaDepartment of Pathology, Indiana University School of Medicine, Indianapolis, IN 46202, USA.ORCID 0000-0003-1833-4642
San Joaquin General Hospital · USAugusta University · USCedars-Sinai Medical Center · USIndiana University School of MedicineNational Cancer Institute · USCharlie Norwood VA Medical Center · USMemorial Regional Medical Center · USVanderbilt University Medical Center · USVirginia Cancer Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Gastrointestinal stromal tumors (GISTs) are the most common mesenchymal neoplasm of the gastrointestinal (GI) system. Most GISTs originate from the interstitial cells of Cajal (ICC), the pacemaker cell situated between the circular and longitudinal layers of the muscularis propria along the GI tract. In this population-based study using the SEER database, we sought to identify demographic, clinical, and pathologic factors that affect the prognosis and survival of patients with this neoplasm. Molecular genetic advances, current management guidelines, and advances in targeted therapy are discussed. Methods: Demographic and clinical data from GIST patients were retrieved from the SEER research plus database for the period 2000−2018. Statistical analysis was performed with IBM SPSS® v20.2 software using the Chi-square test, paired t-test, multivariate analysis, and Kaplan−Meier functions. Results: A total of 10,833 patients with GIST were identified. Most patients were between 60−74 years of age: 40%, Caucasian: 68%, and the male to female ratio was 1.1:1. The most common primary tumor sites were stomach: 63%, small intestine: 30%, rectum: 3%, and esophagus: 0.7%. When reported, the grade of differentiation was well: 38%, moderately: 32%, undifferentiated: 19%, poorly: 12%. The size of most tumors ranged between 6−10 cm: 36% and they were treated by surgical intervention: 82% and/or chemotherapy/targeted therapy: 39%. The stage was localized: 66%, advanced: 19%, and regional: 15%. The 5-year survival was 74% (95% confidence interval (95% CI) = 72.6−74.7), and the 5-year cause-specific survival 82% (95% CI = 80.7−82.6). The 5-year cause-specific survival by treatment included surgery at 86% (95% CI = 85.4−87.3), chemotherapy/targeted therapy with or without surgery at 77% (95% CI = 75.7−78.9), and radiation at 75% (95% CI = 74.5−80). On multivariable analysis tumor size > 5 cm, poorly and undifferentiated grade, age > 60, and distant metastases at presentation were associated with worse overall survival. Conclusion: GISTs comprise 1−2% of malignancies of the GI tract, usually affect male Caucasians between the ages of 60 and 74 years, most tumors occur in the stomach and small intestine, and are usually >5 cm, but still localized, at the time of diagnosis. Most tumors receive multimodality surgical and chemotherapy/targeted therapy treatment, with a 5-year overall survival of 74% and cause-specific survival of 82%. GIST patients would benefit from enrollment in large clinical trials to establish better therapy guidelines for unresectable, treatment-refractory, and recurrent tumors.

Indexed as

DOG1GISTmetastatic GISTsmolecularSDHSEERspindle cell tumors

Identifiers

PMID35954353
PMCPMC9367571
OpenAlexW4288428148

What OpenQuestion holds

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LicenceCC BY
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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.