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Journal ArticleDOI

Prognosis of gastrointestinal smooth-muscle (stromal) tumors: dependence on anatomic site.

TLDR
Tumor location, size, MI, and age have independent value in predicting the prognosis of patients with gastrointestinal smooth-muscle tumors, and better methods are still required to accurately predict clinical course.
Abstract
Although the significance of various prognostic factors, such as tumor size and mitotic index (MI), has been well established for smooth-muscle tumors of the stomach, the significance of these factors in other sites is less well defined. We studied 1004 patients with gastrointestinal smooth-muscle tumors for whom vital status could be determined. The average MI and tumor size varied significantly among the five major sites examined: esophagus (53 cases), stomach (524 cases), small bowel 252 cases), colon/rectum (108 cases), and omentum/mesentery/peritoneum (67 cases). There was a significant difference in site-specific survival (p = 0.001), with 10-year survival varying between 50% and 70%. Multivariate analysis demonstrated tumor location (p = 0.0320), size (p = 0.0003), MI (p < 0.0001), and patient age (p < 0.0001) to each carry independent prognostic value. The significance of MI was highly site dependent. Separation of survival curves for the stomach, using a threshold for analysis of either 5 or 10 mitotic figures/50 high-power fields, was very good. In contrast, small-bowel tumors showed little separation between survival curves, regardless of whether a threshold of 1, 5, or 10 mitotic figures MF/50 high-power fields was used to distinguish groups. In no site were tumor size and MI alone sufficient to provide an accurate long-term prediction of prognosis. Although tumor location, size, MI, and age have independent value in predicting the prognosis of patients with gastrointestinal smooth-muscle tumors, better methods are still required to accurately predict clinical course.

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Journal ArticleDOI

Diagnosis of gastrointestinal stromal tumors: A consensus approach.

TL;DR: Key elements of the consensus are the defining role of KIT immunopositivity in diagnosis and a proposed scheme for estimating metastatic risk in these lesions, based on tumor size and mitotic count, recognizing that it is probably unwise to use the definitive term "benign" for any GIST, at least at the present time.
Journal ArticleDOI

Gastrointestinal stromal tumors--definition, clinical, histological, immunohistochemical, and molecular genetic features and differential diagnosis.

TL;DR: Ligand-independent activation of KIT appears to be a strong candidate for molecular pathogenesis of GISTs, and it may be a target for future treatment for such tumors.
Journal ArticleDOI

Gastrointestinal stromal tumors of the stomach: a clinicopathologic, immunohistochemical, and molecular genetic study of 1765 cases with long-term follow-up.

TL;DR: Tumor location in fundus or gastroesophageal junction, coagulative necrosis, ulceration, and mucosal invasion were unfavorable factors, whereas tumor location in antrum was favorable (P < 0.001).
Journal ArticleDOI

Biology of gastrointestinal stromal tumors.

TL;DR: The rapid progress that has established GIST as a model for understanding the role of oncogenic kinase mutations in human tumorigenesis is charted and a molecular-based classification of GIST is proposed.
References
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Journal ArticleDOI

Test of the National Death Index and Equifax Nationwide Death Search

TL;DR: The authors compared the ability of the National Death Index and the Equifax Nationwide Death Search to ascertain deaths of participants in the Nurses' Health Study and the specificity of both services was approximately 100 percent.
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Smooth muscle tumors of the gastrointestinal tract and retroperitoneum: a pathologic analysis of 100 cases.

TL;DR: One hundred smooth muscle tumors arising in the gastrointestinal tract and retroperitoneum were reviewed in an attempt to define criteria for the diagnosis of leiomyosarcoma in these sites, and mitoses was found to be the most useful indicator of malignancy.
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Differentiation and Risk Assessment of Gastrointestinal Stromal Tumors

TL;DR: This review briefly summarizes ultrastructural studies and then focuses on the many immunohistochemical studies of cellular differentiation in GIST from the perspective of risk assessment.
Journal ArticleDOI

Smooth muscle tumors of the gastrointestinal tract. A study of 56 cases followed for a minimum of 10 years.

TL;DR: The problem of distinguishingLeiomyomas from leiomyosarcomas in sites where the latter did arise could not be resolved, particularly in view of the fact that fatal low‐grade leiomers had diameters as small as 1 cm and maximal mitotic rates as low as one per ten high‐power fields.
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