Evidence map›Paper›PMID 33013109›Full record

ArticleIndian journal of surgical oncology2020

Gastrointestinal Stromal Tumours (GIST): Indian Experience of Rare Malignancy.

Kanuj Malik, Ramakrishnan A Seshadri, Shirley Sundersingh, Manikandan Dhanushkodi

Abstract read
In one paragraph

Article in Indian journal of surgical oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
  2. Gastrointestinal stromal tumors: Clinicopathological features and outcome-Real-world experience.Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology · 2025
    Article
  3. 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

4 authors.

Kanuj MalikDepartment of Surgical Oncology, Cancer Institute (WIA), Chennai, 600020 India.
Ramakrishnan A SeshadriDepartment of Surgical Oncology, Cancer Institute (WIA), Chennai, 600020 India.ORCID https://orcid.org/0000-0003-2471-0237
Shirley SundersinghDepartment of OncoPathology, Cancer Institute (WIA), Chennai, 600020 India.
Manikandan DhanushkodiDepartment of Medical Oncology, Cancer Institute (WIA), Chennai, 600020 India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

GISTs are rare tumours of the GI tract arising from the intestinal cells of Cajal. Though various risk stratification systems have been proposed, none has been universally accepted. We audited the survival and recurrence patterns in our patients and evaluated clinicopathological features to identify prognostic factors affecting survival. We conducted a retrospective analysis of patients treated at our hospital from 1999 to 2012. Patient variables, clinicopathological factors and treatment variables were collected. Sixty-three patients were evaluated and treated at our institute of which 38 were non-metastatic. The most common site of origin was the stomach. On univariate analysis, presence of metastasis, male gender, high mitotic rate, non-gastric primary and epithelioid histology were significantly associated with poor overall survival. Tumour size > 10 cm, mitotic rate > 10/50 hpf and presence of necrosis significantly affected disease-free survival for non-metastatic patients. Multivariate analysis showed higher mitotic rate and non-gastric primary to correlate with worse outcome. In our experience, a high mitotic rate and non-gastric primary independently predicted a poor prognosis in GIST.

Indexed as

Gastrointestinal stromal tumourPrognosisSurvival

Identifiers

PMID33013109
PMCPMC7501329

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.