Evidence map›Paper›PMID 34302255›Full record

ArticleJournal of gastrointestinal cancer2022

Prognostic Factors for Survival in Transverse Colon Cancers.

Ahmet Küçükarda, Ali Gökyer, Sezin Sayın, İvo Gökmen, Erkan Özcan, Osman Köstek, Muhammet Bekir Hacıoğlu, Sernaz Uzunoğlu, İrfan Çiçin, Bülent Erdoğan

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PubMed Publisher
In one paragraph

Article in Journal of gastrointestinal cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 2 pooled it
0.2field-weighted citation impact, top 51% 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

3 citing papers in PubMed, 2 syntheses or guidelines pooled it, 3 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  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

10 authors at 1 institution in 1 country.

Ahmet KüçükardaDivision of Medical Oncology, Department of Internal Medicine, Trakya University School of Medicine, Edirne, Turkey. ahmetkucukarda22@gmail.com.ORCID http://orcid.org/0000-0001-7399-2360
Ali GökyerDivision of Medical Oncology, Department of Internal Medicine, Trakya University School of Medicine, Edirne, Turkey.
Sezin SayınTrakya University School of Medicine, Edirne, Turkey.
İvo GökmenDivision of Medical Oncology, Department of Internal Medicine, Trakya University School of Medicine, Edirne, Turkey.
Erkan ÖzcanDivision of Medical Oncology, Department of Internal Medicine, Trakya University School of Medicine, Edirne, Turkey.
Osman KöstekEdirne Sultan, 1 Murat State Hospital, Edirne, Turkey.
Muhammet Bekir HacıoğluDivision of Medical Oncology, Department of Internal Medicine, Trakya University School of Medicine, Edirne, Turkey.
Sernaz UzunoğluDivision of Medical Oncology, Department of Internal Medicine, Trakya University School of Medicine, Edirne, Turkey.
İrfan ÇiçinDivision of Medical Oncology, Department of Internal Medicine, Trakya University School of Medicine, Edirne, Turkey.
Bülent ErdoğanDivision of Medical Oncology, Department of Internal Medicine, Trakya University School of Medicine, Edirne, Turkey.
Trakya University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTransverse colon cancer (TCC) is a rare condition that accounts for 10% of all colon cancers. TCC was accepted more likely right-sided colon cancers. We aimed to investigate whether TCC differs from other colon tumors by using clinical, pathological, and molecular prognostic factors known to be important in colon cancer and if it differs in its own anatomical structure. PATIENTS AND

methodsWe evaluated local and locally advanced TCC patients between 2007 and 2020 years for demographics data, symptoms, treatment status, and histopathological and molecular features.

resultsOverall, 107 TCC patients were included in this study. According to the molecular data analysis of 44, 35, and 23 patients for MSI, RAS, and BRAF status, respectively, 7 (15.9%) were MSI-H, 13 (37.1%) were RAS mutant, and 11 (47.8%) had BRAF V600E mutation. The median follow-up time was 31.5 months. Median disease-free survival (DFS) was 5.19 months, and median OS was 88.3 months for the whole study population. The tumor stage was the most significant prognostic factor for DFS and OS. Although BRAF mutation was not a significant marker for DFS, it was an independent prognostic marker for OS (HR 3.90 95% CI 1.42-10.7). There were no statistically significant differences between proximal two-thirds and distal one-third tumor location.

conclusionTCC has molecular features and prognostic factors more likely RCC and no differences between proximal and distal sub-parts. BRAF V600E mutation status is an independent predictor of survival even in the early stages of TCC.

Indexed as

Colonic NeoplasmsColon, TransverseHumansMicrosatellite InstabilityMutationPrognosisProto-Oncogene Proteins B-rafProto-Oncogene Proteins B-rafBRAF V600EPathological stagePrognosisSurvivalTransverse colon cancer

Identifiers

PMID34302255
OpenAlexW3185334946

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.