Evidence map›Paper›PMID 32669613›Full record

ArticleModern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc2021

T3 versus T4a staging challenges in deeply invasive colonic adenocarcinomas and correlation with clinical outcomes.

Robert Pantaleon Vasquez, Mustafa Erdem Arslan, Hwajeong Lee, Tonya S King, Deepti Dhall, Dipti M Karamchandani

Abstract read
PubMed Publisher
In one paragraph

Article in Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, 2021. 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. Trial
  2. 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

6 authors.

Robert Pantaleon VasquezDepartment of Pathology, Penn State Health Milton S. Hershey Medical Center/Penn State College of Medicine, Hershey, PA, USA.ORCID http://orcid.org/0000-0003-4416-9652
Mustafa Erdem ArslanDepartment of Pathology and Laboratory Medicine, Albany Medical College, Albany, NY, USA.ORCID http://orcid.org/0000-0002-0683-7421
Hwajeong LeeDepartment of Pathology and Laboratory Medicine, Albany Medical College, Albany, NY, USA.ORCID http://orcid.org/0000-0001-7005-6278
Tonya S KingDepartment of Public Health Sciences, Penn State College of Medicine, Hershey, PA, USA.
Deepti DhallDepartment of Pathology, University of Alabama, Birmingham, AL, USA.
Dipti M KaramchandaniDepartment of Pathology, Penn State Health Milton S. Hershey Medical Center/Penn State College of Medicine, Hershey, PA, USA. dkaramchandani@pennstatehealth.psu.edu.ORCID http://orcid.org/0000-0002-0351-2859

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite the latest 8th edition American Joint Committee on Cancer Staging Manual guidelines, disagreement still exists among pathologists regarding staging deeply invasive colonic adenocarcinomas ≤1 mm to the serosal surface. In this retrospective study, 151 untreated colonic adenocarcinomas staged initially as either pT3 or pT4a and with available 5-year follow-up data were retrieved and re-categorized: Group 1 (38 cases): pT4a with tumor at the serosa; Group 2 (49 cases): tumor ≤1 mm from the serosa, with intervening reactive fibrosis (40/49) or inflammation (9/49); Group 3 (64 cases): pT3 tumor >1 mm from the serosa. Clinical outcomes were analyzed. Groups 1 and 2 tumors showed significantly lower 5-year recurrence-free survival and lower overall survival rates (log-rank p < 0.001 for both), when compared with Group 3 tumors. Even after adjusting for adjuvant therapy and nodal metastases, the proportional hazards ratios for the risk of death (p < 0.001) and risk of recurrence (p = 0.005) showed significantly higher risk in Groups 1 and 2 compared with Group 3. The synchronous nodal (p = 0.012) and metachronous distant metastases (p = 0.004) were also significantly more in Groups 1 and 2 versus Group 3. Colonic adenocarcinomas ≤1 mm from the serosal surface behaved more akin to "bona fide" pT4a tumors at the serosal surface in our study with regards to clinical outcomes. We recommend these tumors be staged as pT4a rather than pT3, as supported by outcome data in our study. We hope this will also ensure reproducibility and consistency in staging these tumors across institutions.

Indexed as

Neoplasm StagingAdenocarcinomaAdultAgedColonic NeoplasmsFemaleHumansMaleMiddle AgedPrognosisRetrospective Studies

Identifiers

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.