Evidence map›Paper›PMID 26832882›Full record

ArticleAnnals of surgical oncology2016

Pancreatic Ductal Adenocarcinoma is Spread to the Peripancreatic Soft Tissue in the Majority of Resected Cases, Rendering the AJCC T-Stage Protocol (7th Edition) Inapplicable and Insignificant: A Size-Based Staging System (pT1: ≤2, pT2: >2-≤4, pT3: >4 cm) is More Valid and Clinically Relevant.

Burcu Saka, Serdar Balci, Olca Basturk, Pelin Bagci, Lauren M Postlewait, Shishir Maithel, Jessica Knight, Bassel El-Rayes, David Kooby, Juan Sarmiento and 9 more

Open access · greenAbstract read
In one paragraph

Article in Annals of surgical oncology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
8.5field-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

52 citing papers in PubMed, 124 citations in OpenAlex.

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  13. Reconsidering the absence of extrapancreatic extension in T staging for pancreatic adenocarcinoma in the AJCC (8Journal of gastrointestinal surgery : official journal of the Society for Surgery of the Alimentary Tract · 2023
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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

19 authors at 5 institutions in 2 countries.

Burcu SakaDepartment of Pathology, Emory University School of Medicine and Winship Cancer Institute, Atlanta, GA, USA.
Serdar BalciDepartment of Pathology, Emory University School of Medicine and Winship Cancer Institute, Atlanta, GA, USA.
Olca BasturkDepartment of Pathology, Wayne State University and Karmanos Cancer Institute, Detroit, MI, USA.
Pelin BagciDepartment of Pathology, Marmara University, Istanbul, Turkey.
Lauren M PostlewaitDepartment of Surgical Oncology, Emory University School of Medicine and Winship Cancer Institute, Atlanta, GA, USA.
Shishir MaithelDepartment of Surgical Oncology, Emory University School of Medicine and Winship Cancer Institute, Atlanta, GA, USA.
Jessica KnightDepartment of Epidemiology, Emory University School of Medicine and Winship Cancer Institute, Atlanta, GA, USA.
Bassel El-RayesDepartment of Medical Oncology, Emory University School of Medicine and Winship Cancer Institute, Atlanta, GA, USA.
David KoobyDepartment of General Surgery, Emory University School of Medicine and Winship Cancer Institute, Atlanta, GA, USA.
Juan SarmientoDepartment of General Surgery, Emory University School of Medicine and Winship Cancer Institute, Atlanta, GA, USA.
Takashi MurakiDepartment of Pathology, Emory University School of Medicine and Winship Cancer Institute, Atlanta, GA, USA.
Irma OlivaDepartment of Pathology, Emory University School of Medicine and Winship Cancer Institute, Atlanta, GA, USA.
Sudeshna BandyopadhyayDepartment of Pathology, Wayne State University and Karmanos Cancer Institute, Detroit, MI, USA.
Gizem AkkasDepartment of Pathology, Emory University School of Medicine and Winship Cancer Institute, Atlanta, GA, USA.
Michael GoodmanDepartment of Epidemiology, Emory University School of Medicine and Winship Cancer Institute, Atlanta, GA, USA.
Michelle D ReidDepartment of Pathology, Emory University School of Medicine and Winship Cancer Institute, Atlanta, GA, USA.
Alyssa KrasinskasDepartment of Pathology, Emory University School of Medicine and Winship Cancer Institute, Atlanta, GA, USA.
Rhonda EverettDepartment of Pathology, Emory University School of Medicine and Winship Cancer Institute, Atlanta, GA, USA.
Volkan AdsayDepartment of Pathology, Emory University School of Medicine and Winship Cancer Institute, Atlanta, GA, USA. volkan.adsay@emory.edu.
Emory University · USWinship Cancer InstituteMarmara University · TRThe Barbara Ann Karmanos Cancer Institute · USWayne State University · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Tumor Antigens for Individual Signatures and TherapyP50CA062924 · NCI · JOHNS HOPKINS UNIVERSITY · PI LENNON, ANNE MARIE · 1993 to 2022
$54.6M
NCI NIH HHS P30 CA008748NCI NIH HHS P50 CA062924
6 · The paper itself

Abstract

backgroundMost studies have failed to identify any prognostic value of the current T-stage protocol for pancreatic ductal adenocarcinoma (PDAC) by the American Joint Committee on Cancer and the Union for International Cancer Control unless some grouping was performed.

methodsTo document the parameters included in this T-stage protocol, 223 consecutive pancreatoduodenectomy specimens with PDAC were processed by a uniform grossing protocol.

resultsPeripancreatic soft tissue (PST) involvement, the main pT3 parameter, was found to be inapplicable and irreproducible due to lack of a true capsule in the pancreas and variability in the amount and distribution of adipose tissue. Furthermore, 91 % of the cases showed carcinoma in the adipose tissue, presumably representing the PST, and thus were classified as pT3. An additional 4.5 % were qualified as pT3 due to extension into adjacent sites. The T-stage defined as such was not found to have any correlation with survival (p = 0.4). A revised T-stage protocol was devised that defined pT1 as 2 cm or smaller, pT2 as >2-4 cm, and pT3 as larger than 4 cm. This revised protocol was tested in 757 consecutive PDACs. The median and 3-year survival rates of this size-based protocol were 26, 18, 13 months, and 40 %, 26 %, 20 %, respectively (p < 0.0001). The association between higher T-stage and shorter survival persisted in N0 cases and in multivariate modeling. Analysis of the Surveillance, Epidemiology, and End Results database also confirmed the survival differences (p < 0.0001).

conclusionsThis study showed that resected PDACs are already spread to various surfaces of the pancreas, leaving only about 4 % of PDACs to truly qualify as pT1/T2, and that the current T-stage protocol does not have any prognostic correlation. In contrast, as shown previously in many studies, size is an important prognosticator, and a size-based T-stage protocol is more applicable and has prognostic value in PDAC.

Indexed as

AdenocarcinomaAdultAgedAged, 80 and overCarcinoma, Pancreatic DuctalFemaleFollow-Up StudiesHumansLymphatic MetastasisMaleMiddle AgedNeoplasm StagingPancreatic NeoplasmsProspective StudiesSurvival Rate

Identifiers

PMID26832882
PMCPMC5389382
OpenAlexW2270145296

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.