Evidence map›Paper›PMID 34790392›Full record

ArticleJournal of gastrointestinal oncology2021

Intact SMAD-4 is a predictor of increased locoregional recurrence in upfront resected pancreas cancer receiving adjuvant therapy.

Hunter C Gits, Amy H Tang, William S Harmsen, William R Bamlet, Rondell P Graham, Gloria M Petersen, Thomas C Smyrk, Amit Mahipal, Roman O Kowalchuk, Jonathan B Ashman and 12 more

Open access · diamondAbstract read
In one paragraph

Article in Journal of gastrointestinal oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 29% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
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  4. The Role ofCancers · 2022
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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

22 authors at 5 institutions in 1 country.

Hunter C GitsDepartment of Radiation Oncology, Mayo Clinic, Rochester, MN, USA.
Amy H TangLeroy T. Canoles Jr. Cancer Research Center, Department of Microbiology and Molecular Cell Biology, Eastern Virginia Medical School, Norfolk, VA, USA.
William S HarmsenDepartment of Biostatistics and Health Sciences Research, Mayo Clinic, Rochester, MN, USA.
William R BamletDepartment of Biostatistics and Health Sciences Research, Mayo Clinic, Rochester, MN, USA.
Rondell P GrahamDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Gloria M PetersenDepartment of Epidemiology and Health Sciences Research, Mayo Clinic, Rochester, MN, USA.
Thomas C SmyrkDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Amit MahipalDepartment of Medical Oncology, Mayo Clinic, Rochester, MN, USA.
Roman O KowalchukDepartment of Radiation Oncology, Mayo Clinic, Rochester, MN, USA.
Jonathan B AshmanDepartment of Radiation Oncology, Mayo Clinic, Phoenix, AZ, USA.
William G RuleDepartment of Radiation Oncology, Mayo Clinic, Phoenix, AZ, USA.
Dawn OwenDepartment of Radiation Oncology, Mayo Clinic, Rochester, MN, USA.
Michelle A Neben WittichDepartment of Radiation Oncology, Mayo Clinic, Rochester, MN, USA.
Robert R McWilliamsDepartment of Medical Oncology, Mayo Clinic, Rochester, MN, USA.
Thorvardur HalfdanarsonDepartment of Medical Oncology, Mayo Clinic, Rochester, MN, USA.
Wen Wee MaDepartment of Medical Oncology, Mayo Clinic, Rochester, MN, USA.
Terence T SioDepartment of Radiation Oncology, Mayo Clinic, Phoenix, AZ, USA.
Sean P ClearyDepartment of Hepatobiliary & Pancreas Surgery, Mayo Clinic, Rochester, MN, USA.
Mark J TrutyDepartment of Hepatobiliary & Pancreas Surgery, Mayo Clinic, Rochester, MN, USA.
Michael G HaddockDepartment of Radiation Oncology, Mayo Clinic, Rochester, MN, USA.
Christopher L HallemeierDepartment of Radiation Oncology, Mayo Clinic, Rochester, MN, USA.
Kenneth W MerrellDepartment of Radiation Oncology, Mayo Clinic, Rochester, MN, USA.
Mayo Clinic in Arizona · USMayo Clinic · USMayo Clinic in Florida · USWinnMed · USCancer Research Center · US

Funding

Women's Cancer ProgramP30CA015083 · NCI · MAYO CLINIC ROCHESTER · PI Felicity Enders · 1985 to 2026
$151.3M
Tissue CoreP50CA102701 · NCI · MAYO CLINIC ROCHESTER · PI PETERSEN, GLORIA M. · 2004 to 2018
$32.7M
SIAH2-Dependent Proteolysis in Cell Migration, Tumor Growth and Cancer MetastasisR01CA140550 · NCI · EASTERN VIRGINIA MEDICAL SCHOOL · PI TANG, AMY H. · 2010 to 2014
$1.4M
Regulated Proteolysis in RAS Signal TransductionR01GM069922 · NIGMS · MAYO CLINIC ROCHESTER · PI TANG, AMY H. · 2004 to 2009
$1.3M
Novel Cilia Trafficking MechanismsR01DK084725 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MARGOLIS, BENJAMIN L · 2009 to 2010
$702k
NCI NIH HHS P30 CA015083NCI NIH HHS P50 CA102701NCI NIH HHS R01 CA140550NIDDK NIH HHS R01 DK084725NIGMS NIH HHS R01 GM069922
6 · The paper itself

Abstract

backgroundPrevious reports suggest that intact SMAD4 expression is associated with a locally aggressive pancreas cancer phenotype. The objectives of this work were to determine the frequency of intact SMAD4 and its association with patterns of recurrence in patients with upfront resected pancreas cancer receiving adjuvant therapy.

methodsA tissue microarray was constructed using resected specimens from patients who underwent upfront surgery and adjuvant gemcitabine with no neoadjuvant treatment for pancreas cancer. SMAD4 expression was determined by immunohistochemical staining. Associations of SMAD4 expression and clinicopathologic parameters with clinical outcomes were evaluated using Cox proportional hazard models.

resultsOne hundred twenty-seven patients were included with a median follow up of 5.7 years. Most patients had stage ≥ pT3 tumors (75%) and pN1 (68%). All patients received adjuvant gemcitabine, and 79% of patients received adjuvant chemoradiotherapy. Ten (8%) patients had intact SMAD4 expression. Grade was the only clinicopathologic parameter statistically associated with SMAD4 expression (P=0.05). Median overall survival was 2.1 years. On univariate analysis, SMAD4 expression was associated with increased locoregional recurrence (hazard ratio 7.0, P<0.01, 95% confidence interval: 2.8-18.0) but not distant recurrence (P=0.06) or overall survival (P=0.73). On multivariable analysis, SMAD4 expression (hazard ratio 9.6, P<0.01, 95% confidence interval: 3.7-24.8) and adjuvant chemoradiotherapy (hazard ratio 0.3, P=0.01, 95% confidence interval: 0.1-0.8) were associated with higher and lower locoregional recurrence, respectively.

conclusionsIn patients with upfront resected pancreas cancer, SMAD4 expression was associated with an increased risk of locoregional recurrence. Prospective evaluation of the frequency of SMAD4 expression and validation of its predictive utility is warranted.

Indexed as

chemoradiotherapy (CRT)mothers against decapentaplegic homolog 4 (SMAD4)Pancreas cancerpatterns of recurrencetissue microarray (TMA)

Identifiers

PMID34790392
PMCPMC8576222
OpenAlexW3197000641

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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.