Evidence map›Paper›PMID 28356064›Full record

Trial reportBMC cancer2017

Protocol of the PANCALYZE trial: a multicenter, prospective study investigating the tumor biomarkers CXCR4, SMAD4, SOX9 and IFIT3 in patients with resected pancreatic adenocarcinoma to predict the pattern of recurrence of the disease.

Felix C Popp, Marie Christine Popp, Yue Zhao, Christopher Betzler, Siegfried Kropf, Benjamin Garlipp, Christoph Benckert, Thomas Kalinski, Hans Lippert, Christiane J Bruns

Open access · goldAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in BMC cancer, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.8field-weighted citation impact, top 26% 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

10 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
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  10. CXCR4 and PD-1 Expression in Head and Neck Cancer with Perineural Spread.Journal of neurological surgery. Part B, Skull base · 2019
    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 4 institutions in 1 country.

Felix C PoppDepartment of General, Visceral and Cancer Surgery, University of Cologne, Cologne, Germany. felix.popp@uk-koeln.de.
Marie Christine PoppDepartment of General, Visceral and Cancer Surgery, University of Cologne, Cologne, Germany.
Yue ZhaoDepartment of General, Visceral and Cancer Surgery, University of Cologne, Cologne, Germany.
Christopher BetzlerDepartment of General, Visceral and Cancer Surgery, University of Cologne, Cologne, Germany.
Siegfried KropfInstitute for Biometrics and Medical Informatics, Otto-von-Guericke University, Magdeburg, Germany.
Benjamin GarlippClinic for General, Visceral and Vascular Surgery, University Clinic Magdeburg, Magdeburg, Germany.
Christoph BenckertDepartment of General and Visceral Surgery, Vivantes Klinikum im Friedrichshain, Berlin, Germany.
Thomas KalinskiDepartment of Pathology, Otto von Guericke University, Magdeburg, Germany.
Hans LippertInstitute for Quality Control in Operative Medicine, Otto von Guericke University, Magdeburg, Germany.
Christiane J BrunsDepartment of General, Visceral and Cancer Surgery, University of Cologne, Cologne, Germany.
University of Cologne · DEOtto-von-Guericke University Magdeburg · DEKlinikum im Friedrichshain · DEUniversity Hospital Magdeburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPancreatic ductal adenocarcinoma (PDAC) is one of the most lethal malignancies today with an urgent need for novel therapeutic strategies. Biomarker analysis helps to better understand tumor biology and might emerge as a tool to develop personalized therapies. The aim of the study is to investigate four promising biomarkers to predict the clinical course and particularly the pattern of tumor recurrence after surgical resection.

designPatients undergoing surgery for PDAC can be enrolled into the PANCALYZE trial. Biomarker expression of CXCR4, SMAD4, SOX9 and IFIT3 will be prospectively assessed by immunohistochemistry and verified by rt.-PCR from tumor and adjacent healthy pancreatic tissue of surgical specimen. Immunohistochemistry expression pattern of all four biomarkers will be combined into a single score. Beginning with the hospital stay clinical data from enrolled patients will be collected and followed. Different adjuvant chemotherapy protocols will be used to create subgroups. The combined biomarker expression score will be correlated with the further clinical course of the patients to test the hypothesis if CXCR4 positive, SMAD4 negative, SOX9 positive, IFIT3 positive tumors will predominantly develop metastatic spread. DISCUSSION: Pancreatic cancer is associated with different patterns of progression requiring personalized therapeutic strategies. Biomarker expression analysis might be a tool to predict the pattern of tumor recurrence and discriminate patients that develop systemic metastatic disease from those with tumors that rather develop local recurrence over time. This data might lead to personalized adjuvant treatment decisions as patients with tumors that stay localized might benefit from adjuvant local therapies like radiochemotherapy as compared to those with systemic recurrence who would benefit exclusively from chemotherapy. Moreover, the pattern of propagation might be a predefined characteristic of pancreatic cancer determined by the genetic signature of the tumor. In the future, biomarker expression analysis could be performed on tumor biopsies to develop personalized therapeutic pathways right after diagnosis of cancer.

trial registrationGerman Clinical Trials Register, DRKS00006179 .

Indexed as

Biomarkers, TumorIntracellular Signaling Peptides and ProteinsPancreatic NeoplasmsReceptors, CXCR4Smad4 ProteinSOX9 Transcription FactorHumansProspective StudiesBiomarkers, TumorCXCR4 protein, humanIFIT3 protein, humanIntracellular Signaling Peptides and ProteinsReceptors, CXCR4Smad4 ProteinSMAD4 protein, humanSOX9 protein, humanSOX9 Transcription FactorBiomarker analysisClinical test developmentImmunohistochemistryPancreatic ductal adenocarcinomaPattern of recurrencePersonalized therapyPrediction of outcomePrognosis of pancreatic cancer, outcomeRt.-PCRSurgery

Identifiers

PMID28356064
PMCPMC5371262
OpenAlexW2602087427

What OpenQuestion holds

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LicenceCC BY
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.