Evidence map›Paper›PMID 29157747›Full record

ArticleInternational journal of radiation oncology, biology, physics2018

Multiplex Proximity Ligation Assay to Identify Potential Prognostic Biomarkers for Improved Survival in Locally Advanced Pancreatic Cancer Patients Treated With Stereotactic Body Radiation Therapy.

Avani D Rao, Yufei Liu, Rie von Eyben, Charles C Hsu, Chen Hu, Lauren M Rosati, Arti Parekh, Kendall Ng, Amy Hacker-Prietz, Lei Zheng and 12 more

Abstract read
In one paragraph

Article in International journal of radiation oncology, biology, physics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. 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

22 authors.

Avani D RaoDepartment of Radiation Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland. Electronic address: avani.rao@jhmi.edu.
Yufei LiuDepartment of Radiation Oncology, Stanford University School of Medicine, Stanford, California.
Rie von EybenDepartment of Radiation Oncology, Stanford University School of Medicine, Stanford, California.
Charles C HsuDepartment of Radiation Oncology, University of Arizona Cancer Center, Tucson, Arizona.
Chen HuDepartment of Radiation Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Lauren M RosatiDepartment of Radiation Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Arti ParekhDepartment of Radiation Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Kendall NgDepartment of Radiation Oncology, Stanford University School of Medicine, Stanford, California.
Amy Hacker-PrietzDepartment of Radiation Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Lei ZhengDivision of Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Timothy M PawlikDepartment of Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Daniel A LaheruDivision of Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Elizabeth M JaffeeDepartment of Radiation Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland; Division of Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Matthew J WeissDepartment of Radiation Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland; Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Dung T LeDivision of Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Ralph H HrubanDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Ana De Jesus-AcostaDivision of Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Christopher L WolfgangDepartment of Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Amol K NarangDepartment of Radiation Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Daniel T ChangDepartment of Radiation Oncology, Stanford University School of Medicine, Stanford, California.
Albert C KoongDepartment of Radiation Oncology, Stanford University School of Medicine, Stanford, California.
Joseph M HermanDepartment of Radiation Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland.

Funding

Translational Research Central ServicesP30CA006973 · NCI · JOHNS HOPKINS UNIVERSITY · PI Rosalie Wollett · 1985 to 2026
$208.6M
Tumor Antigens for Individual Signatures and TherapyP50CA062924 · NCI · JOHNS HOPKINS UNIVERSITY · PI LENNON, ANNE MARIE · 1993 to 2022
$54.6M
NCI NIH HHS P30 CA006973NCI NIH HHS P50 CA062924
6 · The paper itself

Abstract

purposeTo explore seromarker levels for associations with outcomes in locally advanced pancreatic cancer (LAPC) patients who received chemotherapy and stereotactic body radiation therapy (SBRT). METHODS AND MATERIALS: Serum from LAPC patients in 2 prospective trials of hypofractionated SBRT (5-6.6 Gy × 5) was collected before SBRT. Proximity ligation assay quantified the expression levels of 36 pancreatic cancer-specific candidate seromarkers: Axl, BMP2, CA 125, CA 19-9, CEA, CXCL-1/6/9/10, EGFR, Gas6, Her2, IGF-2, IGFBP-2/3/7, IL-6/6Ra/7/8/12, mesothelin, MMP-1/2/3/7, osteopontin, PDGFRa, PDK1, PF4, RegIV, SPARC, TGF-β, VEGF-A/D, and YKL40. Seromarker values were log transformed owing to log-normal distribution of the values, and Cox regression analysis was performed to assess for any association with overall survival. The Benjamini-Hochberg method was used to control for a false discovery rate (FDR) of only 10%.

resultsSixty-four patients with LAPC were included. No clinical factors (including surgical resection, receipt of pre-SBRT chemotherapy, receipt of post-SBRT chemotherapy, performance status, and age) or potential biomarkers in the panel were associated with improved survival in this cohort after application of the FDR correction. Potential prognostic factors for improved survival for future investigation included surgical resection (P=.007, adjusted P=.153) and the serum expression of IL-8 (P=.006, adjusted P=.153), CA 19-9 (P=.031, adjusted P=.377), and MMP-1 (P=.036, adjusted P=.377).

conclusionsThese data explore the expression of a panel of proteins in pre-SBRT serum of LAPC patients in the context of a conservative FDR correction. None of the clinical factors or expression levels of the serum proteins were found to be associated with survival; however, IL-8, CA 19-9, and MMP-1 were highlighted as possible candidates warranting inclusion in future seromarker studies in the ongoing efforts to identify tools for risk stratification and treatment allocation in LAPC.

Indexed as

RadiosurgeryBiomarkers, TumorCA-19-9 AntigenFemaleHumansInterleukin-8MaleMatrix Metalloproteinase 1Nucleic Acid Amplification TechniquesPancreatic NeoplasmsPrognosisProportional Hazards ModelsBiomarkers, TumorCA-19-9 AntigenInterleukin-8Matrix Metalloproteinase 1

Identifiers

PMID29157747
PMCPMC7405990

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.