Evidence map›Paper›PMID 27501955›Full record

ArticleDiagnostic pathology2016

Determination of GP88 (progranulin) expression in breast tumor biopsies improves the risk predictive value of the Nottingham Prognostic Index.

Ginette Serrero, Douglas M Hawkins, Pablo A Bejarano, Olga Ioffe, Katherine R Tkaczuk, Robert E Elliott, Jonathan F Head, Jeffrey Phillips, Andrew K Godwin, JoEllen Weaver and 2 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Diagnostic pathology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05627960 (FIH Phase 1A /1B Study of AG01 Antibody Against Progranulin/GP88 in Advanced Solid Tumor Malignancies With Expansion Cohorts in Advanced Triple Negative Breast Ca, Hormone Resistant Breast Ca, Non Small Cell Lung Cancer and Mesothelioma), which is not on this map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.2field-weighted citation impact, top 35% 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.

NCT05627960 phase1recruitingnot on this mapstarted 2022, after this paper: background citation

FIH Phase 1A /1B Study of AG01 Antibody Against Progranulin/GP88 in Advanced Solid Tumor Malignancies With Expansion Cohorts in Advanced Triple Negative Breast Ca, Hormone Resistant Breast Ca, Non Small Cell Lung Cancer and Mesothelioma

TypeinterventionalSponsorA&G Pharmaceutical Inc.Ran2022 to 2026Enrolled77ConditionsTriple Negative Breast Cancer, Hormone-Resistant Breast Cancer, Non Small Cell Lung Cancer, MesotheliomaArmsAG-01 Compound
3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Observational
  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

12 authors at 8 institutions in 1 country.

Ginette SerreroA&G Pharmaceutical Inc., Columbia, MD, USA. gserrero@agpharma.com.ORCID http://orcid.org/0000-0003-3607-0273
Douglas M HawkinsSchool of Statistics, University of Minnesota, Minneapolis, MN, USA.
Pablo A BejaranoCleveland Clinic Florida, Weston, FL, USA.
Olga IoffeProgram of Oncology, University Maryland Greenebaum Cancer Center, Baltimore, MD, USA.
Katherine R TkaczukProgram of Oncology, University Maryland Greenebaum Cancer Center, Baltimore, MD, USA.
Robert E ElliottElliot, Elliot, Head Breast Cancer Research & Treatment Center, Baton Rouge, LA, USA.
Jonathan F HeadElliot, Elliot, Head Breast Cancer Research & Treatment Center, Baton Rouge, LA, USA.
Jeffrey PhillipsElliot, Elliot, Head Breast Cancer Research & Treatment Center, Baton Rouge, LA, USA.
Andrew K GodwinUniversity of Kansas Medical Center, Kansas City, KS, USA.
JoEllen WeaverUniversity of Pennsylvania School of Medicine, Philadelphia, PA, USA.
David HicksA&G Pharmaceutical Inc., Columbia, MD, USA.
Binbin YueA&G Pharmaceutical Inc., Columbia, MD, USA.
Breast Cancer Research Foundation · USA&G Pharmaceutical (United States) · USU-M Rogel Cancer Center · USCleveland Clinic Florida · USUniversity of Kansas Medical Center · USUniversity of Maryland, Baltimore · USUniversity of Minnesota · USUniversity of Pennsylvania · US

Funding

Fox Chase Clinical Epidemiology and Validation CenterU01CA113916 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI ENGSTROM, PAUL FREDERICK · 2005 to 2015
$8.6M
Novel Targeted Therapy for Breast CancerR43CA124179 · NCI · A AND G PHARMACEUTICAL, INC. · PI SERRERO, GINETTE · 2007 to 2007
$121k
NCI NIH HHS R43 CA124179NCI NIH HHS U01 CA113916
6 · The paper itself

Abstract

backgroundThe Nottingham Prognostic Index (NPI), which combines numerical values for nodal status, tumor size and histological grade, is used in the standard of care to provide predictive value information on post-surgery survival for patients with primary breast cancer. Attempts to improve the performance of the NPI algorithm have been carried out by testing the inclusion of other biomarker expression and morphological features such as vascular invasion. In the present study, we investigated whether expression of the autocrine growth and survival factor GP88 (progranulin), known to be overexpressed in breast cancer, would improve NPI's predictive value.

methodsWe examined by immunohistochemistry (IHC) the GP88 expression in 508 cases of estrogen receptor positive invasive ductal carcinoma with known clinical outcomes and for which NPI had been determined. GP88 IHC expression was scored by two board certified pathologists and classified into two score groups of GP88 <3+ (0, 1+, 2+) and GP88 = 3+. The correlation between GP88 scoring, NPI and disease-free (DFS) or overall survival (OS) outcomes was then examined by Kaplan-Meier analysis, Cox proportional Hazard (CPH) ratio and Pearson's X (2) test.

resultsKaplan-Meier survival graphs of cases categorized by their NPI scores (<3.4, 3.4-5.4, >5.4) and GP88 expression showed that for patients within the same NPI subgroup, patients having tumors with a high GP88 expression (GP88 IHC score of 3+) had a worse DFS than patients with tumors that had a low GP88 expression (GP88 IHC score <3+). When adjusted for NPI, high GP88 score was significantly associated with recurrence with a hazard ratio of 3.30 (95 % CI 2.12 to 5.14).

conclusionsThe data suggest that the determination of GP88 tumor expression at time of diagnosis for early stage breast cancer patients can provide additional survival information to that provided by NPI alone and thus may be useful for risk management of patients diagnosed with breast cancer.

Indexed as

AdultAgedAged, 80 and overBiomarkers, TumorBiopsyBreastBreast NeoplasmsFemaleHumansImmunohistochemistryIntercellular Signaling Peptides and ProteinsKaplan-Meier EstimateMiddle AgedPredictive Value of TestsPrognosisProgranulinsBiomarkers, TumorGRN protein, humanIntercellular Signaling Peptides and ProteinsProgranulinsReceptors, EstrogenBiomarkerBreast CancerGP88ImmunohistochemistryNottingham Prognostic IndexPrognosticProgranulin

Identifiers

PMID27501955
PMCPMC4977669
OpenAlexW2491947130

What OpenQuestion holds

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Registered trials

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.