Evidence map›Paper›PMID 34188166›Full record

ArticleNPJ precision oncology2021

Pentraxin 3 is a stromally-derived biomarker for detection of pancreatic ductal adenocarcinoma.

Michelle R Goulart, Jennifer Watt, Imran Siddiqui, Rita T Lawlor, Ahmet Imrali, Christine Hughes, Amina Saad, Joanne ChinAleong, Chris Hurt, Catrin Cox and 7 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in NPJ precision oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03307148 (A Phase 1B Study Repurposing ATRA as Stromal Targeting Agent Along With Gemcitabine and Nab-Paclitaxel for Pancreatic Cancer), which is not on this map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.7field-weighted citation impact, top 16% 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.

NCT03307148 phase1completednot on this map

A Phase 1B Study Repurposing ATRA as Stromal Targeting Agent Along With Gemcitabine and Nab-Paclitaxel for Pancreatic Cancer (STAR_PAC)

TypeinterventionalSponsorBarts & The London NHS TrustRan2016 to 2019Enrolled29ConditionsPancreatic AdenocarcinomaArmsATRA, Gemcitabine, Nab-paclitaxel
3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Role of long pentraxin PTX3 in cancer.Clinical and experimental medicine · 2023
    Review
  9. Review
  10. Article
  11. Insights into the Relationship between Pentraxin-3 and Cancer.International journal of molecular sciences · 2022
    Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Review
  18. Review
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

17 authors at 6 institutions in 3 countries.

Michelle R GoulartCentre for Tumour Biology, Barts Cancer Institute - a CRUK Centre of Excellence, Queen Mary University of London, London, UK.ORCID http://orcid.org/0000-0001-8333-3908
Jennifer WattCentre for Tumour Biology, Barts Cancer Institute - a CRUK Centre of Excellence, Queen Mary University of London, London, UK.
Imran SiddiquiHumanitas Clinical and Research Center - IRCCS, via Manzoni 56, Rozzano, Italy.
Rita T LawlorARC-NET Research Center for Applied Research on Cancer, and Department of Diagnostics and Public Health, Section of Pathology, University of Verona, Verona, Italy.
Ahmet ImraliBarts Pancreas Tissue Bank, Barts Cancer Institute- a CRUK Centre of Excellence, Queen Mary University London, London, UK.ORCID http://orcid.org/0000-0003-3661-9932
Christine HughesBarts Pancreas Tissue Bank, Barts Cancer Institute- a CRUK Centre of Excellence, Queen Mary University London, London, UK.ORCID http://orcid.org/0000-0002-4477-5305
Amina SaadBarts Pancreas Tissue Bank, Barts Cancer Institute- a CRUK Centre of Excellence, Queen Mary University London, London, UK.ORCID http://orcid.org/0000-0001-6377-196X
Joanne ChinAleongBarts and the London HPB Centre, The Royal London Hospital, Barts Health NHS Trust, London, UK.
Chris HurtCentre for Trials Research, Cardiff University, Cardiff, UK.ORCID http://orcid.org/0000-0003-1206-8355
Catrin CoxCentre for Trials Research, Cardiff University, Cardiff, UK.
Roberto SalviaThe Pancreas Institute and Department of Surgery, University and Hospital Trust of Verona, Verona, Italy.
Alberto MantovaniHumanitas Clinical and Research Center - IRCCS, via Manzoni 56, Rozzano, Italy.
Tatjana Crnogorac-JurcevicCentre for Cancer Biomarkers and Biotherapeutics, Barts Cancer Institute - a CRUK Centre of Excellence, Queen Mary University of London, London, UK.
Somnath MukherjeeOxford Institute for Radiation Oncology, Churchill Hospital - Oxford Cancer Centre, University of Oxford, Oxford, UK.
Aldo ScarpaARC-NET Research Center for Applied Research on Cancer, and Department of Diagnostics and Public Health, Section of Pathology, University of Verona, Verona, Italy.ORCID http://orcid.org/0000-0003-1678-739X
Paola AllavenaHumanitas Clinical and Research Center - IRCCS, via Manzoni 56, Rozzano, Italy.
Hemant M KocherCentre for Tumour Biology, Barts Cancer Institute - a CRUK Centre of Excellence, Queen Mary University of London, London, UK. h.kocher@qmul.ac.uk.ORCID http://orcid.org/0000-0001-6771-1905
Queen Mary University of London · GBHumanitas University · ITCardiff University · GBUniversity of Verona · ITBarts Health NHS Trust · GBChurchill Hospital · GB

Funding

Cancer Research UK 25350
6 · The paper itself

Abstract

Pancreatic ductal adenocarcinoma (PDAC), characterized by dense desmoplastic stroma laid down by pancreatic stellate cells (PSC), has no reliable diagnostic biomarkers for timely detection. A multi-center cohort of PDAC patients and controls (chronic pancreatitis, intra-ductal papillary neoplasms, gallstones and otherwise healthy) donated serum in an ethically approved manner. Serum PTX3 above 4.34 ng/mL has a higher sensitivity (86%, 95% confidence interval (CI): 65-97%) and specificity (86%, 95% CI: 79-91%), positive predictive value (97%) and likelihood ratio (6.05), and is superior when compared to serum CA19-9 and CEA for detection of PDAC. In vitro and ex vivo analyses of PTX3, in human PDAC samples, PSCs, cell lines and transgenic mouse model for PDAC, suggest that PTX3 originates from stromal cells, mainly PSC. In activated PSC, PTX3 secretion could be downregulated by rendering PSC quiescent using all-trans-retinoic acid (ATRA). PTX3 organizes hyaluronan in conjunction with tumor necrosis factor-stimulated gene 6 (TSG-6) and facilitates stellate and cancer cell invasion. In SCALOP clinical trial (ISRCTN96169987) testing chemo-radiotherapy without stromal targeting, PTX3 had no prognostic or predictive role. However, in STARPAC clinical trial (NCT03307148), stromal modulation by ATRA even at first dose is accompanied with serum PTX3 response in patients who later go on to demonstrate disease control but not those in whom the disease progresses. PTX3 is a putative stromally-derived biomarker for PDAC which warrants further testing in prospective, larger, multi-center cohorts and within clinical trials targeting stroma.

Identifiers

PMID34188166
PMCPMC8242009
OpenAlexW3176400724

What OpenQuestion holds

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LicenceCC BY
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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.