Evidence map›Paper›PMID 38926671›Full record

ArticleBMC cancer2024

The Concept of Stroma AReactive Invasion Front Areas (SARIFA) as a new prognostic biomarker for lipid-driven cancers holds true in pancreatic ductal adenocarcinoma.

Przemyslaw Grochowski, Bianca Grosser, Florian Sommer, Andreas Probst, Johanna Waidhauser, Gerhard Schenkirsch, Nic G Reitsam, Bruno Märkl

Abstract read
In one paragraph

Article in BMC cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
–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

14 citing papers in PubMed, 1 synthesis or guideline pooled it.

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  12. [SARIFA-a new multi-entity biomarker].Pathologie (Heidelberg, Germany) · 2024
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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

8 authors.

Przemyslaw GrochowskiPathology, Faculty of Medicine, University of Augsburg, Augsburg, Germany. przemyslaw.grochowski@uk-augsburg.de.
Bianca GrosserPathology, Faculty of Medicine, University of Augsburg, Augsburg, Germany.
Florian SommerGeneral, Visceral and Transplantation Surgery, Faculty of Medicine, University of Augsburg, Augsburg, Germany.
Andreas ProbstGastroenterology, Faculty of Medicine, University of Augsburg, Augsburg, Germany.
Johanna WaidhauserHematology and Oncology, Faculty of Medicine, University of Augsburg, Augsburg, Germany.
Gerhard SchenkirschTumour Data Management, University Hospital Augsburg, Augsburg, Germany.
Nic G Reitsam *Pathology, Faculty of Medicine, University of Augsburg, Augsburg, Germany.
Bruno Märkl *Pathology, Faculty of Medicine, University of Augsburg, Augsburg, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPancreatic ductal adenocarcinoma (PDAC) is a 'difficult-to-treat' entity. To forecast its prognosis, we introduced a new biomarker, SARIFA (stroma areactive invasion front areas), which are areas at the tumour invasion front lacking desmoplastic stroma reaction upon malignant invasion in the surrounding tissue, leading to direct contact between tumour cells and adipocytes. SARIFA showed its significance in gastric and colorectal carcinoma, revealing lipid metabolism alternations that promote tumour progression.

methodsWe reviewed the SARIFA status of 166 PDAC cases on all available H&E-stained tumour slides from archival Whipple-resection specimens. SARIFA positivity was defined as SARIFA detection in at least 66% of the available slides. To investigate alterations in tumour metabolism and microenvironment, we performed immunohistochemical staining for FABP4, CD36 and CD68. To verify and quantify a supposed delipidation of adipocytes, adipose tissue was digitally morphometrised.

resultsIn total, 53 cases (32%) were classified as SARIFA positive and 113 (68%) as SARIFA negative. Patients with SARIFA-positive PDAC showed a significantly worse overall survival compared with SARIFA-negative cases (median overall survival: 11.0 months vs. 22.0 months, HR: 1.570 (1.082-2.278), 95% CI, p = 0.018), which was independent from other prognostic markers (p = 0.014). At the invasion front of SARIFA-positive PDAC, we observed significantly higher expression of FABP4 (p < 0.0001) and higher concentrations of CD68

conclusionsSARIFA is a promising prognostic biomarker for PDAC. Its assessment is characterised by simplicity and low effort. The mechanisms behind SARIFA suggest a tumour-promoting increased lipid metabolism and altered immune background, both showing new therapeutic avenues.

Indexed as

Biomarkers, TumorCarcinoma, Pancreatic DuctalFatty Acid-Binding ProteinsPancreatic NeoplasmsAdipocytesAdultAgedAged, 80 and overAntigens, CDAntigens, Differentiation, MyelomonocyticCD36 AntigensCD68 MoleculeFemaleHumansLipid MetabolismMaleAntigens, CDAntigens, Differentiation, MyelomonocyticBiomarkers, TumorCD36 AntigensCD68 antigen, humanCD68 MoleculeFABP4 protein, humanFatty Acid-Binding ProteinsLipid metabolismPancreasPDACSARIFA

Identifiers

PMID38926671
PMCPMC11210040

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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.