Evidence map›Paper›PMID 30868297›Full record

ArticleVirchows Archiv : an international journal of pathology2019

COPPS, a composite score integrating pathological features, PS100 and SDHB losses, predicts the risk of metastasis and progression-free survival in pheochromocytomas/paragangliomas.

Charlie Pierre, Mikaël Agopiantz, Laurent Brunaud, Shyue-Fang Battaglia-Hsu, Antoine Max, Celso Pouget, Claire Nomine, Sandra Lomazzi, Jean-Michel Vignaud, Georges Weryha and 3 more

Abstract read
PubMed Publisher
In one paragraph

Article in Virchows Archiv : an international journal of pathology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed, 3 pooled it
4.6field-weighted citation impact, top 5% 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

48 citing papers in PubMed, 3 syntheses or guidelines pooled it, 72 citations in OpenAlex.

  1. Guideline
  2. Multidisciplinary practice guidelines for the diagnosis, genetic counseling and treatment of pheochromocytomas and paragangliomas.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2021
    Guideline
  3. Pooled it
  4. Trial
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. The evolving roles of pathologists in paragangliomas and pheochromocytomas.Virchows Archiv : an international journal of pathology · 2026
    Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Approach to the Patient With Metastatic Pheochromocytoma and Paraganglioma.The Journal of clinical endocrinology and metabolism · 2025
    Article
  18. Article
  19. Metastatic Malignant Phaeochromocytoma in Ascitic Fluid: Cytological Diagnosis of a Rare Entity.Cytopathology : official journal of the British Society for Clinical Cytology · 2025
    Article
  20. 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

13 authors at 2 institutions in 1 country.

Charlie PierreDepartment of Pathology, CHRU de Nancy, Université de Lorraine, F-54000, Nancy, France.
Mikaël AgopiantzDepartment of Medical Gynecology, CHRU de Nancy, Université de Lorraine, F-54000, Nancy, France.
Laurent BrunaudDepartment of Endocrine Surgery, CHRU de Nancy, Université de Lorraine, F-54500, Vandœuvre-lès-Nancy, France.
Shyue-Fang Battaglia-HsuINSERM UMRS 1256, Nutrition, Genetics, and Environmental Risk Exposure (NGERE), Faculty of Medicine of Nancy, Université de Lorraine, F-54000, Nancy, France.
Antoine MaxDepartment of Pathology, CHRU de Nancy, Université de Lorraine, F-54000, Nancy, France.
Celso PougetDepartment of Pathology, CHRU de Nancy, Université de Lorraine, F-54000, Nancy, France.
Claire NomineDepartment of Endocrine Surgery, CHRU de Nancy, Université de Lorraine, F-54500, Vandœuvre-lès-Nancy, France.
Sandra LomazziCentre de Ressources Biologiques, BB-0033-00035, CHRU de Nancy, F-54000, Nancy, France.
Jean-Michel VignaudDepartment of Pathology, CHRU de Nancy, Université de Lorraine, F-54000, Nancy, France.
Georges WeryhaDepartment of Endocrinology, CHRU de Nancy, Université de Lorraine, F-54500, Vandœuvre-lès-Nancy, France.
Abderrahim OussalahINSERM UMRS 1256, Nutrition, Genetics, and Environmental Risk Exposure (NGERE), Faculty of Medicine of Nancy, Université de Lorraine, F-54000, Nancy, France.
Guillaume GauchotteDepartment of Pathology, CHRU de Nancy, Université de Lorraine, F-54000, Nancy, France. g.gauchotte@chru-nancy.fr.ORCID http://orcid.org/0000-0001-5585-9195
Hélène Busby-VennerDepartment of Pathology, CHRU de Nancy, Université de Lorraine, F-54000, Nancy, France.
Inserm · FRUniversité de Lorraine · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Current histoprognostic parameters and prognostic scores used in paragangliomas and pheochromocytomas do not adequately predict the risk of metastastic progression and survival. Here, using a series of 147 cases of paraganglioma and pheochromocytoma, we designed and evaluated the potential of a new score, the COPPS (COmposite Pheochromocytoma/paraganglioma Prognostic Score), by taking into consideration three clinico-pathological features (including tumor size, necrosis, and vascular invasion), and the losses of PS100 and SDHB immunostain to predict the risk of metastasis. We compared also the performance of the COPPS with several presently used histoprognostic parameters in risk assessment of these tumors. A PASS score (Pheochromocytoma of the Adrenal gland Scaled Score) ≥ 6 was significantly associated with the occurrence of metastases (P < 0.0001) and shorter PFS (P = 0.013). In addition, both MCM6 and Ki-67 LI correlated with worse PFS (P = 0.004 and P < 0.0001, respectively), and MCM6, but not Ki-67, was significantly higher in metastatic group (P = 0.0004). Loss of PS100 staining correlated with the occurrence of metastasis (P < 0.0001) and shorter PFS (P < 0.0001). At a value of greater or equal to 3, the COPPS correlated with shorter PFS (P < 0.0001), and predicted reproducibly (weighted Kappa coefficient, 0.863) the occurrence of metastases with a sensitivity of 100.0% and specificity of 94.7%. It thus surpassed those found for either PASS, SDHB, MCM6, or Ki-67 alone. In conclusion, while validation is still necessary in independent confirmatory cohorts, COPPS could be of great potential for the risk assessment of metastasis and progression in paragangliomas and pheochromocytomas.

Indexed as

AdolescentAdrenal Gland NeoplasmsAdultAgedAged, 80 and overBiomarkers, TumorChildFemaleHumansMaleMiddle AgedNeoplasm MetastasisNeoplastic ProcessesParagangliomaPheochromocytomaPrognosisBiomarkers, TumorCOPPSKi-67MCM6MetastasisParagangliomaPASSPheochromocytomaPrognosisPS100SDHB

Identifiers

PMID30868297
OpenAlexW2921132243

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.