Evidence map›Paper›PMID 30617596›Full record

ArticleClinical rheumatology2019

Concomitant association of giant cell arteritis and malignancy: a multicenter retrospective case-control study.

S Deshayes, E Liozon, N Chanson, K Sacré, T Moulinet, C Blanchard-Delaunay, O Espitia, M Groh, M Versini, T Le Gallou and 16 more

Abstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Clinical rheumatology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

7 citing papers in PubMed, 14 citations in OpenAlex.

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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

26 authors at 14 institutions in 1 country.

S DeshayesDepartment of Internal Medicine and Clinical Immunology, Normandie Univ, UNICAEN, CHU de Caen Normandie, Avenue de la Côte de Nacre, 14000, Caen, France.
E LiozonDepartment of Internal Medicine, CHU Limoges, Limoges, France.
N ChansonDepartment of Internal Medicine, Hôpital Bichat, Paris, France.
K SacréDepartment of Internal Medicine, Hôpital Bichat, Paris, France.
T MoulinetDepartment of Internal Medicine, Hôpitaux Privés de Metz, Metz, France.
C Blanchard-DelaunayDepartment of Internal Medicine, Centre Hospitalier Georges Renon, Niort, France.
O EspitiaDepartment of Internal Medicine, CHU Nantes, Nantes, France.
M GrohDepartment of Internal Medicine, National Referral Center for Hypereosinophilic Syndromes (CEREO), Hôpital Foch, Suresnes, France.
M VersiniInstitut Arnault Tzanck, Saint Laurent du Var, France.
T Le GallouDepartment of Internal Medicine, CHU Rennes, Rennes, France.
J-E KahnDepartment of Internal Medicine, Hôpital Ambroise Paré, Boulogne Billancourt, France.
V GrobostDepartment of Internal Medicine, CHU Estaing, Clermont-Ferrand, France.
S HumbertDepartment of Internal Medicine, CHU de Besançon, Besançon, France.
M SamsonDepartment of Internal Medicine and Clinical Immunology, CHU Dijon, Dijon, France.
R Mourot CottetDepartment of Internal Medicine, Hôpital Civil, Strasbourg, France.
K MazodierDepartment of Internal Medicine, Hôpital de la Conception, Marseille, France.
A DartevelDepartment of Internal Medicine, CHU Grenoble, Grenoble, France.
J CampagneDepartment of Infectious and Systemic Diseases, Hôpital d'Instruction des Armées, Metz, France.
A DumontDepartment of Internal Medicine and Clinical Immunology, Normandie Univ, UNICAEN, CHU de Caen Normandie, Avenue de la Côte de Nacre, 14000, Caen, France.
B BienvenuDepartment of Internal Medicine, Hôpital Saint Joseph, Marseille, France.
M LambertDepartment of Internal Medicine, CHU de Lille, Lille, France.
A DaumasDepartment of Geriatric and Internal Medicine, CHU de Marseille, Marseille, France.
D SaadounDepartment of Internal Medicine, Hôpital Pitié Salpétrière, Paris, France.
A AoubaDepartment of Internal Medicine and Clinical Immunology, Normandie Univ, UNICAEN, CHU de Caen Normandie, Avenue de la Côte de Nacre, 14000, Caen, France.
H de BoyssonDepartment of Internal Medicine and Clinical Immunology, Normandie Univ, UNICAEN, CHU de Caen Normandie, Avenue de la Côte de Nacre, 14000, Caen, France. deboysson-h@chu-caen.fr.
French Study Group for Large Vessel Vasculitis (GEFA)
Normandie Université · FRCentre Hospitalier Universitaire de Besançon · FRCentre Hospitalier Universitaire de Grenoble · FRCentre Hospitalier Universitaire de Lille · FRCentre Hospitalier Universitaire de Nantes · FRHôpital Bichat-Claude-Bernard · FRInstitut Arnault Tzanck · FRSorbonne Université · FRCentre Hospitalier de Niort · FRCentre Hospitalier Universitaire de Clermont-Ferrand · FRCentre Hospitalier Universitaire de Limoges · FRCHU Dijon Bourgogne · FRHôpital Ambroise-Paré · FRHôpital de la Conception · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionSome studies suggest that there is an increased risk of malignancies in giant cell arteritis (GCA). We aimed to describe the clinical characteristics and outcomes of GCA patients with concomitant malignancy and compare them to a GCA control group.

methodPatients with a diagnosis of GCA and malignancy and with a maximal delay of 12 months between both diagnoses were retrospectively included in this study and compared to a control group of age-matched (3:1) patients from a multicenter cohort of GCA patients.

resultsForty-nine observations were collected (median age 76 years). Malignancies comprised 33 (67%) solid neoplasms and 16 (33%) clonal hematologic disorders. No over-representation of a particular type of malignancy was observed. Diagnosis of GCA and malignancy was synchronous in 7 (14%) patients, while malignancy succeeded GCA in 29 (59%) patients. Malignancy was fortuitously diagnosed based on abnormalities observed in laboratory tests in 26 patients, based on imaging in 14 patients, and based on symptoms or clinical examination in the nine remaining patients. Two patients had a concomitant relapse of both conditions. When compared to the control group, patients with concomitant GCA and malignancy were more frequently male (p < 0.001), with an altered general state (p < 0.001), and polymyalgia rheumatica (p < 0.01).

conclusionsThis study does not indicate an over-representation of any particular type of malignancy in GCA patients. Initial follow-up dictated by vasculitis may have led to an early identification of malignancy. Nevertheless, GCA male patients with an altered general state and polymyalgia rheumatica might more frequently show concomitant malignancies.

Indexed as

AgedFemaleFranceGiant Cell ArteritisHumansMaleNeoplasmsPolymyalgia RheumaticaRetrospective StudiesRisk AssessmentGiant cell arteritisHematologic neoplasmsMalignancyNeoplasms

Identifiers

PMID30617596
OpenAlexW2910898790

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.