Evidence map›Paper›PMID 27310990›Full record

ArticleMedicine2016

Mastocytosis among elderly patients: A multicenter retrospective French study on 53 patients.

Audrey Rouet, Achille Aouba, Gandhi Damaj, Erinn Soucié, Katia Hanssens, Marie-Olivia Chandesris, Cristina Bulai Livideanu, Marine Dutertre, Isabelle Durieu, Catherine Grandpeix-Guyodo and 16 more

Erratum issuedOpen access · goldAbstract readMulticenter Study
In one paragraph

Article in Medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 33% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

26 authors at 16 institutions in 1 country.

Audrey RouetService de médecine interne, Hôpital Tenon, Université Pierre et Marie Curie, Paris, France Service de Médecine Interne, CHU de Caen, Université Basse Normandie, Caen, France Institut d'Hématologie de Basse Normandie, Centre Hospitalier Universitaire, Université de Caen-Basse Normandie, Caen, France Faculté de Médecine et AP-HP Necker-Enfants Malades, Centre de Référence des Mastocytoses, Paris Cedex 15, France Inserm, U1068, CRCM [Signaling, Hematopoiesis and Mechanism of Oncogenesis], Institut Paoli-Calmettes,Marseille, Aix-Marseille Univ, CNRS, UMR7258, Marseille, France Mastocytosis Competence Center of Midi-Pyrénées, Department of Dermatology, Toulouse University Hospital, Toulouse, France Service de Médecine Interne, Université Claude Bernard Lyon1, Groupe Hospitalier Lyon-Sud. Chemin du Grand Revoyet, Pierre Bénite, France Service de Dermatologie, Hôpital Tenon, Université Pierre et Marie Curie-Paris 6, Paris, France Service d'Hématologie Adultes, Université Paris Descartes, Paris Sorbonne Cité, Faculté de Médecine et AP-HP Necker-Enfants Malades, Institut Imagine, Université Paris Descartes, Paris Cedex 15, France Service de Médecine interne, Hôpital St Antoine, Université Pierre et Marie Curie-Paris 6, Paris, France Service de Médecine interne, Université de Rennes 1, Hôpital Sud CHU Rennes, Rennes, France Service de Médecine interne, Hôpital Pitié Salpêtrière, Université Pierre et Marie Curie-Paris 6, Paris, France Service de Médecine interne, CHU, Nantes, France Service de Médecine interne, Hôpital Européen Georges Pompidou, Université Paris 5, Paris, France Université de Lille, UFR Médecine, Lille, France; CHRU Lille, Pôle Spécialités Médicales et Gérontologie, Département de Médecine Interne et Immunologie Clinique, Lille Cedex, France; Centre National de Référence Maladies Systémiques et Auto-immunes Rares (Sclérodermie Systémique), Lille Cedex, France; LIRIC UMR 995, EA2686, France Médecine interne et Maladies vasculaires. Centre de compétences Maladies rares CHU, Angers, France Laboratoire d'Hématologie, Groupe Hospitalier Pitié-Salpêtrière 83, Bd de l'Hôpital, Paris, France LBPA CNRS UMR8113, Ecole Normale Supérieure de Cachan, Cachan, France Université Paris Descartes, Service de Maladies Infectieuses et Tropicales, Université Paris Descartes, Sorbonne, Paris 6, AP-HP, Hôpital Necker-Enfants malades, Centre d'Infectiologie Necker-Pasteur, IHU Imagine, Paris.
Achille Aouba
Gandhi Damaj
Erinn Soucié
Katia Hanssens
Marie-Olivia Chandesris
Cristina Bulai Livideanu
Marine Dutertre
Isabelle Durieu
Catherine Grandpeix-Guyodo
Stéphane Barète
Claude Bachmeyer
Angèle Soria
Laurent Frenzel
Olivier Fain
Bernard Grosbois
Christian de Gennes
Mohamed Hamidou
Jean-Benoit Arlet
David Launay
Christian Lavigne
Michel Arock
Olivier Lortholary
Patrice Dubreuil
Olivier Hermine
Sophie Georgin-Lavialle
Institut Necker Enfants Malades · FRSorbonne Université · FRAssistance Publique – Hôpitaux de Paris · FRCentre National de la Recherche Scientifique · FRDélégation Paris 5 · FRHôpital Lyon Sud · FRInserm · FRCentre Hospitalier Universitaire d'Angers · FRCentre Hospitalier Universitaire de Caen · FRCentre Hospitalier Universitaire de Nantes · FRCentre Hospitalier Universitaire de Rennes · FRHôpital Européen Georges-Pompidou · FRHôpital Tenon · FRPitié-Salpêtrière Hospital · FRUniversité de Lille · FRUniversité Paris Cité · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mastocytosis is a heterogeneous group of diseases with a young median age at diagnosis. Usually indolent and self-limited in childhood, the disease can exhibit aggressive progression in mid-adulthood. Our objectives were to describe the characteristics of the disease when diagnosed among elderly patients, for which rare data are available.The French Reference Center conducted a retrospective multicenter study on 53 patients with mastocytosis >69 years of age, to describe their clinical, biological, and genetic features.The median age of our cohort of patients was 75 years. Mastocytosis variants included were cutaneous (n = 1), indolent systemic (n = 5), aggressive systemic (n = 11), associated with a hematological non-mast cell disease (n = 34), and mast cell leukemia (n = 2). Clinical manifestations were predominantly mast cell activation symptoms (75.5%), poor performance status (50.9%), hepatosplenomegaly (50.9%), skin involvement (49.1%), osteoporosis (47.2%), and portal hypertension and ascites (26.4%). The main biological features were anemia (79.2%), thrombocytopenia (50.9%), leucopenia (20.8%), and liver enzyme abnormalities (32.1%). Of the 40 patients tested, 34 (85%), 2 (5%), and 4 (10%) exhibited the KIT D816V mutant, other KIT mutations and the wild-type form of the KIT gene, respectively. Additional sequencing detected significant genetic defects in 17 of 26 (65.3%) of the patients with associated hematological non-mast cell disease, including TET2, SRSF2, IDH2, and ASLX1 mutations. Death occurred in 19 (35.8%) patients, within a median delay of 9 months, despite the different treatment options available.Mastocytosis among elderly patients has a challenging early detection, rare skin involvement, and/or limited skin disease; it is heterogeneous and has often an aggressive presentation with nonfortuitous associated myeloid lineage malignant clones, and thus a poor overall prognosis.

Indexed as

MutationAgedAged, 80 and overDisease ProgressionDNA Mutational AnalysisDNA, NeoplasmFemaleFranceHumansMaleMast CellsMastocytosisMorbidityOncogenesRetrospective StudiesDNA, Neoplasm

Identifiers

PMID27310990
PMCPMC4998476
OpenAlexW2444144988

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

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.