Evidence map›Paper›PMID 42840804›Full record

ArticleHemaSphere2026

MEK inhibition achieves robust and durable responses in Erdheim-Chester disease.

Francesco Pegoraro, Félicien Triboulet, Matthias Papo, Francesco Peyronel, Anita Argentieri, Jerome Razanamahery, Ahmed Idbaih, Polyzois Makras, Ofer Shpilberg, Oshrat Hershkovitz-Rokah and 25 more

Abstract read
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Article in HemaSphere, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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3 · Its place in the literature

Who cites it

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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

35 authors.

Francesco PegoraroDepartment of Experimental and Clinical Medicine University of Florence Florence Italy.ORCID https://orcid.org/0000-0002-4954-5744
Félicien TribouletInternal Medicine Department 2 Institut E3M, French Reference Centre for Histiocytosis, Pitié-Salpȇtrière Hospital, CIMI INSERM-UMRS 1135, Sorbonne University, Assistance Publique-Hôpitaux de Paris Paris France.
Matthias PapoInternal Medicine Department 2 Institut E3M, French Reference Centre for Histiocytosis, Pitié-Salpȇtrière Hospital, CIMI INSERM-UMRS 1135, Sorbonne University, Assistance Publique-Hôpitaux de Paris Paris France.ORCID https://orcid.org/0000-0003-3389-9473
Francesco PeyronelDepartment of Experimental and Clinical Medicine University of Florence Florence Italy.ORCID https://orcid.org/0000-0001-8470-1952
Anita ArgentieriDepartment of Hematology and Oncology Meyer Children's Hospital IRCCS Florence Italy.ORCID https://orcid.org/0009-0004-0827-3051
Jerome RazanamaheryDepartment of Internal Medicine and Clinical Immunology Dijon University Hospital Dijon France.
Ahmed IdbaihNeuro-Oncology Department Sorbonne University, Paris Brain Institute - ICM, Inserm, CNRS, Pitié-Salpêtrière Hospital, DMU Neurosciences, Assistance Publique-Hôpitaux de Paris Paris France.ORCID https://orcid.org/0000-0001-5290-1204
Polyzois MakrasDepartment of Endocrinology and Diabetes and LCH and ECD Adult Clinic 251 Hellenic Air Force & VA General Hospital Athens Greece.ORCID https://orcid.org/0000-0002-3231-3357
Ofer ShpilbergAdelson School of Medicine Ariel University Ariel Israel.ORCID https://orcid.org/0000-0003-4463-7647
Oshrat Hershkovitz-RokahDepartment of Molecular Biology Faculty of Natural Sciences Ariel University Ariel Israel.ORCID https://orcid.org/0000-0003-4685-0679
Michael GirschikofskyDivision of Hematology With Stem Cell Transplantation, Hemostaseology and Medical Oncology, Department of Internal Medicine I Ordensklinikum Linz Elisabethinen Linz Austria.ORCID https://orcid.org/0000-0003-3270-411X
Matthew CollinFaculty of Medical Sciences Newcastle University Newcastle Upon Tyne United Kingdom.ORCID https://orcid.org/0000-0001-6585-9586
Kristian BowlesNorwich Medical School University of East Anglia Norwich United Kingdom.
Satyen H GohilDeparment of Hematology University College London Hospitals NHS Foundation Trust London United Kingdom.
Rodothea AmerikanouDeparment of Hematology University College London Hospitals NHS Foundation Trust London United Kingdom.ORCID https://orcid.org/0000-0001-6691-9210
Emmanuel LedoultDepartment of Internal Medicine Lille University Hospital Lille France.ORCID https://orcid.org/0000-0002-3925-9541
Tanguy Le ScornetDepartment of Internal Medicine Nantes University Hospital Nantes France.ORCID https://orcid.org/0009-0003-9816-8572
Mathilde de MenthonDepartment of Internal Medicine and Clinical Immunology Bicetre Hospital, Assistance Publique - Hôpitaux de Paris Le Kremlin Bicêtre France.
Etienne RiviereDepartment of Internal Medicine Haut-Lévèque University Hospital Bordeaux France.ORCID https://orcid.org/0000-0003-0254-3394
Xavier BouluDepartment of Internal Medicine Amiens University Medical Center Amiens France.ORCID https://orcid.org/0000-0002-1621-4308
Henry DupuyDepartment of Internal Medicine Ramsay Santé Clinique Aguiléra Biarritz France.
Achille AoubaDepartment of Internal Medicine Caen University Hospital Caen France.
Stanislas FaguerDepartment of Nephrology and Organ Transplantation National Referral Centre for Rare Kidney Diseases-SORARE, Toulouse University Hospital Toulouse France.ORCID https://orcid.org/0000-0003-0553-0927
Xavier SolanichDepartment of Internal Medicine Bellvige University Hospital, Hospitalet de Llobregat Barcelona Spain.ORCID https://orcid.org/0000-0002-2572-2187
Elena SieniDepartment of Hematology and Oncology Meyer Children's Hospital IRCCS Florence Italy.ORCID https://orcid.org/0000-0002-6192-9812
Stéphane BareteUnit of Dermatology Pitié-Salpȇtrière Hospital, Assistance Publique-Hôpitaux de Paris Sorbonne University Paris France.ORCID https://orcid.org/0000-0003-1593-9750
Chiara BellinoUnit of Immunology, Rheumatology, Allegy and Rare Diseases San Raffaele Hospital IRCCS Vita-Salute San Raffaele University Milano Italy.
Alessandro TomelleriUnit of Immunology, Rheumatology, Allegy and Rare Diseases San Raffaele Hospital IRCCS Vita-Salute San Raffaele University Milano Italy.ORCID https://orcid.org/0000-0002-5440-2078
Corrado CampochiaroUnit of Immunology, Rheumatology, Allegy and Rare Diseases San Raffaele Hospital IRCCS Vita-Salute San Raffaele University Milano Italy.ORCID https://orcid.org/0000-0001-6806-3794
Lorenzo DagnaUnit of Immunology, Rheumatology, Allegy and Rare Diseases San Raffaele Hospital IRCCS Vita-Salute San Raffaele University Milano Italy.ORCID https://orcid.org/0000-0002-7428-315X
Zahir AmouraInternal Medicine Department 2 Institut E3M, French Reference Centre for Histiocytosis, Pitié-Salpȇtrière Hospital, CIMI INSERM-UMRS 1135, Sorbonne University, Assistance Publique-Hôpitaux de Paris Paris France.
Jean-François EmileEA4340 BECCOH, Versailles SQY University, Pathology Department, Ambroise Paré Hospital Assistance Publique-Hôpitaux de Paris Boulogne France.ORCID https://orcid.org/0000-0002-6073-4466
Fleur Cohen-AubartInternal Medicine Department 2 Institut E3M, French Reference Centre for Histiocytosis, Pitié-Salpȇtrière Hospital, CIMI INSERM-UMRS 1135, Sorbonne University, Assistance Publique-Hôpitaux de Paris Paris France.
Augusto VaglioDepartment of Biomedical, Experimental and Clinical Sciences "Mario Serio" University of Florence Florence Italy.
Julien HarocheInternal Medicine Department 2 Institut E3M, French Reference Centre for Histiocytosis, Pitié-Salpȇtrière Hospital, CIMI INSERM-UMRS 1135, Sorbonne University, Assistance Publique-Hôpitaux de Paris Paris France.ORCID https://orcid.org/0009-0003-9794-1316

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Erdheim-Chester disease (ECD) is a rare histiocytic neoplasm characterized by heterogeneous clinical manifestations and limited evidence to guide targeted therapy. While MEK inhibitors (MEKi) are increasingly used, data on their real-world efficacy, durability, and safety remain incomplete. We analyzed outcomes of patients with ECD treated with MEKi monotherapy across eight countries and assessed the dynamics and predictors of response, treatment retention, and the safety profile of MEKi. We included 170 patients and were able to evaluate response in 159 (94%) of them. Objective responses were observed in 112 patients (70%), disease stabilization in 35 (22%), and disease progression in 12 (8%). Response rates were independent of treatment lines and underlying molecular alterations. The median time to best response was 14 months, with an estimated 2-year probability of response of 61% (95% CI 51%-67%). In multivariable analysis, dyslipidemia (odds ratio [OR] 0.359, 95% CI 0.171-0.745) and neurodegeneration (OR 0.354, 95% CI 0.144-0.864) were associated with a lower probability of response to MEKi, while cutaneous and gastrointestinal involvement with a higher probability. After a median follow-up of 27 months (interquartile range [IQR] 12-57), the treatment retention rate was 76%, with most discontinuations attributable to toxicity. Adverse events were reported in 106 patients (62%) and were severe in 39 patients (23%). The estimated 2-year event-free survival was 65% (95% CI 57%-72%), and the estimated 2-year overall survival was 80% (95% CI 72%-86%). MEKi monotherapy provides robust and durable clinical efficacy in patients with ECD, with high response rates and favorable long-term outcomes, despite a substantial burden of toxicity.

Identifiers

PMID42840804
PMCPMC13641181

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