Evidence map›Paper›PMID 42642621›Full record

ArticleLeukemia2026

Ivosidenib monotherapy in IDH1 mutated myelodysplastic neoplasm/syndrome.

Marie Sébert, Emmanuelle Clappier, Sylvie Chevret, Hugo Bergugnat, Odile Rauzy, Aspasia Stamatoullas, Sophie Dimicoli-Salazar, Lamya Ait Si Selmi, Cendrine Chaffaut, Fatiha Chermat and 15 more

Registry-linked trialAbstract read
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In one paragraph

Article in Leukemia, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03503409 (A Single-arm Phase II Multicenter Study of IDH1), which is not on this map. Cited by 1 paper.

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

NCT03503409 phase2active not recruitingnot on this map

A Single-arm Phase II Multicenter Study of IDH1 (AG 120) Inhibitor in Patients With IDH1 Mutated Myelodysplastic Syndrome

TypeinterventionalSponsorGroupe Francophone des MyelodysplasiesRan2019 to 2027Enrolled68ConditionsMyelodysplastic Syndromes, Acute Myeloid LeukemiaArmsAG-120
3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
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

25 authors.

Marie SébertClinical Haematology Department, Saint-Louis Hospital, Assistance Publique-Hôpitaux de Paris (APHP), Paris Cité University, Leukemia Institute Paris Saint-Louis, Paris, France. marie.sebert@aphp.fr.ORCID http://orcid.org/0000-0003-4376-4097
Emmanuelle ClappierHaematology Laboratory, Saint-Louis Hospital, Paris Cité University, Leukemia Institute Paris Saint Louis APHP, Paris, France.
Sylvie ChevretBiostatistics Department, Saint Louis Hospital, APHP, Paris, France.
Hugo BergugnatHaematology Laboratory, Saint-Louis Hospital, Paris Cité University, Leukemia Institute Paris Saint Louis APHP, Paris, France.
Odile RauzyGroupe Francophone des Myélodysplasies (GFM), Paris, France.ORCID http://orcid.org/0000-0003-0321-6029
Aspasia StamatoullasGroupe Francophone des Myélodysplasies (GFM), Paris, France.
Sophie Dimicoli-SalazarGroupe Francophone des Myélodysplasies (GFM), Paris, France.
Lamya Ait Si SelmiGroupe Francophone des Myélodysplasies (GFM), Paris, France.
Cendrine ChaffautBiostatistics Department, Saint Louis Hospital, APHP, Paris, France.
Fatiha ChermatGroupe Francophone des Myélodysplasies (GFM), Paris, France.
Lise LarcherHaematology Laboratory, Saint-Louis Hospital, Paris Cité University, Leukemia Institute Paris Saint Louis APHP, Paris, France.ORCID http://orcid.org/0000-0002-9461-0728
Lauriane GoldwirtPharmacological Department, Saint-Louis Hospital, APHP, Paris, France.
Sylvain ThepotGroupe Francophone des Myélodysplasies (GFM), Paris, France.
Pierre PeterlinGroupe Francophone des Myélodysplasies (GFM), Paris, France.
Sophie ParkGroupe Francophone des Myélodysplasies (GFM), Paris, France.
Marie-Pierre GourinGroupe Francophone des Myélodysplasies (GFM), Paris, France.
Norbert VeyGroupe Francophone des Myélodysplasies (GFM), Paris, France.
Cécile BallyClinical Haematology Department, Necker Hospital, APHP, Paris, France.
Sébastien MauryClinical Haematology Department, Henri-Mondor Hospital, APHP, Créteil, France.
Gaelle FossardGroupe Francophone des Myélodysplasies (GFM), Paris, France.
Maud D'AveniGroupe Francophone des Myélodysplasies (GFM), Paris, France.ORCID http://orcid.org/0000-0002-5909-2742
Anne-Laure TaksinGroupe Francophone des Myélodysplasies (GFM), Paris, France.
Thomas CluzeauClinical Haematology Department, Nice University Hospital, Nice, France.ORCID http://orcid.org/0000-0002-6745-1127
Pierre Fenaux *Clinical Haematology Department, Saint-Louis Hospital, Assistance Publique-Hôpitaux de Paris (APHP), Paris Cité University, Leukemia Institute Paris Saint-Louis, Paris, France.
Lionel Adès *Clinical Haematology Department, Saint-Louis Hospital, Assistance Publique-Hôpitaux de Paris (APHP), Paris Cité University, Leukemia Institute Paris Saint-Louis, Paris, France. lionel.ades@aphp.fr.ORCID http://orcid.org/0000-0002-9020-8766

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ivosidenib (IVO) is an oral inhibitor of mutant IDH1 (IDH1m) approved for treatment of IDH1m acute myeloid leukemia (AML) in association with Azacitidine (AZA). We investigated safety and efficacy of IVO monotherapy in patients with IDH1m myelodysplastic neoplasm/syndrome (MDS). This multicenter phase 2 trial enrolled three cohorts: high-risk (HR-) relapse or refractory (R/R) patients after AZA (cohort A), treatment-naïve HR-patients (cohort B) and low-risk patients refractory to erythropoiesis-stimulating agents (cohort C). All patients received 28-day cycles of IVO at 500 mg once daily. Between 2019 and 2023, 48 patients were included (median age 76.5 years). The ORR after 3 cycles was 63.6% (95%CI, 40.7-82.8) in cohort A, and 78.3% (95%CI, 56.3-92.5) in cohort B; the 12-month OS rate in cohorts A and B was 18.2% (95%CI, 7.5-44.1) and 91.3% (95%CI, 80.5-100), respectively. In cohort C, no significant toxicities were reported. Higher baseline IDH1 mutant clone size predicted response, whereas TP53 or IDH2 co-mutations were associated with resistance. Molecular clearance was not required for clinical benefit. IVO monotherapy was well tolerated and demonstrated sustained clinical activity across all IDH1m cohorts representing a potential therapeutic breakthrough in this frail population, particularly as a first-line therapeutic option in treatment naïve IDH1m HR-MDS patients (IDIOME, NCT03503409).

Identifiers

What Socratic holds

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Registered trials

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 Socratic graph.