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Myelodysplastic NeoplasmNCT07825207

Observational Study on Eltrombopag in Hypocellular Myelodysplastic Neoplasms

An observational study of Myelodysplastic Neoplasm and Myelodysplastic Syndrome, run by Fondazione Italiana Sindromi Mielodisplastiche-ETS at 26 sites in Italy.

Active, not recruiting

Under way, not looking for participants. Everyone needed has enrolled. The study is still running.

Official record
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Trial summary

Hypocellular myelodysplastic neoplasms (h-MDS) are a distinct entity introduced in the 2022 WHO classification. They are characterized by reduced bone marrow cellularity and may share several clinical, morphological, immunological, and molecular features with aplastic anemia (AA), making the differential diagnosis… Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
Eltrombopag (ELT)
How many people
100 participants
Where
26 sitesItaly
Study dates
1 May 2026to 31 Jul 2027
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Adult patients diagnosed with h-MDS according to WHO 2022 and treated with eltrombopag included in FISiM registry

Who may be able to join

  • Adult patients (i.e. aged ≥18 years) diagnosed with MDS-h according to WHO 2022
  • IPSS-R risk very-low to intermediate
  • De novo or therapy related MDS
  • Availability of bone marrow sample for central revision
  • Treatment with eltrombopag, in monotherapy or associated with IST, as first -line therapy or as a subsequent therapy to the first line

Who cannot join

  • Unavailability of bone marrow sample for central revision

Trial locations and contacts

26 sites in 1 country.

26 sites in 1 country

Italy26 sites
  • SCDU di Ematologia, AO SS. Antonio e Biagio e Cesare Arrigo

    Alessandria

  • UO Ematologia con Trapianto, Dipartimento di Medicina di Precisione e Rigenerativa e Area Ionica, AOU Consorziale Policlinico, Università degli Studi Aldo Moro

    Bari

  • Istituto di Ematologia L. e A. Seràgnoli, Policlinico di S. Orsola, IRCCS AOU di Bologna

    Bologna

  • Comprehensive Cancer Center, Spedali Civili di Brescia

    Brescia

  • Oncologia Medica, INOC

    Candiolo

  • MDS Unit, AOU Careggi

    Florence

  • UO Ematologia e Terapie Cellulari, IRCCS Ospedale Policlinico San Martino

    Genova

  • SC Immunoematologia e Medicina Trasfusionale, Ospedale Carlo Poma, ASST di Mantova

    Mantua

  • Hematology Unit, IRCCS Istituto Romagnolo per lo Studio dei Tumori Dino Amadori

    Meldola (FC)

  • Oncoematologia, PO Fatebenefratelli, ASST Fatebenefratelli Sacco

    Milan

  • SC Medicina II, PO San Paolo, ASST Santi Paolo e Carlo

    Milan

  • Unità di Ematologia e TMO, IRCCS Ospedale San Raffaele

    Milan

  • UOC Ematologia, Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico

    Milan

  • UOC Ematologia, Dipartimento di Medicina Clinica e Chirurgia, Università di Napoli Federico II

    Naples

  • SCDU Medicina interna ad indirizzo ematologico, AOU San Luigi Gonzaga, Università degli Studi di Torino

    Orbassano

  • UO Ematologia e Immunologia clinica, Dipartimento di Medicina, AOU di Padova

    Padova

  • UOC Ematologia e CTMO, AOU Parma

    Parma

  • UO Ematologia e CTMO, Ospedale Guglielmo da Saliceto

    Piacenza

  • UOC Ematologia, Ospedale S. Eugenio, ASL Roma 2

    Roma

  • Ematologia, Dipartimento di Medicina, Chirurgia e Farmacia, Università degli Studi di Sassari

    Sassari

  • SC Ematologia U, AOU Città della Salute e della Scienza, Università degli Studi di Torino

    Torino

  • SC Ematologia, Dipartimento di Oncologia, AOU Città della Salute e della Scienza

    Torino

  • SCDU Ematologia e Terapie cellulari, AO Ordine Mauriziano, Università degli Studi di Torino

    Torino

  • UOC Ematologia e TMO, Pia Fondazione di Culto e Religione Card. G. Panico

    Tricase

  • UOC Ematologia, Ospedale Maggiore, ASU Giuliano Isontina

    Trieste

  • Hematology Unit, Ospedale di Circolo e Fondazione Macchi, ASST Sette Laghi

    Varese

Other trials in Italy

About this study

Hypocellular myelodysplastic neoplasms (h-MDS) are a distinct entity introduced in the 2022 WHO classification. They are characterized by reduced bone marrow cellularity and may share several clinical, morphological, immunological, and molecular features with aplastic anemia (AA), making the differential diagnosis between the two conditions challenging.

Eltrombopag, a thrombopoietin receptor agonist, has demonstrated efficacy in patients with severe AA and has also shown activity in lower-risk MDS, with bone marrow hypocellularity identified as a potential predictor of response. In Italy, eltrombopag has been used off-label in patients with h-MDS and clinically relevant cytopenias. However, systematic real-world data on its effectiveness and safety in this patient population, either as monotherapy or in combination with immunosuppressive therapy (IST), remain limited.

Read more

This is an observational study. We plan to analyse all patients with h-MDS consecutively diagnosed and included in the FISIM registry in 26 Italian centres.

Study duration: 12 months Data to be collected: demographic, disease characteristics at diagnosis (blood count, morphology, histopathology, cytogenetics, multiparameter flow cytometry, presence of PNH clone, molecular data), response to treatment according to IWG criteria, progression to AML rate and survival.

Centralized revision of bone marrow biopsy: bone marrow biopsy at diagnosis will be centrally reviewed

Read the detailed description

Myelodyspastic neoplasms (MDS) are a heterogeneous group of clonal haematopoietic stem cell disorders characterised by ineffective haematopoiesis, morphological dysplasia and a variable risk of transformation into acute myeloid leukaemia (AML). These diseases generally occur in the elderly, with a median age of onset above 70 years.

Recently, major advances in molecular technology and the development of next-generation sequencing (NGS) have deepened our understanding of MDS pathobiology. Hence, the International Consensus Classification (ICC), and the World Health Organization (WHO) proposed in 2022 a revision to the current classification system.

Hypocellular MDS (h-MDS), defined as a bone marrow cellularity of less than 30% in individuals younger than 60 years of age or less than 20% in those older than 70 years, is a new entity included in the WHO-2022 classification but not present in the ICC, accounting for 10-27% of all MDS cases (2,5-7).

The different prevalences of h-MDS are reported because derive from heterogeneity across the studies in the criteria used to define bone marrow hypocellularity, or the inclusion of de novo or both de novo and secondary cases, or differences in genetic and environmental backgrounds among the populations studied and in the possible contamination with patients with aplastic anaemia (AA). Hypocellular MDS are characterized by bone marrow hypoplasia, a low rate of progression to acute myeloid leukemia (AML), and poor response to conventional MDS therapies. For at least some types of AA and MDS, the overwhelming body of evidence points to a shared pathogenesis and, more speculatively, a shared etiology.

The pathogenesis of h-MDS involves immune system activation against hemopoietic precursor, which may explain the favourable response to immunosuppressive therapy.

Recently, based on clinical features and immunologic and molecular studies, two phenotypes of h-MDS were identified and proposed: one with prevailing inflammation and immune activation defined AA-like, and the other characterized by genetic lesions, clonal selection and clonal evolution, named MDS-like.

Differential diagnosis between h-MDS and AA can be difficult as the two pathologies have partially overlapping diagnostic criteria (8,9). Although cellularity easily differentiates h-MDS from normo/hypercellular cases, the distinction from AA is harder when only clinical features are considered. The presence of >10% dysplasia of one lineage would distinguish h-MDS from AA in hypercellular cases and MDS from Idiopatic Cytopenia of Unknown Significance (ICUS). Compared to AA patients, h-MDS are usually older, show marrow dysplasia, and display more BM blasts and more frequent cytogenetic or molecular alterations. The occasional presence of PNH clones in the setting of h-MDS may point toward the diagnosis of AA. Cytogenetic abnormalities are found in about 50% of MDS and FISH analysis could help to better define category group including chromosome 3, 5, and 7 alterations.

Mutational pattern of h-MDS seems to overlap with the classic MDS pattern except for the relative absence of spliceosoma mutations or myeloproliferative features (SRSF2, ZRSR2, U2AF1) and lower frequency of RUNX1, ASXL1, DNMT3A, EZH2, and TP53 mutations.

Using the Internationally Prognostic Scoring System (IPSS) and its revised version (IPSS-R) , h-MDS are classified as low risk and associated with more favourable outcome versus non h-MDS The treatment options used were mainly directed at controlling cytopenias rather than eradication of disease. Lower Risk patients are commonly treated with lower intensity therapies such as hematopoietic growth factors or immunomodulatory agents, while hypomethylating agents, cytotoxic agents, or allo-HCT are typically reserved for higher risk patients.

In some series a hypocellular marrow predicted a higher likelihood of response, analogous to the response to immunosuppressive therapy (IST) in aplastic anemia.

Younger age, normal karyotype or trisomy 8, lack of transfusion dependence, and the presence of a PNH clone predicted response to immunosuppressive therapy, but none is a robust biomarker as responses have also been noted in lower risk MDS patients without these features.

Beyond IST therapy, thrombopoietin receptor agonists (TPO-RA have been studied in MDS with variable response rates.

Eltrombopag, a TPO-RA, was first used to treat thrombocytopenia in patients with idiopathic thrombocytopenic purpura, but has also been shown to improve hematologic response in patients with refractory severe AA and to increase overall and complete responses when combined with standard immunosuppression in treatment-naïve severe AA.

In a phase III study eltrombopag has shown activity in low risk MDS with thrombocytopenia. In a phase II study on 25 LR-MDS patients eltrombopag lead to a bilineage response in 44% of patients and hypocellularity was a predictor of response.

On the basis of this encouraging data eltrombopag has been used in Italy in h_MDS with clinically relevant cytopenias off-label. Data on eltrombopag use outside from clinical trials in a real-world setting, alone or in combination with other IST are missing.

Being tested
Eltrombopag (ELT)
Keywords
Hypocellular Myelodysplastic Neoplasms, Eltrombopag, Thrombocytopenia, myelodysplastic Syndrome
Medical subject headings
Anemia, Refractory, with Excess of Blasts, Myelodysplastic Syndromes, Thrombocytopenia

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Eltrombopag (ELT)Drug

    Eltrombopag administered as part of routine clinical practice for the treatment of hypocellular myelodysplastic neoplasms. The study retrospectively and prospectively evaluates the effectiveness and safety of eltrombopag in patients treated with eltrombopag monotherapy or in combination with immunosuppressive therapy.

Study groups in NCT07825207
Study groupRoleWhat they receive
Adult patients diagnosed with h-MDS according to WHO 2022 and treated with eltrombopagAdult patients diagnosed with h-MDS according to WHO 2022 and treated with eltrombopag included in FISiM registry * IPSS-R very-low to intermediate * De novo or therapy related Available bone marrow sample for central revision
Receives: Drug: Eltrombopag (ELT)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Overall Response Rate (ORR)

    Overall response rate to eltrombopag according to the International Working Group (IWG) response criteria (Cheson 2006)

    Measured: From initiation of eltrombopag treatment through the last available response assessment, up to study completion.

Secondary outcomes (6)
  1. Overall Response Rate (ORR) of eltrombopag combined with immunosuppressive drugs

    Overall response rate to eltrombopag when administered in combination with immunosuppressive drugs.

    Measured: From initiation of eltrombopag treatment through the last available response assessment, up to study completion.

  2. Overall Survival (OS)

    Overall survival from diagnosis and from initiation of eltrombopag treatment.

    Measured: From diagnosis and from initiation of eltrombopag treatment until death or last available follow-up, up to study completion.

  3. Duration of Response (DoR)

    Duration of response to eltrombopag.

    Measured: From achievement of response until loss of response, death, or last available follow-up, up to study completion.

  4. Adverse Events (AE) and Serious Adverse Events (SAE)

    Percentage of participants experiencing adverse events and serious adverse events reported in relation to eltrombopag treatment.

    Measured: From initiation of eltrombopag treatment through the end of treatment, up to study completion.

  5. Acute Myeloid Leukemia (AML) Rate

    Rate of progression to acute myeloid leukemia.

    Measured: From diagnosis through study completion.

  6. Time to AML Progression

    Time to progression to acute myeloid leukemia from diagnosis and from initiation of eltrombopag treatment

    Measured: From diagnosis and from initiation of eltrombopag treatment until AML progression or last available follow-up, up to study completion.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted17 Sep 2026
  2. Study start1 May 2026
  3. Primary completion30 Nov 2026 (estimated)
  4. Study completion31 Jul 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Retrospective
Enrolment
100 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07825207
Sponsor's protocol ID
FISiM-Eltrombopag-hMDS
Status last verified
Sep 2026
First submitted
11 Sep 2026
Last updated
17 Sep 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
Individual data sharing
No: for national regulations

Questions about this trial

What is this clinical trial studying?

An observational study of Myelodysplastic Neoplasm and Myelodysplastic Syndrome, run by Fondazione Italiana Sindromi Mielodisplastiche-ETS at 26 sites in Italy.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: under way, not looking for participants, as of the sponsor's last update on 17 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 26 sites in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Overall Response Rate (ORR) (time frame: From initiation of eltrombopag treatment through the last available response assessment, up to study completion.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 17 Sep 2026.

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