Eltrombopag in Patients With Delayed Post Transplant Thrombocytopenia. (ITP0511)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details. Identifier: NCT01791101
Recruitment Status : Recruiting
First Posted : February 13, 2013
Last Update Posted : February 21, 2018
Information provided by (Responsible Party):
Gruppo Italiano Malattie EMatologiche dell'Adulto

Brief Summary:
This is a Phase II multicentre study. Patients will be administered eltrombopag 50 mg/daily. If patients don't achieve response after 2 months of therapy they will stop eltrombopag; if patients will achieve response after 2 months of therapy, they will continue eltrombopag for a maximum period of 24 months; 40 patients are needed. In stage I, 22 patients will be enrolled; if ≤ 4 responses at the first evaluation after 2 months (18%) will be seen, the trial will be stopped; if 5 or more responses will be seen, the accrual will continue. In stage II, 18 more patients will be enrolled. If ≤ 12 (30%) responses will be observed out of 40 patients, it will be concluded that the study drug is not active enough. If ≥ 13 responses will be observed, it will be concluded that eltrombopag is worth of further studies.

Condition or disease Intervention/treatment Phase
Thrombocytopenia Drug: Eltrombopag Phase 2

Detailed Description:

The incidence of delayed thrombocytopenia in patients who undergo allogeneic hemopoietic stem cell transplant (SCT) is nearly 20-40% (1-2). Chronic graft versus host disease (cGVHD) seems to be the most frequent pathologic condition associated with post SCT delayed thrombocytopenia. Previous studies indicated the occurrence of delayed thrombocytopenia as a poor prognostic factor for the outcome of patients undergoing SCT, particularly for those patients with cGVHD. In our experience, 27 out of 71 patients (38%) developed post SCT delayed thrombocytopenia, with a median platelet count of 29 x 109/L (range 7-86 x 109/L); cGVHD was associated with delayed thrombocytopenia in 54% of cases. The platelet count was >50 <100 x 109/L in 8 patients (30%) patients and 50 x 109/L in 19 (70%) among whom 9 had 20 x 109/L. The median post SCT survival was 12 months in patients who developed delayed thrombocytopenia vs. > 36 months in patients without delayed thrombocytopenia. The rate of patients alive 12, 24 and 33 months after SCT was 41%, 41% and 7% among patients with delayed thrombocytopenia vs. 93%, 87% and 87% (p< 0.0001). In patients with cGVHD the incidence of mortality was significantly higher in those who developed post SCT thrombocytopenia, i.e. 8 out of 13 (61.5%) vs. 2 out of 19 (10.5%) (p=0.005). Our data confirms the results of previous studies. Therefore, the occurrence of delayed thrombocytopenia in patients undergoing SCT is a very poor prognostic factor and the improvement of this condition may favourably affect patients' outcome. The pathophysiology of cGVHD relayed post SCT delayed thrombocytopenia is complex and only partial understood. Biological and clinical evidences support an autoimmune-like thrombocytopenia with increased platelet destruction; this mechanism is also suggested by the response to some therapeutic strategies generally adopted to treat classical immune thrombocytopenia as steroids, high dose intravenous immunoglobulin, splenectomy, rituximab. However a mechanism consistent with impaired platelet production has also been suggested. Adopting an index for plasma glycocalicin, plasma thrombopoietin (TPO), and circulating B cells producing anti-GPIIb-IIIa antibodies, Yamazaki et al. studied 23 SCT recipients who had prolonged and isolated thrombocytopenia with no apparent causes such as engraftment failure, recurrence of the underlying malignancy, microangiopathy or drugs and compared data with those observed in a similar cohort of SCT recipients with no thrombocytopenia, in patients with primary immune thrombocytopenia (ITP) and aplastic anemia. Despite the frequent occurrence of an antiplatelet antibody response, patients with post SCT thrombocytopenia showed a glycocalicin index and TPO status similar to that seen in aplastic anemia. TPO levels were normal in nearly 30% of patients. Recently, Bao et al. showed an improved regulatory T-cell (T-regs) activity in patients with chronic primary immune thrombocytopenia (ITP) treated with thrombolytic agents, suggesting a possible role of platelet count in improving T-reg function and restore immune tolerance.

On this grounds and similarly to ITP, the stimulation of thrombopoiesis with the thrombolytic agents could be beneficial in some patients with persistent post SCT thrombocytopenia both on platelet count and on cGVHD manifestations. Eltrombopag (Revolade) is a thrombopoietin receptor agonist indicated for the treatment of adult patients with ITP relapsed/refractory to splenectomy; eltrombopag may be considered as second line treatment for adult non-splenectomised patients where surgery is contraindicated. Eltrombopag is also under development for the treatment of thrombocytopenia due to hepatitis C virus HCV, for chemotherapy-induced thrombocytopenia and in MDS/AML.

Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 40 participants
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Eltrombopag in Patients With Delayed Post Transplant Thrombocytopenia.
Study Start Date : September 2013
Estimated Primary Completion Date : March 2018
Estimated Study Completion Date : March 2018

Resource links provided by the National Library of Medicine

Drug Information available for: Eltrombopag

Arm Intervention/treatment
Experimental: Eltrombopag
Eltrombopag 50 mg/daily.
Drug: Eltrombopag

Primary Outcome Measures :
  1. Number of patients who achieve both a platelet count ≥ 50 x 109/L and have doubled their baseline platelet count. [ Time Frame: Two months after treatment with eltrombopag. ]
    Response rate (OR), i.e. the number of patients who achieve both a platelet count ≥ 50 x 109/L and have doubled their baseline platelet count, two months after treatment with eltrombopag. The primary endpoint will be considered for all the treated population according to the intention-to-treat and in the evaluable population, i.e. all patients treated with eltrombopag for at least 3 weeks or who interrupted eltrombopag because of toxic events. A transient increase of platelet count after the administration of iv immunoglobulin given for anti- microbial purpose will not be considered criteria of response.

Secondary Outcome Measures :
  1. Number of adverse events. [ Time Frame: After 4 years from study entry. ]
    Safety profile Incidence of AEs according to NCI Common Terminology Criteria for Adverse Events v 4.0 [NCI CTCAE] toxicity scale.

  2. Number of surviving patients. [ Time Frame: At 4 years from study entry. ]
    Overall Survival OS will be evaluated with Kaplan Meyer and compared with historical patients who developed post SCT delayed thrombocytopenia.

  3. Number of bleeding events. [ Time Frame: After 4 years from study entry. ]
    Bleeding events Bleeding events will be evaluated according to the WHO bleeding scale (grade 0, no bleeding; grade 1, petechiae; grade 2, mild blood loss; grade 3, gross blood loss; grade 4, debilitating blood loss).

  4. Characteristics of TPO serum level. [ Time Frame: After 4 years from study entry. ]
    TPO serum level TPO will be measured using a Human TPO duo-set assay (R&D System). This assay employs the quantitative sandwich enzyme immunoassay technique to evaluate the concentration of TPO in plasma or serum.

  5. Patients T-reg activity. [ Time Frame: After 4 years from study entry. ]
    T-reg activity T-reg activity will be evaluated by flow cytometric analysis of CD4+ CD25+ FOXP3+ lymphocytes in a mixed lymphocyte population.

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Patients develop delayed thrombocytopenia, i.e. Platelet count 50 x 109/l 3 months after SCT;
  • Patients underwent allogeneic SCT with match related or unrelated donor;
  • Patients develop CGVHD-related delayed thrombocytopenia. The definition of cGVHD-related delayed thrombocytopenia is: platelet count 50 x 109/l from month 3 from SCT and presence of any clinical, radiological and/or laboratory finding indicative of cGVHD (all grades); - Patients underwent SCT because of lymphoma (Hodgkin or non-Hodgkin, indolent or aggressive), or multiple myeloma;
  • Sexually active males who accept to use a condom during intercourse while taking the drug and for 12 months after stopping treatment as they should not father a child in this period. A condom is required to be used also by vasectomised men (as well as during intercourse with a male partner) in order to prevent delivery of the drug via seminal fluid. Refer also to Appendix C. Female subjects of non-childbearing potential may be enrolled in the study; For this study population, non-childbearing potential is defined as current tubal ligation, hysterectomy, ovariectomy or post-menopause (please refer to Appendix C);
  • OR Female subjects of childbearing potential may be enrolled in the study, if the subject has practiced adequate contraception for 30 days prior to start of eltrombopag, has a negative pregnancy test prior to start of eltrombopag, and has agreed to continue adequate contraception during the entire treatment period and for 6 months after completion of the treatment.
  • Written informed consent obtained from the subject.

Exclusion Criteria:

  • Patients underwent SCT with aplo-identical donor or cord blood;
  • Patients underwent SCT for diseases different from lymphoma or multiple myeloma;
  • Patients have life threatening bleeding complications;
  • Patients have an expected survival < 1 month;
  • Patients have delayed thrombocytopenia related to medical conditions other then cGVHD;
  • Patients have progressive non stabilized cGVHD necessitating intensification of immune suppressive treatment in the last 2 weeks;
  • Patients need to introduce or increase the dosage of steroids, any other immune suppressive or cytotoxic agent at the time of enrolment into the study or start of eltrombopag; patients already in treatment with a fixed, stabilized dosage of steroids or other immune suppressive agents because of cGVHD may be included into the study;
  • Patients received concomitant erythropoietin treatment; Patients have active deep venous thrombosis (DVT);
  • Patients have venous occlusive disease (VOD);
  • Patients have grade 3-4 hyper bilirubinemia; elevation of hepatic enzymes because of cGVHD should not be considered criteria of exclusion.
  • Patients with baseline elevation of hepatic enzymes will be monitored carefully in order to point out possible addictive eltrombopag- related hepatotoxicity;
  • Patients have hepatic cirrhosis;
  • Patients have transplant related-microangiopathy;
  • Patients have active infections (CMV reactivation included);
  • Patients have hypersensitive to study drug;
  • Patients are unable to stop medications that are known to cause a drug-drug interaction with eltrombopag.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT01791101

Contact: Paola Fazi, Dr.
Contact: Enrico Crea

UO Ematologia con trapianto-Università degli Studi di Bari Aldo Moro Recruiting
Bari, Italy
Contact: Giorgina Specchia, Pr.         
Principal Investigator: Giorgina Specchia, Pr.         
Sub-Investigator: Domenico Pastore, Dr.         
Divisione di Ematologia - Ospedali Riuniti Recruiting
Bergamo, Italy
Contact: Alessandro Rambaldi         
Principal Investigator: Alessandro Rambaldi         
USD Trapianti di midollo per adulti - Cattedra di Ematologia - Università degli Studi di Brescia Recruiting
Brescia, Italy
Contact: Domenico Russo         
Principal Investigator: Domenico Russo         
Ospedale Santa Croce Divisione di Ematologia Cuneo Recruiting
Catania, Italy
Contact: Giuseppe Milone, Dr.         
Principal Investigator: Giuseppe Milone, Dr.         
Sub-Investigator: Salvatore Leotta, Dr.         
Ospedale Santa Croce Divisione di Ematologia Cuneo Recruiting
Cuneo, Italy
Contact: Nicola Mordini, Dr.         
Principal Investigator: Nicola Mordini, Dr.         
Sub-Investigator: Davide Rapezzi, Dr.         
Policlinico di Careggi Recruiting
Firenze, Italy
Contact: Alberto Bosi, Dr.         
Principal Investigator: Alberto Bosi, Dr.         
Sub-Investigator: Stefano Guidi, Dr.         
Divisione Ematologia 2 - Azienda Ospedaliera Universitaria - S.Martino Recruiting
Genova, Italy
Contact: Andrea Bacigalupo, Dr.         
Principal Investigator: Andrea Bacigalupo, Dr.         
Unità Trapianto di Midollo Ist. Nazionale Tumori Recruiting
Milano, Italy
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Principal Investigator: Paolo Corradini         
Sub-Investigator: Francesco Spina         
La Maddalena Casa di Cura di Alta Specialità Dipartimento Oncologico di III Livello Not yet recruiting
Palermo, Italy
Contact: Maurizio Musso, Pr.         
Principal Investigator: Maurizio Musso, Pr.         
Sub-Investigator: Alessandra Crescimano, Dr.         
U.O. Ematologia Clinica - Azienda USL di Pescara Recruiting
Pescara, Italy
Contact: Pasqua Bavaro, Dr.         
Principal Investigator: Pasqua Bavaro, Dr.         
Sub-Investigator: Elsa Pennese, Dr.         
Università Cattolica del Sacro Cuore - Policlinico A. Gemelli Not yet recruiting
Roma, Italy
Contact: Simona Sica         
Principal Investigator: Simona Sica         
Università degli Studi "Sapienza" - Dip Biotecnologie Cellulari ed Ematologia - Divisione di Ematologia Recruiting
Roma, Italy
Contact: Roberto Foà         
Principal Investigator: Roberto Foà         
Sub-Investigator: Anna Paola Iori         
Università degli Studi - Policlinico di Tor Vergata Not yet recruiting
Roma, Italy
Contact: Giorgio Arcese         
Principal Investigator: Giorgio Arcese         
Sub-Investigator: Alessandra Picardi         
Clinica Ematologica - Policlinico Universitario Recruiting
Udine, Italy
Contact: Francesco Zaja, Dr.         
Principal Investigator: Francesco Zaja, Dr.         
Sub-Investigator: Marianna Chizzotto, Dr.         
ULSS N. 6 Ospedale S. Bortolo Recruiting
Vicenza, Italy
Contact: Carlo Borghero         
Principal Investigator: Carlo Borghero         
ULSS N.6 Osp. S. Bortolo Recruiting
Vicenza, Italy
Contact: Carlo Borghero, Dr.         
Principal Investigator: Carlo Borghero, Dr.         
Sponsors and Collaborators
Gruppo Italiano Malattie EMatologiche dell'Adulto
Principal Investigator: Francesco Zaja Clinica Ematologica, DISM, Azienda Ospedaliera Universitaria S. M. Misericordia

Responsible Party: Gruppo Italiano Malattie EMatologiche dell'Adulto Identifier: NCT01791101     History of Changes
Other Study ID Numbers: ITP0511
2011-004608-39 ( EudraCT Number )
First Posted: February 13, 2013    Key Record Dates
Last Update Posted: February 21, 2018
Last Verified: February 2018
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

Keywords provided by Gruppo Italiano Malattie EMatologiche dell'Adulto:

Additional relevant MeSH terms:
Blood Platelet Disorders
Hematologic Diseases