Questa pagina è stata tradotta automaticamente e l'accuratezza della traduzione non è garantita. Si prega di fare riferimento al Versione inglese per un testo di partenza.

A Study of Panobinostat (LBH589) as Second-Line Therapy in Patients With Chronic Graft-Versus-Host Disease

11 febbraio 2013 aggiornato da: SCRI Development Innovations, LLC

A Phase II Study of Panobinostat (LBH589) as Second-Line Therapy in Patients With Chronic Graft-Versus-Host Disease

There is a clear need for effective, steroid-sparing agents for the management of chronic graft-versus-host disease (GVHD). Thus, agents like Histone deacetylase (HDAC) inhibitors, with the potential of decreasing pro-inflammatory events leading to GVHD without affecting graft-versus-leukemia (GVL), may have a central role in the prevention and treatment of GVHD.

This study will look at the efficacy of panobinostat (LBH589), an HDAC inhibitor, in the treatment of patients with chronic GVHD who have failed corticosteroids. In this group of patients, effective steroid-sparing options are limited and are usually associated with profound immunosuppression and decreased GVL effect.

Panoramica dello studio

Descrizione dettagliata

Chronic GVHD is an autoimmune, inflammatory disorder that occurs in the majority of patients who experience acute GVHD. Long-term corticosteroids are still standard therapy for chronic GVHD. Corticosteroids are associated with high morbidity and non-relapse mortality. In addition, corticosteroids are broadly immunosuppressive and can also decrease the GVL effect and increase the incidence of relapse. There is a clear need for effective, steroid-sparing agents for the management of chronic GVHD. Thus, agents like HDAC inhibitors, with the potential of decreasing pro-inflammatory events leading to GVHD without affecting GVL, may have a central role in the prevention and treatment of GVHD.

This study will look at the efficacy of panobinostat (LBH589), an HDAC inhibitor, in the treatment of patients with chronic GVHD who have failed corticosteroids. In this group of patients, effective steroid-sparing options are limited and are usually associated with profound immunosuppression and decreased GVL effect.

Tipo di studio

Interventistico

Fase

  • Fase 2

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

    • Tennessee
      • Nashville, Tennessee, Stati Uniti, 37023
        • Tennessee Oncology, PLLC

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

18 anni e precedenti (Adulto, Adulto più anziano)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Descrizione

Inclusion Criteria:

  1. Chronic GvHD following allogeneic HSCT of any source (bone marrow, peripheral blood, or cord blood stem cells), from any donor type (related, unrelated, or mismatched) and with any type of malignancy. Chronic GvHD will be defined according to NIH Consensus Criteria.
  2. Patients must have had inadequate response to treatment with steroids and calcineurin inhibitors. Patients must have been treated with an initial dose of at least 1 mg/kg/day of methylprednisolone (MP) or equivalent in combination with tacrolimus or cyclosporine and must fulfill the definition of steroid refractoriness or resistance. Steroid refractoriness or resistance will be defined as:

    1. Lack of any response after 1 month of treatment with MP, including 15 days of at least 0.5 mg/kg/day.
    2. Worsening of existing GvHD or new organ involvement at any time following one week of initiation of MP at 1 mg/kg/day.
    3. Reflare or worsening of GvHD at any time during steroid taper.
    4. Patients should not have received any drug or treatment for chronic GvHD other than steroids and calcineurin inhibitors (i.e., cyclosporine or tacrolimus).
  3. Patient must not have evidence of primary disease relapse.
  4. An ECOG (Eastern Cooperative Oncology Group) performance status of ≤2
  5. Baseline MUGA or ECHO must demonstrate left ventricular ejection fraction (LVEF) ≥40%.
  6. No uncontrolled arrhythmias or symptoms of heart disease.
  7. FEV1, FVC, and DLCO ≥40%.
  8. Laboratory values as follows:

    • white blood cell ≥2500/mm³;
    • absolute neutrophil count (ANC) ≥1,000/mm³;
    • hemoglobin ≥9.5 g%;
    • platelets ≥50,000/mm³;
    • total bilirubin <3 x upper limits of normal;
    • aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤5 × the institutional upper limit of normal (ULN);
    • creatinine <1.5 × ULN or creatinine clearance ≥ 50 ml/min;
    • serum potassium ≥ LLN;
    • serum sodium ≥ LLN;
    • serum calcium WNL;
    • serum phosphorus WNL;
    • serum magnesium WNL;
  9. Patients with elevated alkaline phosphatase due to bone metastasis may be enrolled.
  10. TSH and free T4 within normal limits (clinically euthyroid patients are permitted to receive thyroid supplements to treat underlying hypothyroidism).
  11. Age ≥ 18 years, male or female.
  12. Ability to understand and willingness to sign a written informed consent document.

Exclusion Criteria:

  1. Prior HDAC, DAC, HSP90 inhibitors or valproic acid for the treatment of cancer.
  2. Patients who will need valproic acid for any medical condition during the study or ≤5 days prior to first panobinostat treatment.
  3. Use of prior immunosuppressants other than steroids and calcineurin inhibitors(i.e. cyclosporine or tacrolimus).
  4. Chronic active hepatitis or cirrhosis.
  5. Impaired cardiac function including any of the following:

    • Patients with congenital long QT syndrome;
    • Patients with history or presence of sustained ventricular tachyarrhythmias;
    • Patients with any history of ventricular fibrillation or Torsades de Pointes;
    • Patients with bradycardia defined as HR <50 bpm. Patients with pacemakers are eligible if HR ≥50 bpm.
    • Patients with myocardial infarction or unstable angina ≤6 months prior to starting study drug;
    • Right bundle branch block plus left anterior hemiblock (bifasicular block);
    • Screening ECG with QTc >450 msec;
    • Congestive heart failure (CHF) > New York Heart Association (NYHA) Class II (see Appendix D).
  6. Concomitant use of drugs with a risk of causing Torsades de Pointes (see Appendix A).
  7. Other concurrent severe and/or uncontrolled medical conditions.
  8. Any condition that impairs patient's ability to swallow whole pills or gastrointestinal (GI) tract disease that involves an inability to take oral medication, malabsorption syndrome, a requirement for intravenous (IV)

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: N / A
  • Modello interventistico: Assegnazione di gruppo singolo
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: 1
Systemic Therapy
20 mg PO three times weekly
Altri nomi:
  • Panobinostat
1 mg/kg/day PO continuously
Altri nomi:
  • Medrol, Depo-Medrol

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Lasso di tempo
To assess the response rate to panobinostat of patients with cGvHD inadequately treated with steroids and calcineurin inhibitors.
Lasso di tempo: 30 months
30 months

Misure di risultato secondarie

Misura del risultato
Lasso di tempo
To evaluate the safety and tolerability of panobinostat in patients with cGvHD.
Lasso di tempo: 30 months
30 months
To assess the steroid-sparing capacity of panobinostat (as proportion of patients able to discontinue steroids while receiving, or following therapy with, panobinostat).
Lasso di tempo: 30 months
30 months
To assess changes in quality of life (QOL) after treatment with panobinostat.
Lasso di tempo: 30 months
30 months
To analyze survival at 6 and 12 months after initiation of panobinostat.
Lasso di tempo: 30 months
30 months
To evaluate the relapse rate of the underlying malignancy as well as the occurrence of second malignancies at 6 and 12 months after initiation of panobinostat.
Lasso di tempo: 30 months
30 months

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Collaboratori

Investigatori

  • Cattedra di studio: Daniel R Couriel, M.D., SCRI Development Innovations, LLC

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Date di iscrizione allo studio

Primo inviato

7 dicembre 2009

Primo inviato che soddisfa i criteri di controllo qualità

8 dicembre 2009

Primo Inserito (Stima)

9 dicembre 2009

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Stima)

13 febbraio 2013

Ultimo aggiornamento inviato che soddisfa i criteri QC

11 febbraio 2013

Ultimo verificato

1 febbraio 2013

Maggiori informazioni

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

Prove cliniche su LBH589

Sottoscrivi