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

2013년 2월 11일 업데이트: 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.

연구 개요

상세 설명

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.

연구 유형

중재적

단계

  • 2 단계

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 장소

    • Tennessee
      • Nashville, Tennessee, 미국, 37023
        • Tennessee Oncology, PLLC

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

18년 이상 (성인, 고령자)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

모두

설명

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)

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 해당 없음
  • 중재 모델: 단일 그룹 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: 1
Systemic Therapy
20 mg PO three times weekly
다른 이름들:
  • 파노비노스타트
1 mg/kg/day PO continuously
다른 이름들:
  • Medrol, Depo-Medrol

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
기간
To assess the response rate to panobinostat of patients with cGvHD inadequately treated with steroids and calcineurin inhibitors.
기간: 30 months
30 months

2차 결과 측정

결과 측정
기간
To evaluate the safety and tolerability of panobinostat in patients with cGvHD.
기간: 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).
기간: 30 months
30 months
To assess changes in quality of life (QOL) after treatment with panobinostat.
기간: 30 months
30 months
To analyze survival at 6 and 12 months after initiation of panobinostat.
기간: 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.
기간: 30 months
30 months

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

협력자

수사관

  • 연구 의자: Daniel R Couriel, M.D., SCRI Development Innovations, LLC

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 등록 날짜

최초 제출

2009년 12월 7일

QC 기준을 충족하는 최초 제출

2009년 12월 8일

처음 게시됨 (추정)

2009년 12월 9일

연구 기록 업데이트

마지막 업데이트 게시됨 (추정)

2013년 2월 13일

QC 기준을 충족하는 마지막 업데이트 제출

2013년 2월 11일

마지막으로 확인됨

2013년 2월 1일

추가 정보

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

LBH589에 대한 임상 시험

구독하다