Romidepsin in Treating Patients With Steroid-Refractory Graft-versus-Host Disease

This is an interventional supportive care trial for Graft Versus Host Disease Read More

Inclusion Criteria:

• Patients with steroid (or immunosuppressive therapy [IST]) refractory acute GVHD (aGVHD) or chronic GVHD (cGVHD)
• Absolute neutrophil count >= 750/mm^3
• Platelet count >= 50,000/mm^3
• Corrected QT interval (QTc) =< 480 msec
• Bilirubin =< 1.5 x upper limit of normal (ULN)
• Aspartate aminotransferase (AST) (serum glutamic oxaloacetic transaminase [SGOT]) and alanine aminotransferase (ALT) (serum glutamate pyruvate transaminase [SGPT]) =< 3 x ULN
• Serum potassium >= 3.8 mmol/L
• Serum magnesium >= 1.8 mg/dL
• Serum creatinine =< 2.0 mg/dl
• Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0-3
• Patients may undergo electrolyte repletion therapy to meet eligibility requirements

• Patients must be scheduled for tapering doses of (or no longer treated with):

  • Cyclosporine;
  • Tacrolimus;
  • Sirolimus;
  • Steroids (patients may be on physiologic doses of steroids)
• Patients receiving extracorporeal photopheresis must discontinue extracorporeal photopheresis or placed on a tapering schedule;
• Any prior therapy for GVHD must be completed and discontinued with the exception of the above;
• Patients with breakpoint cluster region (bcr)-ABL proto-oncogene 1 (abl) associated malignancies may be on a tyrosine kinase inhibitor as malignant disease therapy or prophylaxis
• There must be no uncontrolled active infections or medical conditions that the investigator feels will compromise the safety of the treatment and/or the assessment of the efficacy of therapy
• The patient must be aware of the high risk and experimental nature of the treatment and provide informed consent
• Negative serum pregnancy test at the time of enrollment for females of childbearing potential
• For males and females of child-producing potential, use of effective contraceptive methods during the study and for at least 6 months after the last dose of romidepsin

Exclusion Criteria:

• Active/uncontrolled infection
• Evidence of relapsed disease
• Life expectancy < 12 weeks
• Pregnant or breast feeding females
• Prior therapy with romidepsin
• Known seropositive for or active viral infection with human immunodeficiency virus (HIV), hepatitis B virus (HBV) or hepatitis C virus (HCV); patients who are seropositive because of hepatitis B virus vaccine are eligible

• Any known cardiac abnormalities such as:

  • Congenital long QT syndrome
  • QTc interval >= 480 milliseconds;
  • Myocardial infarction within 6 months of course 1, day 1 (C1D1); subjects with a history of myocardial infarction between 6 and 12 months prior to C1D1 who are asymptomatic and have had a negative cardiac risk assessment (treadmill stress test, nuclear medicine stress test, or stress echocardiogram) since the event may participate;
  • Other significant electrocardiogram (ECG) abnormalities including 2nd degree atrio-ventricular (AV) block type II, 3rd degree AV block, or bradycardia (ventricular rate less than 50 beats/min);
  • Symptomatic coronary artery disease (CAD), e.g., angina Canadian class II-IV; in any patient in whom there is doubt, the patient should have a stress imaging study and, if abnormal, angiography to define whether or not CAD is present;
  • An ECG recorded at screening showing evidence of cardiac ischemia (ST depression of >= 2 mm, measured from isoelectric line to the ST segment); if in any doubt, the patient should have a stress imaging study and, if abnormal, angiography to define whether or not CAD is present;
  • Congestive heart failure (CHF) that meets New York Heart Association (NYHA) class II to IV definitions and/or ejection fraction < 40% by multi gated acquisition (MUGA) scan or < 50% by echocardiogram and/or magnetic resonance imaging (MRI);
  • A known history of sustained ventricular tachycardia (VT), ventricular fibrillation (VF), Torsade de Pointes, or cardiac arrest unless currently addressed with an automatic implantable cardioverter defibrillator (AICD);
  • Hypertrophic cardiomegaly or restrictive cardiomyopathy from prior treatment or other cause;
  • Any cardiac arrhythmia requiring an anti-arrhythmic medication (excluding stable doses of beta-blockers)
• Uncontrolled hypertension, i.e., blood pressure (BP) of >= 160/95; patients who have a history of hypertension controlled by medication must be on a stable dose (for at least one month) and meet all other inclusion criteria; or
• Patients taking drugs leading to significant QT prolongation must have an ECG prior to each treatment
• Concomitant use of cytochrome P450, family 3, subfamily A, polypeptide 4 (CYP3A4) inhibitors
• Concomitant use of medications known to induce a disulfiram-like reaction to alcohol