A Phase 2 Multicenter Study of High Dose Chemotherapy With Autologous Stem Cell Transplant Followed by Maintenance Therapy With Romidepsin for the Treatment of T Cell Non-Hodgkin Lymphoma
Conditions
T Cell Non-Hodgkin Lymphoma
Conditions: official terms
Lymphoma - Lymphoma, Non-Hodgkin - Lymphoma, T-Cell
Study Type
Interventional
Study Phase
Phase 2
Study Design
Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Intervention
Name: High Dose Chemotherapy with Autologous Stem Cell Transplant Followed by Maintenance Therapy with Romidepsin
Type: Other
Overall Status
Recruiting
Summary
The purpose of this study is to test the benefit of a chemotherapy drug called romidepsin in patients with T Cell Non-Hodgkin Lymphoma (T NHL) who have undergone autologous transplantation.
Detailed Description
The primary aim is to determine a preliminary estimate of the progression-free survival of patients with T NHL who receive maintenance romidepsin at 2 years post-transplant for patients transplanted in CR1 or PR1 with standard risk histologies.

Secondary aims include:

- Determine PFS at 2 yrs for patients transplanted in ≥CR/PR2 or for patients with high risk histologies.

- Determine the toxicities associated with romidepsin following autologous transplantation

- Determine the probability of OS at 2 years post transplant for all patients undergoing transplant

- Characterize the effect of romidepsin on immune recovery post HDT-ASCT

- OS and PFS 1 year after Romidespin completion
Criteria for eligibility
Healthy Volunteers: No
Maximum Age: N/A
Minimum Age: 16 Years
Gender: Both
Criteria: Inclusion Criteria:

- Age: Patients over age 16 who are deemed eligible for transplant by their treating physician Disease status: CR or PR required. Remission status will be assessed at the completion of induction chemotherapy and prior to enrollment on protocol.

Diagnosis: The following histologies will need to be confirmed at MSKCC or locally for participating sites in order to be considered for HDT-ASCT and post-transplant maintenance romidepsin:

- PTCL

- AITL

- ALCL

- EaTCL

- Hepatosplenic Gamma Delta T cell lymphoma

- Adult T-cell leukemia/lymphoma

- Primary cutaneous gamma/delta T-cell lymphoma

- Extranodal NK/T-cell lymphoma, nasal type

- Primary cutaneous anaplastic large cell lymphoma

- Subcutaneous panniculitis-like T-cell lymphoma

- Mycosis fungoides/sezary syndrome Stem cell collection: A minimum of 2 x 106 CD34+ cells must have been collected

Laboratory test results within these ranges:

- Total bilirubin <= 1.5 x ULN

- AST (SGOT) and ALT (SGPT) <= 3 x ULN

Exclusion Criteria:

- • Diagnosis: progressive disease at transplant work-up

- Prior therapy: prior autologous or allogeneic transplant

- Active and uncontrolled infection at time of transplantation including active infection with Aspergillus or other mold, or HIV infection

- Inadequate performance status/organ function defined by DLCO < 50% (adjusted for hgb), cardiac function as defined below, KPS < 60%.

- Pregnant or breast feeding. For males and females of child-producing potential, inability to use effective contraceptive methods during the study

- Prior therapy with romidepsin

- Central nervous system or meningeal involvement

- Any known cardiac abnormalities such as:

- Congenital long QT syndrome

- QTc interval ≥ 500 milliseconds

- Myocardial infarction within 6 months of transplantation. Subjects with a history of myocardial infarction between 6 and 12 months prior to transplant 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 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 (see Appendix 1) 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 (see Appendix 2) and/or ejection fraction <40% by MUGA scan or <50% by echocardiogram and/or 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 causes

- Uncontrolled hypertension, defined as 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

- Any cardiac arrhythmia requiring an anti-arrhythmic medication (excluding stable doses of beta-blockers)

- Patients taking drugs leading to significant QT prolongation within the specified wash out period (See Appendix 3: Medications That May Cause QTc Prolongation).

- Concomitant use of CYP3A4 inhibitors
Locations
Memoral Sloan Kettering Cancer Center
Basking Ridge, New Jersey, United States
Status: Recruiting
Contact: Steven Horwitz, MD - 212-639-3045
Memorial Sloan Kettering Cancer Center @ Suffolk
Commack, New York, United States
Status: Recruiting
Contact: Steven Horwitz, MD - 212-639-3045
Weill Cornell Medical Center
New York, New York, United States
Status: Recruiting
Contact: Jia Ruan, MD
Memorial Sloan Kettering Cancer Center
NY, New York, United States
Status: Recruiting
Contact: Steven Horwitz, MD - 212-639-3045
Memorial Sloan Kettering at Mercy Medical Center
Rockville Centre, New York, United States
Status: Recruiting
Contact: Steven Horwitz, MD
Memoral Sloan Kettering Cancer Center at Phelps
Sleepy Hollow, New York, United States
Status: Recruiting
Contact: Steven Horwitz, MD - 212-639-3045
Memorial Sloan Kettering West Harrison
West Harrison, New York, United States
Status: Recruiting
Contact: Steven Horwitz, MD - 212-639-3045
University of Washington School of Medicine
Seattle, Washington, United States
Status: Recruiting
Contact: Andrei Shustov, MD
Start Date
July 2013
Completion Date
July 2017
Sponsors
Memorial Sloan Kettering Cancer Center
Source
Memorial Sloan Kettering Cancer Center
Record processing date
ClinicalTrials.gov processed this data on July 28, 2015
ClinicalTrials.gov page