Phase 2
Completed N=131
A Trial of Romidepsin for Progressive or Relapsed Peripheral T-cell Lymphoma
Source: ClinicalTrials.gov NCT00426764 ↗Enrolled (actual)
131
Serious AEs
47.3%
Results posted
Aug 2012
Primary outcomePrimary: Percentage of Participants With a Complete Response According to the International Workshop Response Criteria (IWC) for Non-Hodgkin's Lymphomas (NHL) Assessed by an Independent Review Committee — 15.4 percentage of participants
Summary
The purpose of this study is to evaluate the activity of romidepsin in patients with progressive or relapsed peripheral T-cell lymphoma (PTCL) who have already been treated with systemic therapy.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Percentage of Participants With a Complete Response According to the International Workshop Response Criteria (IWC) for Non-Hodgkin's Lymphomas (NHL) Assessed by an Independent Review Committee |
15.4 | — |
| SECONDARY Percentage of Participants With Objective Disease Response |
26.2 | — |
| SECONDARY Duration of Objective Disease Response |
NA | — |
| SECONDARY Duration of Complete Disease Response |
NA | — |
| SECONDARY Time to Disease Progression |
182 | — |
| SECONDARY Change in Eastern Cooperative Oncology Group (ECOG) Performance Status |
1; 0; 0; 0; 0; 0 | — |
| SECONDARY Number of Participants With Treatment Emergent Adverse Events (TEAEs) |
128; 89; 27; 61; 25; 8 | — |
Eligibility Criteria
Inclusion Criteria
Patients must fulfill all of the following criteria to be eligible for study participation and have:
- Histologically confirmed PTCL not otherwise specified, angioimmunoblastic T-cell lymphoma, extranodal natural killer (NK)/T-cell lymphoma nasal type, enteropathy- type T-cell lymphoma, subcutaneous panniculitis-like T-cell lymphoma, cutaneous γδ T-cell lymphoma (excludes mycosis fungoides or Sezary syndrome), transformed mycosis fungoides, hepatosplenic T-cell lymphoma, anaplastic large cell lymphoma (ALCL; anaplastic lymphoma kinase [ALK]-1 negative), or patients with ALK 1 expressing ALCL (ALK-1 positive) who have relapsed disease after autologous stem cell transplant (ASCT);
- Age ≥18 years;
- Written informed consent;
- Progressive disease following at least one systemic therapy or refractory to at least one prior systemic therapy;
- Measurable disease according to the International Workshop Response (IWC) criteria and/or measurable cutaneous disease;
- Eastern Cooperative Oncology Group (ECOG) performance status of 0-2;
- Serum potassium ≥3.8 mmol/L and magnesium ≥0.85 mmol/L (electrolyte abnormalities can be corrected with supplementation to meet inclusion criteria);
- Negative urine or serum pregnancy test on females of childbearing potential; and
- All women of childbearing potential must use an effective barrier method of contraception (either an intrauterine contraceptive device [IUCD] or double barrier method using condoms or a diaphragm plus spermicide) during the treatment period and for at least 1 month thereafter. Male patients should use a barrier method of contraception during the treatment period and for at least 1 month thereafter. Hormonal methods of contraception such as the contraceptive pill or patch (particularly those containing ethinyl-estradiol) should be avoided due to a potential drug interaction.
Exclusion Criteria
Patients are ineligible for entry if any of the following criteria are met:
- Known central nervous system (CNS) lymphoma [computed tomography (CT) or magnetic resonance imaging (MRI) scans are required only if brain metastasis is suspected clinically];
- Chemotherapy or immunotherapy within 4 weeks of study entry (6 weeks if nitrosoureas given);
- Initiation of corticosteroids during study (defined as 7 days prior to Cycle 1 Day 1[C1D1] until study drug discontinuation)
- Patients treated with a pulse of steroids were to discontinue steroid use 7 days prior to C1D1 and have a repeat CT scan and disease assessment after discontinuation of corticosteroids and before starting romidepsin;
- Concomitant use of any other anti-cancer therapy;
- Concomitant use of any investigational agent;
- Use of any investigational agent within 4 weeks of study entry;
- Any known cardiac abnormalities such as:
- Congenital long QT syndrome;
- QTc interval >480 milliseconds (msec);
- A myocardial infarction within 6 months of C1D1. Patients with a history of myocardial infraction 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 be referred to a cardiologist for evaluation;
- An ECG recorded at screening showing significant ST depression (ST depression of ≥2 mm, measured from isoelectric line to the ST segment at a point 60 msec at the end of the QRS complex). 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
Data sourced from ClinicalTrials.gov (NCT00426764). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.