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Phase 2 N=131 Treatment

A Trial of Romidepsin for Progressive or Relapsed Peripheral T-cell Lymphoma

Peripheral T-cell Lymphoma

Enrolled (actual)
131
Serious AEs
47.3%
Results posted
Aug 2012
Primary outcome: 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 percentage of participants

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
Romidepsin (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Celgene
Primary completion
Nov 2010

Outcome Measures

OutcomeResultp-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

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.

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
View full record on ClinicalTrials.gov →

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.

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