Vorinostat Plus FND in Relapsed or Refractory Mantle Cell Lymphoma

Mantle Cell Lymphoma Clinical Trial

— ZOLINZA  

Official title:

A Phase II Investigation of Vorinostat in Combination With Intravenous Fludarabine, Mitoxantrone, and Dexamethasone in Patients With Relapsed or Refractory Mantle Cell Lymphoma

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT01578343
• Other study ID #: SMC2011-11-102-001
• Status: Terminated
• Phase: Phase 2
• First received: March 30, 2012
• Last updated: April 13, 2016
• Start date: June 2012
• Est. completion date: February 2016

Study information

• Verified date: April 2016
• Source: Samsung Medical Center
• Contact: n/a
• Is FDA regulated: No
• Health authority: South Korea: Korea Food and Drug Administration (KFDA)
• Study type: Interventional

Clinical Trial Summary

1. Rationale In mantle cell lymphoma, the conventional chemotherapy achieves only temporary responses with a median duration of remissions only from 1 to 2 years. Therefore, mantle cell lymphoma is known as one of the B-cell lymphomas with poor prognosis. Although the treatment outcome of mantle cell lymphoma has been improved since intensive chemotherapy regimens such as HyperCVAD was used, a substantial number of patients are still frequently relapsed after chemotherapy. After relapse, most of them became refractory to various kinds of salvage treatment. That is why the results of most salvage chemotherapy regimens were disappointing. In addition, mantle cell lymphoma generally occurs in elderly people. Thus, intensive salvage chemotherapy may not be feasible for elderly patients. Therefore, an effective, novel combination treatment is urgently needed in relapsed or refractory mantle cell lymphoma patients.

2. Hypothesis

• Vorinostat will produce synergism with a combination treatment regimen (Fludarabine, mitoxantrone, dexamethasone, FND) without overlapping toxicity

• Vorinostat maintenance treatment will reduce the relapse rate in patients ineligible for autologous stem cell transplantation.

3. Purpose A phase II investigation to determin the effectiveness of vorinostat in combination with intravenous fludarabine, mitoxantrone, and dexamethasone in patients with relapsed or refractory mantle cell lymphomain patients with relapsed or refractory mantle cell lymphoma.

Description:

1. Objectives 1.1 Primary objective • To determine the efficacy of vorinostat plus FND as an induction treatment

• Response rate of vorinostat/FND 1.2 Secondary objective

• Survival outcome

• Overall survival and progression-free survival

• To determine the efficacy of vorinostat maintenance treatment

• Relapse rate • Toxicity of vorinostat/FND

• Hematologic and non-hematologic toxicity

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 20
• Est. completion date: February 2016
• Est. primary completion date: September 2015
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 19 Years to 75 Years

Eligibility

1. Inclusion

• Histologically proven mantle cell lymphoma

• Adequate organ function as defined by the following criteria:

• Serum aspartate transaminase (AST; serum glutamic oxaloacetic transaminase (SGOT)) and serum alanine transaminase (ALT; serum glutamic pyruvic transaminase (SGPT)) =2.5 x local laboratory upper limit of normal (ULN), or AST and ALT less than or equal to 5 x ULN if liver function abnormalities are due to underlying malignancy

• Total serum bilirubin =1.5 x ULN

• Absolute neutrophil count (ANC) =1500/µL

• Platelets =100,000/µL

• Hemoglobin =9.0 g/dL (may be transfused or erythropoietin treated)

• Serum calcium =12.0 mg/dL

• Serum creatinine =1.5 x ULN

• Normal potassium and magnesium at baseline

• All patients should be relapsed or refractory patients after previous treatments including chemotherapy .

• At least one measurable lesion (lymph node or tumor mass)

• The size of lesion must be > 1.0cm in the greatest transverse diameter

• ECOG PS 0-2

• Serum HCG test: negative if a patient is female eligible for pregnancy

2. Exclusion

• Major surgery or radiation therapy within 4 weeks of starting the study treatment.

• History of or known carcinomatous meningitis, or evidence of symptomatic leptomeningeal disease or secondary CNS involvement on CT or MRI scan.

• Ongoing cardiac dysrhythmias of NCI CTCAE grade =2.

• Pregnancy or breastfeeding.

• Patients with HIV positive

• Patients with HBs antigen positive

• Patients with anti-HCV positive

• History of the use of another HDAC inhibitor: e.g. valproic acid

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Lymphoma
• Lymphoma, Mantle-Cell
• Mantle Cell Lymphoma

Intervention

Drug:
• Fludarabine, Mitoxantrone, Dexamethasone, Vorinostat
Induction treatment (Total 4 cycles) FND D1-3 Fludarabine 25mg/m2 + NS 100mL iv over 30 min D1 Mitoxantrone 10mg/m2 + NS 100mL iv over 30 min D1-5 Dexamethasone 20mg IV or PO every 4 weeks Vorinostat D1-10 Vorinostat 200mg once daily PO (When vorinostat is concurrently administered with FND regimen, vorinostat will be administered 3 hours before chemotherapy) Consolidation treatment for responders Patients not eligible for transplantation Vorinostat maintenance up to 6 cycles 200mg twice daily for 14 consecutive days from D1 - 14 in a 21 day cycle Delay of the start of the next cycle by up to 7 days will be acceptable. If relapse or progression during maintenance, it will be stopped. Patients eligible for transplantation High-dose chemotherapy followed by autologous stem cell transplantation

Locations

Country	Name	City	State
Korea, Republic of	Samsung Medical Center	Seoul

Sponsors (2)

Lead Sponsor	Collaborator
Samsung Medical Center	Seok Jin Kim

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	To determine the efficacy of vorinostat plus FND as an induction treatment confirmed by CT or MRI (PET/CT as indicated)	B) Response criteria; 1) Complete response (CR): Disappearance of all detectable clinical and radiographic evidence of disease 2) Partial response (PR): =50% decrease in sum of product diameter (SPD) of 6 nodes/nodal masses 3) Stable disease (SD): Disease status is less than PR, but is not PD 4) Progressive disease (PD): Appearance of any new lesions	A) After 8weeks and 16 weeks of the treatment	Yes
Secondary	To determine the efficacy of vorinostat maintenance treatment, survival outcome and toxicity of vorinostat/FND measured by CT or MRI scan, CTCAE ver 4.0	A) Disease status evaluation every 3 months during the 1st two years after enrollment B) Monitoring survival status during the five years after enrollment C) Toxicity evaluation	every 3 months during the 1st two years after enrollment	Yes