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Vorinostat Plus FND in Relapsed or Refractory Mantle Cell Lymphoma

Information source: Samsung Medical Center
ClinicalTrials.gov processed this data on August 23, 2015
Link to the current ClinicalTrials.gov record.

Condition(s) targeted: Mantle Cell Lymphoma

Intervention: Fludarabine, Mitoxantrone, Dexamethasone, Vorinostat (Drug)

Phase: Phase 2

Status: Not yet recruiting

Sponsored by: Samsung Medical Center

Official(s) and/or principal investigator(s):
Won Seog Kim, MD, PhD, Principal Investigator, Affiliation: Samsung Meical Center

Overall contact:
Won Seog Kim, MD, PhD, Phone: 82-2-3410-6548, Email: wskimsmc@skku.edu

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.

Clinical Details

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

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

Primary outcome: To determine the efficacy of vorinostat plus FND as an induction treatment confirmed by CT or MRI (PET/CT as indicated)

Secondary outcome: 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

Detailed 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

Eligibility

Minimum age: 20 Years. Maximum age: 75 Years. Gender(s): Both.

Criteria:

Inclusion Criteria:

- 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 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

Exclusion Criteria:

- 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

Locations and Contacts

Won Seog Kim, MD, PhD, Phone: 82-2-3410-6548, Email: wskimsmc@skku.edu

Samsung Medical Center, Seoul 135-710, Korea, Republic of; Not yet recruiting
Won Seog Kim, MD, PhD, Principal Investigator
Additional Information

Starting date: January 2013
Last updated: December 30, 2012

Page last updated: August 23, 2015

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