Bortezomib and Ganciclovir in Treating Patients With Relapsed or Refractory Epstein Barr Virus-Positive Lymphoma

Jonsson Comprehensive Cancer Center

Status and phase: Terminated; Phase 1

Conditions: Lymphoproliferative Disorder; Lymphoma

Treatments: Drug: bortezomib + ganciclovir

Study type: Interventional

Funder types: Other

Identifiers

NCT00093704

UCLA-0403021-01

MILLENNIUM-VEL-04-108

CDR0000389476

MILLENNIUM-EBV-NHL-01

Details and patient eligibility

About

RATIONALE: Bortezomib may stop the growth of cancer cells by blocking the enzymes necessary for their growth. The Epstein Barr virus can cause cancer and lymphoproliferative disorders. Ganciclovir is an antiviral drug that acts against the Epstein Barr virus. Giving ganciclovir together with bortezomib may kill more Epstein Barr virus-infected cancer cells.

PURPOSE: This clinical trial is studying how well giving bortezomib together with ganciclovir works in treating patients with relapsed or refractory Epstein Barr virus-positive lymphoma.

Full description

OBJECTIVES:

Primary

• Maximum Tolerated Dose (MTD) of bortezomib in patients with relapsed or refractory Epstein Barr virus-positive lymphoma.

Secondary

• Assess the antitumor effect of this regimen in these patients.

OUTLINE: This is a pilot, open-label, dose-escalation study of bortezomib.

Patients receive bortezomib IV over 3-5 seconds on days 1, 4, 8 and 11. Patients also receive ganciclovir IV twice daily on days 1-14. Treatment repeats every 21 days for a maximum of 3 courses.

Cohorts of 3-6 patients receive escalating doses of bortezomib until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which 2 of 3 or 2 of 6 patients experience dose-limiting toxicity.

Patients are followed every 3 months.

PROJECTED ACCRUAL: A total of 3-9 patients will be accrued for this study.

Enrollment: 1 patient

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Histologically confirmed Epstein Barr virus-positive lymphoma, including the following subtypes:

  • Post-transplantation lymphoma
  • Burkitt's lymphoma
  • Hodgkin's lymphoma
  • T-/NK-cell lymphoma

• Unresponsive to, or relapsed after, at least 1 prior chemotherapy regimen

• Bidimensionally measurable disease by CT scan

• At least 1 lesion ≥ 1.5 cm in the greatest diameter

• Age 18 and over

• ECOG 0-2 OR

• Karnofsky 50-100%

• Life expectancy More than 3 months

• Hematopoietic

  • Absolute neutrophil count ≥ 1,000/mm^3 (no growth factor support within the past 4 weeks)
  • Hemoglobin ≥ 9.0 g/dL
  • Platelet count ≥ 50,000/mm^3 (no platelet transfusions within the past 4 weeks)

• Hepatic

  • Bilirubin ≤ 2.0 times upper limit of normal (ULN)
  • AST and ALT ≤ 2.5 times ULN (5 times ULN in patients with liver involvement)
  • No active hepatitis B or C

• Renal

  • Creatinine clearance ≥ 60 mL/min
  • Sodium > 130 mmol/L

• Negative pregnancy test

• Fertile patients must use effective contraception

• HIV negative

• At least 4 weeks since prior immunotherapy

• At least 4 weeks since prior chemotherapy

• At least 4 weeks since prior radiotherapy

• More than 4 weeks since prior major surgery unless fully recovered

• Recovered from all prior therapy

• At least 4 weeks since prior investigational agents

Exclusion criteria

• primary or secondary CNS lymphoma or HIV-related lymphoma
• known brain metastases
• myocardial infarction within the past 6 months
• acute ischemia or new conduction system abnormalities by electrocardiogram
• symptomatic congestive heart failure
• unstable angina pectoris
• cardiac arrhythmia
• hospitalized
• pregnant or nursing
• other uncontrolled illness
• ongoing or active systemic infection
• psychiatric illness or social situation that would preclude study compliance
• history of allergic reaction attributable to compounds of similar chemical or biological composition to study drugs
• sensitivity to boron, mannitol, bortezomib, or ganciclovir
• concurrent corticosteroids (≥ 10 mg of prednisone or equivalent)
• concurrent radiotherapy
• other concurrent anticancer therapy
• other concurrent investigational agents

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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1 participants in 1 patient group

Bortezomib + ganciclovir

Experimental group

Description:

Patients receive bortezomib IV over 3-5 seconds on days 1, 4, 8 and 11. Patients also receive ganciclovir IV twice daily on days 1-14. Treatment repeats every 21 days for a maximum of 3 courses.

Treatment:

Drug: bortezomib + ganciclovir