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Completed

NCT Number: NCT00201721

Pentostatin, and Rituximab With and Without Cyclophosphamide for Previously Untreated B-Chronic Lymphocytic Leukemia

This study aims to assess the rate of complete and overall response using rituximab and pentostatin with and without cyclophosphamide, to monitor and assess toxicity of this regimen, and to determine the overall and progression-free survival in CLL patients

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Ohio State University

Columbus, Ohio, 43210, United States

About this study

Rationale: Research indicates that both cyclophosphamide and pentostatin work synergistically against cancer cells and have a high response rate against chronic lymphocytic leukemia (CLL) without creating severe side effects in patients. In addition, studies have shown that rituximab, a therapy that targets the immune system, has the highest efficacy against CLL and the lowest toxicity rate when compared with other immunotherapy drugs. Studies also show that rituximab enhances the efficacy of the chemotherapy agents cyclophosphamide and pentostatin. This study offers the combination of immunotherapy with two promising chemotherapy agents against CLL.

Purpose: This study is evaluating the efficacy and safety of combination treatment with cyclophosphamide, pentostatin, and rituximab in patients with CLL. Several tests evaluating the genetic and molecular components of CLL will also be performed. Some of these tests will be conducted before, during, and after treatments to assess changes resulting from the study drugs. Each patient's outcome will be assessed in relation to various aspects of their genes.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosis of B-CLL (no mantle cell)
  • Must have active disease
  • Age >=18 yo
  • ECOG 0-3
  • No radiation or surgery <4 weeks

Exclusion criteria

  • Any of the following comorbid conditions:
  • New York Heart Association Class III or IV heart disease
  • Recent myocardial infarction (<1 month)
  • Uncontrolled infection
  • Active infection with the human immunodeficiency virus (HIV/AIDS) as further severe immunosuppression with this regimen may occur.
  • Pregnant or nursing women
  • Men or women of child bearing potential must use adequate contraception.
  • Active primary malignancy requiring treatment or limits survival to ≤2 years.
  • Any radiation therapy ≤4 weeks prior to study entry.
  • Any major surgery ≤4 weeks prior to study entry.

Treatment and study plan

pentostatin

Drug

2 mg/m2 IV over 30 minutes in 250 mL NS on day 1 during cycles 1-6.

Other names: Nipent®

Rituximab

Drug

For the first week only: Day 1 of therapy 100 mg IV over 4 hours. Day 3 of therapy 375 mg/m2 IV at 50 mg/hr and increase by 100 mg/hr at 30-minute intervals to a maximum of 400 mg/hr. Day 5 of therapy 375 mg/m2 IV at 100 mg/hr for the first 15 minutes the remainder goes in at 45 minutes. The remaining weeks 375 mg/m2 will be repeated as a single IV infusion Day 1 of Week 4, 7, 10, 13 and 16 during cycles 2-6.

Other names: RITUXAN®

Cyclophosphamide

Drug

600 mg/m2 IV in 250 mL NS over 30 minutes on day 1 cycles 1-6

Other names: CTX

Primary outcomes

  1. To assess the rate of complete and overall response using rituximab and pentostatin with and without cyclophosphamide.

    Time frame: up to 5 years

    For this evaluation, patients will be classified as complete responders if either of the following types of response are documented

    • CCR (Clinically based complete remission) denotes NED (No Evidence of Disease) based on baseline clinical parameters.
    • CR denotes CCR and, in bone marrow, no nodules and <30% lymphocytes.

Secondary outcomes

  1. To monitor and assess toxicity of this regimen.

    Time frame: up to 5 years

Sponsors and collaborators

Lead sponsor

Ohio State University Comprehensive Cancer Center

Other

Collaborators

  • Astex Pharmaceuticals, Inc.

Registry information

Official study title

Phase II Trial of Pentostatin, and Rituximab With and Without Cyclophosphamide for Previously Untreated B-Chronic Lymphocytic Leukemia (CLL)

Important dates

Study start
2002
Primary completion
2006
Study completion
2006
First posted
Sep 20, 2005
Registry last updated
Feb 8, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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