Ohio State University
Columbus, Ohio, 43210, United States
NCT Number: NCT00201721
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
Looking for future studies?
Notify Me18 year and older
All sexes
Interventional
Phase 2
Columbus, Ohio, 43210, United States
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
2 mg/m2 IV over 30 minutes in 250 mL NS on day 1 during cycles 1-6.
Other names: Nipent®
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®
600 mg/m2 IV in 250 mL NS over 30 minutes on day 1 cycles 1-6
Other names: CTX
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
Time frame: up to 5 years
Ohio State University Comprehensive Cancer Center
Other
Phase II Trial of Pentostatin, and Rituximab With and Without Cyclophosphamide for Previously Untreated B-Chronic Lymphocytic Leukemia (CLL)
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.
Published trials that share one or more normalized conditions with this study.
NCT01087294
Hematologic Diseases, Hemic and Lymphatic Diseases
Bethesda, Maryland, United States
View Trial DetailsNCT06787131
Chronic Disease, Disease Attributes
Sydney, Randwick NSW, Australia
View Trial DetailsNCT04883749
Chronic Lymphoid Leukemia, Hematologic Diseases
Innsbruck, Austria
View Trial DetailsNCT03448393
Acute Lymphoblastic Leukemia, Acute Lymphocytic Leukemia
Bethesda, Maryland, United States
View Trial Details