CI

At a glance

ClinicalIndex Comparison Record
Phase 2Active· 69 enrolled
Drug / intervention
Pentostatin +9 moredrug
Likely dose
Pentostatin 4 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01059786
NCT01059786Phase 2Active

Randomized Phase II Trial of Rituximab With Either Pentostatin or Bendamustine for Multiply Relapsed or Refractory Hairy Cell Leukemia

National Cancer Institute (NCI)·interventional·Posted Feb 1, 2010·Updated Jun 12, 2025

In Brief

A Phase 2 clinical trial evaluating Pentostatin, Rituximab, and 8 other interventions for Hairy Cell Leukemia. Active but no longer recruiting, targeting 69 participants across 1 site.

Detailed Summary

Background: * Researchers are attempting to develop new treatments for hairy cell leukemia (HCL) that has not responded well to or has recurred after standard HCL therapies. One nonstandard treatment for HCL is rituximab, an antibody that binds to the cancer cells and helps the immune system destroy them. By combining rituximab with other anti-cancer drugs, researchers hope to determine whether the combined drugs are successful in treating HCL. * Pentostatin and bendamustine are two anti-cancer drugs that have been used to treat different kinds of blood and immune system cancers. Bendamustine is approved to treat other kinds of leukemia and lymphoma, but it has not been used to treat HCL. Pentostatin has been used for more than 20 years to treat HCL, but it has not been combined with rituximab in official clinical trials. Objectives: * To determine whether rituximab with either pentostatin or bendamustine is a more effective treatment for HCL than rituximab alone. * To determine whether pentostatin or bendamustine is a more effective treatment for HCL when combined with rituximab. Eligibility: \- Individuals at least 18 years of age who have been diagnosed with hairy cell leukemia that has not responded well to or has relapsed after standard HCL therapies. Design: * The study will last for four treatment cycles of 28 days each. * Prior to the study, participants will be screened with a full medical history and physical exam, bone marrow biopsy (if one has not been performed in the last 6 months), computed tomography (CT) or ultrasound scan, tumor measurements, and other tests as required by the researchers. Participants will provide blood and urine samples at this time as well. * Rituximab with bendamustine: Participants will receive rituximab on Days 1 and 15 of each cycle and bendamustine on Days 1 and 2 of each cycle, for a total of four cycles. * Rituximab with pentostatin: Participants will receive rituximab on Days 1 and 15 of each cycle and pentostatin on rituximab on Days 1 and 15 of each cycle, for a total of four cycles. * Participants will have regular tests during the treatment cycles, including bone marrow biopsies and CT or ultrasound scans. Participants will also provide regular blood and urine samples to assess the results of treatment.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2Active
2010201120122013201420152016201720182019202020212022202320242025202620272028
First PostedFeb 1, 2010
Enrollment StartJul 1, 2010
Primary CompletionDec 15, 2022
Study CompletionDec 31, 2027
TodayJul 2, 2026
Enrollment to primary: 12.5 yearsPosted 16.4 years ago

Interventions

Pentostatindrug

28 participants to pentostatin 4 mg/m\^2 days 1 and 15 of each cycle.

Rituximabdrug

Rituximab 375 mg/m\^2 on day 1, 15 for 6 x 28-day cycles

Bendamustinedrug

1-4 participants to bendamustine 90 mg/m\^2/day, days 1 and 2 each cycle

Acetaminophendrug

Treatment of infusion-related symptoms with acetaminophen is recommended.

Diphenhydraminedrug

Treatment of infusion-related symptoms with diphenhydramine is recommended.

Epinephrinedrug

Epinephrine should be available for immediate use in the event of a hypersensitivity reaction to Rituximab.

Antihistaminesdrug

Antihistamines should be available for immediate use in the event of a hypersensitivity reaction to Rituximab.

Corticosteroidsdrug

Corticosteroids should be available for immediate use in the event of a hypersensitivity reaction to Rituximab.

Bronchodilatorsdrug

Additional treatment with bronchodilators may be indicated.

Intravenous (IV) Salineother

Additional treatment with intravenous (IV) saline may be indicated.