This study is NOT currently recruiting participants.
Number
10-C-0025
Sponsoring Institute
National Cancer Institute (NCI)
Recruitment Detail
Type: No longer recruiting/follow-up only Gender: Male & Female Min Age: 18 Years Max Age: N/A
Referral Letter Required
No
Population Exclusion(s)
Children;Fetuses;Pregnant Women
Keywords
Monoclonal Antibody; Purine Analog; Soluble CD25; Minimal Residual Disease MRD; CD20
Recruitment Keyword(s)
None
Condition(s)
Hairy Cell Leukemia
Investigational Drug(s)
Investigational Device(s)
Intervention(s)
Drug: Pentostatin Drug: Acetaminophen Drug: Rituximab Drug: Bendamustine Drug: Diphenhydramine Drug: Epinephrine Drug: Antihistamines Drug: Corticosteroids Drug: Bronchodilators Other: Intravenous (IV) Saline
Supporting Site
National Cancer Institute
-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.
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INCLUSION CRITERIA: - Evidence of HCL by flow cytometry of blood or a solid (lymph node) mass, confirmed by the Laboratory of Pathology, NCI, including positivity for CD19, CD22, CD20, and CD11c. Patients with flow cytometry consistent with HCL variant (HCLv) are eligible, including those with CD25 and/or CD103 negative disease. - BMBx or BMA consistent with HCL, confirmed by NIH Laboratory of Pathology, NCI, or the Department of Laboratory Medicine, Clinical Center, NIH, unless the diagnosis can be confirmed from a solid (lymph node) mass.. - Treatment indicated based on demonstration of at least one of the following no more than 4 weeks from the time of enrollment, and no less than 6 months after prior cladribine and no less than 4 weeks after other prior treatment, if applicable. --Neutropenia (ANC less than 1000 cells/microl). --Anemia (Hgb less than 10g/dL). --Thrombocytopenia (Plt less than 100,000/microl). --Absolute lymphocyte count (ALC) of greater than 5,000 cells/microL --Symptomatic splenomegaly. --Enlarging lymph nodes greater than 2cm. --Repeated infections requiring oral or i.v. antibiotics. --Increasing lytic bone lesions Patients who have eligible blood counts within 4 weeks from enrollment will not be considered ineligible if subsequent blood counts prior to enrollment fluctuate and become ineligible up until the time of enrollment. - One of the following: --At least 2 prior courses of purine analog --1 prior course of purine analog plus greater than or equal to1 course of rituximab if the response to the course of purine analog lasted less than 1 year. --Diagnosis of HCL variant (HCLv) --Unmutated (>98% homology to germline) IGHV4-34+expressing HCL/HCLv - ECOG performance status (102) of 0-3 - Patients must be able to understand and give informed consent. - Creatinine less than or equal to 1.5 or creatinine clearance greater than or equal to 60 ml/min. - Bilirubin less than or equal to 2 unless consistent with Gilbert s (total/direct greater than 5), ALT and AST less than or equal to 3 x upper limits of normal. - No other therapy (i.e. chemotherapy, interferon) for 4 weeks prior to study entry, or cladribine for 6 months prior to study entry, unless progressive disease more than 2 months after cladribine is documented. - Age at least 18 - Men and women of reproductive potential must agree to use an acceptable method of birth control during treatment and for twelve months after completion of treatment. - Patients must be willing to co-enroll in the investigator s companion protocol 10-C-0066 titled Collection of Human Samples to Study Hairy Cell and other Leukemias, and to Develop Recombinant Immunotoxins for Cancer Treatment . EXCLUSION CRITERIA: - Presence of active untreated infection - Uncontrolled coronary disease or NYHA class III-IV heart disease. - Known infection with HIV, hepatitis B or C. - Pregnant or lactating women. - Presence of active 2nd malignancy requiring treatment. 2nd malignancies with low activity which do not require treatment (i.e. low grade prostate cancer, basal cell or squamous cell skin cancer) do not constitute exclusions. - Inability to comply with study and/or follow-up procedures. - Presence of CNS disease - Patients with history of non-response to both pentostatin plus rituximab and to bendamustine plus rituximab. - Receipt of a live vaccine within 4 weeks prior to randomization. Efficacy and/or safety of immunization during periods of B-cell depletion have not been adequately studied. It is recommended that a patient s vaccination record and possible requirements be reviewed. The patient may have any required vaccination/booster administered at least 4 weeks prior to the initiation of study treatment. Review of the patient s immunization status for the following vaccinations is recommended: tetanus; diphtheria; influenza; Pneumococcal polysaccharide; Varicella; measles, mumps and rubella (MMR); and hepatitis B. Patients who are considered to be at high risk for hepatitis B virus (HBV) infection and for whom the investigator has determined that immunization is indicated should complete the entire HBV vaccine series at least 4 weeks prior to participation in the study.
- Evidence of HCL by flow cytometry of blood or a solid (lymph node) mass, confirmed by the Laboratory of Pathology, NCI, including positivity for CD19, CD22, CD20, and CD11c. Patients with flow cytometry consistent with HCL variant (HCLv) are eligible, including those with CD25 and/or CD103 negative disease.
- BMBx or BMA consistent with HCL, confirmed by NIH Laboratory of Pathology, NCI, or the Department of Laboratory Medicine, Clinical Center, NIH, unless the diagnosis can be confirmed from a solid (lymph node) mass..
- Treatment indicated based on demonstration of at least one of the following no more than 4 weeks from the time of enrollment, and no less than 6 months after prior cladribine and no less than 4 weeks after other prior treatment, if applicable.
--Neutropenia (ANC less than 1000 cells/microl).
--Anemia (Hgb less than 10g/dL).
--Thrombocytopenia (Plt less than 100,000/microl).
--Absolute lymphocyte count (ALC) of greater than 5,000 cells/microL
--Symptomatic splenomegaly.
--Enlarging lymph nodes greater than 2cm.
--Repeated infections requiring oral or i.v. antibiotics.
--Increasing lytic bone lesions
Patients who have eligible blood counts within 4 weeks from enrollment will not be considered ineligible if subsequent blood counts prior to enrollment fluctuate and become ineligible up until the time of enrollment.
- One of the following:
--At least 2 prior courses of purine analog
--1 prior course of purine analog plus greater than or equal to1 course of rituximab if the response to the course of purine analog lasted less than 1 year.
--Diagnosis of HCL variant (HCLv)
--Unmutated (>98% homology to germline) IGHV4-34+expressing HCL/HCLv
- ECOG performance status (102) of 0-3
- Patients must be able to understand and give informed consent.
- Creatinine less than or equal to 1.5 or creatinine clearance greater than or equal to 60 ml/min.
- Bilirubin less than or equal to 2 unless consistent with Gilbert s (total/direct greater than 5), ALT and AST less than or equal to 3 x upper limits of normal.
- No other therapy (i.e. chemotherapy, interferon) for 4 weeks prior to study entry, or cladribine for 6 months prior to study entry, unless progressive disease more than 2 months after cladribine is documented.
- Age at least 18
- Men and women of reproductive potential must agree to use an acceptable method of birth control during treatment and for twelve months after completion of treatment.
- Patients must be willing to co-enroll in the investigator s companion protocol 10-C-0066 titled Collection of Human Samples to Study Hairy Cell and other Leukemias, and to Develop Recombinant Immunotoxins for Cancer Treatment .
EXCLUSION CRITERIA:
- Presence of active untreated infection
- Uncontrolled coronary disease or NYHA class III-IV heart disease.
- Known infection with HIV, hepatitis B or C.
- Pregnant or lactating women.
- Presence of active 2nd malignancy requiring treatment. 2nd malignancies with low activity which do not require treatment (i.e. low grade prostate cancer, basal cell or squamous cell skin cancer) do not constitute exclusions.
- Inability to comply with study and/or follow-up procedures.
- Presence of CNS disease
- Patients with history of non-response to both pentostatin plus rituximab and to bendamustine plus rituximab.
- Receipt of a live vaccine within 4 weeks prior to randomization. Efficacy and/or safety of immunization during periods of B-cell depletion have not been adequately studied. It is recommended that a patient s vaccination record and possible requirements be reviewed. The patient may have any required vaccination/booster administered at least 4 weeks prior to the initiation of study treatment. Review of the patient s immunization status for the following vaccinations is recommended: tetanus; diphtheria; influenza; Pneumococcal polysaccharide; Varicella; measles, mumps and rubella (MMR); and hepatitis B. Patients who are considered to be at high risk for hepatitis B virus (HBV) infection and for whom the investigator has determined that immunization is indicated should complete the entire HBV vaccine series at least 4 weeks prior to participation in the study.
Principal Investigator
Referral Contact
For more information: