Clinical Trials /

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

NCT01059786

Description:

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.

Related Conditions:
  • Hairy Cell Leukemia
  • Hairy Cell Leukemia Variant
Recruiting Status:

Recruiting

Phase:

Phase 2

Trial Eligibility

Document

Title

  • Brief Title: Randomized Phase II Trial of Rituximab With Either Pentostatin or Bendamustine for Multiply Relapsed or Refractory Hairy Cell Leukemia
  • Official Title: Randomized Phase II Trial of Rituximab With Either Pentostatin or Bendamustine for Multiply Relapsed or Refractory Hairy Cell Leukemia

Clinical Trial IDs

  • ORG STUDY ID: 100025
  • SECONDARY ID: 10-C-0025
  • NCT ID: NCT01059786

Conditions

  • Hairy Cell Leukemia

Interventions

DrugSynonymsArms
PentostatinArm 2
RituximabArm 1
BendamustineArm 1

Purpose

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.

Detailed Description

      Background:

        -  Hairy cell leukemia (HCL) is highly responsive to purine analogs cladribine and
           pentostatin, without evidence of cure. Neither is standard after 2 courses, due to
           cumulative marrow and T-cell toxicity and declining remission rates and durations. Once
           resistant, patients after multiple relapses can die of disease-related cytopenias.

        -  Rituximab alone in 51 patients from 5 trials who had cytopenias and at least 1 prior
           purine analog resulted 10 complete + 10 partial remissions (CR+PR= ORR 39%).

        -  Rituximab with cladribine gives high CR rates in 1st or 2nd line, but is not standard.

        -  While cladribine use is more common for 1st and 2nd line, pentostatin is often used for
           subsequent treatment because of < 100% cross-resistance.

        -  Retrospective published data for pentostatin plus rituximab in HCL include 7 of 7
           responses with 6 (86%) CRs, and there are no prospective data.

        -  Recombinant immunotoxins targeting CD25 (LMB-2) and CD22 (BL22 and HA22) are highly
           active in purine analog resistant HCL. Palliative pentostatin-rituximab is often used
           off-protocol for patients with immunogenicity needing more therapy.

        -  Bendamustine is approved for early treatment of CLL, and is effective with rituximab for
           relapsed/refractory CLL. Its use in HCL is unreported.

        -  CRs with minimal residual disease (MRD) by immunohistochemistry of bone marrow biopsy
           (BMBx IHC), can relapse early. Tests for HCL MRD in blood or marrow include flow
           cytometry (FACS) or PCR using consensus primers. The most sensitive MRD test in HCL is
           real-time quantitative PCR using sequence-specific primers (RQ-PCR).

        -  Of 5 HCL-specific trials listed on Cancer.gov, 2 are phase II trials of cladribine +
           rituximab in 1st and 2nd line (1 randomized at NIH, 1 non-randomized at MDA), and 3 NIH
           phase I-II trials of recombinant immunotoxins BL22, HA22 and LMB-2.

      Objectives:

      -Primary:

      --To determine if pentostatin + rituximab and bendamustine + rituximab are each associated
      with adequate response rates (ORR=PR+CR) in patients with relapsed HCL, and, if so, to select
      which combination is likely to be superior.

      Eligibility:

        -  HCL needing therapy, either greater than or equal to 2 prior courses of purine analog, 1
           course purine analog plus greater than or equal to 1 course rituximab if < 1 year
           response to the 1 course purine analog, diagnosis of HCL variant (HCLv), or unmutated
           IGHV4-34+expressing HCL/HCLv.

        -  Prior treatment, ineligibility for, or patient refusal of recombinant immunotoxin.

      Design:

        -  Rituximab 375 mg/m(2) on day 1, 15 for 6 x 28-day cycles (all 68 patients).

        -  Randomize: 1) 28 patients to bendamustine 90 mg/m2/day, days 1 and 2 each

      cycle 2) 28 patients to pentostatin 4 mg/m2 days 1 and 15 of each cycle.

      Initial tolerability study: 12 patients receive rituximab + bendamustine (nonrandom),
      including 6 at 70 mg/ m(2) and 6 at 90 mg/ m(2) of bendamustine.

        -  Statistics: If > 14/28 respond, can conclude with 90% power that response > 40% in that
           arm. >80% probability of selecting the better arm if true response probability is
           approximately 40-50% on the inferior arm and >15% higher on the superior arm.

        -  Stratify to equalize the % of patients/arm refractory to last course of purine analog.

        -  Accrual Ceiling: 74, including 0-6 nonrandomized patients/arm with prior noresponse to
           the other regimen. Allow crossover after failure of either regimen.
    

Trial Arms

NameTypeDescriptionInterventions
Arm 1ExperimentalRituximab + Bendamustine at 70 mg/m2 for initialtolerability study (closed)
  • Rituximab
  • Bendamustine
Arm 2ExperimentalRituximab + bendamustine at 90 mg/m2 for initialtolerability study (closed)
  • Pentostatin
  • Rituximab
Arm 3ExperimentalRituximab + Bendamustine
  • Pentostatin
  • Rituximab
Arm 4Active ComparatorRituximab + Pentostatin
  • Pentostatin
  • Rituximab

Eligibility Criteria

        -  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 (100) 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.
      
Maximum Eligible Age:N/A
Minimum Eligible Age:18 Years
Eligible Gender:All
Healthy Volunteers:No

Primary Outcome Measures

Measure:Overall response rate (PR+CR)
Time Frame:Time of progression
Safety Issue:
Description:Proportion of patients receiving pentostatin + rituximab and bendamustine + rituximab who achieve response

Secondary Outcome Measures

Measure:Response rate
Time Frame:4 years
Safety Issue:
Description:Compare rituximab plus either pentostatin or bendamustinein terms of MRD-free survival, disease-free survival, overall survival and toxicity, including to CD4+ T-cells.
Measure:correlation of MRD levels and tumor markers with response
Time Frame:4 years
Safety Issue:
Description:determine if MRD levels and tumor markers (soluble CD25 and CD22, and RQ-PCR) correlate with response and clinical endpoints, and if bone marrow MRI signal correlates with BMBx results, and whether these tests could in some cases possibly replace BMBx
Measure:two regimens crossover
Time Frame:4 years
Safety Issue:
Description:compare the 2 regimens in crossover when used after failure of the 1st regimen
Measure:mechanism of thrombocytopenia
Time Frame:4 years
Safety Issue:
Description:study the mechanism of thrombocytopenia after purine analog plus rituximab
Measure:HCL biology
Time Frame:4 years
Safety Issue:
Description:study HCL biology by cloning, sequencing and characterizing monoclonal immunoglobulin rearrangements, and other genes

Details

Phase:Phase 2
Primary Purpose:Interventional
Overall Status:Recruiting
Lead Sponsor:National Cancer Institute (NCI)

Trial Keywords

  • Monoclonal Antibody
  • Purine Analog
  • Soluble CD25
  • Minimal Residual Disease MRD
  • CD20

Last Updated

December 14, 2019