Last updated: 11/07/2018 00:26:44

Iodine-131 Anti-B1 Antibody (Tositumomab and Iodine I 131 Tositumomab) for previously untreated, advanced-stage, low grade non-Hodgkin’s lymphoma

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GSK study ID
104517
See study documents
Clinicaltrials.gov ID
NCT00996996
See results summary
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Overview
Eligibility
Locations
Study documents
Results summary
Plain language summaries
Additional information

Trial overview

Official title: Phase II Trial of Iodine-131 Anti-B1 Antibody for Previously Untreated, Advanced Stage, Low Grade Non-Hodgkin’s Lymphoma
Trial description: This is a single-arm, single-institution, phase II study of Iodine-131 Anti-B1 Antibody for patients with previously untreated, advanced-stage (stage III or IV) low-grade non-Hodgkin’s B-cell lymphoma. A total of 75–80 patients will be enrolled.
Patients will undergo two phases of the study. In the first phase, termed the “dosimetric dose”, patients will receive an infusion of unlabeled Anti-B1 Antibody (450 mg) over 70 minutes (including a 10-minute flush) immediately followed by a 30-minute infusion (including a 10-minute flush) of Anti-B1 Antibody (35 mg) which has been trace-labeled with 5 mCi of Iodine-131. Whole body gamma camera scans will be obtained 5 to 8 times between Days 0 and 7 following the dosimetric dose. Using the
dosimetric data from 3 imaging timepoints (the imaging timepoints to be used in decreasing order of preference depending on availability of data are Days 0, 3, and 7; Days 0, 4, and 7; Days 0, 3 and 6; Days 0, 4, and 6; Days 0, 2, and 7; and Days 0, 2, and 6), a patient-specific dose of Iodine-
131 to deliver the desired total body dose of radiotherapy will be calculated. In the second phase, termed the “therapeutic dose”, patients will receive a 70-minute infusion (including a 10-minute flush) of unlabeled Anti-B1 Antibody (450 mg) immediately followed by a 30-minute infusion (including a 10-minute flush) of Anti-B1 Antibody (35 mg) labeled with the patient-specific dose of Iodine-131 to deliver a whole body dose of 75 cGy. Patients who are obese will be dosed based upon 137% of their
calculated lean body mass. Patients will be treated with either saturated solution potassium iodide (SSKI), Lugol’s solution, or potassium iodide tablets starting at least 24 hours prior to the first infusion of the Iodine-131 Anti-B1 Antibody (i.e., dosimetric dose) and continuing for 14 days following the last infusion of Iodine-131 Anti-B1 Antibody (i.e., therapeutic dose).
The primary endpoint of the study is the determination of the response rate with Iodine-131 Anti-B1 Antibody in previously untreated patients with low-grade non-Hodgkin’s lymphoma (NHL). The secondary endpoints include duration of response, safety, radiation dosimetry, and the predictive value of detection of the presence or absence minimal residual disease by molecular techniques on response duration.
Primary purpose:
Treatment
Trial design:
Single Group Assignment
Masking:
None (Open Label)
Allocation:
Not applicable
Primary outcomes:

Number of participants with confirmed response, including participants with Complete Response (CR), Clinical Complete Response (CCR), and Partial Response (PR)

Timeframe: From Study Day 0 (start of treatment) up to 12 years (long-term follow up)

Number of participants with response, including participants with Complete Response (CR), Clinical Complete Response (CCR), or Partial Response (PR)

Timeframe: From Study Day 0 (start of treatment) up to 12 years (long-term follow up)

Number of participants with Confirmed Complete Response (CR, CCR, and CR+CCR) and Partial Response (PR)

Timeframe: From Study Day 0 (start of treatment) up to 12 years (long-term follow up)

Number of participants with Complete Response (CR, CCR, and CR+CCR) and Partial Response (PR)

Timeframe: From Study Day 0 (start of treatment) up to 12 years (long-term follow up)

Secondary outcomes:

The estimated value represents the percentage of participants with a PR

Timeframe: From Study Day 0 (start of treatment) up to 12 years (long-term follow up)

Overall Survival

Timeframe: From Study Day 0 (start of treatment) up to 12 years (long-term follow up)

Time to progression of disease or death (progression-free survival)

Timeframe: From Study Day 0 (start of treatment) up to 12 years (long-term follow up)

Number of participants with resolution of all Baseline B-symptoms by the end of the study

Timeframe: Baseline and up to 12 years (long-term follow up)

Number of participants who were polymerase chain reaction (PCR)-positive at Baseline with bone marrow conversion to a status of PCR positive and negative any time after treatment

Timeframe: Baseline and up to 12 years (long-term follow up)

Duration of response (the time from the first documented response to the first documented progression) for participants who were PCR positive at Baseline and converted to PCR negative status after treatment

Timeframe: Baseline and up to 12 years (long-term follow up)

Progression-free survival (PFS) based on participants’ Baseline PCR status

Timeframe: Baseline and up to 12 years (long-term follow up)

Initial half-life (t1/2alpha)

Timeframe: 0-120 hours from the dosimetric dose (given only on Day 0) and 0-120 hours from the therapeutic dose (given only on Day 7)

Terminal half-life (t1/2beta)

Timeframe: 0-120 hours from the dosimetric dose (given only on Day 0) and 0-120 hours from the therapeutic dose (given only on Day 7)

Area under the curve (AUC) at 0 to 120 hours and 0 to infinity hours

Timeframe: 0-120 hours and 0-infinity hours from the dosimetric dose (given only on Day 0) and 0-120 hours and 0-infinity hours from the therapeutic dose (given only on Day 7)

Clearance values

Timeframe: 0-120 hours from the dosimetric dose (given only on Day 0) and 0-120 hours from the therapeutic dose (given only on Day 7)

Maximum Concentration (Cmax) Values

Timeframe: 0-120 hours from the dosimetric dose (given only on Day 0) and 0-120 hours from the therapeutic dose (given only on Day 7)

Volume of distribution at infusion time 0 (Vd0) and steady state (Vdss)

Timeframe: 0-120 hours from the dosimetric dose (given only on Day 0) and 0-120 hours from the therapeutic dose (given only on Day 7)

Total body effective half-life (EHL)

Timeframe: 0-120 hours from the dosimetric dose (given only on Day 0) and 0-120 hours from the therapeutic dose (given only on Day 7)

Normal organ dosimetry for the indicated organs

Timeframe: 0-120 hours from the dosimetric dose (given only on Day 0) and 0-120 hours from the therapeutic dose (given only on Day 7)

Number of participants with the indicated fatal serious adverse events (SAE)

Timeframe: From Baseline up to 12 years from the start of treatment (long-term follow up)

Number of participants evaluable and not evaluable for Human Anti-Murine Antibodies (HAMA)

Timeframe: From Baseline up to 2 years from the start of treatment

Number of participants with conversion to HAMA positivity any time during the study from Baseline

Timeframe: From Baseline up to 2 years from the start of treatment

Time to HAMA positivity from the first dosimetric dose

Timeframe: From Baseline up to 2 years from the start of treatment

Number of participants with elevated, low, and normal thyroid stimulating hormone (TSH) levels at Baseline

Timeframe: Baseline

Participants with elevated TSH levels at Baseline with post Baseline TSH levels of low/normal and elevated

Timeframe: Baseline and up to 12 years (long-term follow up)

Time to elevated TSH post Baseline for participants who had low or normal TSH levels at Baseline and elevated levels post Baseline

Timeframe: Baseline and up to 12 years from the start of treatment

Number of participants with the adverse event (AEs) of hypothyroidism

Timeframe: Baseline and up to 12 years from the start of treatment

Number of participants with low or normal Baseline TSH levels that developed hypothyroidism

Timeframe: Baseline and up to 12 years from the start of treatment

Number of participants who received thyroid medication after treatment

Timeframe: From Study Day 0 (start of treatment) up to 12 years (long-term follow up)

Interventions:
  • Biological/vaccine: Tositumomab and Iodine I 131 Tositumomab (Anti-B1 Antibody and Iodine-131 Anti-B1 Antibody)
    • Enrollment:
    77
    Primary completion date:
    1999-01-03
    Observational study model:
    Not applicable
    Time perspective:
    Not applicable
    Clinical publications:
    Kaminski MS, Tuck M, Estes J, Kolstad A, Ross CW, Zasadny K, Regan D, Kison P, Fisher S, Kroll S, Wahl RL.. 131I-tositumomab therapy as initial treatment for follicular lymphoma.. N Engl J Med. 2005;352(5):441-9.
    Medical condition
    Lymphoma, Non-Hodgkin
    Product
    tositumomab
    Collaborators
    Not applicable
    Study date(s)
    June 1996 to October 2011
    Type
    Interventional
    Phase
    2

    Participation criteria

    Sex
    Female & Male
    Age
    18+ years
    Accepts healthy volunteers
    No
    • Inclusion Criteria
    • Patients must have a histologically confirmed diagnosis of lowgrade non-Hodgkin’s B-cell lymphoma. The following low-grade histologies are included: small lymphocytic (with or without plasmacytoid differentiation); follicular, small cleaved; follicular, mixed small cleaved and follicular large cell (less than 50% large cell component); and monocytoid B-cell lymphoma.
    Inclusion and exclusion criteria
    Inclusion criteria:
    • Inclusion Criteria
    • Patients must have a histologically confirmed diagnosis of lowgrade non-Hodgkin’s B-cell lymphoma. The following low-grade histologies are included: small lymphocytic (with or without plasmacytoid differentiation); follicular, small cleaved; follicular, mixed small cleaved and follicular large cell (less than 50% large cell component); and monocytoid B-cell lymphoma.
    • Patients must have evidence that their tumor tissue expresses the CD20 antigen. Immunoperoxidase stains of paraffin-embedded tissue showing positive reactivity with L26 antibody or immunoperoxidase stains of frozen tissue showing positive reactivity with Anti-B1 Antibody (Coulter Clone®) or similar commercially available CD20 antibody (>50% of tumor cells are positive) or evidence of CD20 positivity by flow cytometry (>50% of tumor cells are positive) are acceptable evidence of CD20 positivity. Testing of tumor tissue from any time in the course of the patient’s disease is acceptable.
    • Patients must have Ann Arbor stage III or IV extent of disease after complete staging.
    • Patients must not have had any previous treatment for low-grade lymphoma including chemotherapy or radiation. They may be newly diagnosed or observed without treatment after diagnosis. Symptomatic and asymptomatic patients will be eligible.
    • Patients must have a performance status of at least 60% on the Karnofsky Scale and an anticipated survival of at least 3 months.
    • Patients must have an absolute neutrophil count (ANC) >1500 cells/mm3 and a platelet count >100,000 cells/mm3 within 14 days of study entry. These blood counts must be sustained without support of hematopoietic cytokines or transfusion of blood products.
    • Patients must have adequate renal function (defined as serum creatinine <1.5 x upper limit of normal [ULN]) and hepatic function (defined as total bilirubin <1.5 x ULN and aspartate transaminase [AST] <5 x ULN) within 14 days of study entry.
    • Patients must have bi-dimensionally measurable disease. At least one lesion must be ≥2 x 2 cm (by computed tomography [CT] scan).
    • Patients must be at least 18 years of age.
    • Patients must give written informed consent and sign an IRB– approved informed consent form prior to study entry. Exclusion Criteria
    • Patients with more than an average of 25% of the intratrabecular marrow space involved by lymphoma in bone marrow biopsy specimens as assessed microscopically within 42 days of study entry. Bilateral posterior iliac crest core biopsies are required if the percentage of intratrabecular space involved exceeds 10% on a unilateral biopsy. The mean of bilateral biopsies must be no more than 25%.
    • Patients with evidence of active infection requiring intravenous (IV) antibiotics at the time of study entry.
    • Patients with New York Heart Association class III or IV heart disease or other serious illness that would preclude evaluation.
    • Patients with active obstructive hydronephrosis.
    • Patients with prior malignancy other than lymphoma, except for adequately treated skin cancer, in situ cervical cancer, or other cancer for which the patient has been disease-free for 5 years.
    • Patients with known HIV infection.
    • Patients with known brain or leptomeningeal metastases.
    • Patients who are pregnant or nursing. Patients of childbearing potential must undergo a pregnancy test within 7 days of study entry and radiolabeled antibody is not to be administered until a negative result is obtained. Males and females must agree to use effective contraception for 6 months following the radioimmunotherapy.
    • Patients with previous allergic reactions to iodine. This does not include reacting to IV iodine-containing contrast materials.
    • Patients who were previously given any monoclonal or polyclonal antibodies of any non-human species for either diagnostic or therapeutic purposes. This includes engineered chimeric and humanized antibodies.
    • Patients who are concurrently receiving either approved or nonapproved (through another protocol) anti-cancer drugs or biologics.

    Trial location(s)

    This study does not involve prospective enrollment of participants.

    Study documents

    Clinical study report
    Available language(s): English
    Download document(s)
    Scientific result summary
    Available language(s): English
    Download document(s)

    If you wish to request for full study report, please contact - [email protected]

    Results overview

    Results posted on ClinicalTrials.gov

    Recruitment status
    Study complete
    Actual primary completion date
    1999-01-03
    Actual study completion date
    2011-06-10

    Plain language summaries

    Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.

    Additional information about the trial

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