Tositumomab and Iodine I 131 Tositumomab in Treating Patients With Chronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma in First Remission

Fred Hutchinson Cancer Center (FHCC)

Status and phase

Completed

Phase 2

Conditions

Stage IV Small Lymphocytic Lymphoma

Stage IV Chronic Lymphocytic Leukemia

Stage I Chronic Lymphocytic Leukemia

Stage III Chronic Lymphocytic Leukemia

Lymphoid Leukemia in Remission

Stage III Small Lymphocytic Lymphoma

Stage II Chronic Lymphocytic Leukemia

Treatments

Combination Product: Tositumomab and Iodine I 131 Tositumomab

Study type

Interventional

Funder types

Other

NIH

Identifiers

NCT00476047

PSOC 2301 (Other Identifier)

P30CA015704 (U.S. NIH Grant/Contract)

NCI-2011-01311 (Registry Identifier)

Details and patient eligibility

About

This phase II trial studies how well tositumomab and iodine I 131 tositumomab works in treating patients with chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL) that have had their first decrease in or disappearance of signs and symptoms of cancer (first remission). Monoclonal antibodies, such as tositumomab and iodine I 131 tositumomab, may block cancer growth in different ways by targeting certain cells.

Full description

PRIMARY OBJECTIVES:

I. To estimate the progression-free survival at 2 years following administration of 131I-tositumomab (tositumomab and iodine I 131 tositumomab) in patients with CLL/SLL who achieve a complete remission (CR) or partial remission (PR) with prior therapy.

II. To improve the response rate by administering 131I-tositumomab to patients who have achieved a PR not a CR after any prior therapy.

III. To eliminate residual disease (documented by flow cytometry or polymerase chain reaction [PCR]) using 131I-tositumomab in patients who have achieved a CR after any prior therapy.

SECONDARY OBJECTIVES:

I. To evaluate the toxicities of 131I-tositumomab in 1st remission patients with previously treated CLL/SLL.

OUTLINE:

Patients receive tositumomab and iodine I 131 tositumomab intravenously (IV) over 90 minutes on day 0 and then again 7-14 days later over 30-60 minutes.

After completion of study treatment, patients are followed up weekly for 3 months, every 3 months for 2 years, every 6 months for 3 years, and then annually thereafter.

Enrollment

16 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Patients with a diagnosis of cluster of differentiation (CD)20+ CLL/SLL; prior to the first treatment patients with CLL must have been either Rai stage III/IV disease or Rai stage I/II with evidence of disease activity as defined by the National Cancer Institute (NCI) 1996 guidelines, and patients with SLL must have been Stage III or IV per Ann Arbor staging system
Patient has received prior therapy and is in 1st remission with a partial or complete response to treatment
Patients must have no more than 25% of the intratrabecular marrow space involved by leukemia in bone marrow biopsy specimens as assessed microscopically after completion of treatment; 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%
Patient must have consented to participate in the study and signed and dated an appropriate institutional review board (IRB)-approved consent form that conforms to federal and institutional guidelines
Patient must have a Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1 or 2 (0 = fully active, able to carry on all pre-disease performance without restriction; 1 = restricted in physically strenuous activity but ambulatory and ambulatory and able to carry out work of a light or sedentary nature, e.g., light house work, office work; 2 = ambulatory and capable of all self-care but unable to carry out any work activities and is up and about more than 50% of waking hours)
Patient must have an anticipated survival of at least 3 months
Granulocytes >= 1,500/uL within 14 days of planned dosimetric infusion
Platelets >= 100,000/uL within 14 days of planned dosimetric infusion
White blood count =< 20,000/mm^3
Serum creatinine < 2 times upper limit of normal
Total bilirubin < 2 times upper limit of normal
Aspartate aminotransferase (AST) < 5 times upper limit of normal
Males and females must agree to use a contraceptive method from enrollment to 6 months after receiving I-131 labeled tositumomab

Exclusion criteria

Patients who have received prior radiolabeled antibody
Patients with active hemolysis
Patients must not require sustained transfusion support of blood products
Patients in 2nd remission or beyond
Patients who have undergone treatment with either stem cell or bone marrow transplant
Patients with active obstructive hydronephrosis
Patients with evidence of any significant systemic illness, active hepatitis B infection or other active infection 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 known human immunodeficiency virus (HIV) infection
Patients who are pregnant or nursing
Patients with prior malignancy other than CLL/SLL, except for adequately treated skin cancer (basal cell or squamous cell carcinoma), in situ cervical cancer, or other cancer for which the patient has been disease-free for 5 years unless approved by the principal investigator (PI)
Patients with active brain or leptomeningeal involvement by malignancy
Patients who have, in the opinion of the investigator, other medical, social, or psychosocial factors that may negatively impact compliance or their safety by participation in this study