Rasburicase and Allopurinol in Treating Patients With Hematologic Malignancies
Information source: Roswell Park Cancer Institute
ClinicalTrials.gov processed this data on August 23, 2015 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Adult Acute Myeloid Leukemia With 11q23 (MLL) Abnormalities; Adult Acute Myeloid Leukemia With Del(5q); Adult Acute Myeloid Leukemia With Inv(16)(p13;q22); Adult Acute Myeloid Leukemia With t(15;17)(q22;q12); Adult Acute Myeloid Leukemia With t(16;16)(p13;q22); Adult Acute Myeloid Leukemia With t(8;21)(q22;q22); Blastic Phase Chronic Myelogenous Leukemia; Contiguous Stage II Adult Burkitt Lymphoma; de Novo Myelodysplastic Syndromes; Noncontiguous Stage II Adult Burkitt Lymphoma; Previously Treated Myelodysplastic Syndromes; Recurrent Adult Acute Lymphoblastic Leukemia; Recurrent Adult Acute Myeloid Leukemia; Recurrent Adult Burkitt Lymphoma; Stage I Adult Burkitt Lymphoma; Stage III Adult Burkitt Lymphoma; Stage IV Adult Burkitt Lymphoma; Untreated Adult Acute Lymphoblastic Leukemia; Untreated Adult Acute Myeloid Leukemia
Intervention: rasburicase (Drug); allopurinol (Drug)
Phase: Phase 2
Status: Terminated
Sponsored by: Roswell Park Cancer Institute Official(s) and/or principal investigator(s): Eunice Wang, MD, Principal Investigator, Affiliation: Roswell Park Cancer Institute
Summary
This randomized phase II trial studies how well giving rasburicase together with allopurinol
works in treating patients with hematologic malignancies. Rasburicase may reduce the level
of uric acid in the blood. Allopurinol may stop the growth of cancer cells by blocking some
of the enzymes needed for cell growth. It is not yet known which dose of rasburicase is more
effective in treating hematologic malignancies when given together with or without
allopurinol.
Clinical Details
Official title: Efficacy and Safety of Two Comparable Single Low Doses of Rasburicase Followed by Allopurinol in Adult Patients With Malignancy
Study design: Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Primary outcome: Probability of obtaining a uric acid level =< 7.5mg/dL
Secondary outcome: Rate of patients that maintain a uric acid level =< 7.5mg/dLRate of patients requiring additional doses of rasburicase to maintain a uric acid level =< 7.5mg/dL Rate of patients able to maintain a uric acid level =< 7.5mg/dL Differential characteristics of patients unable to achieve and/or maintain a uric acid level =< 7.5mg/dL
Detailed description:
PRIMARY OBJECTIVES:
I. To prospectively evaluate the efficacy, as defined by uric acid response rate, of 2
different single low doses of rasburicase followed by allopurinol in 2 treatment arms.
SECONDARY OBJECTIVES:
I. To estimate the proportion of patients requiring additional doses of rasburicase to
maintain a uric acid level =< 7. 5mg/dL on day 2 through day 6.
II. To identify differential characteristics of the patients who do not respond to
treatment.
III. To measure the area under the plasma uric acid concentration-time curve (AUC) from
baseline (day 1) to day 7, time to plasma uric acid level less than or equal to 7. 5mg/dL.
IV. To evaluate the rate of patients requiring hemodialysis (HD) V. To evaluate the safety
of low single-doses of rasburicase. VI. To evaluate the rate of patients expressing a
doubling of serum creatinine.
OUTLINE: Patients are randomized to 1 of 2 treatment arms.
ARM I: Patients receive 1. 5mg of rasburicase intravenously (IV) over 30 minutes on day 1*
and allopurinol orally (PO) once daily (QD) on days 1-6.
ARM II: Patients receive 3 mg of rasburicase IV over 30 minutes on day 1* and allopurinol PO
QD on days 1-6.
NOTE: *Patients with serum uric acid >= 7. 5mg/dl also receive rasburicase IV on days 2-3.
After completion of study treatment, patients are followed up at 30 days.
Eligibility
Minimum age: 18 Years.
Maximum age: N/A.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- Eastern Cooperative Oncology Group (ECOG) status of 0-3
- Active leukemia and Burkitt leukemia/lymphoma treated in-house that puts them at risk
for tumor lysis syndrome (TLS)
- Serum uric acid level >= 7. 5mg/dL and high risk for TLS as defined by:
- A diagnosis of acute myeloid leukemia (AML), or
- A diagnosis of blast-phase chronic myeloid leukemia (CML), or
- A diagnosis of high-grade myelodysplastic syndrome (MDS) with >= 10% blast bone
marrow blast involvement, or
- Acute lymphoblastic leukemia (ALL), or
- Burkitt leukemia/lymphoma
- Patient or legal representative must understand the investigational nature of this
study and sign an Independent Ethics Committee/Institutional Review Board approved
written informed consent form prior to receiving any study related procedure
Exclusion Criteria:
- History of asthma
- History of severe or life threatening atopic allergy
- Hypersensitivity to uricases
- Known prior sensitivity to allopurinol
- Known glucose-6-phosphate dehydrogenase (G6PD) deficiency
- Recent prior history of uricolytic therapy defined as therapy within the last 7 days
Locations and Contacts
Roswell Park Cancer Institute, Buffalo, New York 14263, United States
Additional Information
Starting date: September 2011
Last updated: May 28, 2015
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