Oncaspar/Doxil/Decadron in Patients With Refractory Lymphoid Malignancies

Multiple Myeloma Clinical Trial

Official title:

Phase II Pilot Efficacy Trial of the Combination Regimen Oncaspar/Doxil/Decadron (ODD) in Patients With Refractory Lymphoid Malignancies

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00837200
• Other study ID #: 08-007
• Status: Completed
• Phase: Phase 2
• First received: February 4, 2009
• Last updated: September 18, 2014
• Start date: March 2009
• Est. completion date: October 2013

Study information

• Verified date: September 2014
• Source: Milton S. Hershey Medical Center
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

This is an exploratory study to study the efficacy of combination regimen of Oncaspar/Doxil/Decadron (ODD) in patients with refractory lymphoid malignancies. Patients with any form of lymphoid malignancy will be eligible: acute lymphoblastic leukemia, chronic lymphocytic leukemia, non-Hodgkin's lymphoma, Hodgkin's lymphoma, multiple myeloma and plasma cell leukemia. Patients must have failed standard regimens for their cancers and could have had unlimited number of prior regimens. Patients will be staged appropriately for their disease with clinical examination, laboratory tests, and imaging studies. Both Oncaspar and Doxil will be given on day 1 and 15. Patients will be clinically evaluated prior to each cycle and will have disease assessments every 2 cycles. Responding patients will continue therapy until disease progression or excessive toxicity. Responders who are candidates for allogenic stem cell transplantation could go to conditioning chemotherapy and stem cell transplant after 4 cycles of ODD.

Description:

This phase II trial will study the effectiveness of a combination regimen which includes Oncaspar (PEG-asparaginase), Doxil (PEG-liposomal doxorubicin), and Decadron (ODD) in terms of disease response against refractory lymphoid malignancies. Asparaginase is an enzyme that depletes asparagines, a key amino acid for survival and growth of malignant lymphocytes. Its depletion results in death of the neoplastic cell. Asparagine depletion has induced a significant improvement of clinical outcomes in acute lymphoblastic leukemia (ALL) and L-asparaginase has been a mainstay for more than 30 years in the treatment of ALL. Although this drug has been used primarily in ALL, promising results have been reported even in other non-ALL lymphoid malignancies, such as chronic lymphocytic leukemia (CLL), prolymphocytic leukemia, refractory non-Hodgkin's lymphoma (NHL) and multiple myeloma (MM). One of the main goals of this trial is to measure the asparaginase level as a surrogate marker of asparagine depletion with Oncaspar, a PEG-enhanced version of E. coli L-asparaginase. The therapeutic value of the simple, non-pegylated form of L-asparaginase is limited by its short half-life and propensity to cause allergic reactions.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 13
• Est. completion date: October 2013
• Est. primary completion date: January 2011
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Histologically documented lymphoid malignancies, regardless of their origin (B,T or NK). These include ALL, CLL, HL, NHL, MM and PCL.

• Patients must have failed at least one standard regimen of chemotherapy for their illness. They may have had unlimited prior regimens.

• Performance status of = 2 as per ECOG scale.

• ALT < 2.5 times the upper limit of normal

• Anticipated life expectancy of at least 12 weeks

• Patients will be allowed to have baseline cytopenias, but ANC should be >200/µl and a platelet count > 25,000/ µl (within 2 weeks of starting therapy).

• Patients must have a serum creatinine level = 2 mg/dL (within 2 weeks of starting therapy).

• Male or female adults of at least 18 years of age.

• Signed written informed consent and willingness to meet follow-up schedule and study procedure obligations

• Left Ventricular Ejection Fraction (LVEF) > 40% by echocardiogram or MUGA scan performed within 60 days prior to registration

• Women and men of childbearing potential must agree to employ adequate contraception to prevent pregnancy while on therapy.

Exclusion Criteria:

• Chemotherapy or radiotherapy received within the previous 2 weeks.

• Uncontrolled, active infection requiring IV antibiotics.

• Psychiatric illness that could potentially interfere with the completion of treatment according to this protocol.

• Pregnant or potential for pregnancy.

• Breast-feeding.

• Prior asparaginase therapy complicated by pancreatitis, allergic reaction, hemorrhagic event, or thrombosis

• Previous treatment with pegylated asparaginase

• Prior doxorubicin exposure, more than 400 mg/m2

• Clinically significant CHF

• No prior malignancy is allowed except for adequately treated basal cell or squamous cell skin cancer, in situ cervical cancer, or other cancer for which the patient has been disease free for at least three years. Prior malignancy is acceptable provided there has been no evidence of disease within the three year interval.

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Hodgkin Disease
• Hodgkins Lymphoma
• Lymphoma
• Lymphoma, Non-Hodgkin
• Multiple Myeloma
• Non-hodgkins Lymphoma

Intervention

Drug:
• Oncaspar, Doxil, Decadron
Once enrolled, patients will receive a cycle (28 days) of Oncaspar (2500 IU/m2 IV on days 1, 15; Doxil 20 mg/m2 IV days 1,15; and Decadron 20 mg PO days 1, 8, 15, 22. Continue until disease progression or unacceptable side effects.

Locations

Country	Name	City	State
United States	Penn State Milton S. Hershey Medical Center	Hershey	Pennsylvania

Sponsors (1)

Lead Sponsor	Collaborator
Milton S. Hershey Medical Center

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Tumor Response	Leukemias mainly w/peripheral blood counts/diff every 2 wks/CLL, CT scan before initiation of study, 2nd CT after EOT, no CT at FU; Lymphomas restaged w/CT scans of chest/abdomen/pelvis or PET/CT scans after 2 cycles; MM monitored w/tumor markers monthly Quantitative immunoglobulins/SPEP w/quantitative M component in MM pts producing full antibody, UPEP w/ quantitative Bence-Jones in MM pts producing only light chains/Serum free light chains obtained all pts/Skeletal surveys at baseline Tumor responses:CR complete resolution of all detectable clinical/radiographic evidence of disease, disappearance of all disease related symptoms, and normalization of biochemical abnormalities for at least 6 wks following treatment and no BM infiltration;PR reduction of all measurable lesions by 50% or more/no new lesions;SD not fulfilling PR criteria/no evidence disease progression;PD increase original tumor mass by more than 25% lesion/new lesion; Stable disease > 2mo was a response	16 weeks	Yes
Primary	Study Specific Measure (Response)		16 Weeks	Yes
Primary	Study Specific Measure (Number of Participants Taken Off Study)		16 weeks	Yes