Natalizumab in Recurrent, Refractory or Progressive Pulmonary Metastatic Osteosarcoma

• Status: Not yet recruiting
• Trial end date: 2023-10-01
• Target enrollment: 0
• Participant gender: All

Summary

The purpose of this study is to evaluate the safety and tolerability of Natalizumab in children, adolescent and young adult patients with pulmonary metastatic osteosarcoma (pOS) and to assess clinical response associated with this treatment as well as overall survival.

• Phase: Phase 1/Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Case Comprehensive Cancer Center
• Treatments: Natalizumab

Criteria

Inclusion Criteria:

• Subjects must have histologic verification of pOS.

• Subjects must have measurable pulmonary disease per RECIST 1.1 documented by clinical, radiographic and histologic criteria, and have progressed, relapsed or become refractory to conventional therapy.

• Subjects must have recovered from the acute toxic effects with ≤ Grade 1 as defined by the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CASE 1718 Page 20 Version date: 9/11/18 CTCAE) Version 5.0 of all prior chemotherapy and immunotherapy with the exception of alopecia, anorexia, bone pain, and tumor pain prior to entering this study.

• Myelosuppressive chemotherapy: Must have adequate recovery of counts from previous treatment prior to entry onto this study.

• Monoclonal antibodies: At least 3 half-lives must have elapsed since prior therapy that included a monoclonal antibody.

• Subjects must have a performance status corresponding to a Karnofsky ≥ 50% for participants > 16 years of age and Lansky ≥ 60 for participants ≤ 16 years of age. Participants who are unable to walk because of paralysis, but who are up in a wheelchair will be considered ambulatory for the purpose of assessing the performance score.

• Subjects must have normal organ and marrow function as defined below:

• Adequate bone marrow function defined as:

• Peripheral absolute neutrophil count (ANC) ≥ 750/mcL

• Platelet count ≥ 75,000/mcL (transfusion independent)

• Hemoglobin ≥ 8.0 g/dL (may receive packed red blood cell transfusions)

• Adequate liver function defined as:

• Total bilirubin ≤ 1.5 times the upper limit of normal for age

• AST (SGOT) and ALT (SGPT) 2.5 X institutional upper limit of normal

• Serum albumin > 2 g/dL

• Adequate cardiac function defined as:

• Ejection fraction of ≥ 50% by echocardiogram

• Subjects must have the ability to understand and the willingness to sign a written informed consent document if ≥ 18 years of age and an assent document if < 18 years of age. If < 7 years of age, no assent document is required.

Exclusion Criteria:

The presence of any of the following will exclude a subject from study enrollment.

• Ongoing prior treatment toxicities > Grade 1 according to NCI CTCAE Version 5.0 with the exception of alopecia, anorexia, bone pain and tumor pain.

• Subjects receiving any other investigational agents.

• History of allergic reactions attributed to compounds of similar chemical or biologic composition to Natalizumab.

• Subjects currently on immunosuppressive therapy.

• Subjects with uncontrolled intercurrent illness including, but not limited to ongoing or active infection, liver failure, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.

• Pregnant or breastfeeding women are excluded from this study because Natalizumab crosses the placenta and can increase the risk of spontaneous abortion. There is an unknown, but potential risk for adverse events in nursing infants secondary to treatment of the mother with Natalizumab, therefore breastfeeding should be discontinued if the mother is treated with Natalizumab.

• Female participants of childbearing potential are not eligible unless a negative pregnancy test result has been obtained.

• Women of childbearing potential and men must agree to use adequate contraception prior to study entry and for the duration of study participation. Should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her treating physician immediately.

• HIV-positive subjects and HIV-positive subjects on antiretroviral therapy are ineligible because of the risk for developing a lethal infection when treated with immunosuppressive therapy.

• Participants who have or have had progressive multifocal leukoencephalopathy (PML).

• Participants whose pulmonary metastatic disease can be completely surgically resected.