Finding studies
Finding studies
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Lead
ECOG-ACRIN Cancer Research Group
With
PRIMARY OBJECTIVE: I. To assess pneumonitis response to additional immunosuppression (infliximab or intravenous immunoglobulin therapy \[IVIG\]) in patients with steroid-refractory pneumonitis at 28-days. SECONDARY OBJECTIVES: I. To assess functional parameters of steroid-refractory pneumonitis at day 1, 14-days and 28-days after day 1 of receipt of additional immunosuppression (infliximab or IVIG). II. To assess radiologic parameters of steroid-refractory pneumonitis at day 1, 14-days and 28-days after day 1 of receipt of additional immunosuppression (infliximab or IVIG). III. To assess patient-reported outcomes of steroid-refractory pneumonitis at day 1, 14-days and 28-days after day 1 of receipt of additional immunosuppression (infliximab or IVIG). IV. To assess death after additional immunosuppression. V. To assess the rate of infections in the 28-day period after additional immunosuppression. EXPLORATORY OBJECTIVES: I. To examine lung tissue, bronchoalveolar lavage (BAL) and serial blood samples in patients who develop steroid-refractory pneumonitis. II. To examine associations between BAL phenotypes and pneumonitis response, functional and radiologic parameters of pneumonitis. III. To evaluate associations between pneumonitis and autoantibodies, T-cell expansion, and baseline cytokines in the blood. OUTLINE: Patients are randomized to 1 of 2 arms. ARM A: Patients receive infliximab intravenously (IV) on day 1 followed by prednisone taper IV or orally (PO) for 4-6 weeks in the absence of disease progression or unacceptable toxicity. Patients may receive an additional dose of infliximab IV on day 14 at the discretion of the treating physician. ARM B: Patients receive intravenous immunoglobulin therapy IV over 2-5 days per institutional guidelines followed by prednisone taper IV or PO for 4-6 weeks in the absence of disease progression or unacceptable toxicity. After completion of study treatment, patients are followed up at 28, 42 and 56 days.
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
