Nanoliposomal Irinotecan and Metronomic Temozolomide for Patients With Recurrent Glioblastoma: BrUOG329, A Phase I Brown University Oncology Research Group Trial. (February 2021)

• Record Type: Journal Article
• Authors: Elinzano, Heinrich; Toms, Steven; Robison, Jordan; Mohler, Alex; Carcieri, Arieana; Cielo, Deus; Donnelly, Jennifer; Disano, Dylan; Vatketich, John; Baekey, John; Sturtevant, Ashlee; MacKinnon, Kelsey; Wood, Roxanne; Safran, Howard
• Is Part Of: American journal of clinical oncology. Volume 44:Number 2(2021)
• Publication Date: 2021-02
• Subjects: glioblastoma -- nanoliposomal irinotecan -- phase I; Cancer -- Treatment -- Periodicals; Oncology -- Periodicals; Tumors -- Periodicals; 616.994005
• DOI: 10.1097/COC.0000000000000780
• Languages: English
• ISSNs: 0277-3732

Abstract

Abstract : Background: Liposomal formulations may improve the solubility and bioavailability of drugs potentially increasing their ability to cross the blood-brain barrier. We performed a phase I study to determine the maximum tolerated dose and preliminary efficacy of pegylated nanoliposomal irinotecan (nal-IRI)+metronomic temozolomide (TMZ) in patients with recurrent glioblastoma. Patients and Methods: Patients with glioblastoma who progressed after at least 1 line of therapy were eligible. All patients received TMZ 50 mg/m 2 /d until disease progression. Three dose levels of nal-IRI were planned, 50, 70, and 80 mg/m 2, intravenously every 2 weeks. Patients were accrued in a 3+3 design. The study included a preliminary assessment after the first 13 evaluable patients. The trial would be terminated early if 0 or 1 responses were observed in these patients. Results: Twelve patients were treated over 2 dose levels (nal-IRI 50 and 70 mg/m 2 ). At dose level 2, nal-IRI 70 mg/m 2, 2 of 3 patients developed dose-limiting toxicities including 1 patient who developed grade 4 neutropenia and grade 3 diarrhea and anorexia and 1 patient with grade 3 diarrhea, hypokalemia fatigue, and anorexia. Accrual to dose level 1 was expanded to 9 patients. The Drug Safety Monitoring Board (DSMB) reviewed the data of the initial 12 patients—there were 0/12 responses (0%) and the median progression-free survival was 2 months and accrual was halted. Conclusions: The maximum tolerated dose of nal-IRI was 50 mg/m 2 every 2 weeks with TMZ 50 mg/m 2 /d. The dose-limiting toxicities were diarrhea and neutropenia. No activity was seen at interim analysis and the study was terminated.