| Title: |
CPX-351 Pharmacokinetics and Safety in Adults with Hematologic Malignancies and Renal Function Impairment: Phase 1 Trial. |
| Authors: |
Solomon, Scott R., Powell, Bayard L., Koprivnikar, Jamie, Lai, Catherine, Male, Heather, Michaelis, Laura C., Newell, Laura F., Sanford, David, Jenkins, Jack, Zelaya, Amy, Coppola, Sheryl, Faderl, Stefan, Walter, Roland B. |
| Source: |
Cancers; Mar2024, Vol. 16 Issue 5, p915, 11p |
| Subject Terms: |
THERAPEUTIC use of antineoplastic agents, PHARMACEUTICAL arithmetic, HEMATOLOGIC malignancies, PATIENT safety, CREATININE, CLINICAL trials, ANTINEOPLASTIC agents, BLOOD collection, DESCRIPTIVE statistics, CYTARABINE, KIDNEY diseases, COMPARATIVE studies, URINE collection & preservation, DAUNOMYCIN |
| Geographic Terms: |
UNITED States |
| Abstract: |
Simple Summary: CPX-351 has been approved for the treatment of acute myeloid leukemia. Previous studies have indicated that dose adjustment is not warranted for patients with mild to moderate renal impairment. However, the effect of severe renal impairment on the use of CPX-351 has not been established. In this study, we evaluated CPX-351 in patients with normal renal function and in patients with moderate and severe renal impairment. We compared how CPX-351 moves through the body, as well as the safety of the drug, in these different patient groups. The results suggest that CPX-351 dose adjustment is not required for patients with hematologic malignancies with moderate or severe renal impairment. This open-label phase 1 study (clinicaltrials.gov, NCT03555955) assessed CPX-351 pharmacokinetics (PK) and safety in patients with hematologic malignancies with normal or impaired renal function. Patients were enrolled into three cohorts based on their creatinine clearance (CrCl): ≥90 mL/min (Cohort 1, normal renal function, n = 7), 30 to <59 mL/min (Cohort 2, moderate renal impairment, n = 8), or <30 mL/min (Cohort 3, severe renal impairment, n = 6). Patients received intravenous CPX-351 for initial induction; blood and urine samples were collected for PK analysis. The primary objective was to assess the PK parameters for cytarabine, daunorubicin, and their respective metabolites, arabinosyluracil (Ara-U) and daunorubicinol. Renal impairment did not significantly impact the cytarabine, daunorubicin, or daunorubicinol exposure, but it caused a slight increase in the Ara-U exposure. The CPX-351 side effect profile was similar in patients with impaired renal function compared to those with normal renal function. All the patients reported ≥1 treatment-emergent adverse event (TEAE), most commonly febrile neutropenia and nausea (57% each) and hyperglycemia (43%); no patients discontinued treatment due to TEAEs. These data suggest that CPX-351 dose adjustment is not required for patients with hematologic malignancies with moderate or severe renal impairment. [ABSTRACT FROM AUTHOR] |
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| Database: |
Complementary Index |
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