Neuroendocrinology · 2025
Real-World Patient Outcomes on the Efficacy of Lanreotide Treatment for Neuroendocrine Tumors: The Influence of Body Mass Index, Body Surface Area, and Renal Function.
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de Weert Ilse, Crul Mirjam, Klümpen Heinz-Josef, Schutte Tim
Аннотация
UNLABELLED: <p>Introduction: Lanreotide is an effective and safe first-line therapy to treat patients with a gastroenteropancreatic (GEP) neuroendocrine tumor (NET). Precision oncology may be used to provide each patient with the right dosage. Pharmacokinetic data suggest lower exposure in higher weight patients. However, no recommendations for dose individualization in specific patient groups exist. Therefore, we aimed to investigate the association of body mass index (BMI), body surface area (BSA), and renal function on the efficacy and toxicity of lanreotide treatment for NETs.
METHODS: GEP-NET patients on lanreotide treatment at Amsterdam UMC from 2016 to 2022 were included. Outcome measures were primarily PFS and secondarily OS and toxicity. Kaplan-Meier analyses and Cox's proportional hazard models were used to calculate median PFS/OS and compare subgroups based on BMI, BSA, and renal function.
RESULTS: A total of 122 patients with NETs of diverse origin, functionality, and grade were included with a median PFS of 28 months (95% CI, 19.3-36.7). The median OS was not reached. No statistically significant difference in PFS among BMI subgroups was observed, although obese patients had the longest PFS (52 months, 95% CI, 27.4-76.7) compared to other BMI categories. No relation between BSA/renal function and PFS or toxicity was found.
CONCLUSION: This large real-world data cohort of NET patients treated with lanreotide found no association of BMI, BSA, or renal function with PFS. Dose individualization of lanreotide treatment based on the patient characteristics BMI, BSA, or renal function does not seem rational based on these findings. </p>.
METHODS: GEP-NET patients on lanreotide treatment at Amsterdam UMC from 2016 to 2022 were included. Outcome measures were primarily PFS and secondarily OS and toxicity. Kaplan-Meier analyses and Cox's proportional hazard models were used to calculate median PFS/OS and compare subgroups based on BMI, BSA, and renal function.
RESULTS: A total of 122 patients with NETs of diverse origin, functionality, and grade were included with a median PFS of 28 months (95% CI, 19.3-36.7). The median OS was not reached. No statistically significant difference in PFS among BMI subgroups was observed, although obese patients had the longest PFS (52 months, 95% CI, 27.4-76.7) compared to other BMI categories. No relation between BSA/renal function and PFS or toxicity was found.
CONCLUSION: This large real-world data cohort of NET patients treated with lanreotide found no association of BMI, BSA, or renal function with PFS. Dose individualization of lanreotide treatment based on the patient characteristics BMI, BSA, or renal function does not seem rational based on these findings. </p>.