Late toxicities burden in patients with radioiodine-refractory differentiated thyroid cancer treated with lenvatinib

• Published in: Endocrine Vol. 73; no. 3; pp. 641 - 647
• Main Authors: Platini, F., Cavalieri, S., Alfieri, S., Bergamini, C., Resteghini, C., Bottiglieri, A., Colombo, E., Mazzeo, L., Licitra, L., Paolini, B., Seregni, E., Locati, L. D.
• Format: Journal Article
• Language: English
• Published: New York Springer US 01.09.2021; Springer Nature B.V
• Subjects: Adverse events; Diabetes; Endocrinology; Humanities and Social Sciences; Internal Medicine; Iodine; Medicine; Medicine & Public Health; multidisciplinary; Original Article; Patients; Science; Side effects; Survival; Thyroid cancer; Toxicity; Lenvatinib; Thyroid cancer; Late toxicities; RAI-resistant
• ISSN: 1355-008X; 1559-0100
• DOI: 10.1007/s12020-021-02702-4

Purpose Radioactive-iodine (RAI)-resistant differentiated thyroid cancer (DTC) patients benefit from multi-kinase inhibitors (MKIs), such as lenvatinib. Incidence of treatment-related (TR) late toxicities has been not yet described. Methods From January 2015 to June 2019 we retrospectively reviewed clinical records of patients with RAI-resistant DTC treated with lenvatinib at Istituto Nazionale dei Tumori (Milan, Italy). New side effect of any grade, appeared after 12 months of lenvatinib, was defined as late adverse event (AE). Descriptive analyses were performed. Survival curves were estimated with Kaplan–Meier method and compared with log-rank test. Results Thirty-seven patients were included, 65% had ≥65 years and 68% were female. Thirty patients received lenvatinib for >12 months. Lenvatinib was started at ≤20 mg/daily in 59% of patients, 64% were ≥65 years. The frequency of late AEs was 80% and cardiovascular toxicity was the most common (57%). There was no difference in the incidence of late AEs between younger/older population (77% and 82%, respectively). Median lenvatinib treatment duration (TD) was 39.96 months (95% CI 21.64-NR): 39.96 months for patients <65 years (95% CI: 13.25-NR) and 37.53 months for those ≥65 years, respectively (95% CI: 15.85-NR). Median overall survival (OS) was 39.96 months (95% CI: 21.84-NR), no statistically differences in OS was observed between younger (<65 years) and older patients (≥65 years) (HR 1.013; 95% CI 0.963–1.065; p  = 0.62). Conclusion Late toxicity burden of lenvatinib is not negligible. Cardiovascular toxicity remains the principal side effect even after a prolonged lenvatinib exposition.