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Therapeutic Efficacy of a Very Low/Low Dose of Lenvatinib in Advanced Radioiodine-Refractory Thyroid Cancer: A Real-World Series from a Single Center.

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Cancers 📖 저널 OA 100% 2021: 20/20 OA 2022: 79/79 OA 2023: 89/89 OA 2024: 156/156 OA 2025: 683/683 OA 2026: 512/512 OA 2021~2026 2025 Vol.17(14)
Retraction 확인
출처

PICO 자동 추출 (휴리스틱, conf 2/4)

유사 논문
P · Population 대상 환자/모집단
15 patients with RAI-RTC who started lenvatinib at a very low/low dose and evaluated the efficacy and safety.
I · Intervention 중재 / 시술
추출되지 않음
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
However, 80% of patients experienced adverse events, mainly of a moderate grade. Although these findings are based on a small sample size and a single-center study, treatment with lenvatinib at very low/low doses in fragile patients seems to be a promising strategy for the management of RAI-RTC, balancing effective disease control with a favorable safety profile.

Oteri V, Gianì F, Sapuppo G, Panebianco S, Marturano I, Blanco G, Malandrino P, Russo M, Frasca F, Pellegriti G

📝 환자 설명용 한 줄

Lenvatinib is a receptor tyrosine kinase inhibitor indicated for advanced radioiodine-refractory thyroid cancer (RAI-RTC).

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↓ .bib ↓ .ris
APA Oteri V, Gianì F, et al. (2025). Therapeutic Efficacy of a Very Low/Low Dose of Lenvatinib in Advanced Radioiodine-Refractory Thyroid Cancer: A Real-World Series from a Single Center.. Cancers, 17(14). https://doi.org/10.3390/cancers17142372
MLA Oteri V, et al.. "Therapeutic Efficacy of a Very Low/Low Dose of Lenvatinib in Advanced Radioiodine-Refractory Thyroid Cancer: A Real-World Series from a Single Center.." Cancers, vol. 17, no. 14, 2025.
PMID 40723255 ↗

Abstract

Lenvatinib is a receptor tyrosine kinase inhibitor indicated for advanced radioiodine-refractory thyroid cancer (RAI-RTC). It is recommended to start at 24 mg per day; however, in patients who are at risk of severe adverse events, it may be reasonable to start at lower doses. We included 15 patients with RAI-RTC who started lenvatinib at a very low/low dose and evaluated the efficacy and safety. Eight patients (53.3%) did not show progression of the disease, and about half of the patients (53.3%) were alive at the last follow-up visit. Up to 26.6% of patients achieved a partial response to therapy, with a notable volume reduction in the local and metastatic lesions. However, 80% of patients experienced adverse events, mainly of a moderate grade. Although these findings are based on a small sample size and a single-center study, treatment with lenvatinib at very low/low doses in fragile patients seems to be a promising strategy for the management of RAI-RTC, balancing effective disease control with a favorable safety profile.

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