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©The Author(s) 2020.
World J Clin Cases. Oct 26, 2020; 8(20): 4883-4894
Published online Oct 26, 2020. doi: 10.12998/wjcc.v8.i20.4883
Published online Oct 26, 2020. doi: 10.12998/wjcc.v8.i20.4883
Trials | Study group with anti-VEGF therapy | Dosage | Median duration of follow-ups | Nephrotoxicity | Strategies during adverse effects |
Brose et al[3] (DECISION trial, phase-3 trial) | RAI-refractory DTC; 207 patients | Sorafenib: 800 mg/d | 10.6 mo | Hypertension: 40.6%/9.7% (all grades/grade ≥ 3) | Dosage would be reduced to 600 mg/d, 400 mg/d or 200 mg/d |
Peripheral edema: not documented | |||||
Proteinuria: not documented | |||||
Schlumberger et al[4] (SELECT trial, phase-3 trial) | RAI-refractory DTC; 261 patients | Lenvatinib: 24 mg/d | 17.1 mo | Hypertension: 67.8%/41.8% (all grades/grade ≥ 3) | Dosage would be reduced to 20 mg/d, 14 mg/d, or 10 mg/d |
Peripheral edema: 11.1%/0.4% (all grades/grade ≥ 3) | |||||
Proteinuria: 31%/10% (all grades/grade ≥ 3) | |||||
Kudo et al[13] (REFLECT trial, phase-3 trial) | Unresectable HCC; 476 patients with lenvatinib; and 475 patients with sorafenib | 1 Lenvatinib: (dosage based on whether body weights above 60 kg or not): (1) 12 mg/d: 325 patients (68%); and (2) 8 mg/d: 153 patients (32%) | 1 Lenvatinib: 27.7 mo | 1 Lenvatinib: (1) Hypertension: 42%/23% (all grades/grade ≥ 3); (2) Peripheral edema: not documented; and (3) Proteinuria: 25%/6% (all grades/grade ≥ 3) | 1 Lenvatinib: Dosage would be reduced to 8 mg (initially with 12 mg/d) and 4 mg/d (initially with 8 mg/d), or 4 mg every other day |
2 Sorafenib: 800 mg/d | 2 Sorafenib: 27.2 mo | 2 Sorafenib: (1) Hypertension: 30%/14% (all grades/grade ≥ 3); (2) Peripheral edema: not documented; and (3) Proteinuria: 11%/2% (all grades/grade ≥ 3 | 2 Sorafenib: Dosage switch was implemented according to prescribing information in each region | ||
Motzer et al[14] (Number NCT01136733, phase-2 trial) | Metastatic RCC; 51 patients with lenvatinib plus everolimus; and 52 patients with lenvatinib | 1 Lenvatinib plus everolimus: Lenvatinib of 18 mg/d plus everolimus of 5 mg/d | 1 Lenvatinib plus everolimus: 18.5 mo | 1 Lenvatinib plus everolimus: (1) Hypertension: 27%/14% (all grades/grade ≥ 3); (2) Peripheral edema: 27%/0% (all grades/grade ≥ 3); and (3) Proteinuria: 18%/4% (all grades/grade ≥ 3) | 1 Lenvatinib plus everolimus: (1) If possibly from lenvatinib: Dosage would be reduced from 18 mg/d to 14 mg/d, 10 mg/d, and 8 mg/d; and (2) If possibly from everolimus: Dosage would be reduced from 5 mg/d to 5 mg every other day. |
2 Lenvatinib: 24 mg/d | 2 Lenvatinib: 17.8 mo | 2 Lenvatinib: (1) Hypertension: 31%/17% (all grades/grade ≥ 3); (2) Peripheral edema: 15%/0% (all grades/grade ≥ 3); and (3) Proteinuria: 12%/19% (all grades/grade ≥ 3) | 2 Lenvatinib: Dosage would be reduced from 24 mg/d to 20 mg/d, 14 mg/d, and 10 mg/d |
- Citation: Yang CH, Chen KT, Lin YS, Hsu CY, Ou YC, Tung MC. Improvement of lenvatinib-induced nephrotic syndrome after adaptation to sorafenib in thyroid cancer: A case report. World J Clin Cases 2020; 8(20): 4883-4894
- URL: https://www.wjgnet.com/2307-8960/full/v8/i20/4883.htm
- DOI: https://dx.doi.org/10.12998/wjcc.v8.i20.4883