Management of treatment-related toxicities in advanced medullary thyroid cancer

被引:8
作者
Tsang, Venessa H. M. [1 ,2 ]
机构
[1] Royal North Shore Hosp, Dept Diabet Endocrinol & Metab, St Leonards, NSW 2065, Australia
[2] Univ Sydney, Fac Med & Hlth, Northern Clin Sch, Sydney, NSW, Australia
关键词
medullary thyroid cancer; toxicities; tyrosine kinase inhibitors; TYROSINE KINASE INHIBITORS; ADVERSE EVENTS; BLOOD-PRESSURE; RISK-FACTORS; CABOZANTINIB; HYPERTENSION; VANDETANIB; CARCINOMA; COMBINATION; DOXORUBICIN;
D O I
10.1097/CCO.0000000000000534
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose of review Tyrosine kinase inhibitors (TKI), predominantly vandetanib and cabozantinib, are increasingly used for management of advanced medullary thyroid cancer. This review aims to discuss the major and serious adverse events associated with TKI. Recent findings The choice of TKI depends on the patient's existing comorbidities. Patients who have long QT interval should avoid vandetanib and those at risk of gastrointestinal perforation should avoid cabozantinib. Hypertension is common during the first 3 months. Treatments include ACE inhibitors, calcium channel blockers (avoiding verapamil and diltiazem, which are CYP3A4 inhibitors), and beta blockers. Diuretics should be second line because of derangement of electrolytes, which may exacerbate QT interval. As nitric oxide (NO) blockade and ET1 are implicated in the mechanism of hypertension, nitrates and endothelin receptor antagonists may be used. Thromboembolism may require anticoagulation or revascularization procedures. Prolonged QT interval should be treated by dose interruption and reduction, correction of electrolytes, and avoidance of medications, which prolong QTc interval. Diarrhoea is managed symptomatically and with electrolyte replacement, dermatological adverse events with avoidance of exacerbating factors and topical therapies. Thyroid function should be monitored. Summary Toxicities are common with TKI use, and management involves symptomatic treatment, avoidance of triggers, dose interruption, and dose reduction.
引用
收藏
页码:236 / 242
页数:7
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