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. 2014 Dec;21(6):309–317. doi: 10.3747/co.21.1647

TABLE III.

Management of selected adverse events in patients receiving sunitinib18,33,34,36

4.1.

Toxicity type Prophylaxis Management
Gastrointestinal toxicity
  Diarrhea Split food and drink into small amounts
Avoid spicy, high-fat, fried foods
Avoid excessive fruit and laxatives
Mild forms: rehydration, electrolytes (early upfront treatment—for example, loperamide—is desirable)
Dose reduction or interruption only for severe diarrhea (grades 3 and 4)
  Nausea and vomiting Bland diet; immediate consultation for any new gastric symptoms Use early intervention to avoid a possible need for sunitinib dose reduction or interruption
Patient should eat smaller meals more often and maintain good fluid intake Antiemetics (for example, metoclopramide) and reduction of stomach acidity (proton pump inhibitors) are recommended; reduce sunitinib dosage by 12.5 mg only in cases of grade 3 and 4 reactions in which other interventions fail
Oral and cutaneous
  Stomatitis or mucositis Avoid irritating foods and drinks
Lip protection; good oral hygiene with mouth rinsing, meticulous dental care, and so on
Hard candies or sugar-free mints can sometimes help with taste disturbance
Early intervention with topical anesthetics, steroids, or anti-infectives
Dose alterations or treatment interruption to be undertaken only if symptoms are pronounced and nutrition inadequate; a treatment-free interval might be necessary
  Exanthema Avoid sun exposure (use sunscreen and a hat) and protect skin
Use moisturizing products after showering; anti-dandruff shampoos can also be useful
Avoid hot showers
Wear loose-fitting clothes
Urea-containing creams or lotions; corticosteroids in more severe cases; antipruritics can also be useful
Treatment-free intervals or dose reductions should not be necessary in most cases
  Hand–foot syndrome Decrease pressure on feet, and avoid friction or pressure on hands; avoid sandals, tight shoes, heavy activity or excessive sport
Manicure and pedicure before starting treatment
Wear loose clothing, and wash with lukewarm water; pat rather than rub dry, and use sunscreens and moisturizing lotions
Fatty ointments or lotions with 10% urea; 35%–40% urea can help with hyperkeratosis
Anti-inflammatory medication or analgesics (for example, ibuprofen, acetaminophen)
Anti-infectives (localized superinfections can be managed with topical antifungals)
Treatment interruption might be necessary in cases of grade 3 or 4 reactions
Constitutional and cardiovascular
  Hypertension Monitor blood pressure
Routine exercise, weight control, and a low-sodium diet are beneficial
Early intervention is recommended: start antihypertensive therapy at grade 2
Treatment interruption might be necessary at uncontrolled grade 3 or greater (need for more than one drug or intensification of therapy) or a systolic pressure exceeding 200 mmHg or a diastolic pressure exceeding 110 mmHg
  Cardiac events Risk–benefit analysis is needed for patients who experienced a cardiac event within 12 months before the consideration of sunitinib; treated patients should be monitored carefully
Baseline and periodic evaluations of left ventricular ejection fraction are recommended for patients with a cardiac history
Consider a baseline ejection fraction evaluation for all patients
Treatment should be withdrawn if clinical signs of congestive heart failure manifest
Dose reduction or interruption is recommended if ejection fraction falls to within 20% and 50% of baseline
Fatigue Maintenance of physical and social activities with balancing of work and sleep schedules
Assess possible secondary conditions (hypothyroidism, anemia, etc.)
Patient diaries may be useful
Treatment of any underlying disorder
Distraction methods such as reading and limitation of daytime naps can be beneficial
Dose reductions can be considered if quality of life is being excessively affected
Laboratory tests
  Hypothyroidism Routine monitoring after baseline measurement is recommended Continue laboratory monitoring and treat per standard practice (hormone replacement)
Treatment interruption is unlikely to be necessary
  Hematology and liver function Complete blood workup to be done before treatment (each cycle) Treatment interruption or dose reduction suggested for grades 3 and 4 abnormalities
Treatment withdrawal if results fail to return to normal
  Hypophosphatemia Electrolyte control
Include serum phosphate in laboratory analyses to be done before each treatment cycle
Alimentary substitution
Treatment interruption or dose reduction should not be necessary