Cardiotoxicity (LVEF decline, cardiomyopathy)
Heart damage from cancer treatment: anthracyclines weaken the heart muscle permanently in a dose-related way, trastuzumab does so reversibly, and some kinase inhibitors raise blood pressure or disturb rhythm. Heart function (LVEF) is monitored by ultrasound during treatment.
Anthracycline cardiomyopathy risk rises steeply above 400-450 mg/m² doxorubicin and with radiotherapy or age; trastuzumab causes asymptomatic LVEF declines in 5-10% and heart failure in 1-4%, more after anthracyclines, monitored every 3 months and usually reversible on stopping. VEGF inhibitors cause hypertension and rarely heart failure; ibrutinib causes atrial fibrillation; immune checkpoint inhibitors cause rare fulminant myocarditis; androgen deprivation and aromatase inhibitors raise cardiovascular risk over years. Cardio-oncology clinics manage risk with ACE inhibitors, beta-blockers, statins and dexrazoxane; anthracycline-free regimens and non-anthracycline ADC payloads reduce exposure. Childhood cancer survivors carry lifelong cardiac risk.
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not linked directly; found by shared links- TermSecondary malignancy (therapy-related cancer)
Shares Late effects and survivorship toxicity, Anthracyclines (doxorubicin, epirubicin).
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- IdeaBiomarker-guided cardioprotection for everyone on cardiotoxic cancer therapy
Shares Cardio-oncology, Trastuzumab.
- PairingCaution: ibrutinib in patients with cardiac risk
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- TermABVD, BEACOPP and BrECADD (Hodgkin lymphoma regimens)
- TermTrastuzumab cardiotoxicity
Shares Cardio-oncology, Trastuzumab.
- TermR-CHOP (lymphoma chemoimmunotherapy)
Shares Anthracyclines (doxorubicin, epirubicin), Doxorubicin.