Breast Cancer and the Heart

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Breast Cancer and the Heart Anne H. Blaes, M.D., M.S. Associate Professor University of Minnesota Hematology/Oncology Director, Adult Cancer Survivor Clinic

No disclosures

Objectives Discuss cardiac complications from cancer treatments Strategies to protect the heart during and after cancer treatment Ongoing research

Background The cardiotoxicity of anticancer agents can lead to significant complications As more and more patients are treated and cured of their malignancies, it is critical for cancer survivors to limit comorbid illnesses Some studies suggest cancer survivors will actually be at as great a risk from cardiac disease as from recurrent cancer

Armenian S, JCO 2017 Breast cancer (IRR, 1.13; P <.01) had significantly higher CVD risk when compared with noncancer controls Cancer survivors with two or more CVRFs had the highest risk of CVD when compared with noncancer controls with less than two CVRFs (IRR, 1.83 to 2.59; P <.01)

Bradshaw et al, Epidemiology 2016

Cardiac Complications from Chemotherapy 1. Anthracycline Induced 2. Radiation Effects 3. Her2 Directed Therapies 4. Vascular Effects (Endothelial Dysfunction) 5. Other (hypertension, etc)

Background - Anthracyclines Doxorubicin AC The Red Devil anthracycline chemotherapeutic agent First approved in the late 1960s Most commonly, it plays an important role in: Breast cancer adjuvant, metastatic setting LV dysfunction could be symptomatic or asymptomatic Clinical manifestations can by acute during therapy or late manifestations after completing therapy

Elderly Breast Cancer Survivors Dose related: 3-4% pts with doses 400-500 mg/m2 18% at 550 mg/m2 30+% at >/= 600 mg/m2 Asymptomatic decrements in EF occur in up to 20-25% of patients treated with moderate doses of doxorubicin (240-400 mg/m2), and up to 30-35% of pts treated at high doses Other risk factors: treatment at a young or old age, mediastinal radiation, history of hypertension, female

Trastuzumab and the Heart Incidence of Cardiomyopathy: 1.7-20% Trastuzumab: significantly improves survival in her2 positive breast cancer Mech: Inhibits cardiomyocyte epidermal growth factor receptor 2 thereby interfering with normal growth, repair and survival of cardiomyocytes Not dose related Histology: no ultrastructural abnormalities Prognosis: often reversible Risk Factors for trastuzumab based cardiomyopathy: Previous or concomitant anthracyclines Age > 65 years BMI > 30 kg/mg2 Previous LV dysfunction Arterial hypertension Prior chest radiation

Other trastuzumab based therapies At this time, we are not seeing cardiac toxicity with pertuzumab (Perjeta) or trastuzumab emtansine (Kadcyla) FDA still recommends cardiac monitoring while on these medications though

Chemotherapy and Ischemia Pathophysiology: Coronary artery thrombosis, arteritis, vasospasm Risk Factors: High doses > 800 mg/m2; continuous infusions of 5-FU

Chemotherapy and HTN Typically our newer small molecule agents or those that affect VEGF (Avastin) Less used in breast cancer Yeh ETH, et al. JACC 2009; 53

Immunotherapy and the Heart

Radiation and the Heart Left sided radiation Left sided breast radiation > right Hodgkin survivors: significant risk with mantle radiation Mulrooney D, BMJ 2009 Henson, Circulation 2016 Darby, NEJM 2013

Effects of Estrogens in Women Cardiovascular system e.g., production of cholesterol, arterial elasticity Central nervous system e.g., temperature regulation, memory mechanisms Breast e.g., development ducts at puberty ESTROGENS Reproductive system e.g., lubrication and thickening of vaginal and urinary tract lining CANCER Increased risk of Breast and Endometrial Musculo skeletal system e.g., bone density Adapted from Clemons, NEJM, 2001

Endocrine Therapy in Breast Cancer Survivors Block estrogen- Tamoxifen (SERM) Lower estrogen- Aromatase inhibitors (steroidal and non-steroidal) Ovarian suppression GnRH Oophorectomy/Ablation Chemotherapy-related amenorrhea (CRA), premature menopause EEstrogen receptor degradation (SERD) fulvestrant

AI trials: Clinical Trial Results: When compared to placebo, slight increases in htn, hyperlipidemia but no real measured CV different outcomes In comparison to tamoxifen, elevations in htn, hyperlipidemia, ischemia in those with preexisting CV disease though the trial results are mixed PA-1 Tamoxifen trials: Fisher et al, JNCI 2005 MA-17, MA-17R, ATAC, IES, BIG 1-98

Multimorbidity after Bilateral Oophorectomy 1653 Premenopausal women undergoing oophorectomy age <50 from 1988-2007 and 1653 age-matched controls Excluded women with ovarian cancer, estrogen sensitive cancer, high risk indication Median followup ~14.5 yrs Analysis adjusted for baseline morbidity, BMI, smoking etc. All women with oophorectomy Women 46-49 at oophorectomy Women < 45 at oophorectomy Rocca et al, Mayo Clin Proc, 2016

San Antonio Breast Cancer Symposium, December 6-10, 2016 Aromatase inhibitors and Endothelial function Large artery elasticity p=0.12 Small artery elasticity p=0.07 EndoPat Ratio p<0.0001 Breast Cancer Controls Breast Cancer Controls Breast Cancer Controls This presentation is the intellectual property of the author/presenter. Contact blaes004@umn.edu for permission to reprint and/or distribute.

Shared Risk Factors: Cancer and Cardiovascular Disease

Overlapping Risk Factors: Age Sex Obesity Diabetes Hypertension Hyperlipidemia Tobacco Use Diet Physical Activity Advancing Age EPIC study N=23,153 individuals ages 35-65 years After f/u 7.8 years, adherence to all 4 vs 0 risk factors: 93% less diabetes 81% less heart attacks 36% less cancer ARIC study N=13,253 individuals Adhering to 6 of 7 risk factors 51% lower incidence of cancer compared to adhering to 0 measures Koene, Prizment, Blaes, Konety. Circulation 2016 Rasmussen-Torvik et al, Circulation 2013 Nothlings U et al, J Diabetes 2010

Novel Inflammatory Targets

What about in breast cancer survivors?

Barac A et al, Journal of Clinical Oncology 2017

Monitoring and Prevention For oncologists: Changes in infusions: liposomal preparations, change in infusion time Alternative therapies? Cardioprotective agents? Dexrazoxane ACE-I B-Blockers Statins? For all: Cardio-oncology Clinic and referral Risk stratify Highest risk - > 65 years, underlying hypertension or heart disease, prior chest radiation (not breast cancer radiation), diabetes, tobacco use

Prevention 1. Medications 2. Biomarkers ACE-I B-blockers Cardinale et al, Circulation 2006; Kalay JACC 2007 Blaes et al, Breast Cancer Res Treat 2010 MANTICORE Pituskin E et al, J Clin Oncol. 2016 Nov 28

Other Practical Tips Avoid Tobacco Use Have a primary care provider Control blood pressure and cholesterol Healthy diet Stay Active *Cancer Rehab, YMCA Livestrong

Cancer and Cardiovascular Disease Risk factors for chemotherapy-related cardiac complications should be assessed in all patients diagnosed with breast cancer Biologic data to support the overlap of the pathogenesis of these two diseases Management of risk factors is important not only during treatment and post treatment, but also in the prevention of these two diseases Treatment of cardiac risk factors including htn, hyperlipidemia, diabetes in cancer patients may actually improve overall outcomes

Questions