Do we have to change our anti-cancer strategy in case of cardiac toxicity? Guy Jerusalem, MD, PhD

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Do we have to change our anti-cancer strategy in case of cardiac toxicity? Point of view of the oncologist Guy Jerusalem, MD, PhD CHU Sart Tilman Liège

Anticancer therapy: cardiac toxicity New anticancer therapies have led to long life expectancy for many patients Treatment related co morbidities have become an issue for cancer survivors Cardiac toxicity vary from mild ECG changes to serious arrhythmias, myocarditis, pericarditis, MI & heart failure

Cardiac disease does matter in early stage breast cancer Patients (age at least 50) with early stage breast cancer are 4x more likely to die of non-cancer conditions (up to 45 % are cardiac in nature) Hanrahan, et al. JCO 25: 4952-4960, 2007

Anticancer therapy and cardiac toxicity: the drug Reversible (at least partially)? Monitoring Cumulative dose-dependent? Adapt regimen Major risk factors well known? Patient selection

Anticancer therapy and cardiotoxicity: specific oncological situations Childhood tumors: - curative treatment, not adjuvant - low incidence - anthracyclines frequently used Very long life expectancy Risk factors? How to adapt treatment?

Anticancer therapy and cardiotoxicity: specific oncological situations Adjuvant treatment of common cancers, such as breast cancer Avoid or reduce exposure to cardiotoxic drugs such as anthracyclines: Anthracycline free adjuvant regimens or sequential therapy with taxanes, reducing cumulative toxicity

Anticancer therapy and cardiotoxicity: specific oncological situations Challenges: - Long term follow-up if late occurrence of cardiotoxicity - Outcome in the real world setting??? (highly selected, exclusion of patients with high risk of cardiotoxicity, younger patients in clinical trials) Patient selection is a key factor (oncological and cardiotoxicity risk?)

Intrinsic molecular subtypes of breast cancer

Therapeutic Strategies L SHC SOS GRB2 RAS MAPK Pathway L PI3K Monoclonal antibodies (Trastuzumab) membrane Small Molecule (Lapatinib) PI3K Pathway No Growth- No Proliferation No Survival Monoclonal antibodies can block the RTK signal from the outside Small molecules can block the RTK signal at the source

Adjuvant Trastuzumab Trials MAJOR IMPROVEMENTS IN DFS Hazard Ratio for Disease Free Survival 1 0.9 0.8 0.7 0.6 0.5 0.4 0.3 0.2 0.1 0 HERA NSABP & NCCTG BCIRG 006 FinHER Telli ML et al: J Clin Oncol 25:3525-3533, 2007

Adjuvant Trastuzumab: Time to First Distant Recurrence Patients, % 100 AC PT 90 80 70 60 AC P 90.4% 89.7% 81.5% AC PT 1672 96 AC P 1679 193 N Events 73.7% Trastuzumabresistant Trastuzumab benefit? No benefit from trastuzumab 50 HR = 0.47, P<.0001 0 1 2 3 4 5 Years From Randomization Trial B31/Trial N9831 AC, cyclophosphamide + doxorubicin; P, paclitaxel; T, trastuzumab. Adapted from Romond EH, et al. New Engl J Med. 2005;353(16):1673-1684.

Cardiac toxicity: trastuzumab (HERA study) Suter et al. J Clin Oncol 25: 3859-65, 2007

Anticancer therapy: HER2 positive breast cancer Use of anthracyclines? Use of trastuzumab? Combined treatment or sequential treatment?

Trastuzumab: Changes in left ventricular ejection fraction Ewer, et al. JCO 23: 7820-6, 2007

Trastuzumab: cardiac monitoring Martin M et al., The Oncologist 14: 1-11, 2009

Adjuvant trastuzumab cardiotoxicity Tarantini et al. Ann Oncol 23: 3058-63, 2012

BCIRG 006: Risk of relapse 33% 39% 6% No statistically significant AC-T TCH AC-TH AC-T TCH AC-TH Risk of relapse AC-T= Anthracycline+Cyclophosphamide +Taxotère TCH= Taxotère +Carboplatine+Herceptin AC-TH= AC-T+Herceptin

BCIRG 006 : cardiotoxicity Cardiac related death CHF NYHA grade III IV AC-T AC-TH TCH N = 1050 N = 1068 N = 1056 0 0 0 4 20 4 Trastuzumab used without prior anthracycline is largely more safe Benefit : difference between AC-TH and TCH isn t statistically significant Why not using Herceptin as first agent?

Cardiac toxicity: trastuzumab Bird B R H, and Swain S M Clin Cancer Res 2008;14:14-24

NSABP B-31 Cardiac Risk Score Factors associated with risk of developing a cardiac event: Use of hypertensive medications Age >49 Baseline LVEF <54 Risk Score = 100 x 7.4(0.03 x Age) (0.10 + baseline LVEF) + (0.68 x C) 4.82 C = HTN medication status: none = 0; yes = 1 Rostagi P, Adjuvant Breast Oral Session, ASCO 2007

NSABP B-31 Cardiac Risk Score Example: 62 yo woman on antihypertensive medication Baseline LVEF = 60% Predicted Cumulative Incidence 0.00 0.05 0.10 0.15 0.20 ( 0. 0 2 4, 5 0 ) o o ( 0. 0 4, 6 2 ) Cardiac Risk Score =82 3-year predicted incidence of symptomatic heart failure/cardiac death 10% 0 2 0 4 0 6 0 8 0 1 0 0 C a r d i a c R i s k S c o r e

PREVENTION? Future Directions Pre-emptive use of ACE inhibitors or beta-blockers in may prevent cardiotoxicity EARLY DETECTION Cardiac biomarkers may help identify high risk patients CLOSE COLLABORATION!!!