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Table 1 Baseline Characteristics for Evaluable Patients (N = 67)

From: Real-world data of cardio-oncologic interventions for cardiovascular adverse events with oral oncolytics

Mean age, years (SD)

69 (± 15)

Mean body-mass index, kg/m2(SD)

28.34 (± 6.73)

Gender (%)

Female

45 (67.2)

Male

22 (32.8)

Race (%)

Caucasian

44 (65.7)

African American

18 (26.9)

Asian

3 (4.5)

Other

2 (3)

Smoking status (%)

Never smoker

43 (64.2)

Former smoker

21 (31.3)

Current smoker

3 (4.5)

Alcohol use (%)

No alcohol use

38 (56.7)

Infrequent to light use

21 (31.3)

Moderate use

7 (10.4)

Heavy use

1 (1.5)

Cancer Diagnosis (%)

Breast cancer

26 (38.8)

Hematological malignancies

22 (32.8)

Other solid tumors

19 (28.4)

Past Medical History (%)

Hypertension

48 (71.6)

Hyperlipidemia

27 (40.3)

Obesity

26 (38.8)

Diabetes

20 (29.9)

Arrhythmias

20 (29.9)

Heart failure (HF)

17 (25.3)

Coronary artery disease (CAD)

14 (20.9)

Treatment History (%)

History of chest radiation

17 (25.4)

History of anthracyclines

15 (22.4)

History of trastuzumab

3 (4.5)

Baseline Cardiovascular Disease (CVD) or CVD Risk Factor (%)

At least one risk factor

65 (97)

None

2 (3)

Classification of Oral Oncolytics (%)

Aromatase inhibitors

25 (36)

BCR-ABL inhibitors

11 (16)

VEGFR inhibitors

9 (13)

Immuno-modulators

7 (10)

Antiandrogens

5 (7)

EGFR inhibitors

4 (6)

mTOR inhibitors

4 (6)

BTK inhibitors

3 (4)

FLT3 inhibitors

1 (2)