As breast cancer survival increases, cardiotoxicity associated with chemotherapeutic regimens such as anthracyclines and trastuzumab becomes a more significant issue. Assessment of the left ventricular (LV) ejection fraction fails to detect subtle alterations in LV function. The objective of this study was to evaluate whether more sensitive echocardiographic measurements and biomarkers could predict future cardiac dysfunction in chemotherapy-treated patients. Forty-three patients diagnosed with breast cancer who received anthracyclines and trastuzumab therapy underwent echocardiography and blood sampling at 3 time points (baseline and 3 and 6 months during the course of chemotherapy). The LV ejection fraction; peak systolic myocardial longitudinal, radial, and circumferential strain; echocardiographic markers of diastolic function; N-terminal pro–B-type natriuretic peptide; and high-sensitivity cardiac troponin I were measured. Nine patients (21%) developed cardiotoxicity (1 at 3 months and 8 at 6 months) as defined by the Cardiac Review and Evaluation Committee reviewing trastuzumab. A decrease in longitudinal strain from baseline to 3 months and detectable high-sensitivity cardiac troponin I at 3 months were independent predictors of the development of cardiotoxicity at 6 months. The LV ejection fraction, parameters of diastolic function, and N-terminal pro–B-type natriuretic peptide did not predict cardiotoxicity. In conclusion, cardiac troponin plasma concentrations and longitudinal strain predict the development of cardiotoxicity in patients treated with anthracyclines and trastuzumab. The 2 parameters may be useful to detect chemotherapy-treated patients who may benefit from alternative therapies, potentially decreasing the incidence of cardiotoxicity and its associated morbidity and mortality.
The overall objective of this study was to assess whether early echocardiographic measurements of myocardial deformation and biomarkers (high-sensitivity troponin I [hsTnI] and N-terminal pro–B-type natriuretic peptide [NT-proBNP]) could predict the development of chemotherapy-induced cardiotoxicity in patients treated with anthracyclines and trastuzumab. Cardiotoxicity was defined according to recent guidelines (Cardiac Review and Evaluation Committee of trastuzumab-associated cardiotoxicity) as a reduction of the left ventricular ejection fraction (LVEF) of ≥5% to <55% with symptoms of heart failure or an asymptomatic reduction of the LVEF of ≥10% to <55%.
Methods
Patients >18 years of age diagnosed with HER-2-overexpressing breast cancer and either scheduled to receive treatment including anthracyclines and trastuzumab or scheduled to receive trastuzumab after previous anthracycline treatment were eligible. Patients with LVEFs <50% were excluded.
Patients were enrolled at 4 institutions. All patients signed informed consent forms, which were approved by the institutional review board of the participating institutions.
Patients were studied before chemotherapy (except 10 patients who had previously been treated with anthracyclines) and at 3 and 6 months of treatment, using questionnaires, echocardiography, and blood samples.
Transthoracic echocardiography was performed using the Vivid 7 or E9 (GE Healthcare, Milwaukee, Wisconsin). The same ultrasound machine was used to acquire all echocardiograms in each patient. All echocardiograms were analyzed in a core laboratory. The LVEF was calculated from the apical 4- and 2-chamber views using a modified Simpson’s biplane method by a single observer (M.S.-C.). All other measurements were acquired by a single observer (H.S.) blinded to the results of the LVEF measurements. The 2 readers were blinded to the treatment that patients were receiving and to the time points during the study. Mitral E and A waves and annular velocities were measured. Left atrial volume was calculated from the apical 4- and 2-chamber views using the area-length method. To measure myocardial strain, 2-dimensional grayscale images were obtained in the parasternal short-axis view at the midpapillary level and the apical 4- and 2-chamber views. The timing of aortic valve closure was obtained using pulsed-wave Doppler traces. Peak systolic radial and circumferential strain were measured by averaging the peak systolic strain values in all 6 segments of the parasternal short-axis view (EchoPAC; GE Healthcare). In 5 patients for radial strain and 11 patients for circumferential strain, >2 of 6 segments could not be reproducibly analyzed at 1 time point. This was especially the case when the sonographer was unable to obtain a perfectly rounded parasternal short-axis view. The values of radial and circumferential strain were excluded for these patients. Furthermore, particularly in patients with left-sided breast cancer, the apex was difficult to visualize (inability to obtain standard apical views, chest pain, scar tissue, expanders). We estimate that in 60% to 70% of the patients, the apex was not analyzable at all time points. Hence, global peak systolic longitudinal strain was calculated by averaging the values of peak systolic strain in the basal and midwall segments of the 4- and 2-chamber views. Longitudinal, radial, and circumferential strain values were averaged over 3 cardiac cycles. The intraobserver variability for longitudinal strain reported as the mean error ± SD of 10 measurements was −0.14 ± 1.1% in absolute values (−0.58 ± 6.5% in percentages) and the interobserver variability as 0.5 ± 1.5% in absolute values (2.7 ± 7.9% in percentages). The variabilities for radial strain were 2 ± 5% (2.5 ± 9.6%) and 2.2 ± 7.5% (4.4 ± 14.4%), respectively. The intraobserver variability for circumferential strain was 0.53 ± 2.82% in absolute values (2 ± 13% in percentages), and the interobserver variability was 3.3 ± 3.5% in absolute values (19 ± 21% in percentages).
NT-proBNP and troponin I were measured using the Dimension Vista 500 Intelligent Laboratory System (Siemens Healthcare Diagnostics, Deerfield, Illinois), using a 1-step, homogenous, sandwich chemiluminescent immunoassay based on LOCI technology (Siemens Healthcare Diagnostics, Deerfield, Illinois). The limit of detection of NT-proBNP assay is 0.8 pg/ml. Typical within-laboratory imprecision for the assay is <3% coefficient of variation at NT-proBNP concentration from 120 to 5,000 pg/ml. The highest value of NT-proBNP reported in healthy subjects aged <75 years is 125 pg/ml. The lower limit of detection of the troponin assay is 0.015 μg/L, and the 10% coefficient of variation is <0.04 μg/L. All values of NT-proBNP >125 pg/ml and of troponin >0.015 μg/L were considered elevated.
Data are expressed as mean ± SD. All statistical analyses were performed using the JMP statistical package (SAS Institute Inc., Cary, North Carolina). Assuming a baseline peak systolic longitudinal strain in healthy patients of 19 ± 5% and a rate of left ventricular dysfunction of 20%, the analysis of 45 patients was expected to allow us to detect a decrease of 14% in longitudinal strain in the left ventricular dysfunction group with power of 80% and a 5% level of significance. Parameters of interest were compared at baseline and at 3 and 6 months in the population using a 1-way analysis of variance for repeated measures. Possible predictors of cardiotoxicity were tested using univariate nominal logistic regression. The primary hypothesis was to test the echocardiographic markers of systolic function and the biomarkers. Echocardiographic markers of diastolic function were also tested because they have been reported to decrease in patients treated with anthracyclines. A multiple nominal logistic regression model including longitudinal strain and troponin levels at 3 months was then applied to the univariate predictors. Because radial strain could not be reliably obtained in all patients, it was excluded from the model. A p value <0.05 was defined as significant.
Results
Forty-five eligible consecutive women were prospectively enrolled in the study. One woman withdrew from the study and 1 was withdrawn because of negative HER-2 status on a second analysis. Therefore, a total of 43 women participated in the study. Ten women received anthracyclines before entering the study. The median delay time between the anthracycline treatment and the initial study time point was 3.5 months (range 2 to 144). There was no difference in the baseline or changes in the clinical parameters, echocardiographic measurements, and biomarker levels between naive and previously treated women. All women were therefore analyzed together. Baseline characteristics of the patients are listed in Table 1 .
| Cardiotoxicity | |||
|---|---|---|---|
| Variable | Yes (n = 9) | No (n = 34) | p Value |
| Age (years) | 47 ± 11 | 49 ± 10 | 0.94 |
| Previous treatment with anthracyclines | 2 (22%) | 8 (23%) | 1.00 |
| Dose of anthracyclines | 1.00 | ||
| Doxorubicin 240 mg/m 2 | 9 (100%) | 30 (88%) | |
| Epirubicin 300 mg/m 2 | 0 (0%) | 4 (12%) | |
| Treatment with taxanes | 9 (100%) | 34 (100%) | 1.00 |
| Radiotherapy | 2 (22%) | 3 (9%) | 0.28 |
| Side of breast cancer | 1.00 | ||
| Right | 3 (33%) | 14 (41%) | |
| Left | 6 (67%) | 19 (56%) | |
| Both | 0 (0%) | 1 (3%) | |
| Cardiac risk factors | |||
| Blood pressure ≥140/≥90 mm Hg | 2 (22%) | 10 (29%) | 1.00 |
| Total cholesterol >200 mg/dl | 0 (0%) | 8 (23%) | 0.66 |
| Diabetes mellitus | 0 (0%) | 1 (3%) | 1.00 |
| Smoker | 1 (11%) | 5 (15%) | 0.31 |
| Cardiovascular therapy | |||
| Angiotensin-converting enzyme inhibitors | 1 (11%) | 3 (9%) | 0.19 |
| β blockers | 0 (0%) | 3 (9%) | 1.00 |
| Body mass index (kg/m 2 ) | 23 ± 2 | 26 ± 4 | 0.74 |
| Systolic blood pressure (mm Hg) | 120 ± 11 | 122 ± 18 | 0.98 |
| Diastolic blood pressure (mm Hg) | 75 ± 10 | 74 ± 9 | 0.19 |
| Heart rate (beats/min) | 71 ± 11 | 69 ± 9 | 0.38 |
At baseline, the LVEF and peak systolic longitudinal and radial strain were within the normal reported range of values ( Table 2 ). When the group was analyzed as a whole, the LVEF decreased by an average of 8%. This decrease was significant at 6 but not at 3 months. Longitudinal strain decreased by 11%; this decrease was significant 3 months after the start of the study period. The decrease in longitudinal strain observed at 3 months was detected in the midwall (p = 0.008) and the lateral (p = 0.01) and anterior (p = 0.01) segments. Circumferential strain decreased by a mean of 15% at 6 months and was already decreased at 3 months. In contrast, radial strain did not decrease at 3 months when all women were studied. No change in hsTnI or NT-proBNP was noted in the course of the study.
| Variable | Baseline | 3 Months | 6 Months | p Value (ANOVA) |
|---|---|---|---|---|
| Systolic blood pressure (mm Hg) | 122 ± 17 | 116 ± 18 | 119 ± 15 | 0.07 |
| Diastolic blood pressure (mm Hg) | 74 ± 9 | 72 ± 10 | 72 ± 9 | 0.33 |
| Heart rate (beats/min) | 69 ± 10 | 72 ± 10 | 73 ± 11 | 0.10 |
| LV end-diastolic volume (ml) | 74 ± 13 | 74 ± 18 | 76 ± 8 | 0.58 |
| LV end-systolic volume (ml) | 26 ± 7 | 28 ± 9 | 33 ± 11 | <0.0001 |
| LVEF | 0.65 ± 0.06 | 0.63 ± 0.06 | 0.59 ± 0.05 | <0.0001 |
| LV end-diastolic diameter (mm) | 43 ± 4 | 43 ± 3 | 44 ± 4 | 0.16 |
| Relative wall thickness | 0.39 ± 0.07 | 0.37 ± 0.06 | 0.37 ± 0.06 | 0.12 |
| Longitudinal strain (%) | 20.5 ± 2.2 | 19.3 ± 2.4 ⁎ | 18.4 ± 3 | <0.0001 |
| Radial strain (%) | 55 ± 12 | 52 ± 12 | 46 ± 14 | 0.02 |
| Circumferential strain (%) | 18 ± 4 | 15 ± 4 ‡ | 14 ± 3 | 0.001 |
| Left atrial volume (ml) | 32 ± 12 | 32 ± 9.5 | 32 ± 11.5 | 0.91 |
| Mitral E-wave filling velocity (cm/s) | 77 ± 17 | 75 ± 19 | 76 ± 18 | 0.36 |
| Mitral A-wave filling velocity (cm/s) | 67 ± 15 | 65 ± 15 | 64 ± 19 | 0.69 |
| Mitral E-wave filling velocity/mitral A-wave filling velocity | 1.2 ± 0.3 | 1.2 ± 0.3 | 1.3 ± 0.4 | 0.44 |
| Peak early diastolic mitral annular velocity (cm/s) | 12.5 ± 2.8 | 11.8 ± 3.1 † | 11 ± 2.5 | 0.004 |
| Peak late diastolic mitral annular velocity (cm/s) | 10 ± 3 | 10 ± 3 | 9 ± 2 | 0.11 |
| Mitral E-wave filling velocity/peak early diastolic mitral annular velocity | 6.7 ± 2 | 6.8 ± 2.6 | 7 ± 2.3 | 0.59 |
| hsTnI (μg/L) | 0.00 ± 0.01 | 0.04 ± 0.13 | 0.02 ± 0.07 | 0.09 |
| NT-proBNP (pg/ml) | 103 ± 73 | 98 ± 105 | 91 ± 114 | 0.12 |
Nine patients (21%) met the criteria for cardiotoxicity. Cardiotoxicity was detected at the 3-month time point in 1 patient (immediately after anthracyclines), whereas 8 other patients developed cardiotoxicity at the 6-month time point. There were no differences in any of the echocardiographic or blood markers at baseline between patients who did or did not develop cardiotoxicity. Importantly, the change of the LVEF from baseline to 3 months was not predictive of later cardiotoxicity (p = 0.19; Table 3 ). This was also true when change in the LVEF was considered a discrete change, and patients were separated by those who did or did not have decreases in the LVEF of >5%. The individual changes in the LVEF and longitudinal strain are shown in Figure 1 in patients who did or did not develop cardiotoxicity.
