- Case report
- Open Access
Delayed contrast enhancement cardiac magnetic resonance imaging in trastuzumab induced cardiomyopathy
Journal of Cardiovascular Magnetic Resonance volume 10, Article number: 5 (2008)
Trastuzumab (Herceptin), an antagonist to the human epidermal growth factor 2 (HER2) receptor significantly decreases the rates of breast cancer recurrence and mortality by 50%. Despite therapeutic benefits, the risk of cardiotoxicity with trastuzumab ranges from 10–15% when administered sequentially following anthraycline chemotherapy. Little is known about the utility of cardiac magnetic resonance (CMR) in the assessment of trastuzumab mediated cardiomyopathy.
Methods and results
Between 2005–2006 inclusive, 160 breast cancer patients were identified at a single tertiary care oncology centre. Of the total population, 10 patients (mean age 40 ± 8 years) were identified with trastuzumab induced cardiomyopathy, based on a LVEF less than 40% on serial MUGA or echocardiography. CMR was performed in all patients to determine LV volumes, systolic function and evidence of late gadolinium enhancement (LGE). At the time of diagnosis of trastuzumab induced cardiomyopathy, the mean LVEF was 29 ± 4%. Subepicardial linear LGE was present in the lateral portion of the left ventricles in all 10 patients.
LGE-CMR is a novel way of detecting early changes in the myocardium due to trastuzumab induced cardiotoxicity.
Breast cancer is a major public health concern that affects 1 in 7 women in their lifetime . Anthracyclines are commonly used in the setting of adjuvant therapy in the treatment of breast cancer patients. While anthracyclines significantly improve clinical morbidity and mortality, there are notable cardiotoxic side effects . Recent understanding of the biology of breast cancer has lead to the introduction of a new therapeutic agent, Trastuzumab (Herceptin), an antagonist to the human epidermal growth factor 2 (HER2) receptor, which is found in 25% of breast cancer patients . When added to conventional anthracycline chemotherapy, trastuzumab significantly decreases the rates of recurrence and mortality by 50% in HER-2 positive breast cancer patients [4–6]. Despite therapeutic benefits however, the risk of cardiotoxicity with trastuzumab ranges from 10–15% when administered in combination with anthracyline therapy [7, 8].
Serial multiple gated acquisition scans (MUGA) are widely used to monitor cardiac dysfunction in breast cancer patients. However, with the improvement in both spatial and temporal resolution of cardiac magnetic resonance (CMR) over the past decade, it has now become the gold standard for the non-invasive assessment of left ventricular (LV) systolic dysfunction. Additionally, late gadolinium enhancement (LGE) can detect myocardial scarring. Although frequently used in the assessment of dilated cardiomyopathies secondary to ischemia or myocarditis , little is known about the utility of CMR in the assessment of trastuzumab induced cardiomyopathy. We report a case series of trastuzumab induced myocarditis characterized by left ventricular dysfunction and focal epicardial LGE using CMR imaging.
Between 2005–2006 inclusive, 160 breast cancer patients who received trastuzamab in addition to anthracyline based adjuvant therapy were identified at a tertiary care oncology centre. All patients received FEC (5-fluorouracil, epirubicin and cyclophoshamide) for a total of 6 cycles. The mean duration between completion of chemotherapy and initiation of trastuzumab was 2 ± 1 months. Of the total population, 10 patients were identified with trastuzumab induced cardiomyopathy based on LV ejection fraction less than 40% on either serial MUGA or echocardiography. The medical records of all 10 patients were extensively reviewed for baseline demographic data. The retrospective study was approved by the local institutional review board.
CMR was performed on all 10 patients using a 1.5 T scanner (Avanto, Siemens, Erlangen, Germany). Morphologic images in the cardiac short axis, 4 chamber long axis and 2 chamber long axis planes were acquired using IR-prepared dark blood HASTE sequences (TR 600 ms, TE 26 ms, 6 mm slice thickness, 1.8 mm interslice gap). In the same planes, cine-CMR was performed using a breath-hold balanced steady state free precession sequence (TrueFISP, TR 42 ms, TE 1.2 ms, FA 70°, 6 mm slice thickness, matrix 192 × 174). The cine-CMR short-axis images encompassed the entire LV from the base to the apex (stack of 10 sequential short-axis slices; TR 64 ms, TE 1 ms, FA 80°, 8 mm slice thickness, 1.6 mm interslice gap, matrix 192 × 132) to obtain a left ventricular ejection fraction (LVEF). Late gadolinium enhancement was performed after 10 minutes of 0.2 mmol/kg injection of Gadolinium (Gd-DTPA, Magnevist, Schering, Germany) using a T1-weighted IR-prepared multislice TrueFISP sequence with magnitude and phase sensitive reconstruction. Images were acquired sequentially in the short axis, followed by horizontal and vertical long axis images (TR 700 ms, TE 1.0 ms, FA 40°, 8 mm slice thickness, 1.6 mm interslice gap, matrix 192 × 144).
The total population included 10 patients (mean age 40 ± 8 years, range 27 to 56 years) with normal LVEF at baseline and preserved systolic function following administration of anthracycline based chemotherapy using serial MUGA scans (Table 1). Cardiovascular risk factors, dose and frequency of chemotherapy, concomitant use of radiation therapy, and duration of trastuzumab therapy (3–5 months) were similar in the entire patient cohort (Table 1).
At the time of diagnosis of trastuzumab induced cardiomyopathy, the left ventricular cavities were dilated with moderate to severe global LV systolic dysfunction on CMR (Table 2). The mean LVEF was for the total population was 29 ± 4% (Table 2). Subepicardial linear LGE was present in the lateral portion of the left ventricles in all 10 patients suggesting the presence of trastuzumab induced myocarditis (Figure 1).
Following the discontinuation of trastuzumab, 6 patients have recovered normal LV systolic function, while 4 patients have persistent LV dysfunction at six month followup, despite appropriate heart failure medications including ACE inhibition and beta blockade (Table 2). The linear LGE-CMR findings persisted at 6 months in all patients despite improvement in LVEF in over half of the patients.
An increasing understanding of the biology of breast cancer has lead to the identification of novel therapeutic targets. The HER2 receptor is a member of the epidermal growth factor receptor family of transmembrane tyrosine kinases and is normally involved in the regulation of cell proliferation. Increased expression of HER2 is detected in 25–30% of breast cancers and is associated with poorly differentiated tumors with a high proliferative rate, positive axially lymph nodes and decreased expression of estrogen and progesterone receptors . These characteristics are associated with an increased risk of disease recurrence and death due to breast cancer .
Trastuzumab (Herceptin) is a relatively new chimerized monoclonal antibody that targets the extracellular portion of the HER2 membrane protein. Previous studies have demonstrated that trastuzumab provides considerable therapeutic benefits, when added to conventional anthracycline chemotherapy, in decreasing the rates of disease recurrence and death in HER2 overexpressed metastatic breast cancers [4–6]. Despite its therapeutic benefit, trastuzumab is cardiotoxic with a 5% prevalence of cardiomyopathy when used as monotherapy and 10–15% prevalence of cardiomyopathy when used in combination with anthracyclines [7, 8].
Various theories have been suggested regarding the possible pathogenetic origin of trastuzumab induced cardiomyopathy. These include potentiation of anthracycline induced cardiotoxicity and immune mediated destruction of cardiomyocytes . There is increasing evidence as well supporting a direct toxic effect of HER2 blockade on the myocardial tissue. HER2 signaling appears to play an important role in the embryonic cardiac development and cardioprotection; the blockade of this pathway by trastuzumab can also lead to myocardial inflammation and damage .
The use of CMR for the non-invasive characterization of trastuzumab induced myocarditis is novel. Whereas CMR has become the standard diagnostic test in the evaluation of suspected myocarditis [9, 12], to date, there are no reports in the literature describing the utility of LGE for the diagnosis of trastuzumab induced cardiomyopathy. The current report demonstrated the common finding of LGE of the subepicardial lateral wall in all patients, which may be a typical distribution and location of myocarditis in this drug induced cardiomyopathy. Although 6 patients recovered LVEF by CMR with appropriate therapy for CHF, it is of interest that the LGE findings persisted up to 6 months in all patients, suggesting persistent injury to the myocardium. A limitation of the current retrospective study however is the small number of individuals. A larger prospective series may enable us to make more substantive conclusions regarding the role of LGE-CMR in the diagnosis and prognosis of this patient population.
Late gadolinium enhancement using CMR is a novel way of detecting early changes in the myocardium due to trastuzumab induced cardiotoxicity. Future studies are required to validate identification of positive delayed enhancement using CMR as a subclinical marker for future LV dysfunction in this select population. Early detection of LV dysfunction using LGE-CMR may allow one to adjust treatment with trastuzumab prior to the development of irreversible heart failure.
Armstrong K, Eisen A, Weber B: Primary care: assessing the risk of breast cancer. N Engl J Med. 2000, 342: 564-571. 10.1056/NEJM200002243420807.
Barry E, Alvarez J, Miller T, Lipshultz S: Anthracycline-induced cardiotoxicity: course, pathophysiology, prevention and management. Expert Opinion. 2007, 8: 1039-1058. 10.1517/14656518.104.22.1689.
Slamon DJ, Clark GM, Wong SG, Levin WJ, Ullrich A, McGuire WL: Human breast cancer: correlation of relapse and survival with amplication of the HER-2/neu oncogene. Science. 1987, 235: 244-707–12. 10.1126/science.3798106.
Slamon DJ, Leland-Jones B, Shak S, Fuchs SH, Paton V, Bajamonder A, Fleming T, Eiermann W, Wolter J, Pegram M, Baselga J, Norton L: Use of chemotherapy plus a monoclonal antibody against HER2 for metastatic breast cancer that overexpresses HER2. N Engl J Med. 2001, 344: 783-92. 10.1056/NEJM200103153441101.
Romond EH, Perez EA, Bryant J, Suman VJ, Geyer CE, Davidson NE, Tan-Chiu E, Martino S, Paik S, Kaufman PA, Swain SM, Pisansky TM, Fehrenbacher L, Kutteh LA, Vogel VG, Visscher DW, Yothers G, Jenkins RB, Brown AM, Dakhil SR, Mamounas EP, Lingle WL, Klein PM, Ingle JN, Wolmark N: Trastuzumab plus adjuvant chemotherapy for operable HER2-positive breast cancer. N Engl J Med. 2005, 353: 1673-84. 10.1056/NEJMoa052122.
Piccart-Gebhart MJ, Procer M, Leyland-Jones B, Goldhirsch A, Untch M, Smith I, Gianni L, Basela J, Bell R, Jackisch C, Cameron D, Dowsett M, Barrios CH, Steger G, Huang CS, Anderson M, Inbar M, Lichinitser M, Lang I, Nutz U, Iawata H, Thomssen C, Lohrisch C, Suter TM, Ruschoff J, Suto T, Greatorex V, Ward C, Straehle C, McFadden E, Dolci MS, Gelber RD: Trasuzumab after adjunctive chemotherapy in HER2-positive breast cancer. N Engl J Med. 2005, 353: 1658-72. 10.1056/NEJMoa052306.
Ewer MS, Gibbs HR, Swafford J, Benjamin RS: Cardiotoxicity in patients receiving trastuzumab (Herceptin): primary toxicity, synergistic or sequential stress, or surveillance artifact?. Semin Oncol. 1999, 26 (Suppl 12): 96-101.
Tan-Chiu E, Yothers G, Romond E, Geyer CE, Ewer M, Leefe D, Shannon RP, Swain SM, Brown A, Fehrenbacher L, Vogel VG, Seay TE, Rastogi P, Mamounas EP, Wolmark N, Bryant J: Assessment of cardiac dysfunction in a randomized trial comparing doxrobucin and cyclophosphamide followed by paclitaxel, with or without trastuzumab as adjuvant therapy in node-positive, human epidermal growth factor receptor 2-overexpressing breast cancer- NSABP B-31. J Clin Oncol. 2005, 23: 7811-9. 10.1200/JCO.2005.02.4091.
Skouri HN, Dec GW, Friedrich MG, Cooper LT: Noninvasive imaging in myocarditis. J Am Coll Cardiol. 2006, 48: 2085-93. 10.1016/j.jacc.2006.08.017.
Chien KR: Herceptin and the heart-a molecular modified of cardiac failure. N Engl J Med. 2006, 354: 789-790. 10.1056/NEJMp058315.
Erickson SL, O'Shea KS, Ghaboosi N, et al: ErbB3 is required for normal cerebellar and cardiac development: a comparison with ErbB2- and heregulin-deficient mice. Development. 1997, 124: 4999-5011.
Dill T, Ekinci O, Hansel J, Kluge A, Briedenbach C, Hamm CW: Delayed contrast-enhanced magnetic resonance imaging for the detection of autoimmune myocarditis and long-term follow-up. J Cardiovasc Magn Reson. 2005, 7 (2): 521-3. 10.1081/JCMR-200053596.
The author(s) declare that they have no competing interests.
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Fallah-Rad, N., Lytwyn, M., Fang, T. et al. Delayed contrast enhancement cardiac magnetic resonance imaging in trastuzumab induced cardiomyopathy. J Cardiovasc Magn Reson 10, 5 (2008). https://doi.org/10.1186/1532-429X-10-5
- Left Ventricular Ejection Fraction
- Cardiac Magnetic Resonance
- Late Gadolinium Enhancement
- Normal Left Ventricular Systolic Function