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Case Report

Case Report: Fatal myocarditis after combination of immune checkpoint inhibitor and platinum doublet chemotherapy

[version 1; peer review: 1 not approved]
PUBLISHED 18 Jan 2021
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Abstract

Myocarditis is a rare but feared adverse event of treatment with immune checkpoint inhibitors. The incidence is about 1%, while the mortality rate is up to 50%. Many physicians treating lung cancer do not have experience with this serious adverse event, and few hospitals in Scandinavia have routines for baseline assessments that may help detect early signs of inflammation of the myocard. Early onset of anti-inflammatory treatment is associated with favourable outcome.  
We present a case report of fatal myocarditis after treatment with check-point inhibitor. The patient was admitted with severe dyspnoea, general body ache, weakness, dysphagia, palpitations and diplopia two weeks after her second infusion of systemic treatment combining chemotherapy and immunotherapy. She had presented vague symptoms at time of the second infusion that were not identified as related to myocarditis/myositis. Upon aggressive treatment with methylprednisolone, mycophenolate mofetil, abatacept and plasmapheresis, her troponins and pro-BNP were reduced, but clinically she deteriorated and her life could not be saved.
We present this case report to increase awareness of the condition and to raise discussion about the role of routine baseline assessments to aid early diagnosis and anti-inflammatory treatment to prevent treatment-related deaths.

Keywords

myocarditis, myositis, immunotherapy, checkpoint inhibitor, adverse events

Introduction

Myocarditis is a rare but feared adverse event of treatment with immune checkpoint inhibitors (ICI). The incidence is about 1%, while the mortality rate is up to 50%. The incidence of lung cancer in Norway is 117 per 100 000 with 3200 patients a year. 30% of patients are treated with surgery or stereotactic radiation. The remaining patients are eligible to treatment with ICI in first or later lines. ICI has been used for lung cancer in Norway since 2016. Still, most physicians in Norway treating lung cancer have not experienced ICI-induced myocarditis. An informal query to six university hospitals and eight local hospitals in the South-East Health Region in Norway revealed no routine examination (blood or imaging) at baseline to help detect development of ICI-induced myocarditis later. An electrocardiogram (ECG) is usually part of the diagnostic work-up before cancer treatment, but only two hospitals specify taking ECG before start of immunotherapy in later lines. Our impression is that the situation is similar in the other Nordic countries (after personal communication through the Nordic Cardio-Oncology Board). The literature indicates the importance of early diagnosis, as a retrospective study found favourable outcome with onset of corticosteroid treatment within 24 hrs of admission to hospital1. We present this case to increase awareness, to advocate early diagnosis and treatment of ICI-related myocarditis.

Case

A woman in her late sixties, working freelance without any exposure and never smoking, with paroxysmal atrial fibrillation and a subvalvular aortic stenosis had a right upper lung lobectomy for an epidermal growth factor receptor (EGFR) positive adenocarcinoma. Post-surgery, she was treated with adjuvant chemotherapy and radiotherapy. A relapse two years later was treated with erlotinib and paused after a year due to gradual progression. After 18 months, upon progression, carboplatin/pemetrexed/pembrolizumab was started. When seen for the second infusion, she had slightly increased dyspnoea and was feeling tender on palpation of the chest wall medial of her right breast and the food felt as if it stopped in her oesophagus if she ate too quickly. There was no cough or fever. Clinical examination, c-reactive protein (CRP), haematology and electrolytes were normal. Troponins and creatine kinase (CK) were not measured. Computerized tomography (CT) showed no signs of pneumonitis and carboplatin/pemetrexed/pembrolizumab treatment was continued.

Two weeks later she was admitted to the oncology department with increased dyspnoea, general body ache, muscular weakness, dysphagia, episodes of palpitations and diplopia. Clinical examination revealed ptosis. Her blood work-up showed troponin T 651 (<14) ng/L, NT-proBNP 6761 (<760) ng/L, CRP 6.4 (<5) mg/L, aspartate aminotransferase (AST) 453 (<35) U/L (grade 3 toxicity), alanine aminotransferase (ALT) 186 (<45) U/L (grade 2), lactate dehydrogenase (LDH) 1111 (<255) U/L and creatine kinase (CK) 5845 (<210) U/L. Her ECG showed sinus rhythm and a new left bundle branch block (Figure 1A). CT excluded pulmonary embolism. Three days later she developed a third-degree atrioventricular block (Figure 1B) and her clinical symptoms progressed. Echocardiography showed no regional wall motion abnormalities. Cardiac magnetic resonance imaging (CMR) was attempted, but aborted as the patient was unstable because of her third-degree atrioventricular block. A two-chamber pacemaker was implanted and a coronary angiography was done and showed no signs of acute coronary syndrome. Later, repeated echocardiography was unchanged from the initial echocardiography, the left ventricular ejection fraction (LVEF) continued to be normal of 58%. With the presenting symptoms, troponin elevation, third degree atrioventricular block and no significant stenosis on the coronary angiogram, the patient fulfilled the criteria of myocarditis2 and it was concluded the patient had ICI-induced myocarditis with myositis and myasthenia gravis-like syndrome.

b1cbdb61-c146-4fc6-8fd8-58d7cb0f3e29_figure1.gif

Figure 1.

Electrocardiogram at admission after the second infusion of combination therapy (A) and three days after admission (B).

Intravenous methylprednisolone 2 mg/kg/day was initiated on day 3 and increased to 1000 mg/day for four days as her troponins increased (Figure 2). As there was a lack of clinical and biochemical response, abatacept 1000 mg once every second week and oral mycophenolate mofetil 750 mg b.i.d was initiated. This improved the biochemical parameters, but the clinical symptoms were unchanged. On day 14 plasmapheresis with exchange of 2l plasma was performed, but could not be repeated as the patient did not tolerate the exchange. However, the biochemical values improved further and her ptosis, dyspnoea and general muscle weakness improved. Unfortunately, her dysphagia and dyspnoea kept deteriorating. On day 25, abatacept and mycophenolate mofetil was stopped and the patient died five days later.

b1cbdb61-c146-4fc6-8fd8-58d7cb0f3e29_figure2.gif

Figure 2. Serum markers of myocardial and muscular damage during hospitalization.

Serum levels of troponin T increase during the first 10 days. Normalization of creatine kinase and myoglobin may reflect improvement of myositis, while the myocarditis did not resolve. Daily treatment regimens are indicated as follows: methylprednisolone X= 2 mg/kg, #= 1000 mg × 1; abatacept X=20 mg/kg; mycophenolate mofetil X= 750 mg × 2, #=500 mg x 2, +=500 mg × 1.

Discussion

Myocarditis is a rare incidence (0.06-1.14%)3,4 off-target effect of ICI with mortality rates up to 50%5. The symptoms are often non-specific as fatigue, dyspnoea or chest pain. In severe cases cardiac arrhythmias as atrioventricular block or ventricular arrhythmias can occur. The myocarditis can be combined with myositis and/or myasthenia gravis like syndrome6. With increasing use of immunotherapy alone and in combination with other therapies, an increase in immune mediated myocarditis can be expected. Combination immunotherapy has a higher incidence than distribution of a PD-1/PD-L1 inhibitor alone7. There are few studies reporting the incidence of myocarditis after combination of ICI and chemotherapy. Keynote 189 reported one case of myocarditis in the treatment arm with pembrolizumab, carboplatin and pemetrexed (of 405 patients)8.

As the incidence of myocarditis is rare, the symptoms non-specific and because in the acute setting, the patients are often seen by medical staff with less experience of immunotherapy off-target effects, the diagnosis may be missed unless there are routines for baseline examinations and pre-defined early diagnostic work-ups. As a minimum, before initiation of immunotherapy, ECG should be taken and troponins and NT-proBNP measured. There should be a low threshold for repeating these measures during treatment, particularly if the patient is admitted to the hospital. After onset of symptoms suspicious of myocarditis, coronary angiography can rule out acute coronary syndrome, while CMR can often detect myocardial oedema along with late gadolinium contrast enhancement (LGE) as a sign of inflamed myocardium. However, in a recent study of 103 patients with ICI-associated myocarditis LGE was only present in 48%, other signs of oedema as elevated T2-weighted short tau inversion recovery (STIR) were present in 28%. The presence of LGE or T2-weighted STIR were not associated with major adverse cardiovascular events (composite of cardiovascular death, cardiogenic shock, cardiac arrest and complete heart block)9. In our patient CMR was not performed as she was unstable because of a third-degree atrioventricular block and implantation of a pacemaker was prioritized. Diagnosis was based on the diagnostic criteria for clinically suspected myocarditis as recommended by the European Society of Cardiology (ESC)2. Early immune suppression is of the essence, and hence, clinical awareness and diagnostic routines are important. In a recent retrospective study, high dose methylprednisolone (1000 mg/d) and early initiation (<24h) were associated with improved cardiac outcomes1. Combination of several anti-inflammatory therapies and plasmapheresis may reverse the serious adverse event6,10.

Conclusion

Education of medical staff in various hospital departments and in the community is necessary and may increase awareness of ICI-associated myocarditis. Clear routines for standard investigations prior to and during treatment with immunotherapy may reduce time to diagnosis, increase awareness and hopefully reduce mortality of myocarditis.

Data availability

All data underlying the results are available as part of the article and no additional source data are required.

Consent

Written informed consent for publication of their clinical details and/or clinical images was obtained from the patient.

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Haakensen VD, Thunold SMH and Gulati G. Case Report: Fatal myocarditis after combination of immune checkpoint inhibitor and platinum doublet chemotherapy [version 1; peer review: 1 not approved]. F1000Research 2021, 10:30 (https://doi.org/10.12688/f1000research.27967.1)
NOTE: If applicable, it is important to ensure the information in square brackets after the title is included in all citations of this article.
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ApprovedThe paper is scientifically sound in its current form and only minor, if any, improvements are suggested
Approved with reservations A number of small changes, sometimes more significant revisions are required to address specific details and improve the papers academic merit.
Not approvedFundamental flaws in the paper seriously undermine the findings and conclusions
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Reviewer Report 15 Feb 2021
Panagiotis T. Diamantopoulos, First Department of Internal Medicine, Laikon General Hospital, National and Kapodistrian University of Athens, Athens, Greece 
Not Approved
VIEWS 64
It was a pleasure to review this interesting case report by Haakensen et al. on the emergence of a complex neurologic/cardiac irAE in a patient with lung adenocarcinoma treated with pembrolizumab. Although the case is interesting, there are already several case ... Continue reading
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HOW TO CITE THIS REPORT
Diamantopoulos PT. Reviewer Report For: Case Report: Fatal myocarditis after combination of immune checkpoint inhibitor and platinum doublet chemotherapy [version 1; peer review: 1 not approved]. F1000Research 2021, 10:30 (https://doi.org/10.5256/f1000research.30933.r79530)
NOTE: it is important to ensure the information in square brackets after the title is included in all citations of this article.
  • Author Response 08 Mar 2021
    Vilde Drageset Haakensen, Department of Oncology, Oslo University Hospital, P.O. Box 4956 Nydalen, Oslo, 0424, Norway
    08 Mar 2021
    Author Response
    We thank Dr Diamantopoulos for reviewing our case report. The first aim of this report was to increase clinicians’ awareness of immune checkpoint inhibitor (ICI) induced myocarditis/myositis. Even though case ... Continue reading
  • Author Response 25 Mar 2021
    Vilde Drageset Haakensen, Department of Oncology, Oslo University Hospital, P.O. Box 4956 Nydalen, Oslo, 0424, Norway
    25 Mar 2021
    Author Response
    We do not wish for additional reviews of this case report.
    Competing Interests: No competing interests were disclosed.
COMMENTS ON THIS REPORT
  • Author Response 08 Mar 2021
    Vilde Drageset Haakensen, Department of Oncology, Oslo University Hospital, P.O. Box 4956 Nydalen, Oslo, 0424, Norway
    08 Mar 2021
    Author Response
    We thank Dr Diamantopoulos for reviewing our case report. The first aim of this report was to increase clinicians’ awareness of immune checkpoint inhibitor (ICI) induced myocarditis/myositis. Even though case ... Continue reading
  • Author Response 25 Mar 2021
    Vilde Drageset Haakensen, Department of Oncology, Oslo University Hospital, P.O. Box 4956 Nydalen, Oslo, 0424, Norway
    25 Mar 2021
    Author Response
    We do not wish for additional reviews of this case report.
    Competing Interests: No competing interests were disclosed.

Comments on this article Comments (0)

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VERSION 1 PUBLISHED 18 Jan 2021
Comment
Alongside their report, reviewers assign a status to the article:
Approved - the paper is scientifically sound in its current form and only minor, if any, improvements are suggested
Approved with reservations - A number of small changes, sometimes more significant revisions are required to address specific details and improve the papers academic merit.
Not approved - fundamental flaws in the paper seriously undermine the findings and conclusions
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