Key result
Immune checkpoint inhibitors show no significant increase in pericardial effusion risk versus chemotherapy.
Why the study?
Cardiovascular toxicity of immunotherapy is an underreported, potentially fatal side effect, with a relatively high incidence of pericardial disease noticed in patients with NSCLC.
Does immunotherapy increase the risk of pericardial effusion compared to chemotherapy in patients with advanced non-small cell lung cancer?
Observational (n=120)
No
Does immunotherapy increase the risk of pericardial effusion compared to chemotherapy in patients with advanced non-small cell lung cancer?
Absolute Event Rate: 6.7% vs 3.3%
p-value: p=not significant
Immunotherapy in advanced NSCLC is associated with a relatively frequent incidence of pericardial effusion (6.7%), highlighting the need for cardiological monitoring.
May support cardiological monitoring with ICIs in advanced NSCLC; leaves open excess risk versus chemotherapy and requires prospective confirmation.
INTRODUCTION: Cardiovascular toxicity of immunotherapy represents an underreported but potentially fatal side effect. A relatively high incidence of pericardial disease has been noticed in patients with non-small cell lung cancer (NSCLC). METHODS: We retrospectively analyzed a population of patients with advanced NSCLC receiving immune checkpoint inhibitors (ICIs) looking for the presence of pericardial effusion at baseline or during treatment. The study population was compared with a control group treated with chemotherapy. All patients were checked for the presence of concomitant pleural effusion. RESULTS: We identify 60 patients (36 male/24 female, median age 70 years [range 43-81]). Prevalent histology was adenocarcinoma (65%) followed by squamous cell carcinoma (28%) and large cell or not otherwise specified (NOS) carcinoma (7%). Treatment consisted of nivolumab 3 mg/kg every 14 days (52 cases; 45 as second-line and 7 as third-line treatment) or pembrolizumab 200 mg (8 cases; all first-line treatment) for a total of 302 cycles delivered. Four out of 60 patients (6.7%) developed pericardial effusion during treatment, in two cases (3.3%) without concomitant pleural effusion, compared to 2 out of 60 (3.3%) in the control group in one case without concomitant pleural effusion (1.6%). Median time of onset was 40 days. Myocarditis was not observed. CONCLUSION: Our findings confirm pericardial effusion as a relatively frequent side effect of immunotherapy in NSCLC. Clinicians should be aware of this specific toxicity in patients with metastatic NSCLC receiving immunotherapy and refer to a cardiologist for a multidisciplinary approach.
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Canale et al. (2020) conducted an observational in Advanced Non-Small Cell Lung Cancer (NSCLC) (n=120). Immune checkpoint inhibitors vs. Chemotherapy was evaluated on Incidence of pericardial effusion (p=not significant). In advanced non-small cell lung cancer, immune checkpoint inhibitors were associated with a 6.7% incidence of pericardial effusion versus 3.3% with chemotherapy (not statistically significant).
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