Next Article in Journal
Upregulation of Cell Surface Glycoproteins in Correlation with KSHV LANA in the Kaposi Sarcoma Tumor Microenvironment
Next Article in Special Issue
Better Late Than Never: The Impact of Steroidal Treatment on the Outcome of Melanoma Patients Treated with Immunotherapy
Previous Article in Journal
The Cell Biology of Metastatic Invasion in Pancreatic Cancer: Updates and Mechanistic Insights
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Cancers
Volume 15
Issue 7
10.3390/cancers15072170
cancers-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Communication

Cardiovascular Immunotoxicity Associated with Immune Checkpoint Inhibitors in Metastatic Melanoma

by
Jean-Matthieu L’Orphelin
1,*,
Charles Dollalille
2,
Julia Akroun
1,
Joachim Alexandre
2 and
Anne Dompmartin
1
1
Department of Dermatology, Caen-Normandie University Hospital, 14033 Caen CEDEX, France
2
Department of Cardiology, Caen-Normandie University Hospital, 14033 Caen CEDEX, France
*
Author to whom correspondence should be addressed.
Cancers 2023, 15(7), 2170; https://doi.org/10.3390/cancers15072170
Submission received: 27 February 2023 / Revised: 27 March 2023 / Accepted: 31 March 2023 / Published: 6 April 2023
(This article belongs to the Special Issue Role of Immune Checkpoint Inhibitors or Targeted Therapy in the Treatment of Patients with Melanoma Volume II)
Browse Figures
Versions Notes

Abstract

:

Simple Summary

PD-1 inhibitors (nivolumab, pembrolizumab) and anti-CTLA-4 (CD152) (ipilimumab) are widely used in metastatic melanoma, and most immune-related adverse events are known. Recently, several cardiovascular AEs (CVAEs, i.e., myocardial infarction, heart failure, stroke, Takotsubo syndrome, and arrhythmia) have been associated with immune checkpoint inhibitor exposure in post-marketing surveillance studies and represent major issues for patients with melanoma during and after cancer treatment. The aim of this study was to estimate the risk of CVAES associated with immune checkpoint inhibitor exposure for melanoma. Among the cancer population of our systematic review, we performed a safety meta-analysis in a subgroup of melanoma patients.

Abstract

Background: Checkpoint inhibitors, such as PD-1 inhibitors (nivolumab, pembrolizumab) and anti-CTLA-4 (CD152) (ipilimumab), are widely used in metastatic melanoma, and most immune-related adverse events are known. Several cardiovascular AEs (CVAEs) associated with immune checkpoint inhibitor exposure have been reported in post-marketing surveillance studies and represent major issues for patients with melanoma during and after cancer treatment. Data on CVAES induced by immune checkpoint inhibitors in melanoma, especially incidence and risk factors, are lacking. Methods: A systematic review of the literature up to 31 August 2020 was performed in Medline, the Cochrane Central Register of Controlled Trials (CENTRAL), and the ClinicalTrials.gov register according to prespecified selection criteria from inception to 7 April 2020. Statistics were performed on 3289 patients from five randomized clinical trials on melanoma. Results: Patients with melanoma treated with immune checkpoint inhibitors had a significant risk of presenting dyslipidemia (Peto OR: 4.74, 95% CI: 2.16–10.41, p < 0.01, I2 = 0%, p = 0.94). The Peto OR was numerically significant for pericarditis, myocarditis, heart failure, myocardial infarction, cerebral ischemia, high pulmonary pressure, blood high pressure, arrhythmias, endocarditis, and conduction disturbances, but the confidence interval was not significant. The risk of CVAEs was not statistically different between melanoma treated with immune checkpoint inhibitors and other tumors treated with immune checkpoint inhibitors (range of p-value from 0.13 to 0.95). No interaction between follow-up length and CVAE reporting was found. Conclusions: Our study underlines that checkpoint inhibitors used for melanoma increase CVAEs, especially dyslipidemia, which could pave the way to chronic inflammatory processes, atherosclerosis, and, finally, ischemic cardiopathy. These cardiovascular adverse events could be acute or delayed, justifying the monitoring of lipidic biology and a baseline cardiology consultation.

1. Introduction

Immune checkpoints inhibitors (ICIs), such as PD-1 inhibitors (e.g., nivolumab or pembrolizumab [1] and ipilimumab (anti-CTLA-4 or CD152)), block prototypical T-cell checkpoints and are now the gold-standard treatment.
Most adverse events (AEs) are immune-related (irAEs) and occur at a median of 40 days [2], whereas 10% are severe (grade III/IV) [3,4].
Overall survival is constantly increasing due to ICI use, and patients with melanoma can become old with a history of treated melanoma; this enables the expression of much later-onset side effects, such as certain cardiovascular effects.
Cardiovascular (CV) irAEs (i.e., myocarditis, pericarditis, and vasculitis) due to ICIs are rare, especially myocarditis (around 1%), but they are usually severe, with high morbidity and mortality rates [5] due to the immune infiltration of CD4+ T cells into the heart [6] when patients are treated with ICIs. Some late-onset and non-inflammatory cardiac irAEs have been reported [7,8].
More recently, several cardiovascular AEs (CVAEs, i.e., myocardial infarction, heart failure, stroke, Takotsubo syndrome, and arrhythmia) have been associated with ICI exposure in post-marketing surveillance studies and represent major issues for patients with cancer during and after cancer treatment. The frequency of CVAEs is higher in cancer patients than in the general population [9,10]. We performed a meta-analysis, which was our previous study, for all types of cancers [11], and we reported a significant risk of myocarditis (Peto OR: 4.42, 95% CI: 1.56–12.50), pericarditis (Peto OR: 2.16, 95% CI: 1.42–3.29), cardiac failure (Peto OR 1.51, 95% CI: 1.01–2.26), and dyslipidemia (Peto OR: 3.68, 95% CI: 1.89–7.19).
Alcoholism and smoking are known risk factors for most solid cancers, altering the epigenome. They are also cardiovascular risk factors. However, these risk factors are not found in melanoma. We conducted this ancillary study to determine whether melanoma treated with immunotherapy presents a similar risk of CVAEs compared with other solid cancers.

2. Materials and Methods

2.1. Registration

The study protocol was prospectively registered to the International Prospective Register of Systematic Reviews (registration number: CRD42020165672) and was conducted according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) Guidelines. No ethics committee approval or subject informed consent was obtained, as this was a retrospective analysis of already published studies.

2.2. Data Sources, Search Strategy, and Data Extraction

For the meta-analysis source, a systematic review of the literature up to 31 August 2020 was performed in Medline, the Cochrane Central Register of Controlled Trials (CENTRAL), and the ClinicalTrials.gov register according to prespecified selection criteria from inception to 7 April 2020. We used both controlled terms (i.e., MeSH terms in MEDLINE) and free-text terms related to ICIs, with the language restricted to English.
Second, we focused on terms related to ICIs used in melanoma only (anti-PD-1 antibodies (nivolumab and pembrolizumab) and anti-CTLA-4 antibodies (ipilimumab)) in the title or abstract (or both) that were considered the sole research domain, and the search strategy included the Cochrane Highly Sensitive Search Strategy for identifying RCTs in Medline. RCTs including at least one ICI-containing arm (including ICI monotherapy or a combination of ICIs) that enrolled adult patients (age ≥18 years) with melanoma and provided information on CVAEs were eligible for inclusion. Case reports or case series, case–control studies, observational studies, single-arm studies, and nonrandomized trials were excluded. Patients with risk factors related to the development of cardiovascular disease prior to the initiation of ICIs were not excluded from the analysis.
First, all available CVAEs, classified according to the Common Terminology Criteria for Adverse Events (CTCAE), in RCTs on ICIs reported on ClinicalTrials.gov were extracted. Second, if the reported CVAEs were not available on ClinicalTrials.gov, all reported CVAEs were extracted from published RCTs. RCTs without data related to the CVAEs of interest were not included.
Additional data from eligible studies were collected, including the ICI regimen, control arm regimen, median age, median/mean follow-up duration, and overall number of patients analyzed. All results, including follow-up data posted on ClinicalTrials.gov, were collected at the time of the searches.
Two authors evaluated the risk of bias in individual studies using the Pharmacoepidemiological Research on Outcomes of Therapeutics by a European Consortium (also known as PROTECT) checklist tool, which is specially designed to assess bias in safety meta-analyses [12]. In cases of disagreements, a third author was consulted.
The study flowchart is given in Figure 1.

2.3. Outcomes

The primary outcome was the summarized risk of CVAEs associated with ICI exposure (ICI monotherapy—pembrolizumab, nivolumab, or ipilimumab—or a combination of ICIs). The control arms could be either placebo or non-placebo agents (kinase inhibitors, vascular endothelial growth factor pathway inhibitors, or chemotherapy).
The CVAEs we gathered were ventricular and supraventricular arrhythmias, cardiogenic shock, dyslipidemia, venous thrombo-embolic issues, high blood pressure, high pulmonary pressure, myocardial infarction, cerebral ischemia, heart failure, myocarditis, pericarditis, QT/QTc prolongation and torsade de pointe, valvopathy, and conduction disturbances. All CVAEs were defined by MedDRA terminology.

2.4. Statistical Analysis

We performed a random-effects meta-analysis to compute the Peto odds ratios (ORs) with 95% confidence intervals (CIs), which has been described as the most accurate method for binary studies on rare events (<1%) [13]. Assuming that CV irAEs were not frequent events (incidence <10%), we interpreted the OR as a measure of risk [14,15].
In this study, specific subgroup analyses were performed regarding the types of tumors: MM vs. other tumors. “Other tumors” comprised bronchial adenocarcinomas, small cells carcinomas, colorectal cancer, gastric cancer, glioblastoma, hepatocellular carcinoma, mesothelioma, myeloma, ovarian cancer, pancreatic adenocarcinoma, prostate cancer, breast cancer, and urothelial cancer.
A two-sided p-value of <0.05 in Z-tests (for overall effect) or v2 tests (for overall subgroup comparison) in all analyses was considered statistically significant.

3. Results

3.1. Descriptions of Included Studies

The PRISMA flow diagram of study selection is presented in Figure 1. The details of the study characteristics are presented in Table 1. Among the 63 RCTs included in our previous study, 8 phase III studies dedicated to melanoma were kept. Three studies were excluded since no control arm was available; only five studies with a control arm out of the eight clinical trials were considered. A total of 3289 adult patients with melanoma were enrolled, with 1824 (55%) patients in the ICI arm, of whom 1353 were treated with PD-1i and 471 were treated with CTLA-4i.
In the control arm, 1465 patients received placebo or chemotherapy; 979 patients (67%) received placebo, and 486 (33%) received chemotherapy. In the ICI arm, 28% of the immunotherapy regimens were nivolumab, 29% were pembrolizumab, 28% were ipilimumab monotherapy, and 15% were double immunotherapy with ipilimumab–nivolumab.
The population was 62% male, and the mean age was 58.9 years old. Follow-up ranged from 5.2 months to 32.8 months.

3.2. Risk of CVAEs Associated with ICI Exposure and Incidence of CV irAEs with an Increased Risk Associated with ICI Exposure in Melanoma

Patients with MM treated with ICI had a significant risk of presenting dyslipidemia (Peto OR: 4.74, 95% CI: 2.16–10.41, p < 0.01, I2 = 0%, p = 0.94). The Peto OR was numerically significant for pericarditis, myocarditis, heart failure, myocardial infarction, cerebral ischemia, high pulmonary pressure, high blood pressure, arrhythmias, endocarditis, and conduction disturbances, but the confidence interval was not significant.
The risk of CVAEs was not statistically different between MM treated with ICI and other tumors treated with ICI (range of p-value from 0.13–0.95). No interaction between the follow-up length and CVAE reporting was found.
When data were disaggregated by sex, no statistical differences were found for cardiac conductive disorders (p = 0.16), cardiac death or shock (p = 0.62), cardiac supra-ventricular (p = 0.19) or ventricular (p = 0.59) arrhythmias, heart failure (p = 0.3), hypertension (p = 0.52), myocarditis (p = 0.84), or cerebral arterial ischemia (p = 0.57), and data were not available for dyslipidemia.
In three studies, patients had previous treatment before ICI, but it was not statistically significant.
All results are summarized in Figure 2, and details are given in Table 2. We reported no statistical differences between melanoma and “other solid cancers” regarding CVAEs (p ranging from 0.13 to 0.95).

4. Discussion

There was a higher incidence of melanoma in males than in females, with differences between the location of primary tumors and mortality, due to discovery at later stages in males. However, the purpose of our study was to investigate the cardiovascular risk factors of immunotherapy in melanoma and assess the potential difference from other cancers independent of overall survival and mortality. Our study showed that the population was comparable between patients with melanoma and patients with other cancers When treated with immunotherapy, melanoma patients had the same risk of developing CVAEs as those with other solid cancers, and alcohol and tobacco intake played a role in both cardiovascular risk factors and oncogenesis.
Dyslipidemia was significantly associated with ICIs, whereas the previous study showed a significant Peto OR for a higher risk of myocarditis, pericarditis, heart failure, dyslipidemia, and myocardial infarction. Autoimmunity can be ascribed among the potential mechanisms of ICI-associated CVAEs, and to a greater extent, although not unique, myocarditis [16]. Nevertheless, we have to point out that several CVAEs (arrhythmias, myocarditis, coronary artery disease, valvopathies, and cardiomyopathy) have a sharply different pathologic basis, making it difficult to define a common origin when they are considered secondary events associated with the use of anti-neoplastic drugs.
In our cohort, the sex ratio was 2/3, whereas the sex ratio of melanoma is around 1. It is well-known that males over 45 years old have a higher cardiovascular risk regarding SCORE (European Society of Cardiology 2019) [17], which could maximize the baseline cardiovascular risk. Women may have more misleading presentations of cardiovascular pathology, leading to delayed management or misdiagnosis. In our study, we did not find a gender-related excess risk. Nevertheless, atypical presentations in females might not have been taken into account in clinical studies and should be a cause for vigilance in future studies.
We reported that 35% of melanomas were treated with ipilimumab monotherapy, which is not a common or universal practice. We could suppose that this over-representation of ipilimumab overestimates CVAEs in real-life data since ipilimumab is more of a provider of irAEs than PD-1i.
We reported a strong tendency toward myocardial infarction and stroke, whereas the previous study reported significant results. The non-significance can be explained by a lack of power (fewer patients were included when focusing on melanoma only). Atherosclerosis is reported in 45 to 75% of patients with cancers [18], and the incidence rate of atherosclerosis with ICIs is underestimated because of the slow development and potential manifestations after the end point of clinical trials [19]. Classically, inflammation in atherosclerosis is mediated by macrophages present in atheroma plaque [20], but when treated with ICIs, T lymphocytes stimulated by ICIs are involved in the atherosclerosis process [21], and atheroma plaque is mostly made of lymphocytes [22]. CVAEs increased threefold under ICI treatment, and atheroma plaque progression was three times higher with ICIs [23].
Atherosclerosis phenomena under ICI treatment are increased by dyslipidemia [24]. We reported that the risk of development of dyslipidemia was four times higher in melanoma treated with ICIs. In [25], an animal model carrying a myeloid cell-specific PD-1 ablation implicated in the anti-tumor immune response by effector myeloid cells underlined that PD-1-deficient mice synthesized more cholesterol by glycolysis mechanism alteration. It has been suggested that baseline dyslipidemia under ICIs is a good prognosis factor [26], as most irAEs are [27]. In our study, we reported the occurrence of dyslipidemia under treatment, and we did not study this parameter as a baseline characteristic.
Statins are known to have a benefit on CV mortality [28] thanks to anti-inflammatory effects and hypolipemiant properties, stifling the increase in atherosclerosis [29]. Some studies have suggested that statins could have a protective effect against MM [30,31] by modulating the immune response with a higher innate response and tumoral immunity. Nevertheless, the use of cholesterol-lowering drugs, such as statins or fibrates, in melanoma is controversial [32,33], specifically in terms of its potential to increase PCSK9 [34], which is associated with platelet reactivity, leading to acute coronary syndrome. Novel lipid-lowering drugs, such as PCSK9 inhibitors, could be proposed, as Quagliariello [35] did, putting forward the argument that PCSK9 inhibition in patients with cancer treated with ICI therapies enables a reduction in atherosclerotic cardiovascular events and potentially improves ICs-related anticancer functions. This meta-analysis did not have the sensitivity to determine whether subjects who developed dyslipidemia under immunotherapy were carriers of a predisposing genetic mutation [36].
Dyslipidemia and atherosclerosis risks are not currently monitored during ICI treatment. Regarding our results, it seems relevant to propose quarterly lipid biology, ECG monitoring, and cardiac echography at baseline, before treatment initiation. Troponin could be also monitored since 94% of myocarditis patients treated with ICIs have increased troponin [37] and normal morphologic parameters before event occurrence. Efficient cooperation between dermatologists and cardiologists should be implemented. Further prospective studies should be implemented to assess whether any CVAEs exist before ICI treatment initiation; cholesterol-lowering drugs have to be proposed, considering that ICI treatment is a cardiovascular risk factor in its own right.
We can consider ICIs as a large part of the CV risk factor since the risk of CVAEs is similar between melanoma patients and those with other solid cancers, i.e., a population in which alcohol and tobacco consumption, a major cardiovascular risk factor, is less represented than in other solid cancers. Currently, there is no standardized consensus on the choice of surveillance strategies and management algorithms for CVAEs in patients participating in oncological RCTs. Annual cardio-oncology monitoring is recommended. Further studies could be implemented to study late-onset CVAEs [38] since irAEs can occur 2 years after the initiation of immunotherapy, even if it has been stopped, suggesting that risk factors are sustainable over time.

5. Conclusions

The incidence CVAEs ranged from 3 to 20 per 1000 patients, but it might be underestimated in clinical trials, as cardiac monitoring is usually lacking in melanoma trials involving ICIs. We report a significant risk of dyslipidemia, and our study suggests that we could consider ICIs to be a large part of the cardiovascular risk factor. Dyslipidemia and, more broadly, CVAE could occur in melanoma as in other cancers treated with ICIs. This suggests that the risk of dyslipidemia with ICIs cannot be attributed to alcoholism and smoking since they are not risk factors for melanoma.
Our study underlines that ICIs used in melanoma increase CVAEs, especially dyslipidemia, which could pave the way to chronic inflammatory processes, atherosclerosis, and, finally, ischemic cardiopathy. This assertion is all the more interesting because the average lifespan of melanoma patients is increasing, allowing slowly evolving side effects, such as dyslipidemia, to appear.
These cardiovascular irAEs could be acute or delayed, justifying the monitoring of lipid biology and a baseline cardiology consultation. Further prospective studies could assess cholesterol-lowering drug use to reduce late-onset CVAEs in melanoma patients treated with immunotherapy.

Author Contributions

Conceptualization, J.-M.L.; Methodology, J.A. (Joachim Alexandre); Formal analysis, C.D. and J.A. (Joachim Alexandre); Data curation, J.A. (Julia Akroun); Writing—original draft, J.-M.L.; Writing—review & editing, J.-M.L.; Supervision, J.A. (Joachim Alexandre) and A.D.; Project administration, J.A. (Joachim Alexandre). All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

The study protocol was prospectively registered to the International Prospective Register of Systematic Reviews (registration number: CRD42020165672).

Informed Consent Statement

No informed consent was obtained from the subjects, as this was a retrospective analysis of already published studies.

Data Availability Statement

The data presented in this study are available upon request from the corresponding author. Public data are available on ClinicalTrials.gov.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Lipson, E.J.; Sharfman, W.H.; Drake, C.G.; Wollner, I.; Taube, J.M.; Anders, R.A.; Xu, H.; Yao, S.; Pons, A.; Chen, L.; et al. Durable Cancer Regression Off-Treatment and Effective Reinduction Therapy with an Anti-PD-1 Antibody. Clin. Cancer Res. 2013, 19, 462–468. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  2. Wang, D.Y.; Salem, J.E.; Cohen, J.V.; Chandra, S.; Menzer, C.; Ye, F.; Zhao, S.; Das, S.; Beckermann, K.E.; Ha, L.; et al. Fatal Toxic Effects Associated with Immune Checkpoint Inhibitors: A Systematic Review and Meta-analysis. JAMA Oncol. 2018, 4, 1721–1728. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  3. Freeman-Keller, M.; Kim, Y.; Cronin, H.; Richards, A.; Gibney, G.; Weber, J.S. Nivolumab in Resected and Unresectable Metastatic Melanoma: Characteristics of Immune-Related Adverse Events and Association with Outcomes. Clin. Cancer Res. 2016, 22, 886–894. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  4. Naidoo, J.; Page, D.B.; Li, B.T.; Connell, L.C.; Schindler, K.; Lacouture, M.E.; Postow, M.A.; Wolchok, J.D. Toxicities of the anti-PD-1 and anti-PD-L1 immune checkpoint antibodies. Ann. Oncol. Off. J. Eur. Soc. Med. Oncol. 2015, 26, 2375–2391. [Google Scholar] [CrossRef]
  5. Diamantopoulos, P.T.; Tsatsou, K.; Benopoulou, O.; Bonou, M.; Anastasopoulou, A.; Mastrogianni, E.; Gogas, H. Concomitant development of neurologic and cardiac immune-related adverse effects in patients treated with immune checkpoint inhibitors for melanoma. Melanoma Res. 2020, 30, 484–491. [Google Scholar] [CrossRef]
  6. Reuben, A.; de Macedo, M.P.; McQuade, J.; Joon, A.; Ren, Z.; Calderone, T.; Conner, B.; Wani, K.; Cooper, Z.; Tawbi, H.; et al. Comparative immunologic charac-terization of autoimmune giant cell myocarditis with ipilimumab. Oncoimmunology 2017, 6, e1361097. [Google Scholar] [CrossRef]
  7. Dasanu, C.A.; Jen, T.; Skulski, R. Late-onset pericardial tamponade, bilateral pleural effusions and recurrent immune monoarthritis induced by ipilimumab use for metastatic melanoma. J. Oncol. Pharm. Pr. 2016, 23, 231–234. [Google Scholar] [CrossRef]
  8. Yamaguchi, S.; Morimoto, R.; Okumura, T.; Yamashita, Y.; Haga, T.; Kuwayama, T.; Yokoi, T.; Hiraiwa, H.; Kondo, T.; Sugiura, Y.; et al. Late-Onset Fulminant Myocar-ditis With Immune Checkpoint Inhibitor Nivolumab. Can. J. Cardiol. 2018, 34, 812.e1–812.e3. [Google Scholar] [CrossRef]
  9. Zamorano, J.L.; Gottfridsson, C.; Asteggiano, R.; Atar, D.; Badimon, L.; Bax, J.J.; Cardinale, D.; Cardone, A.; Feijen, E.A.M.; Ferdinandy, P.; et al. The cancer patient and cardiology. Eur. J. Hear. Fail. 2020, 22, 2290–2309. [Google Scholar] [CrossRef]
  10. Zamorano, J.L.; Lancellotti, P.; Rodriguez Munoz, D.; Aboyans, V.; Asteggiano, R.; Galderisi, M.; Habib, G.; Lenihan, D.J.; Lip, G.Y.; Lyon, A.R.; et al. 2016 ESC Position Paper on cancer treatments and cardiovascular toxicity developed under the auspices of the ESC Committee for Practice Guidelines: The Task Force for cancer treatments and cardiovascular toxicity of the European Society of Cardiology (ESC). Eur. Heart J. 2016, 37, 2768–2801. [Google Scholar] [CrossRef]
  11. Dolladille, C.; Akroun, J.; Morice, P.-M.; Dompmartin, A.; Ezine, E.; Sassier, M.; Da-Silva, A.; Plane, A.-F.; Legallois, D.; L’Orphelin, J.-M.; et al. Cardiovascular immunotoxicities as-sociated with immune checkpoint inhibitors: A safety meta-analysis. Eur. Heart J. 2021, 42, 4964–4977. [Google Scholar] [CrossRef] [PubMed]
  12. Faillie, J.L.; Ferrer, P.; Gouverneur, A.; Driot, D.; Berkemeyer, S.; Vidal, X.; Martínez-Zapata, M.J.; Huerta, C.; Castells, X.; Rottenkolber, M.; et al. A new risk of bias checklist applicable to randomized trials, observational studies, and systematic reviews was developed and validated to be used for sys-tematic reviews focusing on drug adverse events. J. Clin. Epidemiol. 2017, 86, 168–175. [Google Scholar] [CrossRef] [PubMed]
  13. Rockville, M.D. Methods Guide for Effectiveness and Comparative Effectiveness Reviews; Agency for Healthcare Research and Quality (US): Rockville, MD, USA, 2008. [Google Scholar]
  14. Ranganathan, P.; Aggarwal, R.; Pramesh, C. Common pitfalls in statistical analysis: Odds versus risk. Perspect. Clin. Res. 2015, 6, 222–224. [Google Scholar] [CrossRef] [PubMed]
  15. Sedgwick, P. Relative risks versus odds ratios. BMJ 2014, 348, g1407. [Google Scholar] [CrossRef] [Green Version]
  16. Okazaki, T.; Tanaka, Y.; Nishio, R.; Mitsuiye, T.; Mizoguchi, A.; Wang, J.; Ishida, M.; Hiai, H.; Matsumori, A.; Minato, N.; et al. Autoantibodies against cardiac troponin I are responsible for dilated cardiomyopathy in PD-1-deficient mice. Nat. Med. 2003, 9, 1477–1483. [Google Scholar] [CrossRef]
  17. Escardio. Available online: www.escardio.org/static-file/Escardio/Subspecialty/EACPR/Documents/score-charts.pdf (accessed on 25 February 2023).
  18. Vincent, L.; Leedy, D.; Masri, S.C.; Cheng, R.K. Cardiovascular Disease and Cancer: Is There Increasing Overlap? Curr. Oncol. Rep. 2019, 21, 1–13. [Google Scholar] [CrossRef]
  19. Lutgens, E.; Seijkens, T.T. Cancer patients receiving immune checkpoint inhibitor therapy are at an increased risk for atherosclerotic cardiovascular disease. J. Immunother. Cancer 2019, 8, e000300. [Google Scholar] [CrossRef]
  20. Tall, A.R.; Yvan-Charvet, L. Cholesterol, inflammation and innate immunity. Nat. Rev. Immunol. 2015, 15, 104–116. [Google Scholar] [CrossRef] [Green Version]
  21. Wolf, D.; Ley, K. Immunity and Inflammation in Atherosclerosis. Circ. Res. 2019, 124, 315–327. [Google Scholar] [CrossRef]
  22. Newman, J.L.; Stone, J.R. Immune checkpoint inhibition alters the inflammatory cell composition of human coronary artery atherosclerosis. Cardiovasc. Pathol. 2019, 43, 107148. [Google Scholar] [CrossRef]
  23. Drobni, Z.D.; Alvi, R.M.; Taron, J.; Zafar, A.; Murphy, S.P.; Rambarat, P.K.; Mosarla, R.C.; Lee, C.; Zlotoff, D.A.; Raghu, V.K.; et al. Association Between Immune Checkpoint Inhibitors with Cardiovascular Events and Atherosclerotic Plaque. Circulation 2020, 142, 2299–2311. [Google Scholar] [CrossRef] [PubMed]
  24. Nicholls, S.J.; Ballantyne, C.M.; Barter, P.J.; Chapman, M.J.; Erbel, R.M.; Libby, P.; Raichlen, J.S.; Uno, K.; Borgman, M.; Wolski, K.; et al. Effect of two intensive statin regimens on progression of coronary disease. N. Engl. J. Med. 2011, 365, 2078–2087. [Google Scholar] [CrossRef] [Green Version]
  25. Strauss, L.; Mahmoud, M.A.A.; Weaver, J.D.; Tijaro-Ovalle, N.M.; Christofides, A.; Wang, Q.; Pal, R.; Yuan, M.; Asara, J.; Patsoukis, N.; et al. Targeted deletion of PD-1 in myeloid cells induces antitumor immunity. Sci. Immunol. 2020, 5, eaay1863. [Google Scholar] [CrossRef]
  26. Perrone, F.; Minari, R.; Bersanelli, M.; Bordi, P.; Tiseo, M.; Favari, E.; Sabato, R.; Buti, S. The Prognostic Role of High Blood Cholesterol in Advanced Cancer Patients Treated with Immune Checkpoint Inhibitors. J. Immunother. 2020, 43, 196–203. [Google Scholar] [CrossRef] [PubMed]
  27. Suo, A.; Chan, Y.; Beaulieu, C.; Kong, S.; Cheung, W.Y.; Monzon, J.G.; Smylie, M.; Walker, J.; Morris, D.; Cheng, T. Anti-PD1-Induced Immune-Related Adverse Events and Survival Outcomes in Advanced Melanoma. Oncology 2020, 25, 438–446. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  28. Orkaby, A.R.; Driver, J.A.; Ho, Y.L.; Lu, B.; Costa, L.; Honerlaw, J.; Galloway, A.; Vassy, J.L.; Forman, D.E.; Gaziano, J.M.; et al. Association of Statin Use with All-Cause and Cardiovascular Mortality in US Veterans 75 Years and Older. JAMA 2020, 324, 68–78. [Google Scholar] [CrossRef]
  29. Todoric, J.; Antonucci, L.; Karin, M. Targeting Inflammation in Cancer Prevention and Therapy. Cancer Prev. Res. 2016, 9, 895–905. [Google Scholar] [CrossRef] [Green Version]
  30. Sarrabayrouse, G.; Pich-Bavastro, C.; Teiti, I.; Tilkin-Mariame, A.F. Regulatory properties of statins and rho gtpases prenylation inhibitiors to stimulate melanoma immunogenicity and promote anti-melanoma immune response. Int. J. Cancer 2016, 140, 747–755. [Google Scholar] [CrossRef]
  31. Boudreau, D.M.; Yu, O.; Johnson, J. Statin use and cancer risk: A comprehensive review. Expert Opin. Drug Saf. 2010, 9, 603–621. [Google Scholar] [CrossRef] [Green Version]
  32. Li, X.; Wu, X.B.; Chen, Q. Statin use is not associated with reduced risk of skin cancer: A meta-analysis. Br. J. Cancer 2013, 110, 802–807. [Google Scholar] [CrossRef] [Green Version]
  33. Freeman, S.R.; Drake, A.L.; Heilig, L.F.; Graber, M.; McNealy, K.; Schilling, L.M.; Dellavalle, R.P. Statins, fibrates, and melanoma risk: A systematic review and meta-analysis. J. Natl. Cancer Inst. 2006, 98, 1538–1546. [Google Scholar] [CrossRef] [PubMed]
  34. Wang, S.; Fu, D.; Liu, H.; Peng, D. Independent association of PCSK9 with platelet reactivity in subjects without statin or antiplatelet agents. Front. Cardiovasc. Med. 2022, 9, 934914. [Google Scholar] [CrossRef] [PubMed]
  35. Quagliariello, V.; Bisceglia, I.; Berretta, M.; Iovine, M.; Canale, M.L.; Maurea, C.; Giordano, V.; Paccone, A.; Inno, A.; Maurea, N. PCSK9 Inhibitors in Cancer Patients Treated with Immune-Checkpoint Inhibitors to Reduce Cardiovascular Events: New Frontiers in Cardioncology. Cancers 2023, 15, 1397. [Google Scholar] [CrossRef] [PubMed]
  36. Gratton, J.; Finan, C.; Hingorani, A.D.; Humphries, S.E.; Futema, M. LDL-C Concentrations and the 12-SNP LDL-C Score for Polygenic Hypercholesterolaemia in Self-Reported South Asian, Black and Caribbean Participants of the UK Biobank. Front. Genet. 2022, 13, 845498. [Google Scholar] [CrossRef]
  37. Mahmood, S.S.; Fradley, M.G.; Cohen, J.V.; Nohria, A.; Reynolds, K.L.; Heinzerling, L.M.; Sullivan, R.J.; Damrongwatanasuk, R.; Chen, C.L.; Gupta, D.; et al. Myocarditis in Patients Treated with Immune Checkpoint Inhibitors. J. Am. Coll. Cardiol. 2018, 71, 1755–1764. [Google Scholar] [CrossRef]
  38. L’Orphelin, J.M.; Varey, E.; Khammari, A.; Dreno, B.; Dompmartin, A. Severe Late-Onset Grade III-IV Adverse Events un-der Immunotherapy: A Retrospective Study of 79 Cases. Cancers 2021, 13, 4928. [Google Scholar] [CrossRef]
Cancers 15 02170 g001 550
Figure 1. Study flowchart: PRISMA flow diagram of systematic review and meta-analysis in ClinicalTrials.gov registries, Medline, and Cochrane CENTRAL up to 7 April 2020.
Figure 1. Study flowchart: PRISMA flow diagram of systematic review and meta-analysis in ClinicalTrials.gov registries, Medline, and Cochrane CENTRAL up to 7 April 2020.
Cancers 15 02170 g001
Cancers 15 02170 g002 550
Figure 2. Risk of CVAEs for MM treated with ICI. The line represents the confidence interval and the size of the circle/dot represents the strength of the association (i.e., peto OR).
Figure 2. Risk of CVAEs for MM treated with ICI. The line represents the confidence interval and the size of the circle/dot represents the strength of the association (i.e., peto OR).
Cancers 15 02170 g002
Table
Table 1. Characteristics of the included randomized clinical trials.
Table 1. Characteristics of the included randomized clinical trials.
ClinicalTrials.gov IdentifierStudyStudy DesignComparisonAdvanced or Metastatic CancerPrior Systemic Therapy (%)Mean Patient Age (years)Follow up Duration (months)Number of Patients in the ICI Mono Therapy GroupNumber of Patients in the Combination ICI Therapy GroupNumber of Patients in the Control Group
NCT00636168Eggermont Lancet Oncol. 2015Phase 3 RCTIpilimumab 10 mg/kg vs. placeboNo051.132.8471-474
NCT01704287Ribas Lancet Oncol. 2015Phase 2 RCTPembrolizumab 2 or 10 mg/kg vs. chemotherapy (paclitaxel + carboplatin, paclitaxel, carboplatin, dacarbazine or temozolomide)Yes46–5060.110357-171
NCT01721746Weber Lancet Oncol. 2015Phase 3 RCTNivolumab 3 mg/kg vs. chemotherapy (dacarbazine, or carboplatin + paclitaxel)Yes10059.28.4268-102
NCT01721772Robert N. Engl. J. Med. 2015Phase 3 RCTNivolumab 3 mg/kg + placebo vs. dacarbazine + placeboYes16.862.75.2206-205
NCT01844505Larkin N. Engl. J Med. 2015Phase 3 RCTNivolumab 3 mg/kg vs. Nivolumab 1 mg/kg + Ipilimumab 3 mg/kg vs. Ipilimumab 3 mg/kgYes059.612.2624313-
NCT01927419Postow N. Engl. J. Med. 2015Phase 3 RCTIpilimumab 3 mg/kg + placebo vs. nivolumab 1 mg/kg + Ipilimumab 3 mg/kgYes063.7114694-
NCT02362594Eggermont N. Engl. J. Med. 2018Phase 3 RCTPembrolizumab 200 mg vs. placeboNo053.815509-502
NCT02374242Long Lancet Oncol. 2018Phase 2 RCTNivolumab 3 mg/kg vs. Nivolumab 1 mg/kg + Ipilimumab 3 mg/kgYes-61.1142535
Table
Table 2. Comparison of CVAEs for MM patients versus patients with other cancers.
Table 2. Comparison of CVAEs for MM patients versus patients with other cancers.
Immune Checkpoint Inhibitors Arm
(n/N)		Control Arm
(n/N)		n Study/.I2OR (IC95%)p
MelanomasOther TumorsMelanomasOther TumorsMelanomasOther TumorsMelanomasOther Tumors
Supraventricular arrhythmias13/181185/11,2175/145460/74065/0%29/27%1.74 (0.66–4.58)0.77 (0.50–1.20)0.13
Ventricular arrhythmias2/7774/25910/6042/15722/0%6/31%5.57 (0.30–103.56)1.18 (0.16–8.80)0.39
Cardiogenic shock7/160560/10,3382/124927/68734/0%26/0%1.88 (0.47–7.58)1.45 (0.93–2.24)0.73
Dyslipidemia30/6259/14220/2732/6612/0%2/0%4.74 (2.16–10.41)1.91 (0.54–6.79)0.23
Venous thromboembolic events 15/1811231/12,15410/1454162/83035/52%34/26%1.01 (0.30–3.39)0.97 (0.74–1.25)0.95
High blood pressure122/1811376/766887/1454208/47585/62%18/76%1.71 (0.86–3.40)1.12 (0.74–1.70)0.30
High pulmonary pressure 2/2710 5/1696 6/3% 0.26 (0.05–1.23)0.42
Myocardial infarction4/160566/11,0931/124930/76313/0%28/0%2.50 (0.40–15.57)1.47 (0.97–2.22)0.58
Cerebral ischemia5/160593/10,7315/124936/74544/0%29/0%0.59 (0.16–2.16)1.68 (1.17–2.40)0.13
Heart failure7/181182/99031/145428/66345/0%27/0%3.62 (0.87–15.07)1.90 (1.28–2.80)0.39
Myocarditis1/50913/48570/5021/35871/NA%11/0%7.29 (0.14–367.33)4.25 (1.44–12.51)0.79
Pericarditis1/35770/89060/17122/67021/NA%23/2%4.39 (0.07–289.28)2.17 (1.41–3.32)0.74
Torsades de pointes/QT prolongation1/5092/12110/5021/5891/NA%3/37%7.29 (0.14–367.33)0.96 (0.05–19.87)0.42
Conduction disturbance1/8282/30041/6454/17822/29%6/0%0.71 (0.02–21.34)0.29 (0.05–1.52)0.64
Valvulopathy 1/1769 2/1363 3/41% 0.37 (0.02–7.64)0.39
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

L’Orphelin, J.-M.; Dollalille, C.; Akroun, J.; Alexandre, J.; Dompmartin, A. Cardiovascular Immunotoxicity Associated with Immune Checkpoint Inhibitors in Metastatic Melanoma. Cancers 2023, 15, 2170. https://doi.org/10.3390/cancers15072170

AMA Style

L’Orphelin J-M, Dollalille C, Akroun J, Alexandre J, Dompmartin A. Cardiovascular Immunotoxicity Associated with Immune Checkpoint Inhibitors in Metastatic Melanoma. Cancers. 2023; 15(7):2170. https://doi.org/10.3390/cancers15072170

Chicago/Turabian Style

L’Orphelin, Jean-Matthieu, Charles Dollalille, Julia Akroun, Joachim Alexandre, and Anne Dompmartin. 2023. "Cardiovascular Immunotoxicity Associated with Immune Checkpoint Inhibitors in Metastatic Melanoma" Cancers 15, no. 7: 2170. https://doi.org/10.3390/cancers15072170

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop