Prospective Cardiovascular Surveillance of Immune Checkpoint Inhibitor–Based Combination Therapy in Patients With Advanced Renal Cell Cancer: Data From the Phase III JAVELIN Renal 101 Trial

Author:

Rini Brian I.1ORCID,Moslehi Javid J.23,Bonaca Marc4,Schmidinger Manuela5,Albiges Laurence6ORCID,Choueiri Toni K.7ORCID,Motzer Robert J.8ORCID,Atkins Michael B.9ORCID,Haanen John10ORCID,Mariani Mariangela11,Wang Jing12,Hariharan Subramanian13,Larkin James14ORCID

Affiliation:

1. Department of Medicine, Division of Hematology and Oncology, Vanderbilt University Medical Center, Nashville, TN

2. Section of Cardio-Oncology & Immunology, Division of Cardiology, Cardiovascular Research Institute, University of California San Francisco School of Medicine, San Francisco, CA

3. Vanderbilt University Medical Center, Nashville, TN

4. Colorado Prevention Center Clinical Research, Division of Cardiology, Department of Medicine, University of Colorado School of Medicine, Aurora, CO

5. Department of Urology and Comprehensive Cancer Center, Medical University of Vienna, Waehringer Guertel, Vienna, Austria

6. Medical Oncology Department, Institut Gustave Roussy, Villejuif, France

7. Lank Center for Genitourinary Oncology, Dana-Farber Cancer Institute and Brigham and Women's Hospital, Boston, MA

8. Memorial Sloan Kettering Cancer Center, New York, NY

9. Georgetown Lombardi Comprehensive Cancer Center, Washington, DC

10. Netherlands Cancer Institute, Amsterdam, the Netherlands

11. Oncology Research Unit, Pfizer srl, Milano, Italy

12. Statistics, Pfizer, Cambridge, MA

13. Oncology, Pfizer, New York, NY

14. Royal Marsden NHS Foundation Trust, London, United Kingdom

Abstract

PURPOSE Both immune checkpoint inhibitors (ICIs) and vascular endothelial growth factor receptor (VEGFR) inhibitors are approved for advanced renal cell carcinoma treatment and can cause cardiovascular events (CVs); thus, combination therapy could lead to major adverse CV events (MACE). Cardiac serum biomarker assessment and imaging, including left ventricular ejection fraction (LVEF) monitoring, can be used to evaluate MACE. METHODS To our knowledge, the JAVELIN Renal 101 trial, assessing avelumab plus axitinib versus sunitinib in patients with advanced renal cell carcinoma, is the first randomized study of ICI plus VEGFR inhibitor treatment to include prospective serial cardiac monitoring of LVEF and serum cardiac biomarkers. RESULTS MACE (defined as grade ≥ 3 CV AEs) occurred in 31 patients (7.1%) in the combination arm and 17 patients (3.9%) in the sunitinib arm. Patients in the combination arm who had high baseline troponin T values were at higher risk of MACE versus patients with low values (MACE in 6/35 v 7/135, respectively; relative risk, 3.31; 95% CI, 1.19 to 9.22). This association was not observed in patients treated with sunitinib. Other CV baseline risk factors and serum cardiac biomarkers were not significantly predictive for MACE, although a trend toward an association with dyslipidemia was seen in the combination arm. No clinical value of on-treatment routine monitoring of LVEF in relation to MACE was observed. Although LVEF decline was significantly more frequent in the combination arm, most patients recovered, and decline was not associated with other significant cardiac events or symptoms. CONCLUSION Patients with high baseline troponin T levels receiving ICI and VEGFR combinations may need to be monitored more closely for MACE. Routine monitoring of LVEF in asymptomatic patients is not recommended.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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