Cited by 77Renal cell carcinoma treatmentChemotherapy-induced cardiotoxicity and mitigationCancer Immunotherapy and Biomarkers

The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.

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

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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.

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  • Troponin T is more sensitive for surveillance in patients with ICI myocarditis.

    “and is more sensitive for surveillance in patients.”

    From Autoimmune Myocarditis, Old Dogs and New Tricks. (2024) · cites this paper as [236]

    The Methods section (page unavailable) says the trial monitored either troponin T or I to assess early detection of myocarditis, and the Discussion reports that troponin T was elevated in 94% of cases in another study. It does not establish that troponin T is more sensitive for surveillance than troponin I; the Results say baseline cardiac biomarkers were not predictive of myocarditis. (LLM, conf=0.84)

    Experimental — accuracy not yet measured
  • In ICI myocarditis, troponin T is specifically associated with adverse outcomes.

    “In ICI myocarditis, troponin T is specifically associated with adverse outcomes”

    From Autoimmune Myocarditis, Old Dogs and New Tricks. (2024) · cites this paper as [236]

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Metadata

Authors
Rini, B. I., Moslehi, J. J., Bonaca, M., Schmidinger, M., Albiges, L., Choueiri, T. K., Motzer, R. J., Atkins, M. B., Haanen, J., Mariani, M., Wang, J., Hariharan, S., & Larkin, J.
Affiliations
  • Vanderbilt University Medical Center (US)
  • University of California, San Francisco (US)
  • University of Colorado Anschutz (US)
  • Comprehensive Cancer Center Vienna (AT)
  • Institut Gustave Roussy (FR)
  • Brigham and Women's Hospital (US)
  • Memorial Sloan Kettering Cancer Center (US)
  • Georgetown University Medical Center (US)
  • The Netherlands Cancer Institute (NL)
  • Oncology Research Unit, Pfizer srl, Milano, Italy
  • Pfizer (United States) (US)
  • Royal Marsden NHS Foundation Trust (GB)
Corresponding author
Rini, Brian I.
Venue
Journal of Clinical Oncology
Published
2022-06-10
Volume
40
Issue
17
Pages
1929-1938
ISSN
  • 0732-183X (ISSN-L)
  • 1527-7755
OpenAlex
W4214924062
Cited by
77
References
2
Citations by year
2026: 6 · 2025: 18 · 2024: 19 · 2023: 20 · 2022: 14
FWCI
11.45
Type
journal article
Language
en
Open access
Licence
cc-by-nc-nd
Locations
  • Journal of Clinical Oncology (publishedVersion, cc-by-nc-nd)
  • PubMed Central (publishedVersion, cc-by-nc-nd)
  • PubMed (publishedVersion)
  • eScholarship (California Digital Library) (submittedVersion, cc-by-nc-nd)
Funders
  • National Heart, Lung, and Blood Institute (R01HL141466, R01HL156021, R01HL155990)
  • National Cancer Institute (P30CA008748)
Topics
  • Health Sciences › Medicine › Oncology › Renal cell carcinoma treatment
  • Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Chemotherapy-induced cardiotoxicity and mitigation
  • Health Sciences › Medicine › Oncology › Cancer Immunotherapy and Biomarkers
Keywords
immune checkpoint inhibitors, VEGFR inhibitors, advanced renal cell carcinoma, cardiovascular adverse events, major adverse cardiovascular events, avelumab, axitinib, sunitinib, troponin T, cardiac biomarkers, cardiotoxicity, JAVELIN Renal 101
MeSH terms
Sunitinib, Immune Checkpoint Inhibitors, Antineoplastic Combined Chemotherapy Protocols, Carcinoma, Renal Cell, Cardiovascular System, Humans, Kidney Neoplasms, Prospective Studies, Randomized Controlled Trials as Topic, Ventricular Function, Left, Troponin T, Vascular Endothelial Growth Factor A

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