Italian survey on managing immune checkpoint inhibitors in oncology during COVID-19 outbreak
- PMID: 32535890
- PMCID: PMC7323025
- DOI: 10.1111/eci.13315
Italian survey on managing immune checkpoint inhibitors in oncology during COVID-19 outbreak
Abstract
Background: During COVID-19 outbreak, oncological care has been reorganized. Patients with cancer have been reported to experience a more severe COVID-19 syndrome; moreover, there are concerns of a potential interference between immune checkpoint inhibitors (ICIs) and SARS-CoV-2 pathogenesis.
Materials and methods: Between 6 and 16 May 2020, a 22-item survey was sent to Italian physicians involved in administering ICIs. It aimed at exploring the perception about SARS-CoV-2-related risks in cancer patients receiving ICIs, and the attitudes towards their management.
Results: The 104 respondents had a median age of 35.5 years, 58.7% were females and 71.2% worked in Northern Italy. 47.1% of respondents argued a synergism between ICIs and SARS-CoV-2 pathogenesis leading to worse outcomes, but 97.1% would not deny an ICI only for the risk of infection. During COVID-19 outbreak, to reduce hospital visits, 55.8% and 30.8% opted for the highest labelled dose of each ICI and/or, among different ICIs for the same indication, for the one with the longer interval between cycles, respectively. 53.8% of respondents suggested testing for SARS-CoV-2 every cancer patient candidate to ICIs. 71.2% declared to manage patients with onset of dyspnoea and cough as infected by SARS-CoV-2 until otherwise proven; however, 96.2% did not reduce the use of steroids to manage immune-related toxicities. The administration of ICIs in specific situations for different cancer types has not been drastically conditioned.
Conclusions: These results highlight the uncertainties around the perception of a potential interference between ICIs and COVID-19, supporting the need of focused studies on this topic.
Keywords: COVID-19; SARS-CoV-2; cancer; immune checkpoint inhibitors; immunotherapy.
© 2020 Stichting European Society for Clinical Investigation Journal Foundation.
Conflict of interest statement
All authors have completed and submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Dr Tagliamento reported travel grants from Roche, Bristol‐Myers Squibb, AstraZeneca, Takeda and Honoraria as medical writer from Novartis outside the submitted work. Dr Poggio declares travel, accommodations, expenses supported by Takeda, Ely Lilly, and received honoraria from Merck Sharp & Dohme, Ely Lilly, Novartis outside the submitted work. Dr Del Mastro declares personal fees from Roche, Pfeizer, Ipsen, Eli Lilly, Novartis, Takeda, Merck Sharp & Dohme, Genomic Health and Seattle Genetics, and non‐financial support from Celgene, outside the submitted work. Dr Di Maio acted as consultant for Eisai, Takeda, Janssen, Astellas, Pfizer and AstraZeneca, outside the submitted work. Dr Lambertini acted as a consultant for Roche and Novartis, and received honoraria from Theramex, Roche, Lilly, Pfizer and Novartisoutside the submitted work. Dr Spagnolo, Dr Soldato, Dr Conte, Dr Ruelle, Dr Barisione and Dr De Maria declare no competing interests.
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References
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