Serveur d'exploration sur la COVID en France

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Impact of COVID-19 pandemic on treatment patterns in metastatic clear cell renal cell carcinoma.

Identifieur interne : 000D44 ( Main/Exploration ); précédent : 000D43; suivant : 000D45

Impact of COVID-19 pandemic on treatment patterns in metastatic clear cell renal cell carcinoma.

Auteurs : Stefanie Aeppli [Suisse] ; Eric Innocents Eboulet [Suisse] ; Tim Eisen [Royaume-Uni] ; Bernard Escudier [France] ; Stefanie Fischer [Suisse] ; James Larkin [Royaume-Uni] ; Viktor Gruenwald [Allemagne] ; David Mcdermott [États-Unis] ; Jan Oldenburg [Norvège] ; Aurelius Omlin [Suisse] ; Camillo Porta [Italie] ; Brian Rini [États-Unis] ; Manuela Schmidinger [Autriche] ; Cora Sternberg [États-Unis] ; Christian Rothermundt [Suisse]

Source :

RBID : pubmed:32669298

Descripteurs français

English descriptors

Abstract

BACKGROUND

The coronavirus pandemic has provoked discussions among healthcare providers how to manage cancer patients when faced with the threat of severe acute respiratory syndrome related coronavirus 2 (SARS-CoV-2) infection. Immune checkpoint inhibitor (ICI) containing regimens are standard of care in the majority of metastatic clear cell renal cell carcinoma (mccRCC) patients. It remains unclear whether therapies should be modified in response to the COVID-19 pandemic.

METHODS

We performed an online survey among physicians involved in the treatment of mccRCC, and 41 experts responded. Questions focused on criteria relevant for treatment decision outside the pandemic and the modifications of systemic therapy during COVID-19.

FINDINGS

For the majority of experts (73%), the combination of International metastatic renal cell carcinoma Database Consortium (IMDC) risk category and patient fitness are two important factors for decision-making. The main treatment choice in fit, favourable risk patients outside the pandemic is pembrolizumab/axitinib for 53%, avelumab/axitinib, sunitinib or pazopanib for 13% of experts each. During the pandemic, ICI-containing regimens are chosen less often in favour of a tyrosine kinase inhibitors (TKI) monotherapy, mainly sunitinib or pazopanib (35%).In fit, intermediate/poor-risk patients outside the pandemic, over 80% of experts choose ipilimumab/nivolumab, in contrast to only 41% of physicians during COVID-19, instead more TKI monotherapies are given. In patients responding to established therapies with ICI/ICI or ICI/TKI combinations, most participants modify treatment regimen by extending cycle length, holding one ICI or even both.

CONCLUSION

mccRCC treatment modifications in light of the coronavirus pandemic are variable, with a shift from ICI/ICI to ICI/TKI or TKI monotherapy.


DOI: 10.1136/esmoopen-2020-000852
PubMed: 32669298
PubMed Central: PMC7368485


Affiliations:


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Le document en format XML

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<settlement type="city">Londres</settlement>
<region type="country">Angleterre</region>
<region type="région" nuts="1">Grand Londres</region>
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<name sortKey="Gruenwald, Viktor" sort="Gruenwald, Viktor" uniqKey="Gruenwald V" first="Viktor" last="Gruenwald">Viktor Gruenwald</name>
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<nlm:affiliation>Clinic for Internal Medicine (Tumor Research) and Clinic for Urology, University Hospital Essen, Essen, Germany.</nlm:affiliation>
<country xml:lang="fr">Allemagne</country>
<wicri:regionArea>Clinic for Internal Medicine (Tumor Research) and Clinic for Urology, University Hospital Essen, Essen</wicri:regionArea>
<wicri:noRegion>Essen</wicri:noRegion>
<wicri:noRegion>Essen</wicri:noRegion>
<wicri:noRegion>Essen</wicri:noRegion>
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<name sortKey="Mcdermott, David" sort="Mcdermott, David" uniqKey="Mcdermott D" first="David" last="Mcdermott">David Mcdermott</name>
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<nlm:affiliation>Kidney Cancer Program, Dana-Farber/Harvard Cancer Center, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Kidney Cancer Program, Dana-Farber/Harvard Cancer Center, Beth Israel Deaconess Medical Center, Boston, Massachusetts</wicri:regionArea>
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<name sortKey="Oldenburg, Jan" sort="Oldenburg, Jan" uniqKey="Oldenburg J" first="Jan" last="Oldenburg">Jan Oldenburg</name>
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<nlm:affiliation>Division of Medicine an Laboratory Sciences, Akershus University Hospital, Lorenskog, Norway.</nlm:affiliation>
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<name sortKey="Omlin, Aurelius" sort="Omlin, Aurelius" uniqKey="Omlin A" first="Aurelius" last="Omlin">Aurelius Omlin</name>
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<name sortKey="Porta, Camillo" sort="Porta, Camillo" uniqKey="Porta C" first="Camillo" last="Porta">Camillo Porta</name>
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<nlm:affiliation>Biomedical Sciences and Human Oncology, Università degli Studi di Bari Aldo Moro, Bari, Italy.</nlm:affiliation>
<country xml:lang="fr">Italie</country>
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<wicri:noRegion>Bari</wicri:noRegion>
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<name sortKey="Rini, Brian" sort="Rini, Brian" uniqKey="Rini B" first="Brian" last="Rini">Brian Rini</name>
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<nlm:affiliation>Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee</wicri:regionArea>
<placeName>
<region type="state">Tennessee</region>
</placeName>
</affiliation>
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<name sortKey="Schmidinger, Manuela" sort="Schmidinger, Manuela" uniqKey="Schmidinger M" first="Manuela" last="Schmidinger">Manuela Schmidinger</name>
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<name sortKey="Sternberg, Cora" sort="Sternberg, Cora" uniqKey="Sternberg C" first="Cora" last="Sternberg">Cora Sternberg</name>
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<nlm:affiliation>Medical Oncology, Weill Cornell Medicine, New York, New York, USA.</nlm:affiliation>
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<placeName>
<region type="state">État de New York</region>
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<name sortKey="Rothermundt, Christian" sort="Rothermundt, Christian" uniqKey="Rothermundt C" first="Christian" last="Rothermundt">Christian Rothermundt</name>
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<title level="j">ESMO open</title>
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<term>Antineoplastic Agents (therapeutic use)</term>
<term>Betacoronavirus (MeSH)</term>
<term>Carcinoma, Renal Cell (drug therapy)</term>
<term>Carcinoma, Renal Cell (secondary)</term>
<term>Clinical Decision-Making (MeSH)</term>
<term>Coronavirus Infections (epidemiology)</term>
<term>Coronavirus Infections (prevention & control)</term>
<term>Humans (MeSH)</term>
<term>Immunologic Factors (therapeutic use)</term>
<term>Kidney Neoplasms (drug therapy)</term>
<term>Kidney Neoplasms (pathology)</term>
<term>Medical Oncology (statistics & numerical data)</term>
<term>Pandemics (prevention & control)</term>
<term>Pneumonia, Viral (epidemiology)</term>
<term>Pneumonia, Viral (prevention & control)</term>
<term>Practice Patterns, Physicians' (statistics & numerical data)</term>
<term>Protein Kinase Inhibitors (therapeutic use)</term>
<term>Urology (statistics & numerical data)</term>
</keywords>
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<term>Antinéoplasiques (usage thérapeutique)</term>
<term>Betacoronavirus (MeSH)</term>
<term>Facteurs immunologiques (usage thérapeutique)</term>
<term>Humains (MeSH)</term>
<term>Infections à coronavirus (prévention et contrôle)</term>
<term>Infections à coronavirus (épidémiologie)</term>
<term>Inhibiteurs de protéines kinases (usage thérapeutique)</term>
<term>Néphrocarcinome (secondaire)</term>
<term>Néphrocarcinome (traitement médicamenteux)</term>
<term>Oncologie médicale (statistiques et données numériques)</term>
<term>Pandémies (prévention et contrôle)</term>
<term>Pneumopathie virale (prévention et contrôle)</term>
<term>Pneumopathie virale (épidémiologie)</term>
<term>Prise de décision clinique (MeSH)</term>
<term>Tumeurs du rein (anatomopathologie)</term>
<term>Tumeurs du rein (traitement médicamenteux)</term>
<term>Types de pratiques des médecins (statistiques et données numériques)</term>
<term>Urologie (statistiques et données numériques)</term>
</keywords>
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<term>Antineoplastic Agents</term>
<term>Immunologic Factors</term>
<term>Protein Kinase Inhibitors</term>
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<keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr">
<term>Tumeurs du rein</term>
</keywords>
<keywords scheme="MESH" qualifier="drug therapy" xml:lang="en">
<term>Carcinoma, Renal Cell</term>
<term>Kidney Neoplasms</term>
</keywords>
<keywords scheme="MESH" qualifier="epidemiology" xml:lang="en">
<term>Coronavirus Infections</term>
<term>Pneumonia, Viral</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en">
<term>Kidney Neoplasms</term>
</keywords>
<keywords scheme="MESH" qualifier="prevention & control" xml:lang="en">
<term>Coronavirus Infections</term>
<term>Pandemics</term>
<term>Pneumonia, Viral</term>
</keywords>
<keywords scheme="MESH" qualifier="prévention et contrôle" xml:lang="fr">
<term>Infections à coronavirus</term>
<term>Pandémies</term>
<term>Pneumopathie virale</term>
</keywords>
<keywords scheme="MESH" qualifier="secondaire" xml:lang="fr">
<term>Néphrocarcinome</term>
</keywords>
<keywords scheme="MESH" qualifier="secondary" xml:lang="en">
<term>Carcinoma, Renal Cell</term>
</keywords>
<keywords scheme="MESH" qualifier="statistics & numerical data" xml:lang="en">
<term>Medical Oncology</term>
<term>Practice Patterns, Physicians'</term>
<term>Urology</term>
</keywords>
<keywords scheme="MESH" qualifier="statistiques et données numériques" xml:lang="fr">
<term>Oncologie médicale</term>
<term>Types de pratiques des médecins</term>
<term>Urologie</term>
</keywords>
<keywords scheme="MESH" qualifier="traitement médicamenteux" xml:lang="fr">
<term>Néphrocarcinome</term>
<term>Tumeurs du rein</term>
</keywords>
<keywords scheme="MESH" qualifier="usage thérapeutique" xml:lang="fr">
<term>Antinéoplasiques</term>
<term>Facteurs immunologiques</term>
<term>Inhibiteurs de protéines kinases</term>
</keywords>
<keywords scheme="MESH" qualifier="épidémiologie" xml:lang="fr">
<term>Infections à coronavirus</term>
<term>Pneumopathie virale</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Betacoronavirus</term>
<term>Clinical Decision-Making</term>
<term>Humans</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Betacoronavirus</term>
<term>Humains</term>
<term>Prise de décision clinique</term>
</keywords>
</textClass>
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<front>
<div type="abstract" xml:lang="en">
<p>
<b>BACKGROUND</b>
</p>
<p>The coronavirus pandemic has provoked discussions among healthcare providers how to manage cancer patients when faced with the threat of severe acute respiratory syndrome related coronavirus 2 (SARS-CoV-2) infection. Immune checkpoint inhibitor (ICI) containing regimens are standard of care in the majority of metastatic clear cell renal cell carcinoma (mccRCC) patients. It remains unclear whether therapies should be modified in response to the COVID-19 pandemic.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>METHODS</b>
</p>
<p>We performed an online survey among physicians involved in the treatment of mccRCC, and 41 experts responded. Questions focused on criteria relevant for treatment decision outside the pandemic and the modifications of systemic therapy during COVID-19.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>FINDINGS</b>
</p>
<p>For the majority of experts (73%), the combination of International metastatic renal cell carcinoma Database Consortium (IMDC) risk category and patient fitness are two important factors for decision-making. The main treatment choice in fit, favourable risk patients outside the pandemic is pembrolizumab/axitinib for 53%, avelumab/axitinib, sunitinib or pazopanib for 13% of experts each. During the pandemic, ICI-containing regimens are chosen less often in favour of a tyrosine kinase inhibitors (TKI) monotherapy, mainly sunitinib or pazopanib (35%).In fit, intermediate/poor-risk patients outside the pandemic, over 80% of experts choose ipilimumab/nivolumab, in contrast to only 41% of physicians during COVID-19, instead more TKI monotherapies are given. In patients responding to established therapies with ICI/ICI or ICI/TKI combinations, most participants modify treatment regimen by extending cycle length, holding one ICI or even both.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>CONCLUSION</b>
</p>
<p>mccRCC treatment modifications in light of the coronavirus pandemic are variable, with a shift from ICI/ICI to ICI/TKI or TKI monotherapy.</p>
</div>
</front>
</TEI>
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<DateCompleted>
<Year>2020</Year>
<Month>07</Month>
<Day>24</Day>
</DateCompleted>
<DateRevised>
<Year>2020</Year>
<Month>07</Month>
<Day>24</Day>
</DateRevised>
<Article PubModel="Print">
<Journal>
<ISSN IssnType="Electronic">2059-7029</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>5</Volume>
<Issue>Suppl 3</Issue>
<PubDate>
<Year>2020</Year>
<Month>07</Month>
</PubDate>
</JournalIssue>
<Title>ESMO open</Title>
<ISOAbbreviation>ESMO Open</ISOAbbreviation>
</Journal>
<ArticleTitle>Impact of COVID-19 pandemic on treatment patterns in metastatic clear cell renal cell carcinoma.</ArticleTitle>
<ELocationID EIdType="pii" ValidYN="Y">e000852</ELocationID>
<ELocationID EIdType="doi" ValidYN="Y">10.1136/esmoopen-2020-000852</ELocationID>
<Abstract>
<AbstractText Label="BACKGROUND">The coronavirus pandemic has provoked discussions among healthcare providers how to manage cancer patients when faced with the threat of severe acute respiratory syndrome related coronavirus 2 (SARS-CoV-2) infection. Immune checkpoint inhibitor (ICI) containing regimens are standard of care in the majority of metastatic clear cell renal cell carcinoma (mccRCC) patients. It remains unclear whether therapies should be modified in response to the COVID-19 pandemic.</AbstractText>
<AbstractText Label="METHODS">We performed an online survey among physicians involved in the treatment of mccRCC, and 41 experts responded. Questions focused on criteria relevant for treatment decision outside the pandemic and the modifications of systemic therapy during COVID-19.</AbstractText>
<AbstractText Label="FINDINGS">For the majority of experts (73%), the combination of International metastatic renal cell carcinoma Database Consortium (IMDC) risk category and patient fitness are two important factors for decision-making. The main treatment choice in fit, favourable risk patients outside the pandemic is pembrolizumab/axitinib for 53%, avelumab/axitinib, sunitinib or pazopanib for 13% of experts each. During the pandemic, ICI-containing regimens are chosen less often in favour of a tyrosine kinase inhibitors (TKI) monotherapy, mainly sunitinib or pazopanib (35%).In fit, intermediate/poor-risk patients outside the pandemic, over 80% of experts choose ipilimumab/nivolumab, in contrast to only 41% of physicians during COVID-19, instead more TKI monotherapies are given. In patients responding to established therapies with ICI/ICI or ICI/TKI combinations, most participants modify treatment regimen by extending cycle length, holding one ICI or even both.</AbstractText>
<AbstractText Label="CONCLUSION">mccRCC treatment modifications in light of the coronavirus pandemic are variable, with a shift from ICI/ICI to ICI/TKI or TKI monotherapy.</AbstractText>
<CopyrightInformation>© Author (s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. Published by BMJ on behalf of the European Society for Medical Oncology.</CopyrightInformation>
</Abstract>
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<LastName>Aeppli</LastName>
<ForeName>Stefanie</ForeName>
<Initials>S</Initials>
<AffiliationInfo>
<Affiliation>Medical Oncology and Haematology, Kantonsspital St Gallen, Sankt Gallen, Switzerland.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Eboulet</LastName>
<ForeName>Eric Innocents</ForeName>
<Initials>EI</Initials>
<AffiliationInfo>
<Affiliation>Coordinating Center, Swiss Group for Clinical Cancer Research (SAKK), Bern, Switzerland.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Eisen</LastName>
<ForeName>Tim</ForeName>
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<AffiliationInfo>
<Affiliation>Department of Oncology, Cambridge University Hospitals NHS Foundation Trust, Cambridge, Cambridgeshire, UK.</Affiliation>
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<LastName>Escudier</LastName>
<ForeName>Bernard</ForeName>
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<Affiliation>Department Medical Oncology, Gustave Roussy, Villejuif, Île-de-France, France.</Affiliation>
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<LastName>Fischer</LastName>
<ForeName>Stefanie</ForeName>
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<LastName>Gruenwald</LastName>
<ForeName>Viktor</ForeName>
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<AffiliationInfo>
<Affiliation>Clinic for Internal Medicine (Tumor Research) and Clinic for Urology, University Hospital Essen, Essen, Germany.</Affiliation>
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<Affiliation>Kidney Cancer Program, Dana-Farber/Harvard Cancer Center, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.</Affiliation>
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<LastName>Oldenburg</LastName>
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<Affiliation>Division of Medicine an Laboratory Sciences, Akershus University Hospital, Lorenskog, Norway.</Affiliation>
</AffiliationInfo>
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<LastName>Omlin</LastName>
<ForeName>Aurelius</ForeName>
<Initials>A</Initials>
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<Affiliation>Medical Oncology and Haematology, Kantonsspital St Gallen, Sankt Gallen, Switzerland.</Affiliation>
</AffiliationInfo>
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<ForeName>Camillo</ForeName>
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<Identifier Source="ORCID">0000-0003-2412-1563</Identifier>
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<Affiliation>Biomedical Sciences and Human Oncology, Università degli Studi di Bari Aldo Moro, Bari, Italy.</Affiliation>
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<LastName>Rini</LastName>
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<Initials>B</Initials>
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<Affiliation>Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.</Affiliation>
</AffiliationInfo>
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<LastName>Schmidinger</LastName>
<ForeName>Manuela</ForeName>
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<Identifier Source="ORCID">0000-0002-2567-2749</Identifier>
<AffiliationInfo>
<Affiliation>Medicine I, Clinical Division of Oncology, Vienna, Austria.</Affiliation>
</AffiliationInfo>
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<LastName>Sternberg</LastName>
<ForeName>Cora</ForeName>
<Initials>C</Initials>
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<Affiliation>Medical Oncology, Weill Cornell Medicine, New York, New York, USA.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Rothermundt</LastName>
<ForeName>Christian</ForeName>
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<Identifier Source="ORCID">0000-0002-2104-7794</Identifier>
<AffiliationInfo>
<Affiliation>Medical Oncology and Haematology, Kantonsspital St Gallen, Sankt Gallen, Switzerland christian.rothermundt@kssg.ch.</Affiliation>
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<Keyword MajorTopicYN="Y">decision criteria</Keyword>
<Keyword MajorTopicYN="Y">pandemic</Keyword>
<Keyword MajorTopicYN="Y">renal cell carcinoma</Keyword>
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<CoiStatement>Competing interests: SA: MSD (C/A), Sanofi-Genzyme (C/A) recipient: my institution. TE: Personal: AstraZeneca (RF, E, OI), Bayer (RF), Pfizer (RF), Roche (E, OI); Institution: AstraZeneca (RF), Roche (RF). BE: Pfizer (C/A), BMS (C/A), Ipsen (C/A), Roche (C/A), Oncorena (C/A), Aveo (C/A). SF: Bayer (TS), Astellas (RF, TS). VG: Astra Zeneca (C/A, H, OI, RF), Bristol-Myers Squibb (C/A, H, OI, RF), Roche Pharma AG (C/A, H), MSD Oncology (C/A, H, OI, RF), Ipsen (C/A, H, RF), Bayer (H, RF), Merck Serono (C/A, H), Janssen Cliag (C/A, H), Pfizer (C/A, H), Lilly (C/A, H), PharmaMar (H), EUSAPharm (C/A, H), Novartis (C/A, H, RF), EISAI (H), Onkowissen (C/A). JML: Achilles Therapeutics (C/A, grant support), Bristol-Myers Squibb (C/A, grant support), Merck Sharp & Dohme (C/A, grant support), Nektar (C/A, grant support), Novartis (C/A, grant support), Pfizer (C/A, grant support), Roche–Genentech (C/A, grant support), Immunocore (C/A, grant support), AstraZeneca (C/A), Boston Biomedical (C/A), Eisai (C/A), EUSA Pharma (C/A), GlaxoSmithKline (C/A), Ipsen (C/A), Imugen (C/A), Incyte (C/A), iOnctura (C/A), Kymab (C/A), Merck Serono (C/A), Pierre Fabre (C/A), Secama (C/A), Vitaccess (C/A), Covance (C/A), Aveo (C/A), Pharmacyclics (C/A). DM: BMS (H, C/A), Pfizer (H, C/A), Merck (H, C/A), Alkermes, Inc. (H, C/A). AO: Personal: Astellas (TS), Bayer (TS), Sanofi (TS), Janssen (TS). Instituional: Astellas (C/A, SB), Bayer (C/A, SB), Sanofi (C/A), Roche (C/A), Janssen (C/A, RF, SB), MSD (C/A), Molecular Partners (C/A), Teva (RF). CP: Bristol-Myers Squibb (personal fees), Merck Sharpe & Dohme (personal fees), Novartis (personal fees), Ipsen (personal fees), EUSA (personal fees), Eisai (personal fees), Janssen (personal fees), AstraZeneca (personal fees), General Electric (personal fees), Pfizer (grants and personal fees). BR: Merck (C/A), BMS (C/A), AVEO (C/A), Pfizer (C/A), Roche(C/A), Pfizer (RF), Merck (RF), BMS (RF), AVEO (RF), Astra-Zeneca (RF), Roche (RF). MS: Pfizer, BMS, Ipsen, MSD, Merck, Exelixis, EISAI, EUSA, Roche, Novartis, Alkermes. CS: Pfizer (C/A), MSD (C/A), Merck (C/A), AstraZeneca (C/A), Astellas (C/A), Sanofi-Genzyme (C/A), Roche-Genentech (C/A), Incyte (C/A). CR: Pfizer (C/A), Bristol-Myers Squibb (C/A), Roche Pharma AG (C/A), MSD Oncology (C/A), Merck (Schweiz) AG (C/A) recipient for all: my institution. Astellas Pharma (RF) recipient: my institution. Legend: (C/A) Consulting/advisory relationship; (RF) Research funding; (E) Employment; (ET) Expert testimony; (H) Honoraria received; (TS) Travel Support; (OI) Ownership interests; (IP) Intellectual property rights/inventor/patent holder; (SAB) Scientific advisory board, Speaker Bureau (SB).</CoiStatement>
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