Abstract
Background & Aims: The coronavirus disease 2019 (COVID-19) pandemic has posed unprecedented challenges to healthcare systems and it may have heavily impacted patients with liver cancer (LC). Herein, we evaluated whether the schedule of LC screening or procedures has been interrupted or delayed because of the COVID-19 pandemic. Methods: An international survey evaluated the impact of the COVID-19 pandemic on clinical practice and clinical trials from March 2020 to June 2020, as the first phase of a multicentre, international, and observational project. The focus was on patients with hepatocellular carcinoma or intrahepatic cholangiocarcinoma, cared for around the world during the first COVID-19 pandemic wave. Results: Ninety-one centres expressed interest to participate and 76 were included in the analysis, from Europe, South America, North America, Asia, and Africa (73.7%, 17.1%, 5.3%, 2.6%, and 1.3% per continent, respectively). Eighty-seven percent of the centres modified their clinical practice: 40.8% the diagnostic procedures, 80.9% the screening programme, 50% cancelled curative and/or palliative treatments for LC, and 41.7% modified the liver transplantation programme. Forty-five out of 69 (65.2%) centres in which clinical trials were running modified their treatments in that setting, but 58.1% were able to recruit new patients. The phone call service was modified in 51.4% of centres which had this service before the COVID-19 pandemic (n = 19/37). Conclusions: The first wave of the COVID-19 pandemic had a tremendous impact on the routine care of patients with liver cancer. Modifications in screening, diagnostic, and treatment algorithms may have significantly impaired the outcome of patients. Ongoing data collection and future analyses will report the benefits and disadvantages of the strategies implemented, aiding future decision-making. Lay summary: The coronavirus disease 2019 (COVID-19) pandemic has posed unprecedented challenges to healthcare systems globally. Herein, we assessed the impact of the first wave pandemic on patients with liver cancer and found that routine care for these patients has been majorly disrupted, which could have a significant impact on outcomes.
Original language | English (US) |
---|---|
Article number | 100260 |
Journal | JHEP Reports |
Volume | 3 |
Issue number | 3 |
DOIs | |
State | Published - Jun 2021 |
Externally published | Yes |
Keywords
- COVID-19
- Cholangiocarcinoma
- Clinical trials
- Hepatocellular carcinoma
- Liver cancer
- Management
- Nurses
ASJC Scopus subject areas
- Internal Medicine
- Immunology and Allergy
- Hepatology
- Gastroenterology
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In: JHEP Reports, Vol. 3, No. 3, 100260, 06.2021.
Research output: Contribution to journal › Article › peer-review
}
TY - JOUR
T1 - Assessing the impact of COVID-19 on liver cancer management (CERO-19)
AU - Muñoz-Martínez, Sergio
AU - Sapena, Victor
AU - Forner, Alejandro
AU - Nault, Jean Charles
AU - Sapisochin, Gonzalo
AU - Rimassa, Lorenza
AU - Sangro, Bruno
AU - Bruix, Jordi
AU - Sanduzzi-Zamparelli, Marco
AU - Hołówko, Wacław
AU - El Kassas, Mohamed
AU - Mocan, Tudor
AU - Bouattour, Mohamed
AU - Merle, Philippe
AU - Hoogwater, Frederik J.H.
AU - Alqahtani, Saleh A.
AU - Reeves, Helen L.
AU - Pinato, David J.
AU - Giorgakis, Emmanouil
AU - Meyer, Tim
AU - Villadsen, Gerda Elisabeth
AU - Wege, Henning
AU - Salati, Massimiliano
AU - Mínguez, Beatriz
AU - Di Costanzo, Giovan Giuseppe
AU - Roderburg, Christoph
AU - Tacke, Frank
AU - Varela, María
AU - Galle, Peter R.
AU - Alvares-da-Silva, Mario Reis
AU - Trojan, Jörg
AU - Bridgewater, John
AU - Cabibbo, Giuseppe
AU - Toso, Christian
AU - Lachenmayer, Anja
AU - Casadei-Gardini, Andrea
AU - Toyoda, Hidenori
AU - Lüdde, Tom
AU - Villani, Rosanna
AU - Matilla Peña, Ana María
AU - Guedes Leal, Cassia Regina
AU - Ronzoni, Monica
AU - Delgado, Manuel
AU - Perelló, Christie
AU - Pascual, Sonia
AU - Lledó, José Luis
AU - Argemi, Josepmaria
AU - Basu, Bristi
AU - da Fonseca, Leonardo
AU - Acevedo, Juan
AU - Siebenhüner, Alexander R.
AU - Braconi, Chiara
AU - Meyers, Brandon M.
AU - Granito, Alessandro
AU - Sala, Margarita
AU - Rodríguez-Lope, Carlos
AU - Blaise, Lorraine
AU - Romero-Gómez, Manuel
AU - Piñero, Federico
AU - Gomez, Dhanny
AU - Mello, Vivianne
AU - Pinheiro Alves, Rogerio Camargo
AU - França, Alex
AU - Branco, Fernanda
AU - Brandi, Giovanni
AU - Pereira, Gustavo
AU - Coll, Susanna
AU - Guarino, Maria
AU - Benítez, Carlos
AU - Anders, Maria Margarita
AU - Bandi, Juan C.
AU - Vergara, Mercedes
AU - Calvo, Mariona
AU - Peck-Radosavljevic, Markus
AU - García-Juárez, Ignacio
AU - Cardinale, Vincenzo
AU - Lozano, Mar
AU - Gambato, Martina
AU - Okolicsanyi, Stefano
AU - Morales-Arraez, Dalia
AU - Elvevi, Alessandra
AU - Muñoz, Alberto E.
AU - Lué, Alberto
AU - Iavarone, Massimo
AU - Reig, Maria
N1 - Funding Information: SM.-M.: Speaker fees from Bayer and travel funding from Bayer and Eisai. V.S.: Travel grants from Bayer. A.F.: Lecture fees from Bayer, Gilead and MSD; consultancy fees from Bayer, AstraZeneca, Roche and Guerbert. J-C.N.: Received research grant from Bayer for Inserm UMR1138. L.R.: Reports receiving consulting fees from Amgen, ArQule, AstraZeneca, Basilea, Bayer, Celgene, Eisai, Exelixis, Hengrui, Incyte, Ipsen, Lilly, MSD, Nerviano Medical Sciences, Roche, Sanofi; lectures fees from AbbVie, Amgen, Eisai, Gilead, Incyte, Ipsen, Lilly, Roche, Sanofi; travel fees from Ipsen; and institutional research funding from Agios, ARMO BioSciences, AstraZeneca, BeiGene, Eisai, Exelixis, Fibrogen, Incyte, Ipsen, Lilly, MSD, Roche. B.S.: Reports consultancy fees from Adaptimmune, AstraZeneca, Bayer, BMS, BTG, Eli Lilly, Ipsen, Novartis, Merck, Roche, Sirtex Medical, Terumo; and research grants from BMS and Sirtex Medical. J. Bruix: Consultancy: AbbVie, ArQule, Astra, Basilea, Bayer, BMS, Daiichi Sankyo, GlaxoSmithKline, Gilead, Kowa, Lilly, Medimune, Novartis, Onxeo, Polaris, Quirem, Roche, Sanofi-Aventis, Sirtex, Terumo/Grants: Bayer and Ipsen. M.S.Z.: Received speaker fees and travel grants from Bayer and BTG, MSD. M.B.: Consultant and Advisory Board for: Bayer Pharma, Ipsen, BMS, Eisai, Roche, AstraZeneca, Sirtex Medical. D.J.P.: Received lecture fees from ViiV Healthcare and Bayer Healthcare and travel expenses from BMS and Bayer Healthcare; consulting fees for Mina Therapeutics, EISAI, Roche, and AstraZeneca; received research funding (to institution) from MSD and BMS. T.M.: Consultancy: Eisai, Roche, BTG, Ipsen, Bayer, Adaptimmune. Research funding: Bayer, BTG. H.W.: Served as speaker for Bayer, Eisai, and Ipsen, and as a consultant for Bayer, Eisai, Lilly, BMS, Roche, and Ipsen. B.M.: Consultancy: Bayer-Shering Pharma /Speaker fees: Eisai, MSDG. C. Consultancy fees from Bayer, Ipsen. P.R.G.: Bayer, BMS, MSD, AstraZeneca, Adaptimmune, Sirtex, Lilly Ipsen, Roche, Eisai. M.R.A.S.: Has received Research grants, advisory board or speaker fees for AbbVie, Bayer, Biolab, Intercept, Ipsen, Gilead, MSD, Novartis, and Roche. J.T.: Has received research grants from Roche and Ipsen. He has received speaker and consulting honoraria from AstraZeneca, Amgen, Bayer Healthcare, Bristol Myers-Squibb, Eisai, Ipsen, Merck Serono, Merck Sharp & Dome, Lilly Imclone, and Roche. J. Bridgewater: Consultancy Bayer, BMS, Incyte, Taiho, Roche, MSD and Merck Serono. Research funding from Incyte. G.C.: Consultancy fees from Bayer, Ipsen. A.L.: Consultancy CAScination, Advisory Board Neuwave and Histosonics. H.T.: Speaker fees from AbbVie, Gilead, MSD, and Bayer. R.V.: Research grant from Abbvie. A.M.M.P.: Speaker honorarium from Bayer, BMS, Boston Scientific and EISAI. Consulting honorarium from Bayer, AstraZeneca and EISAI. Advisory honorarium from Bayer, AstraZeneca and EISAI. Grants from Bayer and Boston Scientific. M.D.: Has received consulting and training fees from Bayer and Eisai. B.B.: Reports Consultancy for GenMab (paid to Institution); Advisory Boards for Roche (paid to Institution), Eisai Europe Limited (paid to Institution), research grant from Celgene Ltd (paid to Institution), Speakers Bureau for Eisai Europe Limited (paid to Institution), Travel and registration for Congress from Bayer. L.d.F.: Lectures fees from BMS, Roche and Bayer. B.M.M.: Advisory/Speaker: Amgen, AstraZeneca, Bayer, BMS, Eisai, Ipsen, Merck, Roche, Sanoffi Genzyme, Taiho. Expert Testimony: Eisai, Roche. Travel: Eisai, Merck. Research: Sillajen (Individual); AstraZeneca, H3/Eisai, Galera, GSK, Exelixis (Institution). M.S.: Travel/ accommodation/meeting expenses: Bayer. Eisai. Speaker fees: Bayer. C.R.L.: Travel grants from Bayer. M.R-G.: Reports grants from Intercept, grants from Gilead-Sciences, personal fees from Shionogi, personal fees from Alfa-Wasserman, personal fees from Prosciento, personal fees from Kaleido, personal fees from Novonrdisk, personal fees from MSD, personal fees from BMS, personal fees from Allergan, personal fees from Boehriger-Ingelheim, personal fees from Zydus, personal fees from Intercept Pharma, personal fees from Gilead-Sciences, outside the submitted work. F.P.: Disclosures: Received speaker honoraria from Bayer, Roche, LKM-Biotoscana, RAFFO. Research Grants from INC Argentinean National Institute of Corrections, Roche. V.M.: Lectures sponsored by Bayer. G.B.: Advisory board Eli-Lilly and Incyte. M. Vergara: Travel grants from Bayer, Gilead, MSD and Abbvie. Lectures sponsored by Gilead, Abbvie, Intercept, and MSD. M.L.: Lectures and educational presentations: Abbvie. Travel/accommodation, meeting expenses covered by Bayer, Gilead, Abbvie. M.I.: Received speaker honoraria from Bayer, Gilead Sciences, BMS, Janssen, Ipsen, MSD, BTG-Boston Scientific, AbbVie, EISAI, and was consultant for BTG-Boston Scientific, Bayer, and Guerbet. M.R.: Consultancy: Bayer-Schering Pharma, BMS, Roche, Ipsen, AstraZeneca, Lilly, BTG/Paid conferences: Bayer-Schering Pharma, BMS, Gilead, Lilly/Research Grants: Bayer-Schering Pharma, Ipsen.S.M.-M. received the grant support “Beca para Perfeccionamiento en Gastroenterología en el Extranjero” from Asociación Mexicana de Gastroenterología, A.C. A.F. received grant support from Instituto de Salud Carlos III (PI13/01229 and PI18/00542). J. Bruix received grant support from Instituto de Salud Carlos III (PI18/00768), AECC (PI044031), and WCR (AICR) 16-0026. M.S.Z. was supported by “Ajuts per a la iniciació a la recerca 2019 from Societat Catalana de Digestologia (SCD)” and received grant support from Instituto de Salud Carlos III (FI19/00222). H.L.R. is supported by funding from Cancer Research UK (CR UK) centre grant C9380/A18084; CR UK programme grant C18342/A23390 and CR UK Accelerator award HUNTER C9380/A26813. D.J.P. is supported by grant funding from the Wellcome Trust Strategic Fund (PS3416) and acknowledges grant support from the Cancer Treatment and Research Trust (CTRT) and infrastructural support by the Cancer Research UK Imperial Centre, the Imperial College Experimental Cancer Medicine Centre (ECMC) and the NIHR Imperial Biomedical Research Centre. B.M. received grant support from Instituto de Salud Carlos III (PI18/00961). J. Bridgewater is in part funded by the UCLH / UCL Biomedical Research Centre. M.S. received funding from CIBEREHD (CB06/04/0033) and AGAUR (2017-SGR-490). M.R. received grant support from Instituto de Salud Carlos III (PI15/00145 and PI18/0358). Some of the authors of this article are members of the European Reference Network (ERN) RARE-LIVER. Some of the authors of this article are members of the European Network for the Study of Cholangiocarcinoma (ENS-CCA).This article/publication is based upon work from COST Action CA18122 European Cholangiocarcinoma Network supported by COST (European Cooperation in Science and Technology) www.cost.eu Funding Information: S.M.-M. received the grant support “Beca para Perfeccionamiento en Gastroenterología en el Extranjero” from Asociación Mexicana de Gastroenterología , A.C. A.F. received grant support from Instituto de Salud Carlos III ( PI13/01229 and PI18/00542 ). J. Bruix received grant support from Instituto de Salud Carlos III ( PI18/00768 ), AECC ( PI044031 ), and WCR (AICR) 16-0026. M.S.Z. was supported by “ Ajuts per a la iniciació a la recerca 2019 from Societat Catalana de Digestologia (SCD) ” and received grant support from Instituto de Salud Carlos III ( FI19/00222 ). H.L.R. is supported by funding from Cancer Research UK (CR UK) centre grant C9380/A18084 ; CR UK programme grant C18342/A23390 and CR UK Accelerator award HUNTER C9380 / A26813 . D.J.P. is supported by grant funding from the Wellcome Trust Strategic Fund ( PS3416 ) and acknowledges grant support from the Cancer Treatment and Research Trust (CTRT) and infrastructural support by the Cancer Research UK Imperial Centre, the Imperial College Experimental Cancer Medicine Centre (ECMC) and the NIHR Imperial Biomedical Research Centre . B.M. received grant support from Instituto de Salud Carlos III ( PI18/00961 ). J. Bridgewater is in part funded by the UCLH / UCL Biomedical Research Centre . M.S. received funding from CIBEREHD ( CB06/04/0033 ) and AGAUR ( 2017-SGR-490 ). M.R. received grant support from Instituto de Salud Carlos III ( PI15/00145 and PI18/0358 ). Funding Information: Some of the authors of this article are members of the European Reference Network (ERN) RARE-LIVER. Some of the authors of this article are members of the European Network for the Study of Cholangiocarcinoma (ENS-CCA).This article/publication is based upon work from COST Action CA18122 European Cholangiocarcinoma Network supported by COST (European Cooperation in Science and Technology) www.cost.eu Publisher Copyright: © 2021 The Authors
PY - 2021/6
Y1 - 2021/6
N2 - Background & Aims: The coronavirus disease 2019 (COVID-19) pandemic has posed unprecedented challenges to healthcare systems and it may have heavily impacted patients with liver cancer (LC). Herein, we evaluated whether the schedule of LC screening or procedures has been interrupted or delayed because of the COVID-19 pandemic. Methods: An international survey evaluated the impact of the COVID-19 pandemic on clinical practice and clinical trials from March 2020 to June 2020, as the first phase of a multicentre, international, and observational project. The focus was on patients with hepatocellular carcinoma or intrahepatic cholangiocarcinoma, cared for around the world during the first COVID-19 pandemic wave. Results: Ninety-one centres expressed interest to participate and 76 were included in the analysis, from Europe, South America, North America, Asia, and Africa (73.7%, 17.1%, 5.3%, 2.6%, and 1.3% per continent, respectively). Eighty-seven percent of the centres modified their clinical practice: 40.8% the diagnostic procedures, 80.9% the screening programme, 50% cancelled curative and/or palliative treatments for LC, and 41.7% modified the liver transplantation programme. Forty-five out of 69 (65.2%) centres in which clinical trials were running modified their treatments in that setting, but 58.1% were able to recruit new patients. The phone call service was modified in 51.4% of centres which had this service before the COVID-19 pandemic (n = 19/37). Conclusions: The first wave of the COVID-19 pandemic had a tremendous impact on the routine care of patients with liver cancer. Modifications in screening, diagnostic, and treatment algorithms may have significantly impaired the outcome of patients. Ongoing data collection and future analyses will report the benefits and disadvantages of the strategies implemented, aiding future decision-making. Lay summary: The coronavirus disease 2019 (COVID-19) pandemic has posed unprecedented challenges to healthcare systems globally. Herein, we assessed the impact of the first wave pandemic on patients with liver cancer and found that routine care for these patients has been majorly disrupted, which could have a significant impact on outcomes.
AB - Background & Aims: The coronavirus disease 2019 (COVID-19) pandemic has posed unprecedented challenges to healthcare systems and it may have heavily impacted patients with liver cancer (LC). Herein, we evaluated whether the schedule of LC screening or procedures has been interrupted or delayed because of the COVID-19 pandemic. Methods: An international survey evaluated the impact of the COVID-19 pandemic on clinical practice and clinical trials from March 2020 to June 2020, as the first phase of a multicentre, international, and observational project. The focus was on patients with hepatocellular carcinoma or intrahepatic cholangiocarcinoma, cared for around the world during the first COVID-19 pandemic wave. Results: Ninety-one centres expressed interest to participate and 76 were included in the analysis, from Europe, South America, North America, Asia, and Africa (73.7%, 17.1%, 5.3%, 2.6%, and 1.3% per continent, respectively). Eighty-seven percent of the centres modified their clinical practice: 40.8% the diagnostic procedures, 80.9% the screening programme, 50% cancelled curative and/or palliative treatments for LC, and 41.7% modified the liver transplantation programme. Forty-five out of 69 (65.2%) centres in which clinical trials were running modified their treatments in that setting, but 58.1% were able to recruit new patients. The phone call service was modified in 51.4% of centres which had this service before the COVID-19 pandemic (n = 19/37). Conclusions: The first wave of the COVID-19 pandemic had a tremendous impact on the routine care of patients with liver cancer. Modifications in screening, diagnostic, and treatment algorithms may have significantly impaired the outcome of patients. Ongoing data collection and future analyses will report the benefits and disadvantages of the strategies implemented, aiding future decision-making. Lay summary: The coronavirus disease 2019 (COVID-19) pandemic has posed unprecedented challenges to healthcare systems globally. Herein, we assessed the impact of the first wave pandemic on patients with liver cancer and found that routine care for these patients has been majorly disrupted, which could have a significant impact on outcomes.
KW - COVID-19
KW - Cholangiocarcinoma
KW - Clinical trials
KW - Hepatocellular carcinoma
KW - Liver cancer
KW - Management
KW - Nurses
UR - http://www.scopus.com/inward/record.url?scp=85105461585&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85105461585&partnerID=8YFLogxK
U2 - 10.1016/j.jhepr.2021.100260
DO - 10.1016/j.jhepr.2021.100260
M3 - Article
C2 - 33644725
AN - SCOPUS:85105461585
SN - 2589-5559
VL - 3
JO - JHEP Reports
JF - JHEP Reports
IS - 3
M1 - 100260
ER -