Abstract 962P
Background
Multi-disciplinary teams (MDTs) are key in the hepatocellular carcinoma (HCC) care pathway. They leverage the diverse member expertise to achieve better treatment decisions and patient outcomes compared to a single discipline without peer-discussion. MDTs drive earlier treatment initiation and improved guideline concordant care, positively impacting survival outcomes. Despite their common objective, the constitution and operations of HCC MDTs are variable across hospitals and regions, which may lead to sub-optimal outcomes, such as inconsistencies from numbers of patients treated to survival rates. The previously published framework by the MDT Aid Program (MAP) was used to gather best practices and perceived impact of HCC MDTs.
Methods
Over 130 semi-structured interviews were conducted with MDT members from 24 hospitals across Europe, Canada, US and China. A questionnaire was used to assess MDT member’s perceived impact of HCC MDTs on: MDT status quo (team composition, process), patient pathway (scale, time) and qualitative impact (patient outcomes, cost). Best practices and perceived impact were then pressure tested with 24 working groups within respective hospitals, and a cross-country panel of international HCC experts in a knowledge exchange session.
Results
We obtained 3 sets of results: (1) an optimal HCC MDT structure reflecting the dimensions stated above, (2) 40+ best practices encompassing patient access, MDT operations, technology utilisation, medical practice quality, team capabilities, and (3) insights on MDT members’ perception on the impact of HCC MDTs on patient outcomes and satisfaction. With this, hospital gaps were identified and matched to actionable best practices ready for implementation.
Conclusions
This is the first study to provide insights into specific HCC MDTs ways of working and recommended best practices. This can improve how MDTs are organized and managed globally, ultimately improving patient outcomes. The account of MDT members’ perceived impact of HCC MDTs will be used to inform the design of a real-world evidence study, aiming to quantitatively assess HCC MDTs impact on patient outcomes and healthcare resource utilisation.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
AstraZeneca.
Funding
AstraZeneca.
Disclosure
M.T. Campos Partera: Financial Interests, Personal, Stocks/Shares: AstraZeneca. A. Vogel: Financial Interests, Personal, Advisory Board: Amgen, AstraZeneca, Boehringer Mannheim, Eisai, Incyte, Ipsen, Janssen, MSD, Pierre Fabre, Roche, Servier, Tyra, Tahio; Financial Interests, Personal, Invited Speaker: BMS, Eisai, Ipsen, Lilly, MSD, Roche, AstraZeneca; Financial Interests, Personal, Steering Committee Member: Roche, MSD, BeiGene, Jiangsu Hengrui Medicines. G. Sapisochin: Financial Interests, Personal, Advisory Board: AstraZeneca, Roche, HeparRegeniX; Financial Interests, Personal, Invited Speaker: AstraZeneca, Integra, Chiesi; Financial Interests, Personal, Other, Research study: Novartis; Financial Interests, Personal, Stocks/Shares: Amgen, CVS Health, Gilead, J&J, Merck, Pfizer, UnitedHealth; Financial Interests, Institutional, Coordinating PI: AstraZeneca; Financial Interests, Institutional, Funding: Roche, Stryker. A. Digklia: Financial Interests, Institutional, Invited Speaker: BMS, Roche; Financial Interests, Institutional, Advisory Board: AstraZeneca. G.E. Villadsen: Financial Interests, Personal, Invited Speaker: Sirtex C. Schnatwinkel: Financial Interests, Personal, Stocks/Shares: AstraZeneca, Ipsen. L. Turner: Financial Interests, Personal, Stocks/Shares: AstraZeneca. W. Vereecken: Financial Interests, Personal, Stocks/Shares: AstraZeneca, Merck. A. Moucquot: Financial Interests, Personal, Stocks/Shares: Pfizer, Moderna. H. Naqvi: Financial Interests, Personal, Stocks/Shares: AstraZeneca, Roche, Pfizer, Lily, GE, IBM. All other authors have declared no conflicts of interest.
Resources from the same session
961P - Sodium-glucose co-transporter 2 inhibitors (SGLT2i) improve oncologic outcomes in diabetic patients with hepatocellular carcinoma (HCC): A nationwide database study
Presenter: Chien-Huai Chuang
Session: Poster session 17
963P - Quality-adjusted time without symptoms or toxicity (Q-TWiST) analysis to assess the impact of treatment with camrelizumab + rivoceranib (cam+rivo) on quality of life vs sorafenib (sora) in patients (pts) with unresectable hepatocellular carcinoma (uHCC): Study CARES-310
Presenter: Andrew Moon
Session: Poster session 17
964P - Lenvatinib (L) and sorafenib (S) in patients (pts) with advanced or unresectable hepatocellular carcinoma (uHCC): An international, multicenter, phase IV study (STELLAR)
Presenter: Markus Peck Radosavljevic
Session: Poster session 17
967P - Lenvatinib (L) versus sorafenib (S) second-line therapy in hepatocellular carcinoma (HCC) patients (P) progressed to atezolizumab plus bevacizumab (AB)
Presenter: Mara Persano
Session: Poster session 17
968P - HAIC combined with lenvatinib and PD-1 inhibitors versus lenvatinib plus PD-1 inhibitors for advanced HCC with portal vein tumor thrombosis: A prospective controlled trial
Presenter: Xiaodong Wang
Session: Poster session 17
969P - Lenvatinib versus sorafenib as a second-line option in patients with unresectable hepatocellular carcinoma previously treated with atezolizumab plus bevacizumab: An observational study
Presenter: Pasquale Lombardi
Session: Poster session 17
970P - Comparing clinical outcomes between PD-1 and PD-L1 inhibitors plus bevacizumab combined with hepatic arterial interventional therapies in unresectable hepatocellular carcinoma: A single-center, real-world study
Presenter: Yangxun Pan
Session: Poster session 17
Resources:
Abstract
971P - Chemotherapy combined with lenvatinib and PD-1 may be a potential better alternative optionfor advanced unresectable intrahepatic cholangiocarcinoma: A retrospective real-world study
Presenter: binghua dai
Session: Poster session 17
972P - Efficacy and safety of lenvatinib vs sorafenib in hepatocellular carcinoma: A multi-center real-world study from the LINK Research Network
Presenter: Jung Yong Hong
Session: Poster session 17