Transarterial chemoembolization (TACE) combined with donafenib as first-line therapy for unresectable hepatocellular carcinoma (uHCC): A real-world clinical study
e16145Background: To evaluate the efficacy and safety of TACE combined with Donafenib, which is as a new tyrosine kinase inhibitors therapy recommended by the China liver cancer staging (CNLC) system for the treatment of unresectable hepatocellular carcinoma (uHCC). Methods: We conducted a single-ce...
Saved in:
Published in | Journal of clinical oncology Vol. 42; no. 16_suppl; p. e16145 |
---|---|
Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
American Society of Clinical Oncology
01.06.2024
|
Online Access | Get full text |
ISSN | 0732-183X 1527-7755 |
DOI | 10.1200/JCO.2024.42.16_suppl.e16145 |
Cover
Abstract | e16145Background: To evaluate the efficacy and safety of TACE combined with Donafenib, which is as a new tyrosine kinase inhibitors therapy recommended by the China liver cancer staging (CNLC) system for the treatment of unresectable hepatocellular carcinoma (uHCC). Methods: We conducted a single-center, retrospective study on patients diagnosed with uHCC treated by TACE plus Donafenib as the first-line therapy between May 2021 and September 2023 at The First Affiliated Hospital of Sun Yat-sen University. The primary outcomes evaluated in this study were progression-free survival (PFS) and overall survival (OS). Local response, one-year survival rate, safety and tolerability were the secondary outcomes. Results: All of 48 eligible patients by August, 2023, with the median age of 59 years. The clinical characteristics were as follows: BCLC stage A:2 (4.2%), B:16 (33.3%), and C:30 (62.5%); Child-Pugh class A:33 (68.8%) and B:15 (31.2%); ECOG PS 0: 27 (56.2%) and 1: 21 (43.7%). In this study, 10 (20.8%) patients had huge intrahepatic lesions, 15 (31.2%) subjects exhibited extrahepatic metastases at multiple sites, 19 (42.2%) patients presented with portal vein tumor thrombus, and 4 patients were diffuse-type HCC.107 TACE sessions were performed. Three patients had liver transplantation as frequent therapy, and histopathological examination of tissue from these subjects revealed complete necrotic foci. The median PFS was 12.8 months (95% CI: 8.66-NA) , mOS was not reached and the one-year OS rate was 87.5% (95% CI: 77%-97%) in the survival results. The tumor objective response rate was 58.3% with 14.5% complete response and 43.7% partial response based on mRECIST assessment. The disease control rate of the study group was 81.3%. The most common treatment-related adverse events (TRAEs) observed were elevated aspartate aminotransferase (AST) levels (75.0%), increase in bilirubin level (72.9%), elevated alanine aminotransferase (ALT) levels (54.2%), hand-foot syndrome (53.1%), diarrhea (29.1%), rashes (22.9%), hair loss (18.4%) and hypertension (12.5%). Twenty-three (46.9%) patients presented with grade 3 or 4 TRAEs including elevated AST levels (22.4%), elevated ALT levels (16.3%), increase in bilirubin level (4%), diarrhea (4%) and hypertension (2%). No Grade 5 TRAEs were observed. Conclusions: The combination of TACE and Donafenib presented good efficacy and tolerability, which could be potentially used as the first-line treatment of Chinese uHCC patients. |
---|---|
AbstractList | e16145Background: To evaluate the efficacy and safety of TACE combined with Donafenib, which is as a new tyrosine kinase inhibitors therapy recommended by the China liver cancer staging (CNLC) system for the treatment of unresectable hepatocellular carcinoma (uHCC). Methods: We conducted a single-center, retrospective study on patients diagnosed with uHCC treated by TACE plus Donafenib as the first-line therapy between May 2021 and September 2023 at The First Affiliated Hospital of Sun Yat-sen University. The primary outcomes evaluated in this study were progression-free survival (PFS) and overall survival (OS). Local response, one-year survival rate, safety and tolerability were the secondary outcomes. Results: All of 48 eligible patients by August, 2023, with the median age of 59 years. The clinical characteristics were as follows: BCLC stage A:2 (4.2%), B:16 (33.3%), and C:30 (62.5%); Child-Pugh class A:33 (68.8%) and B:15 (31.2%); ECOG PS 0: 27 (56.2%) and 1: 21 (43.7%). In this study, 10 (20.8%) patients had huge intrahepatic lesions, 15 (31.2%) subjects exhibited extrahepatic metastases at multiple sites, 19 (42.2%) patients presented with portal vein tumor thrombus, and 4 patients were diffuse-type HCC.107 TACE sessions were performed. Three patients had liver transplantation as frequent therapy, and histopathological examination of tissue from these subjects revealed complete necrotic foci. The median PFS was 12.8 months (95% CI: 8.66-NA) , mOS was not reached and the one-year OS rate was 87.5% (95% CI: 77%-97%) in the survival results. The tumor objective response rate was 58.3% with 14.5% complete response and 43.7% partial response based on mRECIST assessment. The disease control rate of the study group was 81.3%. The most common treatment-related adverse events (TRAEs) observed were elevated aspartate aminotransferase (AST) levels (75.0%), increase in bilirubin level (72.9%), elevated alanine aminotransferase (ALT) levels (54.2%), hand-foot syndrome (53.1%), diarrhea (29.1%), rashes (22.9%), hair loss (18.4%) and hypertension (12.5%). Twenty-three (46.9%) patients presented with grade 3 or 4 TRAEs including elevated AST levels (22.4%), elevated ALT levels (16.3%), increase in bilirubin level (4%), diarrhea (4%) and hypertension (2%). No Grade 5 TRAEs were observed. Conclusions: The combination of TACE and Donafenib presented good efficacy and tolerability, which could be potentially used as the first-line treatment of Chinese uHCC patients. e16145 Background: To evaluate the efficacy and safety of TACE combined with Donafenib, which is as a new tyrosine kinase inhibitors therapy recommended by the China liver cancer staging (CNLC) system for the treatment of unresectable hepatocellular carcinoma (uHCC). Methods: We conducted a single-center, retrospective study on patients diagnosed with uHCC treated by TACE plus Donafenib as the first-line therapy between May 2021 and September 2023 at The First Affiliated Hospital of Sun Yat-sen University. The primary outcomes evaluated in this study were progression-free survival (PFS) and overall survival (OS). Local response, one-year survival rate, safety and tolerability were the secondary outcomes. Results: All of 48 eligible patients by August, 2023, with the median age of 59 years. The clinical characteristics were as follows: BCLC stage A:2 (4.2%), B:16 (33.3%), and C:30 (62.5%); Child-Pugh class A:33 (68.8%) and B:15 (31.2%); ECOG PS 0: 27 (56.2%) and 1: 21 (43.7%). In this study, 10 (20.8%) patients had huge intrahepatic lesions, 15 (31.2%) subjects exhibited extrahepatic metastases at multiple sites, 19 (42.2%) patients presented with portal vein tumor thrombus, and 4 patients were diffuse-type HCC.107 TACE sessions were performed. Three patients had liver transplantation as frequent therapy, and histopathological examination of tissue from these subjects revealed complete necrotic foci. The median PFS was 12.8 months (95% CI: 8.66–NA) , mOS was not reached and the one-year OS rate was 87.5% (95% CI: 77%-97%) in the survival results. The tumor objective response rate was 58.3% with 14.5% complete response and 43.7% partial response based on mRECIST assessment. The disease control rate of the study group was 81.3%. The most common treatment-related adverse events (TRAEs) observed were elevated aspartate aminotransferase (AST) levels (75.0%), increase in bilirubin level (72.9%), elevated alanine aminotransferase (ALT) levels (54.2%), hand-foot syndrome (53.1%), diarrhea (29.1%), rashes (22.9%), hair loss (18.4%) and hypertension (12.5%). Twenty-three (46.9%) patients presented with grade 3 or 4 TRAEs including elevated AST levels (22.4%), elevated ALT levels (16.3%), increase in bilirubin level (4%), diarrhea (4%) and hypertension (2%). No Grade 5 TRAEs were observed. Conclusions: The combination of TACE and Donafenib presented good efficacy and tolerability, which could be potentially used as the first-line treatment of Chinese uHCC patients. |
Author | Tang, Yiyang Zhao, Yue Zhu, Bowen Wu, Yanqin Fan, Wenzhe Xue, Miao |
Author_xml | – sequence: 1 givenname: Bowen surname: Zhu fullname: Zhu, Bowen – sequence: 2 givenname: Yiyang surname: Tang fullname: Tang, Yiyang – sequence: 3 givenname: Miao surname: Xue fullname: Xue, Miao – sequence: 4 givenname: Yanqin surname: Wu fullname: Wu, Yanqin – sequence: 5 givenname: Yue surname: Zhao fullname: Zhao, Yue – sequence: 6 givenname: Wenzhe surname: Fan fullname: Fan, Wenzhe |
BookMark | eNqN0E1r3DAQBmBRUugm6X8Q9JIc7Eqy5I_2UBaTj4ZALlvoTYzlMVYrW0aSWbY_p7-0Dtvee5rD8L7MPJfkYvYzEvKBs5wLxj4-tS-5YELmUuS81HFdFpcjL7lUb8iOK1FlVaXUBdmxqhAZr4vv78hljD8Y47Iu1I78PgSYI4SEwYKjZsTJ49R5Z39Bsn6mN4d9e3dLjZ86O2NPjzaNtPczDDjbjkKkgw0xZW7b0jRigOVEBx_oOgeMaBJ0DumICyRv0LnVQaAGgrGzn4DerI9te_uJ7mlAcNnRB9dTs5VZs50T09qfrsnbAVzE93_nFfl2f3doH7Pnl4ev7f45M5zVKisGMxS8Y6U0HW96VTQDVliaAlQpBPLO9Ir1YmhAyh6FUE2JHCWwmhlooC6uyOdzrwk-xoCDXoKdIJw0Z_qVW2_c-pVbS6H_cesz95b-ck4fvdsw40-3HjHocfsqjf_V8Adj5JE4 |
ContentType | Journal Article |
Copyright | 2024 by American Society of Clinical Oncology |
Copyright_xml | – notice: 2024 by American Society of Clinical Oncology |
DBID | AAYXX CITATION |
DOI | 10.1200/JCO.2024.42.16_suppl.e16145 |
DatabaseName | CrossRef |
DatabaseTitle | CrossRef |
DatabaseTitleList | CrossRef |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine Pharmacy, Therapeutics, & Pharmacology |
EISSN | 1527-7755 |
EndPage | e16145 |
ExternalDocumentID | 10_1200_JCO_2024_42_16_suppl_e16145 444924 |
Genre | meeting-report |
GrantInformation_xml | – fundername: None. |
GroupedDBID | --- .55 0R~ 18M 34G 39C 4.4 53G 5GY 5RE 8F7 AAQQT AARDX AAWTL AAYEP ABJNI ABOCM ACGFO ACGFS ACGUR ADBBV AEGXH AENEX AIAGR ALMA_UNASSIGNED_HOLDINGS BAWUL BYPQX C45 CS3 DIK EBS EJD F5P F9R FBNNL FD8 GX1 HZ~ IH2 IPNFZ K-O KQ8 L7B LSO MJL N9A O9- OK1 OVD OWW P2P QTD R1G RHI RIG RLZ RUC SJN TEORI TR2 TWZ UDS VVN WH7 X7M YFH YQY 2WC AAYXX ABBLC CITATION |
ID | FETCH-LOGICAL-c1085-3fcf31b064cb19d539fe7e6c3a5622e1bcd50d2f9a44de22596e1e4a080ca9a83 |
ISSN | 0732-183X |
IngestDate | Tue Jul 01 01:38:06 EDT 2025 Wed Apr 16 02:24:34 EDT 2025 |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 16_suppl |
Language | English |
LinkModel | OpenURL |
MergedId | FETCHMERGED-LOGICAL-c1085-3fcf31b064cb19d539fe7e6c3a5622e1bcd50d2f9a44de22596e1e4a080ca9a83 |
Notes | Abstract Disclosures |
PageCount | 334 |
ParticipantIDs | crossref_primary_10_1200_JCO_2024_42_16_suppl_e16145 wolterskluwer_health_10_1200_JCO_2024_42_16_suppl_e16145 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 20240601 2024-06-01 |
PublicationDateYYYYMMDD | 2024-06-01 |
PublicationDate_xml | – month: 6 year: 2024 text: 20240601 day: 1 |
PublicationDecade | 2020 |
PublicationTitle | Journal of clinical oncology |
PublicationTitleAbbrev | ASCO MEETING ABSTRACTS |
PublicationYear | 2024 |
Publisher | American Society of Clinical Oncology |
Publisher_xml | – name: American Society of Clinical Oncology |
SSID | ssj0014835 |
Score | 2.4562366 |
Snippet | e16145Background: To evaluate the efficacy and safety of TACE combined with Donafenib, which is as a new tyrosine kinase inhibitors therapy recommended by the... e16145 Background: To evaluate the efficacy and safety of TACE combined with Donafenib, which is as a new tyrosine kinase inhibitors therapy recommended by the... |
SourceID | crossref wolterskluwer |
SourceType | Index Database Publisher |
StartPage | e16145 |
Title | Transarterial chemoembolization (TACE) combined with donafenib as first-line therapy for unresectable hepatocellular carcinoma (uHCC): A real-world clinical study |
URI | https://ovidsp.ovid.com/ovidweb.cgi?T=JS&NEWS=n&CSC=Y&PAGE=fulltext&D=ovft&DO=10.1200/JCO.2024.42.16_suppl.e16145 |
Volume | 42 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
journalDatabaseRights | – providerCode: PRVAFT databaseName: Open Access Digital Library customDbUrl: eissn: 1527-7755 dateEnd: 99991231 omitProxy: true ssIdentifier: ssj0014835 issn: 0732-183X databaseCode: KQ8 dateStart: 19990101 isFulltext: true titleUrlDefault: http://grweb.coalliance.org/oadl/oadl.html providerName: Colorado Alliance of Research Libraries – providerCode: PRVBFR databaseName: Free Medical Journals customDbUrl: eissn: 1527-7755 dateEnd: 20241003 omitProxy: true ssIdentifier: ssj0014835 issn: 0732-183X databaseCode: DIK dateStart: 20040101 isFulltext: true titleUrlDefault: http://www.freemedicaljournals.com providerName: Flying Publisher – providerCode: PRVFQY databaseName: GFMER Free Medical Journals customDbUrl: eissn: 1527-7755 dateEnd: 20241003 omitProxy: true ssIdentifier: ssj0014835 issn: 0732-183X databaseCode: GX1 dateStart: 20040101 isFulltext: true titleUrlDefault: http://www.gfmer.ch/Medical_journals/Free_medical.php providerName: Geneva Foundation for Medical Education and Research |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1ba9swFBZtB2VsjK3bWHdDsFFaqNNEVux6b8FryW5JHlJI92IkW6Zhjb0tMaX7OfulO0eSb2SMri8myDc55_O5yOc7h5C32LoKlKN0-lL4Dvc85oARTuC94okMEoYmF7MtRt7wjH-c9Wcbm_caWUvFSnbiX3_lldxGqjAGckWW7H9ItrooDMBvkC9sQcKwvZmMdbNvTMrEdW_4-xe5Wsj80nIr0XucDsITjPzh9hADl7nmCfjfqcrmEtvMpHPwAB3tbho2lsnhLHQhoHiluVUXYLVWOa7y67TVGDsQZflC4C2KYRjCLQzHHXzQS0eXYW2QLqsStutecHVQnsWtFf6vF4XGXn5Vk9WmdnH7fH4trMWF0VlhVtfnIq9MjD73XGQ_bGFxu67BeJ1_1aASoI6z2auYnVJOadycklGWvsscUE8zY9esMmc-RA-mDHCp7TlrotqLltg8taHBFbjApsCl9QfqgTVrw0wj7XDcwQfocNYpL9hpXqZZ43s0jibvT6PPH0af2ju1S8E5h3h4k9xhPrw1SF2fVQlLELeadrHlk26TN3YSR_-YQsvfun-VYw7G8pumYDQcqelD8sDKng4MnB-RDZXtkO0vNsdjh-xNTDX160M6rcmBy0O6Ryd1nfXrx-R3C_50Df50H8F_QEvoU4Q-raBPxZLW0KcW-hSgT5vQp23o0wr6dB-Bf_CODmgNelrimWrQPyFnpyfTcOjYliNOrGk4bhqnbk-Cnx7LXpD03SBVvvJiV4DSYqon46TfTVgaCM4TBbYw8FRPcQFxVywCcew-JVtZnqlnhErl-YnPmQ97eTd2pdcTARybdhXS49Qu4aVgou-mskyEETnDz8vhOEJ5RpxFpTwjI89dctwSYmT40jc59fntT31B7tbv6EuytfpZqFfgja_kaw3SP24g5AA |
linkProvider | Geneva Foundation for Medical Education and Research |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Transarterial+chemoembolization+%28TACE%29+combined+with+donafenib+as+first-line+therapy+for+unresectable+hepatocellular+carcinoma+%28uHCC%29%3A+A+real-world+clinical+study&rft.jtitle=Journal+of+clinical+oncology&rft.au=Zhu%2C+Bowen&rft.au=Tang%2C+Yiyang&rft.au=Xue%2C+Miao&rft.au=Wu%2C+Yanqin&rft.date=2024-06-01&rft.pub=American+Society+of+Clinical+Oncology&rft.issn=0732-183X&rft.eissn=1527-7755&rft.volume=42&rft.issue=16_suppl&rft.spage=e16145&rft.epage=e16145&rft_id=info:doi/10.1200%2FJCO.2024.42.16_suppl.e16145&rft.externalDBID=NO_PDF_LINK&rft.externalDocID=444924 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0732-183X&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0732-183X&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0732-183X&client=summon |