Real-world efficacy and safety of TACE-HAIC combined with TKIs and PD-1 inhibitors in initially unresectable hepatocellular carcinoma
•Efficacy and safety of TACE and HAIC combined with TKIs and PD-1 inhibitors in unresectable hepatocellular carcinoma (uHCC) were evaluated.•Key findings: median overall survival (OS) 18.2 months, progression-free survival (PFS) 9.2 months, objective response rate (ORR) 67.7 %, disease control rate...
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creator | Pang, Beichuan Zuo, Bangyou Huang, Liang You, Xinyu Liu, Tao Hao, Jianjie Yuan, Chengxiang Yang, Chong Yee Lau, Wan Zhang, Yu |
description | •Efficacy and safety of TACE and HAIC combined with TKIs and PD-1 inhibitors in unresectable hepatocellular carcinoma (uHCC) were evaluated.•Key findings: median overall survival (OS) 18.2 months, progression-free survival (PFS) 9.2 months, objective response rate (ORR) 67.7 %, disease control rate (DCR) 90.3 %, and conversion surgery rate (CSR) 27.4 %.•Converted patients is superior to that of other enrolled patients on OS and PFS.•Main adverse events included transaminitis, nausea, and fever.•This combination therapy demonstrates effectiveness, particularly in enhancing survival post-surgery in uHCC patients.
Local treatment may function synergistically with immunotherapy and targeted agents. This study aimed to assess the effectiveness and safety of transcatheter arterial chemoembolization (TACE) and hepatic artery infusion chemotherapy (HAIC) combined with tyrosine kinase inhibitors (TKIs) and programmed death-1 (PD-1) inhibitors in patients with initially unresectable hepatocellular carcinoma (uHCC).
A retrospective study was conducted on patients diagnosed with initially uHCC who received combined treatment of TACE-HAIC combined with TKIs and PD-1 inhibitors from July 2020 to February 2023. The primary endpoints were overall survival (OS) and progression free survival (PFS) and adverse events (AEs). Objective response rate (ORR), disease control rate (DCR) and conversion surgery rate (CSR), whereas the secondary endpoints.
After screening, a total of 62 patients were selected for this study. The overall median OS was 18.2 (95% CI 16.24–20.16) months and median PFS was 9.2 (95% CI 7.24–11.16) months. Based on the modified Response Evaluation Criteria in Solid Tumors (mRECIST) criteria and RECIST v1.1 criteria, ORR was 67.7% (42/62), and the DCR was 90.3% (56/62), the CSR was 27.4% (17/62). The most common treatment-emergent adverse events (TEAEs) were transaminitis (56.4%, 35/62), nausea and vomiting (43.5%, 27/62), thrombocytopenia (37.1%, 23/62), abdominal pain (33.9%, 21/62), and fever (33.9%, 21/62).
TKIs combined with PD-1 inhibitors plus TACE-HAIC therapy represents an effective and tolerable treatment option in patients with uHCC. Patients undergoing surgery after combination therapy may have survival benefits. |
doi_str_mv | 10.1016/j.intimp.2024.112492 |
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Local treatment may function synergistically with immunotherapy and targeted agents. This study aimed to assess the effectiveness and safety of transcatheter arterial chemoembolization (TACE) and hepatic artery infusion chemotherapy (HAIC) combined with tyrosine kinase inhibitors (TKIs) and programmed death-1 (PD-1) inhibitors in patients with initially unresectable hepatocellular carcinoma (uHCC).
A retrospective study was conducted on patients diagnosed with initially uHCC who received combined treatment of TACE-HAIC combined with TKIs and PD-1 inhibitors from July 2020 to February 2023. The primary endpoints were overall survival (OS) and progression free survival (PFS) and adverse events (AEs). Objective response rate (ORR), disease control rate (DCR) and conversion surgery rate (CSR), whereas the secondary endpoints.
After screening, a total of 62 patients were selected for this study. The overall median OS was 18.2 (95% CI 16.24–20.16) months and median PFS was 9.2 (95% CI 7.24–11.16) months. Based on the modified Response Evaluation Criteria in Solid Tumors (mRECIST) criteria and RECIST v1.1 criteria, ORR was 67.7% (42/62), and the DCR was 90.3% (56/62), the CSR was 27.4% (17/62). The most common treatment-emergent adverse events (TEAEs) were transaminitis (56.4%, 35/62), nausea and vomiting (43.5%, 27/62), thrombocytopenia (37.1%, 23/62), abdominal pain (33.9%, 21/62), and fever (33.9%, 21/62).
TKIs combined with PD-1 inhibitors plus TACE-HAIC therapy represents an effective and tolerable treatment option in patients with uHCC. Patients undergoing surgery after combination therapy may have survival benefits.</description><identifier>ISSN: 1567-5769</identifier><identifier>ISSN: 1878-1705</identifier><identifier>EISSN: 1878-1705</identifier><identifier>DOI: 10.1016/j.intimp.2024.112492</identifier><identifier>PMID: 38906005</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Adult ; Aged ; Antineoplastic Combined Chemotherapy Protocols - adverse effects ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Carcinoma, Hepatocellular - drug therapy ; Carcinoma, Hepatocellular - mortality ; Carcinoma, Hepatocellular - therapy ; Chemoembolization, Therapeutic - adverse effects ; Chemoembolization, Therapeutic - methods ; Combined Modality Therapy ; Conversion therapy ; Female ; HAIC ; Hepatic Artery ; Hepatocellular carcinoma ; Humans ; Immune Checkpoint Inhibitors - adverse effects ; Immune Checkpoint Inhibitors - therapeutic use ; Infusions, Intra-Arterial ; Liver Neoplasms - drug therapy ; Liver Neoplasms - mortality ; Liver Neoplasms - therapy ; Male ; Middle Aged ; Programmed Cell Death 1 Receptor - antagonists & inhibitors ; Protein Kinase Inhibitors - administration & dosage ; Protein Kinase Inhibitors - adverse effects ; Protein Kinase Inhibitors - therapeutic use ; Retrospective Studies ; Systemic treatment ; TACE ; Treatment Outcome</subject><ispartof>International immunopharmacology, 2024-08, Vol.137, p.112492, Article 112492</ispartof><rights>2024 Elsevier B.V.</rights><rights>Copyright © 2024 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c241t-54c562a9325ad98053cdeac3087ed26fd0bb34f88542e7e95b9f020154fb9823</cites><orcidid>0000-0002-9191-7708</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.intimp.2024.112492$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38906005$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pang, Beichuan</creatorcontrib><creatorcontrib>Zuo, Bangyou</creatorcontrib><creatorcontrib>Huang, Liang</creatorcontrib><creatorcontrib>You, Xinyu</creatorcontrib><creatorcontrib>Liu, Tao</creatorcontrib><creatorcontrib>Hao, Jianjie</creatorcontrib><creatorcontrib>Yuan, Chengxiang</creatorcontrib><creatorcontrib>Yang, Chong</creatorcontrib><creatorcontrib>Yee Lau, Wan</creatorcontrib><creatorcontrib>Zhang, Yu</creatorcontrib><title>Real-world efficacy and safety of TACE-HAIC combined with TKIs and PD-1 inhibitors in initially unresectable hepatocellular carcinoma</title><title>International immunopharmacology</title><addtitle>Int Immunopharmacol</addtitle><description>•Efficacy and safety of TACE and HAIC combined with TKIs and PD-1 inhibitors in unresectable hepatocellular carcinoma (uHCC) were evaluated.•Key findings: median overall survival (OS) 18.2 months, progression-free survival (PFS) 9.2 months, objective response rate (ORR) 67.7 %, disease control rate (DCR) 90.3 %, and conversion surgery rate (CSR) 27.4 %.•Converted patients is superior to that of other enrolled patients on OS and PFS.•Main adverse events included transaminitis, nausea, and fever.•This combination therapy demonstrates effectiveness, particularly in enhancing survival post-surgery in uHCC patients.
Local treatment may function synergistically with immunotherapy and targeted agents. This study aimed to assess the effectiveness and safety of transcatheter arterial chemoembolization (TACE) and hepatic artery infusion chemotherapy (HAIC) combined with tyrosine kinase inhibitors (TKIs) and programmed death-1 (PD-1) inhibitors in patients with initially unresectable hepatocellular carcinoma (uHCC).
A retrospective study was conducted on patients diagnosed with initially uHCC who received combined treatment of TACE-HAIC combined with TKIs and PD-1 inhibitors from July 2020 to February 2023. The primary endpoints were overall survival (OS) and progression free survival (PFS) and adverse events (AEs). Objective response rate (ORR), disease control rate (DCR) and conversion surgery rate (CSR), whereas the secondary endpoints.
After screening, a total of 62 patients were selected for this study. The overall median OS was 18.2 (95% CI 16.24–20.16) months and median PFS was 9.2 (95% CI 7.24–11.16) months. Based on the modified Response Evaluation Criteria in Solid Tumors (mRECIST) criteria and RECIST v1.1 criteria, ORR was 67.7% (42/62), and the DCR was 90.3% (56/62), the CSR was 27.4% (17/62). The most common treatment-emergent adverse events (TEAEs) were transaminitis (56.4%, 35/62), nausea and vomiting (43.5%, 27/62), thrombocytopenia (37.1%, 23/62), abdominal pain (33.9%, 21/62), and fever (33.9%, 21/62).
TKIs combined with PD-1 inhibitors plus TACE-HAIC therapy represents an effective and tolerable treatment option in patients with uHCC. Patients undergoing surgery after combination therapy may have survival benefits.</description><subject>Adult</subject><subject>Aged</subject><subject>Antineoplastic Combined Chemotherapy Protocols - adverse effects</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Carcinoma, Hepatocellular - drug therapy</subject><subject>Carcinoma, Hepatocellular - mortality</subject><subject>Carcinoma, Hepatocellular - therapy</subject><subject>Chemoembolization, Therapeutic - adverse effects</subject><subject>Chemoembolization, Therapeutic - methods</subject><subject>Combined Modality Therapy</subject><subject>Conversion therapy</subject><subject>Female</subject><subject>HAIC</subject><subject>Hepatic Artery</subject><subject>Hepatocellular carcinoma</subject><subject>Humans</subject><subject>Immune Checkpoint Inhibitors - adverse effects</subject><subject>Immune Checkpoint Inhibitors - therapeutic use</subject><subject>Infusions, Intra-Arterial</subject><subject>Liver Neoplasms - drug therapy</subject><subject>Liver Neoplasms - mortality</subject><subject>Liver Neoplasms - therapy</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Programmed Cell Death 1 Receptor - antagonists & inhibitors</subject><subject>Protein Kinase Inhibitors - administration & dosage</subject><subject>Protein Kinase Inhibitors - adverse effects</subject><subject>Protein Kinase Inhibitors - therapeutic use</subject><subject>Retrospective Studies</subject><subject>Systemic treatment</subject><subject>TACE</subject><subject>Treatment Outcome</subject><issn>1567-5769</issn><issn>1878-1705</issn><issn>1878-1705</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kN1qFDEUgINYbK2-gUguvZk1ySQzkxthWatdWmiRvQ-Z5ITNMjNZk0zLPoDvbdapXgqBHA7f-fsQ-kDJihLafD6s_JT9eFwxwviKUsYle4WuaNd2FW2JeF1i0bSVaBt5id6mdCCk5Dl9gy7rTpKGEHGFfv0APVTPIQ4Wg3PeaHPCerI4aQf5hIPDu_XmprpdbzfYhLH3E1j87PMe7-626Q_6-LWi2E973_scYipheT57PQwnPE8REpis-wHwHo46BwPDMA86YqOj8VMY9Tt04fSQ4P3Lf4123252m9vq_uH7drO-rwzjNFeCG9EwLWsmtJUdEbWxoE1NuhYsa5wlfV9z13WCM2hBil46wggV3PWyY_U1-rS0Pcbwc4aU1ejTeRs9QZiTqklLS6-ulQXlC2piSCmCU8foRx1PihJ19q8OavGvzv7V4r-UfXyZMPcj2H9Ff4UX4MsCQDnzyUNUyXiYDFgfiyVlg___hN-utZjB</recordid><startdate>20240820</startdate><enddate>20240820</enddate><creator>Pang, Beichuan</creator><creator>Zuo, Bangyou</creator><creator>Huang, Liang</creator><creator>You, Xinyu</creator><creator>Liu, Tao</creator><creator>Hao, Jianjie</creator><creator>Yuan, Chengxiang</creator><creator>Yang, Chong</creator><creator>Yee Lau, Wan</creator><creator>Zhang, Yu</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-9191-7708</orcidid></search><sort><creationdate>20240820</creationdate><title>Real-world efficacy and safety of TACE-HAIC combined with TKIs and PD-1 inhibitors in initially unresectable hepatocellular carcinoma</title><author>Pang, Beichuan ; Zuo, Bangyou ; Huang, Liang ; You, Xinyu ; Liu, Tao ; Hao, Jianjie ; Yuan, Chengxiang ; Yang, Chong ; Yee Lau, Wan ; Zhang, Yu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c241t-54c562a9325ad98053cdeac3087ed26fd0bb34f88542e7e95b9f020154fb9823</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Antineoplastic Combined Chemotherapy Protocols - adverse effects</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Carcinoma, Hepatocellular - drug therapy</topic><topic>Carcinoma, Hepatocellular - mortality</topic><topic>Carcinoma, Hepatocellular - therapy</topic><topic>Chemoembolization, Therapeutic - adverse effects</topic><topic>Chemoembolization, Therapeutic - methods</topic><topic>Combined Modality Therapy</topic><topic>Conversion therapy</topic><topic>Female</topic><topic>HAIC</topic><topic>Hepatic Artery</topic><topic>Hepatocellular carcinoma</topic><topic>Humans</topic><topic>Immune Checkpoint Inhibitors - adverse effects</topic><topic>Immune Checkpoint Inhibitors - therapeutic use</topic><topic>Infusions, Intra-Arterial</topic><topic>Liver Neoplasms - drug therapy</topic><topic>Liver Neoplasms - mortality</topic><topic>Liver Neoplasms - therapy</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Programmed Cell Death 1 Receptor - antagonists & inhibitors</topic><topic>Protein Kinase Inhibitors - administration & dosage</topic><topic>Protein Kinase Inhibitors - adverse effects</topic><topic>Protein Kinase Inhibitors - therapeutic use</topic><topic>Retrospective Studies</topic><topic>Systemic treatment</topic><topic>TACE</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pang, Beichuan</creatorcontrib><creatorcontrib>Zuo, Bangyou</creatorcontrib><creatorcontrib>Huang, Liang</creatorcontrib><creatorcontrib>You, Xinyu</creatorcontrib><creatorcontrib>Liu, Tao</creatorcontrib><creatorcontrib>Hao, Jianjie</creatorcontrib><creatorcontrib>Yuan, Chengxiang</creatorcontrib><creatorcontrib>Yang, Chong</creatorcontrib><creatorcontrib>Yee Lau, Wan</creatorcontrib><creatorcontrib>Zhang, Yu</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>International immunopharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pang, Beichuan</au><au>Zuo, Bangyou</au><au>Huang, Liang</au><au>You, Xinyu</au><au>Liu, Tao</au><au>Hao, Jianjie</au><au>Yuan, Chengxiang</au><au>Yang, Chong</au><au>Yee Lau, Wan</au><au>Zhang, Yu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Real-world efficacy and safety of TACE-HAIC combined with TKIs and PD-1 inhibitors in initially unresectable hepatocellular carcinoma</atitle><jtitle>International immunopharmacology</jtitle><addtitle>Int Immunopharmacol</addtitle><date>2024-08-20</date><risdate>2024</risdate><volume>137</volume><spage>112492</spage><pages>112492-</pages><artnum>112492</artnum><issn>1567-5769</issn><issn>1878-1705</issn><eissn>1878-1705</eissn><abstract>•Efficacy and safety of TACE and HAIC combined with TKIs and PD-1 inhibitors in unresectable hepatocellular carcinoma (uHCC) were evaluated.•Key findings: median overall survival (OS) 18.2 months, progression-free survival (PFS) 9.2 months, objective response rate (ORR) 67.7 %, disease control rate (DCR) 90.3 %, and conversion surgery rate (CSR) 27.4 %.•Converted patients is superior to that of other enrolled patients on OS and PFS.•Main adverse events included transaminitis, nausea, and fever.•This combination therapy demonstrates effectiveness, particularly in enhancing survival post-surgery in uHCC patients.
Local treatment may function synergistically with immunotherapy and targeted agents. This study aimed to assess the effectiveness and safety of transcatheter arterial chemoembolization (TACE) and hepatic artery infusion chemotherapy (HAIC) combined with tyrosine kinase inhibitors (TKIs) and programmed death-1 (PD-1) inhibitors in patients with initially unresectable hepatocellular carcinoma (uHCC).
A retrospective study was conducted on patients diagnosed with initially uHCC who received combined treatment of TACE-HAIC combined with TKIs and PD-1 inhibitors from July 2020 to February 2023. The primary endpoints were overall survival (OS) and progression free survival (PFS) and adverse events (AEs). Objective response rate (ORR), disease control rate (DCR) and conversion surgery rate (CSR), whereas the secondary endpoints.
After screening, a total of 62 patients were selected for this study. The overall median OS was 18.2 (95% CI 16.24–20.16) months and median PFS was 9.2 (95% CI 7.24–11.16) months. Based on the modified Response Evaluation Criteria in Solid Tumors (mRECIST) criteria and RECIST v1.1 criteria, ORR was 67.7% (42/62), and the DCR was 90.3% (56/62), the CSR was 27.4% (17/62). The most common treatment-emergent adverse events (TEAEs) were transaminitis (56.4%, 35/62), nausea and vomiting (43.5%, 27/62), thrombocytopenia (37.1%, 23/62), abdominal pain (33.9%, 21/62), and fever (33.9%, 21/62).
TKIs combined with PD-1 inhibitors plus TACE-HAIC therapy represents an effective and tolerable treatment option in patients with uHCC. Patients undergoing surgery after combination therapy may have survival benefits.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>38906005</pmid><doi>10.1016/j.intimp.2024.112492</doi><orcidid>https://orcid.org/0000-0002-9191-7708</orcidid></addata></record> |
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subjects | Adult Aged Antineoplastic Combined Chemotherapy Protocols - adverse effects Antineoplastic Combined Chemotherapy Protocols - therapeutic use Carcinoma, Hepatocellular - drug therapy Carcinoma, Hepatocellular - mortality Carcinoma, Hepatocellular - therapy Chemoembolization, Therapeutic - adverse effects Chemoembolization, Therapeutic - methods Combined Modality Therapy Conversion therapy Female HAIC Hepatic Artery Hepatocellular carcinoma Humans Immune Checkpoint Inhibitors - adverse effects Immune Checkpoint Inhibitors - therapeutic use Infusions, Intra-Arterial Liver Neoplasms - drug therapy Liver Neoplasms - mortality Liver Neoplasms - therapy Male Middle Aged Programmed Cell Death 1 Receptor - antagonists & inhibitors Protein Kinase Inhibitors - administration & dosage Protein Kinase Inhibitors - adverse effects Protein Kinase Inhibitors - therapeutic use Retrospective Studies Systemic treatment TACE Treatment Outcome |
title | Real-world efficacy and safety of TACE-HAIC combined with TKIs and PD-1 inhibitors in initially unresectable hepatocellular carcinoma |
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