Clinical Characteristics, Treatment Patterns, and Outcomes of Patients With Locally Advanced/Metastatic Hepatocellular Carcinoma Treated at the Veterans Health Administration
This study retrospectively reviewed the outcomes of patients with advanced hepatocellular carcinoma (HCC) receiving atezolizumab with bevacizumab (A + B) therapy at the Veterans Health Administration (VHA). Patients with advanced HCC who received first-line systemic therapy with A + B at the VHA bet...
Gespeichert in:
Veröffentlicht in: | The oncologist (Dayton, Ohio) Ohio), 2024-05, Vol.29 (5), p.369-376 |
---|---|
Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 376 |
---|---|
container_issue | 5 |
container_start_page | 369 |
container_title | The oncologist (Dayton, Ohio) |
container_volume | 29 |
creator | Alkadimi, Munaf A Aldawoodi, Tamarah A Lucero, Kana T Fierro, Maria E Boyle, Lauren D Mader, Michael J Franklin, Kathleen R Arora, Sukeshi P Nooruddin, Zohra |
description | This study retrospectively reviewed the outcomes of patients with advanced hepatocellular carcinoma (HCC) receiving atezolizumab with bevacizumab (A + B) therapy at the Veterans Health Administration (VHA).
Patients with advanced HCC who received first-line systemic therapy with A + B at the VHA between December 1, 2019, and March 1, 2022, were selected from electronic medical records (EMR) using ICD-9 and ICD-10 codes. Abstractors reviewed the EMR of the patients from their index date of A + B initiation until death or their last VHA visit, with the study period ending on January 31, 2023. The chi-square test was used to compare rates, and the Mann-Whitney test was used to compare medians.
A total of 332 patients met the study criteria. The median age was 67 years; 99% were male, 63% were non-Hispanic Whites, 26% were Black, and 66% had an Eastern Cooperative Oncology Group performance status of ≥1. 84% had child Pugh score (CPS) class A, 16% had CPS classes B and C, 62% had a grade 2 albumin-bilirubin score, 56% had HCC caused by viral hepatitis, 80% had cirrhosis, and 67% had received prior local therapies. The 6-month progression-free survival (PFS) was 59%, while the 1-year PFS rate was 36%. Overall survival (OS) at 1-year was 52% in our study.
In real world, despite having similar PFS as the phase III IMbrave 150 trial, our OS at 12 months was lower (52% vs. 67%) because our study included a higher proportion of elderly patients with moderate liver dysfunction and a 40% non-White. This study provided real-world outcomes that differed from the study population in a pivotal trial. |
doi_str_mv | 10.1093/oncolo/oyad343 |
format | Article |
fullrecord | <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_miscellaneous_2917860459</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A795056541</galeid><sourcerecordid>A795056541</sourcerecordid><originalsourceid>FETCH-LOGICAL-c357t-22318985147900d80030ec58d9dba06dfcebba84de83489ab9ced08420ca5f753</originalsourceid><addsrcrecordid>eNptkU-P0zAQxS0EYpfClSOyxIUD2Tqx3djHKgIWqWg5LH9u0cSeUKPELraD1C_FZ8RVC6eVDx6Nf_PmyY-QlzW7qZnm6-BNmMI6HMFywR-R61oKXQnNvj8uNVO8amupr8izlH4yVkrePCVXXDVSNKK5Jn-6yXlnYKLdHiKYjNGl7Ex6S-8jQp7RZ_oZcun70gNv6d2STZgx0TCeXlwhEv3m8p7uQhGajnRrf4M3aNefMEPKhTH0Fg-Qg8FpWiaItINonA8znNegpZBp3iP9imUV-FQGYCqaWzsXgynHohL8c_JkhCnhi8u9Il_ev7vvbqvd3YeP3XZXGS7bXDUNr5VWshatZswqxjhDI5XVdgC2saPBYQAlLCoulIZBF7dMiYYZkGMr-Yq8OeseYvi1YMr97NLJPHgMS-obXbdqw0T5zxV5fUZ_wIS982MoXs0J77etlkxupKgLdfMAVY7F2ZngcXSl_9CAiSGliGN_iG6GeOxr1p-i78_R95foy8Cri-VlmNH-x_9lzf8CuJ-vNQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2917860459</pqid></control><display><type>article</type><title>Clinical Characteristics, Treatment Patterns, and Outcomes of Patients With Locally Advanced/Metastatic Hepatocellular Carcinoma Treated at the Veterans Health Administration</title><source>Oxford Journals Open Access Collection</source><source>MEDLINE</source><source>DOAJ Directory of Open Access Journals</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><creator>Alkadimi, Munaf A ; Aldawoodi, Tamarah A ; Lucero, Kana T ; Fierro, Maria E ; Boyle, Lauren D ; Mader, Michael J ; Franklin, Kathleen R ; Arora, Sukeshi P ; Nooruddin, Zohra</creator><creatorcontrib>Alkadimi, Munaf A ; Aldawoodi, Tamarah A ; Lucero, Kana T ; Fierro, Maria E ; Boyle, Lauren D ; Mader, Michael J ; Franklin, Kathleen R ; Arora, Sukeshi P ; Nooruddin, Zohra</creatorcontrib><description>This study retrospectively reviewed the outcomes of patients with advanced hepatocellular carcinoma (HCC) receiving atezolizumab with bevacizumab (A + B) therapy at the Veterans Health Administration (VHA).
Patients with advanced HCC who received first-line systemic therapy with A + B at the VHA between December 1, 2019, and March 1, 2022, were selected from electronic medical records (EMR) using ICD-9 and ICD-10 codes. Abstractors reviewed the EMR of the patients from their index date of A + B initiation until death or their last VHA visit, with the study period ending on January 31, 2023. The chi-square test was used to compare rates, and the Mann-Whitney test was used to compare medians.
A total of 332 patients met the study criteria. The median age was 67 years; 99% were male, 63% were non-Hispanic Whites, 26% were Black, and 66% had an Eastern Cooperative Oncology Group performance status of ≥1. 84% had child Pugh score (CPS) class A, 16% had CPS classes B and C, 62% had a grade 2 albumin-bilirubin score, 56% had HCC caused by viral hepatitis, 80% had cirrhosis, and 67% had received prior local therapies. The 6-month progression-free survival (PFS) was 59%, while the 1-year PFS rate was 36%. Overall survival (OS) at 1-year was 52% in our study.
In real world, despite having similar PFS as the phase III IMbrave 150 trial, our OS at 12 months was lower (52% vs. 67%) because our study included a higher proportion of elderly patients with moderate liver dysfunction and a 40% non-White. This study provided real-world outcomes that differed from the study population in a pivotal trial.</description><identifier>ISSN: 1083-7159</identifier><identifier>ISSN: 1549-490X</identifier><identifier>EISSN: 1549-490X</identifier><identifier>DOI: 10.1093/oncolo/oyad343</identifier><identifier>PMID: 38254242</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Aged ; Antibodies, Monoclonal, Humanized - therapeutic use ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Bevacizumab - therapeutic use ; Carcinoma, Hepatocellular - drug therapy ; Carcinoma, Hepatocellular - mortality ; Carcinoma, Hepatocellular - pathology ; Carcinoma, Hepatocellular - therapy ; Demographic aspects ; Drug therapy ; Female ; Hepatoma ; Humans ; Liver Neoplasms - drug therapy ; Liver Neoplasms - mortality ; Liver Neoplasms - pathology ; Liver Neoplasms - therapy ; Male ; Middle Aged ; Patient outcomes ; Retrospective Studies ; Treatment Outcome ; United States - epidemiology ; United States Department of Veterans Affairs - statistics & numerical data ; Veterans Health - statistics & numerical data</subject><ispartof>The oncologist (Dayton, Ohio), 2024-05, Vol.29 (5), p.369-376</ispartof><rights>Published by Oxford University Press 2024.</rights><rights>COPYRIGHT 2024 Oxford University Press</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c357t-22318985147900d80030ec58d9dba06dfcebba84de83489ab9ced08420ca5f753</cites><orcidid>0000-0003-3363-730X ; 0000-0003-4659-4310</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,860,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38254242$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Alkadimi, Munaf A</creatorcontrib><creatorcontrib>Aldawoodi, Tamarah A</creatorcontrib><creatorcontrib>Lucero, Kana T</creatorcontrib><creatorcontrib>Fierro, Maria E</creatorcontrib><creatorcontrib>Boyle, Lauren D</creatorcontrib><creatorcontrib>Mader, Michael J</creatorcontrib><creatorcontrib>Franklin, Kathleen R</creatorcontrib><creatorcontrib>Arora, Sukeshi P</creatorcontrib><creatorcontrib>Nooruddin, Zohra</creatorcontrib><title>Clinical Characteristics, Treatment Patterns, and Outcomes of Patients With Locally Advanced/Metastatic Hepatocellular Carcinoma Treated at the Veterans Health Administration</title><title>The oncologist (Dayton, Ohio)</title><addtitle>Oncologist</addtitle><description>This study retrospectively reviewed the outcomes of patients with advanced hepatocellular carcinoma (HCC) receiving atezolizumab with bevacizumab (A + B) therapy at the Veterans Health Administration (VHA).
Patients with advanced HCC who received first-line systemic therapy with A + B at the VHA between December 1, 2019, and March 1, 2022, were selected from electronic medical records (EMR) using ICD-9 and ICD-10 codes. Abstractors reviewed the EMR of the patients from their index date of A + B initiation until death or their last VHA visit, with the study period ending on January 31, 2023. The chi-square test was used to compare rates, and the Mann-Whitney test was used to compare medians.
A total of 332 patients met the study criteria. The median age was 67 years; 99% were male, 63% were non-Hispanic Whites, 26% were Black, and 66% had an Eastern Cooperative Oncology Group performance status of ≥1. 84% had child Pugh score (CPS) class A, 16% had CPS classes B and C, 62% had a grade 2 albumin-bilirubin score, 56% had HCC caused by viral hepatitis, 80% had cirrhosis, and 67% had received prior local therapies. The 6-month progression-free survival (PFS) was 59%, while the 1-year PFS rate was 36%. Overall survival (OS) at 1-year was 52% in our study.
In real world, despite having similar PFS as the phase III IMbrave 150 trial, our OS at 12 months was lower (52% vs. 67%) because our study included a higher proportion of elderly patients with moderate liver dysfunction and a 40% non-White. This study provided real-world outcomes that differed from the study population in a pivotal trial.</description><subject>Aged</subject><subject>Antibodies, Monoclonal, Humanized - therapeutic use</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Bevacizumab - therapeutic use</subject><subject>Carcinoma, Hepatocellular - drug therapy</subject><subject>Carcinoma, Hepatocellular - mortality</subject><subject>Carcinoma, Hepatocellular - pathology</subject><subject>Carcinoma, Hepatocellular - therapy</subject><subject>Demographic aspects</subject><subject>Drug therapy</subject><subject>Female</subject><subject>Hepatoma</subject><subject>Humans</subject><subject>Liver Neoplasms - drug therapy</subject><subject>Liver Neoplasms - mortality</subject><subject>Liver Neoplasms - pathology</subject><subject>Liver Neoplasms - therapy</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Patient outcomes</subject><subject>Retrospective Studies</subject><subject>Treatment Outcome</subject><subject>United States - epidemiology</subject><subject>United States Department of Veterans Affairs - statistics & numerical data</subject><subject>Veterans Health - statistics & numerical data</subject><issn>1083-7159</issn><issn>1549-490X</issn><issn>1549-490X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkU-P0zAQxS0EYpfClSOyxIUD2Tqx3djHKgIWqWg5LH9u0cSeUKPELraD1C_FZ8RVC6eVDx6Nf_PmyY-QlzW7qZnm6-BNmMI6HMFywR-R61oKXQnNvj8uNVO8amupr8izlH4yVkrePCVXXDVSNKK5Jn-6yXlnYKLdHiKYjNGl7Ex6S-8jQp7RZ_oZcun70gNv6d2STZgx0TCeXlwhEv3m8p7uQhGajnRrf4M3aNefMEPKhTH0Fg-Qg8FpWiaItINonA8znNegpZBp3iP9imUV-FQGYCqaWzsXgynHohL8c_JkhCnhi8u9Il_ev7vvbqvd3YeP3XZXGS7bXDUNr5VWshatZswqxjhDI5XVdgC2saPBYQAlLCoulIZBF7dMiYYZkGMr-Yq8OeseYvi1YMr97NLJPHgMS-obXbdqw0T5zxV5fUZ_wIS982MoXs0J77etlkxupKgLdfMAVY7F2ZngcXSl_9CAiSGliGN_iG6GeOxr1p-i78_R95foy8Cri-VlmNH-x_9lzf8CuJ-vNQ</recordid><startdate>20240503</startdate><enddate>20240503</enddate><creator>Alkadimi, Munaf A</creator><creator>Aldawoodi, Tamarah A</creator><creator>Lucero, Kana T</creator><creator>Fierro, Maria E</creator><creator>Boyle, Lauren D</creator><creator>Mader, Michael J</creator><creator>Franklin, Kathleen R</creator><creator>Arora, Sukeshi P</creator><creator>Nooruddin, Zohra</creator><general>Oxford University Press</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/0000-0003-3363-730X</orcidid><orcidid>https://orcid.org/0000-0003-4659-4310</orcidid></search><sort><creationdate>20240503</creationdate><title>Clinical Characteristics, Treatment Patterns, and Outcomes of Patients With Locally Advanced/Metastatic Hepatocellular Carcinoma Treated at the Veterans Health Administration</title><author>Alkadimi, Munaf A ; Aldawoodi, Tamarah A ; Lucero, Kana T ; Fierro, Maria E ; Boyle, Lauren D ; Mader, Michael J ; Franklin, Kathleen R ; Arora, Sukeshi P ; Nooruddin, Zohra</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c357t-22318985147900d80030ec58d9dba06dfcebba84de83489ab9ced08420ca5f753</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Aged</topic><topic>Antibodies, Monoclonal, Humanized - therapeutic use</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Bevacizumab - therapeutic use</topic><topic>Carcinoma, Hepatocellular - drug therapy</topic><topic>Carcinoma, Hepatocellular - mortality</topic><topic>Carcinoma, Hepatocellular - pathology</topic><topic>Carcinoma, Hepatocellular - therapy</topic><topic>Demographic aspects</topic><topic>Drug therapy</topic><topic>Female</topic><topic>Hepatoma</topic><topic>Humans</topic><topic>Liver Neoplasms - drug therapy</topic><topic>Liver Neoplasms - mortality</topic><topic>Liver Neoplasms - pathology</topic><topic>Liver Neoplasms - therapy</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Patient outcomes</topic><topic>Retrospective Studies</topic><topic>Treatment Outcome</topic><topic>United States - epidemiology</topic><topic>United States Department of Veterans Affairs - statistics & numerical data</topic><topic>Veterans Health - statistics & numerical data</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Alkadimi, Munaf A</creatorcontrib><creatorcontrib>Aldawoodi, Tamarah A</creatorcontrib><creatorcontrib>Lucero, Kana T</creatorcontrib><creatorcontrib>Fierro, Maria E</creatorcontrib><creatorcontrib>Boyle, Lauren D</creatorcontrib><creatorcontrib>Mader, Michael J</creatorcontrib><creatorcontrib>Franklin, Kathleen R</creatorcontrib><creatorcontrib>Arora, Sukeshi P</creatorcontrib><creatorcontrib>Nooruddin, Zohra</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>The oncologist (Dayton, Ohio)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Alkadimi, Munaf A</au><au>Aldawoodi, Tamarah A</au><au>Lucero, Kana T</au><au>Fierro, Maria E</au><au>Boyle, Lauren D</au><au>Mader, Michael J</au><au>Franklin, Kathleen R</au><au>Arora, Sukeshi P</au><au>Nooruddin, Zohra</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinical Characteristics, Treatment Patterns, and Outcomes of Patients With Locally Advanced/Metastatic Hepatocellular Carcinoma Treated at the Veterans Health Administration</atitle><jtitle>The oncologist (Dayton, Ohio)</jtitle><addtitle>Oncologist</addtitle><date>2024-05-03</date><risdate>2024</risdate><volume>29</volume><issue>5</issue><spage>369</spage><epage>376</epage><pages>369-376</pages><issn>1083-7159</issn><issn>1549-490X</issn><eissn>1549-490X</eissn><abstract>This study retrospectively reviewed the outcomes of patients with advanced hepatocellular carcinoma (HCC) receiving atezolizumab with bevacizumab (A + B) therapy at the Veterans Health Administration (VHA).
Patients with advanced HCC who received first-line systemic therapy with A + B at the VHA between December 1, 2019, and March 1, 2022, were selected from electronic medical records (EMR) using ICD-9 and ICD-10 codes. Abstractors reviewed the EMR of the patients from their index date of A + B initiation until death or their last VHA visit, with the study period ending on January 31, 2023. The chi-square test was used to compare rates, and the Mann-Whitney test was used to compare medians.
A total of 332 patients met the study criteria. The median age was 67 years; 99% were male, 63% were non-Hispanic Whites, 26% were Black, and 66% had an Eastern Cooperative Oncology Group performance status of ≥1. 84% had child Pugh score (CPS) class A, 16% had CPS classes B and C, 62% had a grade 2 albumin-bilirubin score, 56% had HCC caused by viral hepatitis, 80% had cirrhosis, and 67% had received prior local therapies. The 6-month progression-free survival (PFS) was 59%, while the 1-year PFS rate was 36%. Overall survival (OS) at 1-year was 52% in our study.
In real world, despite having similar PFS as the phase III IMbrave 150 trial, our OS at 12 months was lower (52% vs. 67%) because our study included a higher proportion of elderly patients with moderate liver dysfunction and a 40% non-White. This study provided real-world outcomes that differed from the study population in a pivotal trial.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>38254242</pmid><doi>10.1093/oncolo/oyad343</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0003-3363-730X</orcidid><orcidid>https://orcid.org/0000-0003-4659-4310</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1083-7159 |
ispartof | The oncologist (Dayton, Ohio), 2024-05, Vol.29 (5), p.369-376 |
issn | 1083-7159 1549-490X 1549-490X |
language | eng |
recordid | cdi_proquest_miscellaneous_2917860459 |
source | Oxford Journals Open Access Collection; MEDLINE; DOAJ Directory of Open Access Journals; EZB-FREE-00999 freely available EZB journals; PubMed Central |
subjects | Aged Antibodies, Monoclonal, Humanized - therapeutic use Antineoplastic Combined Chemotherapy Protocols - therapeutic use Bevacizumab - therapeutic use Carcinoma, Hepatocellular - drug therapy Carcinoma, Hepatocellular - mortality Carcinoma, Hepatocellular - pathology Carcinoma, Hepatocellular - therapy Demographic aspects Drug therapy Female Hepatoma Humans Liver Neoplasms - drug therapy Liver Neoplasms - mortality Liver Neoplasms - pathology Liver Neoplasms - therapy Male Middle Aged Patient outcomes Retrospective Studies Treatment Outcome United States - epidemiology United States Department of Veterans Affairs - statistics & numerical data Veterans Health - statistics & numerical data |
title | Clinical Characteristics, Treatment Patterns, and Outcomes of Patients With Locally Advanced/Metastatic Hepatocellular Carcinoma Treated at the Veterans Health Administration |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-05T14%3A35%3A40IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Clinical%20Characteristics,%20Treatment%20Patterns,%20and%20Outcomes%20of%20Patients%20With%20Locally%20Advanced/Metastatic%20Hepatocellular%20Carcinoma%20Treated%20at%20the%20Veterans%20Health%20Administration&rft.jtitle=The%20oncologist%20(Dayton,%20Ohio)&rft.au=Alkadimi,%20Munaf%20A&rft.date=2024-05-03&rft.volume=29&rft.issue=5&rft.spage=369&rft.epage=376&rft.pages=369-376&rft.issn=1083-7159&rft.eissn=1549-490X&rft_id=info:doi/10.1093/oncolo/oyad343&rft_dat=%3Cgale_proqu%3EA795056541%3C/gale_proqu%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2917860459&rft_id=info:pmid/38254242&rft_galeid=A795056541&rfr_iscdi=true |