CheckMate 040 cohort 5: A phase I/II study of nivolumab in patients with advanced hepatocellular carcinoma and Child-Pugh B cirrhosis
Patients with advanced hepatocellular carcinoma (aHCC) and Child-Pugh B liver function are often excluded from clinical trials. In previous studies, overall survival for these patients treated with sorafenib was ∼3–5 months; thus, new treatments are needed. Nivolumab, alone or in combination with ip...
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creator | Kudo, Masatoshi Matilla, Ana Santoro, Armando Melero, Ignacio Gracián, Antonio Cubillo Acosta-Rivera, Mirelis Choo, Su-Pin El-Khoueiry, Anthony B. Kuromatsu, Ryoko El-Rayes, Bassel Numata, Kazushi Itoh, Yoshito Di Costanzo, Francesco Crysler, Oxana Reig, Maria Shen, Yun Neely, Jaclyn Tschaika, Marina Wisniewski, Tami Sangro, Bruno |
description | Patients with advanced hepatocellular carcinoma (aHCC) and Child-Pugh B liver function are often excluded from clinical trials. In previous studies, overall survival for these patients treated with sorafenib was ∼3–5 months; thus, new treatments are needed. Nivolumab, alone or in combination with ipilimumab, is conditionally approved in the United States to treat patients with aHCC who previously received sorafenib. We describe nivolumab monotherapy outcomes in patients with Child-Pugh B status.
This phase I/II, open-label, non-comparative, multicentre trial (27 centres) included patients with Child-Pugh B (B7–B8) aHCC. Patients received intravenous nivolumab 240 mg every 2 weeks until unacceptable toxicity or disease progression. Primary endpoints were objective response rate (ORR) by investigator assessment (using Response Evaluation Criteria in Solid Tumors v1.1) and duration of response. Safety was assessed using National Cancer Institute Common Terminology Criteria for Adverse Events v4.0.
Twenty-five sorafenib-naive and 24 sorafenib-treated patients began treatment between November 2016 and October 2017 (median follow-up, 16.3 months). Investigator-assessed ORR was 12% (95% CI 5–25%) with 6 patients responding; disease control rate was 55% (95% CI 40–69%). Median time to response was 2.7 months (interquartile range, 1.4–4.2), and median duration of response was 9.9 months (95% CI 9.7–9.9). Treatment-related adverse events (TRAEs) were reported in 25 patients (51%) and led to discontinuation in 2 patients (4%). The most frequent grade 3/4 TRAEs were hypertransaminasemia (n = 2), amylase increase (n = 2), and aspartate aminotransferase increase (n = 2). The safety of nivolumab was comparable to that in patients with Child-Pugh A aHCC.
Nivolumab showed clinical activity and favourable safety with manageable toxicities, suggesting it could be suitable for patients with Child-Pugh B aHCC.
In patients with advanced hepatocellular carcinoma, almost all systemic therapies require very good liver function, i.e. Child-Pugh A status. The evidence from this study suggests that nivolumab shows clinical activity and an acceptable safety profile in patients with hepatocellular carcinoma with Child-Pugh B status who have mild to moderate impairment of liver function or liver decompensation that might rule out other therapies. Further studies are warranted to assess the safety and efficacy of nivolumab in this patient population.
NCT01658878.
[Display omitted]
•This |
doi_str_mv | 10.1016/j.jhep.2021.04.047 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2534618962</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0168827821003135</els_id><sourcerecordid>2576698843</sourcerecordid><originalsourceid>FETCH-LOGICAL-c428t-21f634963ce060b6d5ef416399e28947c120d81ab9d4dcc4bbbb1c1214a316743</originalsourceid><addsrcrecordid>eNp9kc2KFDEUhYMoTjv6Ai7kghs31ZO_TlXEzUzjT8OILnQdUknKSllVKZNUyzyA722aHl24MFwIXL57OJyD0HOCtwQTcTVsh94tW4op2WJepn6ANkRgXGHByUO0KVBTNbRuLtCTlAaMMcOSP0YXjOMdYVRu0K9978z3jzo7wByDCX2IGXav4RqWXicHh6vDAVJe7R2EDmZ_DOM66Rb8DIvO3s05wU-fe9D2qGfjLBRPOgfjxnEddQSjo_FzmDTo2cK-96OtPq_fergB42PsQ_LpKXrU6TG5Z_f_Jfr67u2X_Yfq9tP7w_76tjKcNrmipBOMS8GMwwK3wu5cx4lgUjraSF4bQrFtiG6l5dYY3pZHypJwzYioObtEr866Sww_Vpeymnw6OdWzC2tSdMe4II0UtKAv_0GHsMa5uCtULYRsGs4KRc-UiSGl6Dq1RD_peKcIVqeS1KBOJalTSQrzMnU5enEvvbaTs39P_rRSgDdnwJUsjt5FlUxJuoTrozNZ2eD_p_8bjlWhUg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2576698843</pqid></control><display><type>article</type><title>CheckMate 040 cohort 5: A phase I/II study of nivolumab in patients with advanced hepatocellular carcinoma and Child-Pugh B cirrhosis</title><source>MEDLINE</source><source>Access via ScienceDirect (Elsevier)</source><creator>Kudo, Masatoshi ; Matilla, Ana ; Santoro, Armando ; Melero, Ignacio ; Gracián, Antonio Cubillo ; Acosta-Rivera, Mirelis ; Choo, Su-Pin ; El-Khoueiry, Anthony B. ; Kuromatsu, Ryoko ; El-Rayes, Bassel ; Numata, Kazushi ; Itoh, Yoshito ; Di Costanzo, Francesco ; Crysler, Oxana ; Reig, Maria ; Shen, Yun ; Neely, Jaclyn ; Tschaika, Marina ; Wisniewski, Tami ; Sangro, Bruno</creator><creatorcontrib>Kudo, Masatoshi ; Matilla, Ana ; Santoro, Armando ; Melero, Ignacio ; Gracián, Antonio Cubillo ; Acosta-Rivera, Mirelis ; Choo, Su-Pin ; El-Khoueiry, Anthony B. ; Kuromatsu, Ryoko ; El-Rayes, Bassel ; Numata, Kazushi ; Itoh, Yoshito ; Di Costanzo, Francesco ; Crysler, Oxana ; Reig, Maria ; Shen, Yun ; Neely, Jaclyn ; Tschaika, Marina ; Wisniewski, Tami ; Sangro, Bruno</creatorcontrib><description>Patients with advanced hepatocellular carcinoma (aHCC) and Child-Pugh B liver function are often excluded from clinical trials. In previous studies, overall survival for these patients treated with sorafenib was ∼3–5 months; thus, new treatments are needed. Nivolumab, alone or in combination with ipilimumab, is conditionally approved in the United States to treat patients with aHCC who previously received sorafenib. We describe nivolumab monotherapy outcomes in patients with Child-Pugh B status.
This phase I/II, open-label, non-comparative, multicentre trial (27 centres) included patients with Child-Pugh B (B7–B8) aHCC. Patients received intravenous nivolumab 240 mg every 2 weeks until unacceptable toxicity or disease progression. Primary endpoints were objective response rate (ORR) by investigator assessment (using Response Evaluation Criteria in Solid Tumors v1.1) and duration of response. Safety was assessed using National Cancer Institute Common Terminology Criteria for Adverse Events v4.0.
Twenty-five sorafenib-naive and 24 sorafenib-treated patients began treatment between November 2016 and October 2017 (median follow-up, 16.3 months). Investigator-assessed ORR was 12% (95% CI 5–25%) with 6 patients responding; disease control rate was 55% (95% CI 40–69%). Median time to response was 2.7 months (interquartile range, 1.4–4.2), and median duration of response was 9.9 months (95% CI 9.7–9.9). Treatment-related adverse events (TRAEs) were reported in 25 patients (51%) and led to discontinuation in 2 patients (4%). The most frequent grade 3/4 TRAEs were hypertransaminasemia (n = 2), amylase increase (n = 2), and aspartate aminotransferase increase (n = 2). The safety of nivolumab was comparable to that in patients with Child-Pugh A aHCC.
Nivolumab showed clinical activity and favourable safety with manageable toxicities, suggesting it could be suitable for patients with Child-Pugh B aHCC.
In patients with advanced hepatocellular carcinoma, almost all systemic therapies require very good liver function, i.e. Child-Pugh A status. The evidence from this study suggests that nivolumab shows clinical activity and an acceptable safety profile in patients with hepatocellular carcinoma with Child-Pugh B status who have mild to moderate impairment of liver function or liver decompensation that might rule out other therapies. Further studies are warranted to assess the safety and efficacy of nivolumab in this patient population.
NCT01658878.
[Display omitted]
•This is the first report, to our knowledge, of immune checkpoint inhibitor therapy in patients with advanced HCC and Child-Pugh B liver function status.•Median OS with nivolumab was longer than the historical OS rate for patients treated with sorafenib (7.6 months vs. 2.5–5.4 months, respectively).•Clinically meaningful stabilisation of liver function was observed, as evidenced by maintained or improved Child-Pugh scores and albumin-bilirubin scores.•Nivolumab had a favourable safety profile with manageable toxicities when used in patients with Child-Pugh B advanced HCC and was comparable to that seen in patients with Child-Pugh A HCC.</description><identifier>ISSN: 0168-8278</identifier><identifier>EISSN: 1600-0641</identifier><identifier>DOI: 10.1016/j.jhep.2021.04.047</identifier><identifier>PMID: 34051329</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Adult ; Adverse events ; Aged ; anti-PD-1 ; Aspartate aminotransferase ; Carcinoma, Hepatocellular - drug therapy ; checkpoint inhibitors ; Cirrhosis ; Clinical trials ; Cohort Studies ; Disease control ; Female ; Hepatocellular carcinoma ; Humans ; Immune Checkpoint Inhibitors - pharmacology ; Immune Checkpoint Inhibitors - therapeutic use ; immunotherapy ; Intravenous administration ; Liver cancer ; Liver cirrhosis ; liver decompensation ; Liver Neoplasms - drug therapy ; Male ; Middle Aged ; Nivolumab - pharmacology ; Nivolumab - therapeutic use ; objective response ; overall survival ; Patients ; Safety ; Solid tumors ; Toxicity</subject><ispartof>Journal of hepatology, 2021-09, Vol.75 (3), p.600-609</ispartof><rights>2021 The Authors</rights><rights>Copyright © 2021 The Authors. Published by Elsevier B.V. All rights reserved.</rights><rights>Copyright Elsevier Science Ltd. Sep 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c428t-21f634963ce060b6d5ef416399e28947c120d81ab9d4dcc4bbbb1c1214a316743</citedby><cites>FETCH-LOGICAL-c428t-21f634963ce060b6d5ef416399e28947c120d81ab9d4dcc4bbbb1c1214a316743</cites><orcidid>0000-0002-2078-1161 ; 0000-0002-4177-6417 ; 0000-0002-4102-3474 ; 0000-0001-7137-3953</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jhep.2021.04.047$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>315,781,785,3551,27926,27927,45997</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34051329$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kudo, Masatoshi</creatorcontrib><creatorcontrib>Matilla, Ana</creatorcontrib><creatorcontrib>Santoro, Armando</creatorcontrib><creatorcontrib>Melero, Ignacio</creatorcontrib><creatorcontrib>Gracián, Antonio Cubillo</creatorcontrib><creatorcontrib>Acosta-Rivera, Mirelis</creatorcontrib><creatorcontrib>Choo, Su-Pin</creatorcontrib><creatorcontrib>El-Khoueiry, Anthony B.</creatorcontrib><creatorcontrib>Kuromatsu, Ryoko</creatorcontrib><creatorcontrib>El-Rayes, Bassel</creatorcontrib><creatorcontrib>Numata, Kazushi</creatorcontrib><creatorcontrib>Itoh, Yoshito</creatorcontrib><creatorcontrib>Di Costanzo, Francesco</creatorcontrib><creatorcontrib>Crysler, Oxana</creatorcontrib><creatorcontrib>Reig, Maria</creatorcontrib><creatorcontrib>Shen, Yun</creatorcontrib><creatorcontrib>Neely, Jaclyn</creatorcontrib><creatorcontrib>Tschaika, Marina</creatorcontrib><creatorcontrib>Wisniewski, Tami</creatorcontrib><creatorcontrib>Sangro, Bruno</creatorcontrib><title>CheckMate 040 cohort 5: A phase I/II study of nivolumab in patients with advanced hepatocellular carcinoma and Child-Pugh B cirrhosis</title><title>Journal of hepatology</title><addtitle>J Hepatol</addtitle><description>Patients with advanced hepatocellular carcinoma (aHCC) and Child-Pugh B liver function are often excluded from clinical trials. In previous studies, overall survival for these patients treated with sorafenib was ∼3–5 months; thus, new treatments are needed. Nivolumab, alone or in combination with ipilimumab, is conditionally approved in the United States to treat patients with aHCC who previously received sorafenib. We describe nivolumab monotherapy outcomes in patients with Child-Pugh B status.
This phase I/II, open-label, non-comparative, multicentre trial (27 centres) included patients with Child-Pugh B (B7–B8) aHCC. Patients received intravenous nivolumab 240 mg every 2 weeks until unacceptable toxicity or disease progression. Primary endpoints were objective response rate (ORR) by investigator assessment (using Response Evaluation Criteria in Solid Tumors v1.1) and duration of response. Safety was assessed using National Cancer Institute Common Terminology Criteria for Adverse Events v4.0.
Twenty-five sorafenib-naive and 24 sorafenib-treated patients began treatment between November 2016 and October 2017 (median follow-up, 16.3 months). Investigator-assessed ORR was 12% (95% CI 5–25%) with 6 patients responding; disease control rate was 55% (95% CI 40–69%). Median time to response was 2.7 months (interquartile range, 1.4–4.2), and median duration of response was 9.9 months (95% CI 9.7–9.9). Treatment-related adverse events (TRAEs) were reported in 25 patients (51%) and led to discontinuation in 2 patients (4%). The most frequent grade 3/4 TRAEs were hypertransaminasemia (n = 2), amylase increase (n = 2), and aspartate aminotransferase increase (n = 2). The safety of nivolumab was comparable to that in patients with Child-Pugh A aHCC.
Nivolumab showed clinical activity and favourable safety with manageable toxicities, suggesting it could be suitable for patients with Child-Pugh B aHCC.
In patients with advanced hepatocellular carcinoma, almost all systemic therapies require very good liver function, i.e. Child-Pugh A status. The evidence from this study suggests that nivolumab shows clinical activity and an acceptable safety profile in patients with hepatocellular carcinoma with Child-Pugh B status who have mild to moderate impairment of liver function or liver decompensation that might rule out other therapies. Further studies are warranted to assess the safety and efficacy of nivolumab in this patient population.
NCT01658878.
[Display omitted]
•This is the first report, to our knowledge, of immune checkpoint inhibitor therapy in patients with advanced HCC and Child-Pugh B liver function status.•Median OS with nivolumab was longer than the historical OS rate for patients treated with sorafenib (7.6 months vs. 2.5–5.4 months, respectively).•Clinically meaningful stabilisation of liver function was observed, as evidenced by maintained or improved Child-Pugh scores and albumin-bilirubin scores.•Nivolumab had a favourable safety profile with manageable toxicities when used in patients with Child-Pugh B advanced HCC and was comparable to that seen in patients with Child-Pugh A HCC.</description><subject>Adult</subject><subject>Adverse events</subject><subject>Aged</subject><subject>anti-PD-1</subject><subject>Aspartate aminotransferase</subject><subject>Carcinoma, Hepatocellular - drug therapy</subject><subject>checkpoint inhibitors</subject><subject>Cirrhosis</subject><subject>Clinical trials</subject><subject>Cohort Studies</subject><subject>Disease control</subject><subject>Female</subject><subject>Hepatocellular carcinoma</subject><subject>Humans</subject><subject>Immune Checkpoint Inhibitors - pharmacology</subject><subject>Immune Checkpoint Inhibitors - therapeutic use</subject><subject>immunotherapy</subject><subject>Intravenous administration</subject><subject>Liver cancer</subject><subject>Liver cirrhosis</subject><subject>liver decompensation</subject><subject>Liver Neoplasms - drug therapy</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Nivolumab - pharmacology</subject><subject>Nivolumab - therapeutic use</subject><subject>objective response</subject><subject>overall survival</subject><subject>Patients</subject><subject>Safety</subject><subject>Solid tumors</subject><subject>Toxicity</subject><issn>0168-8278</issn><issn>1600-0641</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kc2KFDEUhYMoTjv6Ai7kghs31ZO_TlXEzUzjT8OILnQdUknKSllVKZNUyzyA722aHl24MFwIXL57OJyD0HOCtwQTcTVsh94tW4op2WJepn6ANkRgXGHByUO0KVBTNbRuLtCTlAaMMcOSP0YXjOMdYVRu0K9978z3jzo7wByDCX2IGXav4RqWXicHh6vDAVJe7R2EDmZ_DOM66Rb8DIvO3s05wU-fe9D2qGfjLBRPOgfjxnEddQSjo_FzmDTo2cK-96OtPq_fergB42PsQ_LpKXrU6TG5Z_f_Jfr67u2X_Yfq9tP7w_76tjKcNrmipBOMS8GMwwK3wu5cx4lgUjraSF4bQrFtiG6l5dYY3pZHypJwzYioObtEr866Sww_Vpeymnw6OdWzC2tSdMe4II0UtKAv_0GHsMa5uCtULYRsGs4KRc-UiSGl6Dq1RD_peKcIVqeS1KBOJalTSQrzMnU5enEvvbaTs39P_rRSgDdnwJUsjt5FlUxJuoTrozNZ2eD_p_8bjlWhUg</recordid><startdate>202109</startdate><enddate>202109</enddate><creator>Kudo, Masatoshi</creator><creator>Matilla, Ana</creator><creator>Santoro, Armando</creator><creator>Melero, Ignacio</creator><creator>Gracián, Antonio Cubillo</creator><creator>Acosta-Rivera, Mirelis</creator><creator>Choo, Su-Pin</creator><creator>El-Khoueiry, Anthony B.</creator><creator>Kuromatsu, Ryoko</creator><creator>El-Rayes, Bassel</creator><creator>Numata, Kazushi</creator><creator>Itoh, Yoshito</creator><creator>Di Costanzo, Francesco</creator><creator>Crysler, Oxana</creator><creator>Reig, Maria</creator><creator>Shen, Yun</creator><creator>Neely, Jaclyn</creator><creator>Tschaika, Marina</creator><creator>Wisniewski, Tami</creator><creator>Sangro, Bruno</creator><general>Elsevier B.V</general><general>Elsevier Science Ltd</general><scope>6I.</scope><scope>AAFTH</scope><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>7T5</scope><scope>H94</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-2078-1161</orcidid><orcidid>https://orcid.org/0000-0002-4177-6417</orcidid><orcidid>https://orcid.org/0000-0002-4102-3474</orcidid><orcidid>https://orcid.org/0000-0001-7137-3953</orcidid></search><sort><creationdate>202109</creationdate><title>CheckMate 040 cohort 5: A phase I/II study of nivolumab in patients with advanced hepatocellular carcinoma and Child-Pugh B cirrhosis</title><author>Kudo, Masatoshi ; Matilla, Ana ; Santoro, Armando ; Melero, Ignacio ; Gracián, Antonio Cubillo ; Acosta-Rivera, Mirelis ; Choo, Su-Pin ; El-Khoueiry, Anthony B. ; Kuromatsu, Ryoko ; El-Rayes, Bassel ; Numata, Kazushi ; Itoh, Yoshito ; Di Costanzo, Francesco ; Crysler, Oxana ; Reig, Maria ; Shen, Yun ; Neely, Jaclyn ; Tschaika, Marina ; Wisniewski, Tami ; Sangro, Bruno</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c428t-21f634963ce060b6d5ef416399e28947c120d81ab9d4dcc4bbbb1c1214a316743</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adult</topic><topic>Adverse events</topic><topic>Aged</topic><topic>anti-PD-1</topic><topic>Aspartate aminotransferase</topic><topic>Carcinoma, Hepatocellular - drug therapy</topic><topic>checkpoint inhibitors</topic><topic>Cirrhosis</topic><topic>Clinical trials</topic><topic>Cohort Studies</topic><topic>Disease control</topic><topic>Female</topic><topic>Hepatocellular carcinoma</topic><topic>Humans</topic><topic>Immune Checkpoint Inhibitors - pharmacology</topic><topic>Immune Checkpoint Inhibitors - therapeutic use</topic><topic>immunotherapy</topic><topic>Intravenous administration</topic><topic>Liver cancer</topic><topic>Liver cirrhosis</topic><topic>liver decompensation</topic><topic>Liver Neoplasms - drug therapy</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Nivolumab - pharmacology</topic><topic>Nivolumab - therapeutic use</topic><topic>objective response</topic><topic>overall survival</topic><topic>Patients</topic><topic>Safety</topic><topic>Solid tumors</topic><topic>Toxicity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kudo, Masatoshi</creatorcontrib><creatorcontrib>Matilla, Ana</creatorcontrib><creatorcontrib>Santoro, Armando</creatorcontrib><creatorcontrib>Melero, Ignacio</creatorcontrib><creatorcontrib>Gracián, Antonio Cubillo</creatorcontrib><creatorcontrib>Acosta-Rivera, Mirelis</creatorcontrib><creatorcontrib>Choo, Su-Pin</creatorcontrib><creatorcontrib>El-Khoueiry, Anthony B.</creatorcontrib><creatorcontrib>Kuromatsu, Ryoko</creatorcontrib><creatorcontrib>El-Rayes, Bassel</creatorcontrib><creatorcontrib>Numata, Kazushi</creatorcontrib><creatorcontrib>Itoh, Yoshito</creatorcontrib><creatorcontrib>Di Costanzo, Francesco</creatorcontrib><creatorcontrib>Crysler, Oxana</creatorcontrib><creatorcontrib>Reig, Maria</creatorcontrib><creatorcontrib>Shen, Yun</creatorcontrib><creatorcontrib>Neely, Jaclyn</creatorcontrib><creatorcontrib>Tschaika, Marina</creatorcontrib><creatorcontrib>Wisniewski, Tami</creatorcontrib><creatorcontrib>Sangro, Bruno</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of hepatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kudo, Masatoshi</au><au>Matilla, Ana</au><au>Santoro, Armando</au><au>Melero, Ignacio</au><au>Gracián, Antonio Cubillo</au><au>Acosta-Rivera, Mirelis</au><au>Choo, Su-Pin</au><au>El-Khoueiry, Anthony B.</au><au>Kuromatsu, Ryoko</au><au>El-Rayes, Bassel</au><au>Numata, Kazushi</au><au>Itoh, Yoshito</au><au>Di Costanzo, Francesco</au><au>Crysler, Oxana</au><au>Reig, Maria</au><au>Shen, Yun</au><au>Neely, Jaclyn</au><au>Tschaika, Marina</au><au>Wisniewski, Tami</au><au>Sangro, Bruno</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>CheckMate 040 cohort 5: A phase I/II study of nivolumab in patients with advanced hepatocellular carcinoma and Child-Pugh B cirrhosis</atitle><jtitle>Journal of hepatology</jtitle><addtitle>J Hepatol</addtitle><date>2021-09</date><risdate>2021</risdate><volume>75</volume><issue>3</issue><spage>600</spage><epage>609</epage><pages>600-609</pages><issn>0168-8278</issn><eissn>1600-0641</eissn><abstract>Patients with advanced hepatocellular carcinoma (aHCC) and Child-Pugh B liver function are often excluded from clinical trials. In previous studies, overall survival for these patients treated with sorafenib was ∼3–5 months; thus, new treatments are needed. Nivolumab, alone or in combination with ipilimumab, is conditionally approved in the United States to treat patients with aHCC who previously received sorafenib. We describe nivolumab monotherapy outcomes in patients with Child-Pugh B status.
This phase I/II, open-label, non-comparative, multicentre trial (27 centres) included patients with Child-Pugh B (B7–B8) aHCC. Patients received intravenous nivolumab 240 mg every 2 weeks until unacceptable toxicity or disease progression. Primary endpoints were objective response rate (ORR) by investigator assessment (using Response Evaluation Criteria in Solid Tumors v1.1) and duration of response. Safety was assessed using National Cancer Institute Common Terminology Criteria for Adverse Events v4.0.
Twenty-five sorafenib-naive and 24 sorafenib-treated patients began treatment between November 2016 and October 2017 (median follow-up, 16.3 months). Investigator-assessed ORR was 12% (95% CI 5–25%) with 6 patients responding; disease control rate was 55% (95% CI 40–69%). Median time to response was 2.7 months (interquartile range, 1.4–4.2), and median duration of response was 9.9 months (95% CI 9.7–9.9). Treatment-related adverse events (TRAEs) were reported in 25 patients (51%) and led to discontinuation in 2 patients (4%). The most frequent grade 3/4 TRAEs were hypertransaminasemia (n = 2), amylase increase (n = 2), and aspartate aminotransferase increase (n = 2). The safety of nivolumab was comparable to that in patients with Child-Pugh A aHCC.
Nivolumab showed clinical activity and favourable safety with manageable toxicities, suggesting it could be suitable for patients with Child-Pugh B aHCC.
In patients with advanced hepatocellular carcinoma, almost all systemic therapies require very good liver function, i.e. Child-Pugh A status. The evidence from this study suggests that nivolumab shows clinical activity and an acceptable safety profile in patients with hepatocellular carcinoma with Child-Pugh B status who have mild to moderate impairment of liver function or liver decompensation that might rule out other therapies. Further studies are warranted to assess the safety and efficacy of nivolumab in this patient population.
NCT01658878.
[Display omitted]
•This is the first report, to our knowledge, of immune checkpoint inhibitor therapy in patients with advanced HCC and Child-Pugh B liver function status.•Median OS with nivolumab was longer than the historical OS rate for patients treated with sorafenib (7.6 months vs. 2.5–5.4 months, respectively).•Clinically meaningful stabilisation of liver function was observed, as evidenced by maintained or improved Child-Pugh scores and albumin-bilirubin scores.•Nivolumab had a favourable safety profile with manageable toxicities when used in patients with Child-Pugh B advanced HCC and was comparable to that seen in patients with Child-Pugh A HCC.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>34051329</pmid><doi>10.1016/j.jhep.2021.04.047</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-2078-1161</orcidid><orcidid>https://orcid.org/0000-0002-4177-6417</orcidid><orcidid>https://orcid.org/0000-0002-4102-3474</orcidid><orcidid>https://orcid.org/0000-0001-7137-3953</orcidid><oa>free_for_read</oa></addata></record> |
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identifier | ISSN: 0168-8278 |
ispartof | Journal of hepatology, 2021-09, Vol.75 (3), p.600-609 |
issn | 0168-8278 1600-0641 |
language | eng |
recordid | cdi_proquest_miscellaneous_2534618962 |
source | MEDLINE; Access via ScienceDirect (Elsevier) |
subjects | Adult Adverse events Aged anti-PD-1 Aspartate aminotransferase Carcinoma, Hepatocellular - drug therapy checkpoint inhibitors Cirrhosis Clinical trials Cohort Studies Disease control Female Hepatocellular carcinoma Humans Immune Checkpoint Inhibitors - pharmacology Immune Checkpoint Inhibitors - therapeutic use immunotherapy Intravenous administration Liver cancer Liver cirrhosis liver decompensation Liver Neoplasms - drug therapy Male Middle Aged Nivolumab - pharmacology Nivolumab - therapeutic use objective response overall survival Patients Safety Solid tumors Toxicity |
title | CheckMate 040 cohort 5: A phase I/II study of nivolumab in patients with advanced hepatocellular carcinoma and Child-Pugh B cirrhosis |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-18T09%3A29%3A46IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=CheckMate%20040%20cohort%205:%20A%20phase%20I/II%20study%20of%20nivolumab%20in%20patients%20with%20advanced%20hepatocellular%20carcinoma%20and%20Child-Pugh%20B%20cirrhosis&rft.jtitle=Journal%20of%20hepatology&rft.au=Kudo,%20Masatoshi&rft.date=2021-09&rft.volume=75&rft.issue=3&rft.spage=600&rft.epage=609&rft.pages=600-609&rft.issn=0168-8278&rft.eissn=1600-0641&rft_id=info:doi/10.1016/j.jhep.2021.04.047&rft_dat=%3Cproquest_cross%3E2576698843%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2576698843&rft_id=info:pmid/34051329&rft_els_id=S0168827821003135&rfr_iscdi=true |