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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Veröffentlicht in:Journal of hepatology 2021-09, Vol.75 (3), p.600-609
Hauptverfasser: 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
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container_end_page 609
container_issue 3
container_start_page 600
container_title Journal of hepatology
container_volume 75
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
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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 ; 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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
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