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HATT: a phase IV, single-arm, open-label study of sorafenib in Taiwanese patients with advanced hepatocellular carcinoma
BACKGROUND: Sorafenib significantly improves survival in patients with advanced hepatocellular carcinoma (HCC). This phase IV study assessed sorafenib efficacy/safety in Taiwanese patients with advanced HCC and Child–Pugh A status. METHODS: All patients received 400 mg sorafenib BID. Safety, efficac...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer India
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5362674/ https://www.ncbi.nlm.nih.gov/pubmed/27909950 http://dx.doi.org/10.1007/s12072-016-9774-x |
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author | Lin, Shi-Ming Lu, Sheng-Nan Chen, Ping-Tsung Jeng, Long-Bin Chen, Shinn-Cherng Hu, Chi-Tan Yang, Sien-Sing Le Berre, Marie-Aude Liu, Xuan Mitchell, David Y. Prins, Klaas Grevel, Joachim Peña, Carol A. E. Meinhardt, Gerold |
author_facet | Lin, Shi-Ming Lu, Sheng-Nan Chen, Ping-Tsung Jeng, Long-Bin Chen, Shinn-Cherng Hu, Chi-Tan Yang, Sien-Sing Le Berre, Marie-Aude Liu, Xuan Mitchell, David Y. Prins, Klaas Grevel, Joachim Peña, Carol A. E. Meinhardt, Gerold |
author_sort | Lin, Shi-Ming |
collection | PubMed |
description | BACKGROUND: Sorafenib significantly improves survival in patients with advanced hepatocellular carcinoma (HCC). This phase IV study assessed sorafenib efficacy/safety in Taiwanese patients with advanced HCC and Child–Pugh A status. METHODS: All patients received 400 mg sorafenib BID. Safety, efficacy, sorafenib pharmacokinetics, and Child–Pugh progression were evaluated. A hand-foot skin reaction (HFSR) prevention substudy assessed HFSR incidence and grade/severity and time to HFSR in 29 and 34 patients randomized to corticosteroid and noncorticosteroid ointments, respectively, and in 88 nonrandomized patients. RESULTS: The 151 patients included 120 (80%) male patients and 81 (54%) with stage IV disease. Mean sorafenib dose was 626 mg/day, and median treatment duration was 4.2 months. Median overall survival (OS), progression-free survival, and time to progression (TTP) were 8.6, 2.7, and 3.8 months, respectively. Disease control and response rates (partial responses only) were 48 and 6.6%, respectively. Median TTP from Child–Pugh A to B/C was 88 days. Drug-related adverse events (AEs) occurred in 89.4% of patients; none were new or unexpected. The most frequent grade ≥3 drug-related, treatment-emergent AEs were HFSR (13.2%), diarrhea (11.9%), and hypertension (6.6%). Corticosteroid ointment tended to reduce the severity and incidence of all HFSR-associated parameters. Pharmacokinetic exposure was unaltered by Child–Pugh progression. The final pharmacokinetic model predicted 13.1 and 33.8% reductions in sorafenib exposure over 6 and 12 months, respectively. CONCLUSIONS: There was a trend of longer OS and TTP in Taiwanese patients with advanced HCC compared with patients with advanced HCC in the Asia–Pacific trial. Sorafenib exposure did not correlate with liver function. Reduced pharmacokinetic exposure over time was unrelated to reduced or interrupted dosing. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s12072-016-9774-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5362674 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer India |
record_format | MEDLINE/PubMed |
spelling | pubmed-53626742017-04-04 HATT: a phase IV, single-arm, open-label study of sorafenib in Taiwanese patients with advanced hepatocellular carcinoma Lin, Shi-Ming Lu, Sheng-Nan Chen, Ping-Tsung Jeng, Long-Bin Chen, Shinn-Cherng Hu, Chi-Tan Yang, Sien-Sing Le Berre, Marie-Aude Liu, Xuan Mitchell, David Y. Prins, Klaas Grevel, Joachim Peña, Carol A. E. Meinhardt, Gerold Hepatol Int Original Article BACKGROUND: Sorafenib significantly improves survival in patients with advanced hepatocellular carcinoma (HCC). This phase IV study assessed sorafenib efficacy/safety in Taiwanese patients with advanced HCC and Child–Pugh A status. METHODS: All patients received 400 mg sorafenib BID. Safety, efficacy, sorafenib pharmacokinetics, and Child–Pugh progression were evaluated. A hand-foot skin reaction (HFSR) prevention substudy assessed HFSR incidence and grade/severity and time to HFSR in 29 and 34 patients randomized to corticosteroid and noncorticosteroid ointments, respectively, and in 88 nonrandomized patients. RESULTS: The 151 patients included 120 (80%) male patients and 81 (54%) with stage IV disease. Mean sorafenib dose was 626 mg/day, and median treatment duration was 4.2 months. Median overall survival (OS), progression-free survival, and time to progression (TTP) were 8.6, 2.7, and 3.8 months, respectively. Disease control and response rates (partial responses only) were 48 and 6.6%, respectively. Median TTP from Child–Pugh A to B/C was 88 days. Drug-related adverse events (AEs) occurred in 89.4% of patients; none were new or unexpected. The most frequent grade ≥3 drug-related, treatment-emergent AEs were HFSR (13.2%), diarrhea (11.9%), and hypertension (6.6%). Corticosteroid ointment tended to reduce the severity and incidence of all HFSR-associated parameters. Pharmacokinetic exposure was unaltered by Child–Pugh progression. The final pharmacokinetic model predicted 13.1 and 33.8% reductions in sorafenib exposure over 6 and 12 months, respectively. CONCLUSIONS: There was a trend of longer OS and TTP in Taiwanese patients with advanced HCC compared with patients with advanced HCC in the Asia–Pacific trial. Sorafenib exposure did not correlate with liver function. Reduced pharmacokinetic exposure over time was unrelated to reduced or interrupted dosing. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s12072-016-9774-x) contains supplementary material, which is available to authorized users. Springer India 2016-12-01 /pmc/articles/PMC5362674/ /pubmed/27909950 http://dx.doi.org/10.1007/s12072-016-9774-x Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article Lin, Shi-Ming Lu, Sheng-Nan Chen, Ping-Tsung Jeng, Long-Bin Chen, Shinn-Cherng Hu, Chi-Tan Yang, Sien-Sing Le Berre, Marie-Aude Liu, Xuan Mitchell, David Y. Prins, Klaas Grevel, Joachim Peña, Carol A. E. Meinhardt, Gerold HATT: a phase IV, single-arm, open-label study of sorafenib in Taiwanese patients with advanced hepatocellular carcinoma |
title | HATT: a phase IV, single-arm, open-label study of sorafenib in Taiwanese patients with advanced hepatocellular carcinoma |
title_full | HATT: a phase IV, single-arm, open-label study of sorafenib in Taiwanese patients with advanced hepatocellular carcinoma |
title_fullStr | HATT: a phase IV, single-arm, open-label study of sorafenib in Taiwanese patients with advanced hepatocellular carcinoma |
title_full_unstemmed | HATT: a phase IV, single-arm, open-label study of sorafenib in Taiwanese patients with advanced hepatocellular carcinoma |
title_short | HATT: a phase IV, single-arm, open-label study of sorafenib in Taiwanese patients with advanced hepatocellular carcinoma |
title_sort | hatt: a phase iv, single-arm, open-label study of sorafenib in taiwanese patients with advanced hepatocellular carcinoma |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5362674/ https://www.ncbi.nlm.nih.gov/pubmed/27909950 http://dx.doi.org/10.1007/s12072-016-9774-x |
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