Systemic Cytotoxic Chemotherapy of Patients With Advanced Hepatocellular Carcinoma in the Era of Sorafenib Nonavailability
DC Field | Value | Language |
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dc.contributor.author | Yoon, Eileen L. | - |
dc.contributor.author | Yeon, Jong Eun | - |
dc.contributor.author | Lee, Hyun Jung | - |
dc.contributor.author | Suh, Sang Jun | - |
dc.contributor.author | Lee, Sun Jae | - |
dc.contributor.author | Kang, Seong Hee | - |
dc.contributor.author | Kang, Keunhee | - |
dc.contributor.author | Yoo, Yang Jae | - |
dc.contributor.author | Kim, Ji Hoon | - |
dc.contributor.author | Yim, Hyung Joon | - |
dc.contributor.author | Byun, Kwan Soo | - |
dc.date.accessioned | 2021-09-05T10:59:51Z | - |
dc.date.available | 2021-09-05T10:59:51Z | - |
dc.date.created | 2021-06-15 | - |
dc.date.issued | 2014-03 | - |
dc.identifier.issn | 0192-0790 | - |
dc.identifier.uri | https://scholar.korea.ac.kr/handle/2021.sw.korea/99136 | - |
dc.description.abstract | Goals:The goal of the study was to compare the efficacy and safety of sorafenib with those of systemic cytotoxic chemotherapy.Background:Sorafenib treatment has shown to improve the survival in patients with advanced hepatocellular carcinoma (HCC) when compared with placebo. However, whether sorafenib controls advanced-stage HCC better than systemic cytotoxic chemotherapy has not been elucidated.Study:We retrospectively reviewed the medical records of 220 patients with measurable advanced HCC who had not received systemic treatment previously between January 2007 and April 2012. Among these patients, 78 had been treated with sorafenib. Another 14 patients who were treated with a 4-weekly regimen of adriamycin, cisplatin, and capecitabine were included as the historical control group for comparison. The median overall survival, the progression-free survival, response rates, and safety profiles were evaluated.Results:Baseline characteristics were similar between the treatment groups. The median overall survival was 7.2 months [95% confidence interval (CI), 5.6-8.8] in the sorafenib group and 11.2 months (95% CI, 8.1-14.2) in the cytotoxic chemotherapy group (P=0.10). The median progression-free survival was 3.2 months (95% CI, 2.2-4.3) in the sorafenib group and 5.9 months (95% CI, 3.6-8.2) in the cytotoxic chemotherapy group (P=0.07). The deterioration of liver function and neutropenia were the most frequent serious adverse events in the sorafenib and the systemic chemotherapy group.Conclusions:Although a direct head-to-head comparison could not be done, there were some patients who showed a good response to systemic cytotoxic chemotherapy. Further assessment is necessary to study the role of chemotherapy in patients who are intolerant or intractable to sorafenib. | - |
dc.language | English | - |
dc.language.iso | en | - |
dc.publisher | LIPPINCOTT WILLIAMS & WILKINS | - |
dc.subject | CLINICAL-PRACTICE GUIDELINES | - |
dc.subject | PHASE-III | - |
dc.subject | SURVIVAL | - |
dc.subject | DOXORUBICIN | - |
dc.subject | TRIAL | - |
dc.subject | THERAPY | - |
dc.subject | CANCER | - |
dc.title | Systemic Cytotoxic Chemotherapy of Patients With Advanced Hepatocellular Carcinoma in the Era of Sorafenib Nonavailability | - |
dc.type | Article | - |
dc.contributor.affiliatedAuthor | Yeon, Jong Eun | - |
dc.contributor.affiliatedAuthor | Kim, Ji Hoon | - |
dc.contributor.affiliatedAuthor | Yim, Hyung Joon | - |
dc.contributor.affiliatedAuthor | Byun, Kwan Soo | - |
dc.identifier.doi | 10.1097/MCG.0b013e3182a54ec8 | - |
dc.identifier.scopusid | 2-s2.0-84894044560 | - |
dc.identifier.wosid | 000334921100001 | - |
dc.identifier.bibliographicCitation | JOURNAL OF CLINICAL GASTROENTEROLOGY, v.48, no.3, pp.E22 - E29 | - |
dc.relation.isPartOf | JOURNAL OF CLINICAL GASTROENTEROLOGY | - |
dc.citation.title | JOURNAL OF CLINICAL GASTROENTEROLOGY | - |
dc.citation.volume | 48 | - |
dc.citation.number | 3 | - |
dc.citation.startPage | E22 | - |
dc.citation.endPage | E29 | - |
dc.type.rims | ART | - |
dc.type.docType | Article | - |
dc.description.journalClass | 1 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Gastroenterology & Hepatology | - |
dc.relation.journalWebOfScienceCategory | Gastroenterology & Hepatology | - |
dc.subject.keywordPlus | CLINICAL-PRACTICE GUIDELINES | - |
dc.subject.keywordPlus | PHASE-III | - |
dc.subject.keywordPlus | SURVIVAL | - |
dc.subject.keywordPlus | DOXORUBICIN | - |
dc.subject.keywordPlus | TRIAL | - |
dc.subject.keywordPlus | THERAPY | - |
dc.subject.keywordPlus | CANCER | - |
dc.subject.keywordAuthor | hepatocellular carcinoma | - |
dc.subject.keywordAuthor | sorafenib | - |
dc.subject.keywordAuthor | cytotoxic chemotherapy | - |
dc.subject.keywordAuthor | survival rate | - |
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