Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/74571
Full metadata record
DC FieldValueLanguage
dc.contributor.authorSongporn Oranratnachaien_US
dc.contributor.authorSasivimol Rattanasirien_US
dc.contributor.authorEkaphop Sirachainanen_US
dc.contributor.authorAmarit Tansaweten_US
dc.contributor.authorNilubol Raunroadroongen_US
dc.contributor.authorGareth J. McKayen_US
dc.contributor.authorJohn Attiaen_US
dc.contributor.authorAmmarin Thakkinstianen_US
dc.date.accessioned2022-10-16T06:44:38Z-
dc.date.available2022-10-16T06:44:38Z-
dc.date.issued2022-01-01en_US
dc.identifier.issn20457634en_US
dc.identifier.other2-s2.0-85137516771en_US
dc.identifier.other10.1002/cam4.5224en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85137516771&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/74571-
dc.description.abstractBackground: Multikinase inhibitors (MKIs) represent the main treatment options for advanced hepatocellular carcinoma (aHCC). However, accessibility in developing countries is limited. A chemotherapy, Fluorouracil and Oxaliplatin (FOLFOX), offers a less expensive treatment. Therefore, this study sought to compare the clinical effectiveness of FOLFOX with Sorafenib as a first-line treatment for aHCC in real-life practice. Methods: A retrospective aHCC cohort from four Thai hospitals was investigated for patients who received FOLFOX or Sorafenib between 2013–2019. Multiple imputation by chained equations addressed missing covariate data in a treatment effect model using Weight-adjusted-censoring inverse-probability-weighted regression adjustment; overall survival (OS) and progression-free survival (PFS) were estimated. Results: A total of 504 patients were included, (Sorafenib [n = 382] and FOLFOX [n = 122]). The treatment effect model estimated a median OS for Sorafenib and FOLFOX of 11.38 and 8.22 months, representing a significantly shorter OS (95% confidence interval) of −3.16 (−6.21, −0.11) months for FOLFOX, p = 0.042. A significant shorter median PFS of FOLFOX to Sorafenib of −2.13 (−3.03, −1.24) months, p < 0.001, was reported. Conclusion: Despite significantly shorter median OS and PFS than Sorafenib, FOLFOX still extended OS by 8.22 months. This evidence may offer clinical utility to physicians considering treatment options for aHCC in low resource settings.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectMedicineen_US
dc.titleTreatment outcomes of advanced hepatocellular carcinoma in real-life practice: Chemotherapy versus multikinase inhibitorsen_US
dc.typeJournalen_US
article.title.sourcetitleCancer Medicineen_US
article.stream.affiliationsSchool of Medicine and Public Healthen_US
article.stream.affiliationsFaculty of Medicine, Chiang Mai Universityen_US
article.stream.affiliationsVajira Hospitalen_US
article.stream.affiliationsFaculty of Medicine Ramathibodi Hospital, Mahidol Universityen_US
article.stream.affiliationsSchool of Medicine, Dentistry and Biomedical Sciencesen_US
article.stream.affiliationsLampang Cancer Hospitalen_US
Appears in Collections:CMUL: Journal Articles

Files in This Item:
There are no files associated with this item.


Items in CMUIR are protected by copyright, with all rights reserved, unless otherwise indicated.