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Long-term Survival, Tolerability, and Safety of First-Line Bevacizumab and FOLFIRI in Combination With Ginsenoside-Modified Nanostructured Lipid Carrier Containing Curcumin in Patients With Unresectable Metastatic Colorectal Cancer

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dc.contributor.authorJeon, Youngbae-
dc.contributor.authorSym, Sun Jin-
dc.contributor.authorYoo, Bong Kyu-
dc.contributor.authorBaek, Jeong-Heum-
dc.date.accessioned2022-07-19T02:40:53Z-
dc.date.available2022-07-19T02:40:53Z-
dc.date.created2022-07-19-
dc.date.issued2022-06-
dc.identifier.issn1534-7354-
dc.identifier.urihttps://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/85020-
dc.description.abstractBackground: Colorectal cancer is the third most common malignant disease and the second leading cause of death worldwide. Previous studies showed improved bioavailability and cytotoxicity of ginsenoside-modified nanostructured lipid carrier containing curcumin (G-NLC) in human colon cancer cell lines. This study aimed to evaluate the safety and tolerability with long-term survival rates in patients with colorectal cancer with unresectable metastases after treatment with first-line bevacizumab/FOLFIRI (folinic acid, bolus/continuous fluorouracil, and irinotecan) in combination with a dietary supplement of G-NLC. Methods: This study was a prospective, observational, single-group analysis. The enrolled patients had colorectal cancer with unresectable metastases and were administered bevacizumab and FOLFIRI in combination with daily oral G-NLC as first-line treatment. Overall survival, progression-free survival, tumor response, and adverse events were evaluated. Results: A total of 44 patients were enrolled between 2015 and 2019. The median age was 65 (range 45-81) years and the sex ratio was 31:13 (male:female). The primary tumor locations were the colon (31 patients) and rectum (13 patients). The metastatic sites included, liver only (n = 20), lung only (n = 6), both liver and lung (n = 12), and others (n = 6). The median duration of curcumin supply was 7.9 (range 0.9-16.6) months. The most common grade 3 or higher adverse events were neutropenia (n = 15, 34.1%), followed by nausea (n = 4, 9.1%) and vomiting (n = 4, 9.1%). Within the median follow-up period of 22.8 months, the median overall survival was 30.7 months, and the median progression-free survival was 12.8 months. None of the patients achieved complete response (CR); however, 9 patients showed partial response (PR), and 3 patients underwent conversion surgery. Conclusions: Bevacizumab/FOLFIRI with G-NLC as first-line chemotherapy in patients with colorectal cancer with unresectable metastases presented comparable long-term survival outcomes with acceptable toxicity outcomes. Additional randomized controlled studies are needed to establish definitive conclusions regarding this new regimen for metastatic colorectal cancer.-
dc.language영어-
dc.language.isoen-
dc.publisherSAGE PUBLICATIONS INC-
dc.relation.isPartOfINTEGRATIVE CANCER THERAPIES-
dc.titleLong-term Survival, Tolerability, and Safety of First-Line Bevacizumab and FOLFIRI in Combination With Ginsenoside-Modified Nanostructured Lipid Carrier Containing Curcumin in Patients With Unresectable Metastatic Colorectal Cancer-
dc.typeArticle-
dc.type.rimsART-
dc.description.journalClass1-
dc.identifier.wosid000813691700001-
dc.identifier.doi10.1177/15347354221105498-
dc.identifier.bibliographicCitationINTEGRATIVE CANCER THERAPIES, v.21-
dc.description.isOpenAccessY-
dc.identifier.scopusid2-s2.0-85131849492-
dc.citation.titleINTEGRATIVE CANCER THERAPIES-
dc.citation.volume21-
dc.contributor.affiliatedAuthorJeon, Youngbae-
dc.contributor.affiliatedAuthorSym, Sun Jin-
dc.contributor.affiliatedAuthorYoo, Bong Kyu-
dc.contributor.affiliatedAuthorBaek, Jeong-Heum-
dc.type.docTypeArticle-
dc.subject.keywordAuthorcurcumin-
dc.subject.keywordAuthormetastatic colorectal cancer-
dc.subject.keywordAuthorchemotherapy-
dc.subject.keywordAuthorsurvival-
dc.subject.keywordAuthoradverse event-
dc.subject.keywordPlusPHYSICOCHEMICAL PROPERTIES-
dc.subject.keywordPlusNANOPARTICLE DISPERSION-
dc.subject.keywordPlusRANDOMIZED-TRIALS-
dc.subject.keywordPlusPLUS BEVACIZUMAB-
dc.subject.keywordPlusPHASE-III-
dc.subject.keywordPlusTUMORS-
dc.subject.keywordPlusBIOAVAILABILITY-
dc.subject.keywordPlusDOCETAXEL-
dc.subject.keywordPlusCETUXIMAB-
dc.subject.keywordPlusRESECTION-
dc.relation.journalResearchAreaOncology-
dc.relation.journalResearchAreaIntegrative & Complementary Medicine-
dc.relation.journalWebOfScienceCategoryOncology-
dc.relation.journalWebOfScienceCategoryIntegrative & Complementary Medicine-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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