Publication:
Single-agent temozolomide may be an effective option for late adjuvant therapy in patients with melanoma

dc.contributor.coauthorTas, Faruk
dc.contributor.departmentN/A
dc.contributor.kuauthorErtürk, Kayhan
dc.contributor.kuprofileFaculty Member
dc.contributor.schoolcollegeinstituteSchool of Medicine
dc.contributor.unitKoç University Hospital
dc.contributor.yokidN/A
dc.date.accessioned2024-11-09T23:58:37Z
dc.date.issued2021
dc.description.abstractBackground Late adjuvant therapy is the term to define the treatment administered following complete resection of metastatic or relapsed disease. Objective To assess the efficacy of single-agent temozolomide, a standard agent is used for metastatic melanoma in late adjuvant chemotherapy for cutaneous melanoma. Methods Twenty-seven adult cutaneous melanoma patients whose relapses were completely resected were included in this study. Temozolomide was administered as follows: peroral, 200 mg/m(2) once daily for five consecutive days of a 28-day treatment cycle for six cycles. Results The median age was 55 years and men were predominant (74%). Median follow-up time was 23.6 months (range, 3.6-122.6 months). Any type of relapse occurred in 14 (51.9%) patients, and five patients relapsed while on chemotherapy. Almost all relapses (n = 13, 93%) occurred within the first two years of follow-up. The relapse rates were found 37.4 and 49.1% in the first and second years of follow-up, respectively. Moreover, after fifth year of onset of chemotherapy, relapse rate was found only 51.9%. The median relapse-free survival (RFS) was 12.9 months, and 1-, 2-, 3-, and 5-year RFS rates were 60, 46, 39, and 39%, respectively. The estimated median overall survival was 23.6 months. All patients survived first year (n = 27, 100%), and the overall survival rates for 2, 3, and 5 years were 81, 48, and 48%, respectively. Conclusion Single-agent temozolomide may be a rational and prudent option for late adjuvant therapy in melanoma patients if/when novel therapies, such as targeting and immune therapies, are not accessible or available.
dc.description.indexedbyWoS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.issue1
dc.description.openaccessNO
dc.description.publisherscopeInternational
dc.description.volume27
dc.identifier.doi10.1177/1078155220909426
dc.identifier.eissn1477-092X
dc.identifier.issn1078-1552
dc.identifier.scopus2-s2.0-85082109214
dc.identifier.urihttp://dx.doi.org/10.1177/1078155220909426
dc.identifier.urihttps://hdl.handle.net/20.500.14288/15493
dc.identifier.wos524151100001
dc.keywordsTemozolomide
dc.keywordsMelanoma
dc.keywordsLate adjuvant therapy
dc.keywordsSurvival stage-III
dc.keywordsDouble-blind
dc.keywordsCombination
dc.keywordsIpilimumab
dc.keywordsPlacebo
dc.languageEnglish
dc.publisherSage Publications Ltd
dc.sourceJournal of Oncology Pharmacy Practice
dc.subjectOncology
dc.subjectPharmacology
dc.subjectPharmacy
dc.titleSingle-agent temozolomide may be an effective option for late adjuvant therapy in patients with melanoma
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.authorid0000-0001-5804-6800
local.contributor.kuauthorErtürk, Kayhan

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