Publication: Single-agent temozolomide may be an effective option for late adjuvant therapy in patients with melanoma
dc.contributor.coauthor | Tas, Faruk | |
dc.contributor.department | N/A | |
dc.contributor.kuauthor | Ertürk, Kayhan | |
dc.contributor.kuprofile | Faculty Member | |
dc.contributor.schoolcollegeinstitute | School of Medicine | |
dc.contributor.unit | Koç University Hospital | |
dc.contributor.yokid | N/A | |
dc.date.accessioned | 2024-11-09T23:58:37Z | |
dc.date.issued | 2021 | |
dc.description.abstract | Background 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.indexedby | WoS | |
dc.description.indexedby | Scopus | |
dc.description.indexedby | PubMed | |
dc.description.issue | 1 | |
dc.description.openaccess | NO | |
dc.description.publisherscope | International | |
dc.description.volume | 27 | |
dc.identifier.doi | 10.1177/1078155220909426 | |
dc.identifier.eissn | 1477-092X | |
dc.identifier.issn | 1078-1552 | |
dc.identifier.scopus | 2-s2.0-85082109214 | |
dc.identifier.uri | http://dx.doi.org/10.1177/1078155220909426 | |
dc.identifier.uri | https://hdl.handle.net/20.500.14288/15493 | |
dc.identifier.wos | 524151100001 | |
dc.keywords | Temozolomide | |
dc.keywords | Melanoma | |
dc.keywords | Late adjuvant therapy | |
dc.keywords | Survival stage-III | |
dc.keywords | Double-blind | |
dc.keywords | Combination | |
dc.keywords | Ipilimumab | |
dc.keywords | Placebo | |
dc.language | English | |
dc.publisher | Sage Publications Ltd | |
dc.source | Journal of Oncology Pharmacy Practice | |
dc.subject | Oncology | |
dc.subject | Pharmacology | |
dc.subject | Pharmacy | |
dc.title | Single-agent temozolomide may be an effective option for late adjuvant therapy in patients with melanoma | |
dc.type | Journal Article | |
dspace.entity.type | Publication | |
local.contributor.authorid | 0000-0001-5804-6800 | |
local.contributor.kuauthor | Ertürk, Kayhan |