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dc.contributor.authorOzguroglu, M
dc.contributor.authorBerkarda, B
dc.contributor.authorSerdengecti, S
dc.contributor.authorDemirelli, F
dc.contributor.authorDemir, G
dc.contributor.authorBelentepe, S
dc.contributor.authorBuyukunal, E
dc.contributor.authorMandel, N
dc.date.accessioned2021-03-03T21:02:45Z
dc.date.available2021-03-03T21:02:45Z
dc.identifier.citationDemir G., Ozguroglu M., Belentepe S., Demirelli F., Mandel N., Buyukunal E., Serdengecti S., Berkarda B., "Chemoimmunotherapy protocol in patients with advanced gastric cancer", 2nd Congress of the Balkan-Union-of-Oncology, İzmir, Türkiye, 10 - 14 Eylül 1998, ss.407-411
dc.identifier.othervv_1032021
dc.identifier.otherav_5d26b245-07ac-43eb-89d3-bb815b349d83
dc.identifier.urihttp://hdl.handle.net/20.500.12627/65244
dc.description.abstractWe tested in a prospective phase II study a chemo-immuno therapy protocol in advanced gastric cancer patients. The regimen consisted of Cisplatin 50 mg/m(2) D3, 5-FU 375 mg/m(2) D1-3, Folinic Acid 20 mg/m(2) D1-3, IFN-alpha 2b 3 Mio U sc. D1-3, every 28d; and IFN-alpha 2b 3 Mio U sc. 3 times weekly between the cycles. Twentyfive patients were included (20 males, 5 females). Mean age was 54,3 yr (25-75). Five presented with locally advanced disease and 20 had metastatic disease. Response rate was 40% (1 CR, 7 PR). Median overall survival was 9+/-3 months (95% CI 7-10 months). The toxicity profile of this regimen was: G I-II Fever: 14 patients, G II Neutropenia: 3 patients, G I Renal toxicity: 2 patients. We conclude that, this regimen is well tolerated on an outpatient basis, and effective in advanced gastric cancer patients.
dc.language.isoeng
dc.subjectDahili Tıp Bilimleri
dc.subjectİç Hastalıkları
dc.subjectOnkoloji
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp
dc.subjectONKOLOJİ
dc.subjectKlinik Tıp (MED)
dc.titleChemoimmunotherapy protocol in patients with advanced gastric cancer
dc.typeBildiri
dc.contributor.department, ,
dc.contributor.firstauthorID122233


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