Concurrent chemobiotherapy with cisplatin, dacarbazine, decrescendo interleukin-2 and interferon α2b in patients with metastatic melanoma

被引:4
|
作者
Bar, Jair [2 ]
Yerushalmi, Rinat [2 ,4 ]
Shapira-Frummer, Roni
Kutchuk, Irena
Sulkes, Aaron [2 ,4 ]
Gutman, Haim [2 ,3 ]
Catane, Raphael [2 ]
Schachter, Jacob [1 ,2 ]
机构
[1] Chaim Sheba Med Ctr, Inst Oncol, Div Oncol, IL-52621 Tel Hashomer, Israel
[2] Tel Aviv Univ, Sackler Fac Med, IL-69978 Tel Aviv, Israel
[3] RMC, Dept Surg B, IL-49100 Petah Tiqwa, Israel
[4] Rabin Med Ctr, Davidoff Ctr, Inst Oncol, IL-49100 Petah Tiqwa, Israel
关键词
metastatic melanoma; chemobiotherapy; complete response;
D O I
10.3892/or_00000176
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We aimed to evaluate a Concurrent chemobiotherapy (CBT) regimen consisting of cisplatin (CDDP), dacarbazine (DTIC), decrescendo interleukin-2 (IL-2). and interferon alpha 2b (INF-alpha 2b), in metastatic melanoma patients. A total of 60 patients with biopsy proven, metastatic melanoma were treated between October 2000 and November 2005 at the Oncology Institutes of RMC and CSMC. Patients received Concurrent CBT for 5 clays, consisting of CDDP, DTIC, decrescendo IL-2, and subcutaneous INF-alpha x2b. GM-CSF was given Subcutaneously on clays 8 to 12 of each cycle, to the first 26 patients. Treatment was administered q21d for a total of six cycles or until severe toxicity or progression; 57 patients who received at least two cycles, followed for atleast 24 months, were included in response analysis. The overall response rate (RR) reached 44% (28/57 patients), 14 patients had a complete response (CR, 25%); 11 (19%) reached a partial response. The median progression-free survival was 7 months. Median overall survival (OS) was 11.7 months. At a median follow-up of 29 months, 8 of 14 complete responders remain alive for more than two years, with no clinical evidence of disease. Median OS of patients with CR has not been reached 17% of the Courses were modified due to toxicity, and 20% of the patients were removed from the protocol due to toxicity or refusal to continue. The data from this study indicate that this protocol of concomitant CBT is feasible with a fraction of the patients achieving a durable CR.
引用
收藏
页码:1533 / 1538
页数:6
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