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达卡巴嗪联合α-2a干扰素、粒细胞集落刺激因子及昂丹司琼用于转移性黑色素瘤患者的剂量递增研究。

Dose escalation of dacarbazine combined with interferon alpha-2a, G-CSF and ondansetron in patients with metastatic melanoma.

作者信息

Buter J, Sleijfer D T, Willemse P H, van der Graaf W T, de Vries E G, Schraffordt Koops H, Mulder N H

机构信息

Department of Medical Oncology, University Hospital, Groningen, The Netherlands.

出版信息

Anticancer Res. 1994 May-Jun;14(3B):1325-8.

PMID:7520681
Abstract

To define the activity of an individually escalated dacarbazine (DTIC) dose combined with interferon-alpha-2a (IFN), granulocyte-colony stimulating-factor (G-CSF) and ondansetron, 20 patients (pts) with metastatic melanoma were treated with DTIC, ondansetron 8 mg iv, G-CSF 300 micrograms sc and IFN 9 MU sc. Treatment was performed every 21 days to a maximum of 6 courses. DTIC dose was escalated with 250 mg/m2 in case of acceptable toxicity to 1250, 1500 and 1750 mg/m2 in (projected/realized), 14/19, 8/11 and 0/5 pts, respectively. Dose escalation prohibiting toxicities were thrombocytopenia (10 pts), leukopenia (9 pts), and nausea/vomiting (2 pts). Four partial remissions were observed, for a response rate of 20% (95% confidence interval, 6 to 44%). Duration of responses was 1, 2, 3 and 3 months. Median overall survival was 8 months.

摘要

为明确个体化递增剂量的达卡巴嗪(DTIC)联合α-2a干扰素(IFN)、粒细胞集落刺激因子(G-CSF)和昂丹司琼的活性,对20例转移性黑色素瘤患者采用DTIC、静脉注射8mg昂丹司琼、皮下注射300μg G-CSF和皮下注射9MU IFN进行治疗。每21天进行一次治疗,最多6个疗程。若毒性可接受,DTIC剂量从250mg/m²递增至(预计/实际)1250、1500和1750mg/m²,分别有14/19、8/11和0/5例患者。剂量递增的禁止毒性为血小板减少(10例患者)、白细胞减少(9例患者)和恶心/呕吐(2例患者)。观察到4例部分缓解,缓解率为20%(95%置信区间,6%至44%)。缓解持续时间分别为1、2、3和3个月。中位总生存期为8个月。

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