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递增剂量的干扰素α-2A联合顺铂及同步放疗:一项I期研究。

Escalating doses of interferon alpha-2A with cisplatin and concomitant radiotherapy: a phase I study.

作者信息

Vokes E E, Haraf D J, Hoffman P C

机构信息

Department of Medicine, University of Chicago, IL 60637.

出版信息

Cancer Chemother Pharmacol. 1993;33(3):203-9. doi: 10.1007/BF00686217.

DOI:10.1007/BF00686217
PMID:8269601
Abstract

In this phase I study, we added escalating doses of interferon-alpha 2A (IFN) to cisplatin and twice-daily radiotherapy based on the following rationale. Radiation enhancement has been shown for both interferon and cisplatin; in addition, potentiation of the cytotoxic activity of cisplatin by interferon has been demonstrated. A total of 48 patients with advanced solid tumors were treated with radiotherapy in 2 daily fractions of 125 cGy plus cisplatin at 8-10 mg/m2 per day delivered on 3 different schedules (continuous infusion, daily short-term infusion, and single short-term infusion of 50 mg/m2). IFN was injected s.c. 2 h preceding the first daily fraction of radiation. IFN doses ranged from 0 to 5.0 x 10(6) U/m2 per day. All therapy was given over 5 days of every other week until completion of the radiotherapy. Treatment at all dose levels was well tolerated during cycles 1 and 2, with no instance of acute grade 3 or 4 toxicity being noted. However, cumulative myelosuppression in patients receiving more than two treatment cycles was seen at all dose levels and was attributed to the repeated administration of cisplatin. Alteration of the cisplatin schedule did not allow for further dose escalation of cisplatin. Our recommended doses are cisplatin given at 8 mg/m2 per day as a continuous infusion with IFN at 5.0 x 10(6) U/m2 per day. Among 24 patients with non-small-cell lung cancer, 2 had a complete response, 9 had a partial response, and 7 had stable disease. We conclude that this concomitant cisplatin-IFN-radiotherapy regimen is feasible. Activity was seen in non-small-cell lung cancer, and further studies of this regimen in that disease appear indicated.

摘要

在这项I期研究中,基于以下理论依据,我们在顺铂和每日两次放疗基础上加用递增剂量的干扰素-α 2A(IFN)。干扰素和顺铂均已显示出放射增敏作用;此外,干扰素增强顺铂细胞毒活性的作用也已得到证实。共有48例晚期实体瘤患者接受放疗,每日分2次给予125 cGy,同时每日给予顺铂8 - 10 mg/m²,采用3种不同给药方案(持续输注、每日短期输注和单次短期输注50 mg/m²)。IFN在每日首次放疗前2小时皮下注射。IFN剂量范围为0至5.0×10⁶ U/m²/天。所有治疗每两周进行5天,直至放疗结束。在第1和第2周期,所有剂量水平的治疗耐受性良好,未观察到急性3级或4级毒性反应。然而,所有剂量水平下接受超过两个治疗周期的患者均出现累积性骨髓抑制,这归因于顺铂的重复给药。顺铂给药方案的改变并未允许顺铂进一步增加剂量。我们推荐的剂量是顺铂每日8 mg/m²持续输注,同时IFN每日5.0×10⁶ U/m²。在24例非小细胞肺癌患者中,2例完全缓解,9例部分缓解,7例病情稳定。我们得出结论,这种顺铂 - IFN - 放疗联合方案是可行的。在非小细胞肺癌中观察到了活性,似乎有必要对该疾病的这一方案进行进一步研究。

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引用本文的文献

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A phase I trial of concomitant chemoradiotherapy with cisplatin dose intensification and granulocyte-colony stimulating factor support for advanced malignancies of the chest.一项关于顺铂剂量强化及粒细胞集落刺激因子支持的同步放化疗用于胸部晚期恶性肿瘤的I期试验。
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2
A phase I trial of 5-day continuous infusion cisplatin and interferon alpha.
Cancer Chemother Pharmacol. 1995;37(1-2):39-46. doi: 10.1007/BF00685627.

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