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AK-2123作为一种乏氧细胞增敏剂联合放疗治疗晚期头颈癌的初步经验概述。

An overview of the initial experience with AK-2123 as a hypoxic cell sensitizer with radiation in the treatment of advanced head and neck cancers.

作者信息

Huilgol N G, Chatterjee N, Mehta A R

机构信息

Division of Radiation Oncology, Dr. Balabhai Nanavati Hospital, Bombay, India.

出版信息

Int J Radiat Oncol Biol Phys. 1996 Mar 15;34(5):1121-4. doi: 10.1016/0360-3016(95)02181-7.

Abstract

PURPOSE

AK-2123 (Senazole) is a nitrotriazole with a reported potential for hypoxic cell sensitization. The present study was conducted to evaluate hypoxic cell potentiation in patients with advanced head and neck cancer treated with discontinuous accelerated hyperfractionated radiation.

METHODS AND MATERIALS

Histologically proven unresectable oro-pharyngeal cancers Stage T3-4, NO-3 and M0 were randomly allocated to receive discontinuous accelerated hyperfractionated radiation alone or with AK-2123. AK-2123 (880 and 990 mg) was administered as an i.v. infusion between the first and second fraction of radiation for 10 days in two groups of patients. Initial response as a surrogate end point has been analyzed for comparison and documented for follow-up status.

RESULTS

A 100% complete response was observed in both the AK-2123-treated groups (880 mg and 990 mg), while a 44.4% complete response was observed in the control group. There were no treatment-related deaths. Neurotoxicity was not reported.

CONCLUSION

AK-2123 (Senazole) when administered with discontinuous accelerated hyperfractionated radiation showed a significant potentiation that, therefore, requires further evaluation.

摘要

目的

AK - 2123(司那唑)是一种硝基三唑,据报道具有使缺氧细胞增敏的潜力。本研究旨在评估在接受间断加速超分割放疗的晚期头颈癌患者中缺氧细胞的增敏作用。

方法和材料

组织学确诊为不可切除的口咽癌(T3 - 4期、NO - 3期和M0期)患者被随机分配,分别接受单纯间断加速超分割放疗或联合AK - 2123治疗。两组患者中,AK - 2123(880毫克和990毫克)在放疗的第一和第二分次之间静脉输注,共10天。已分析初始反应作为替代终点进行比较,并记录随访状态。

结果

在接受AK - 2123治疗的两组(880毫克组和990毫克组)中均观察到100%的完全缓解,而对照组的完全缓解率为44.4%。未出现与治疗相关的死亡病例。未报告神经毒性。

结论

AK - 2123(司那唑)与间断加速超分割放疗联合使用时显示出显著的增敏作用,因此需要进一步评估。

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