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[每周紫杉醇联合调强适形放疗治疗鼻咽癌:耐受性试验结果]

[Weekly paclitaxel with concurrent intensity-modulated radiotherapy for nasopharyngeal carcinoma: outcomes of a tolerance trial].

作者信息

Chen Chun-Yan, Lu Tai-Xiang, Zhao Chong, Lu Li-Xia, Han Fei, Sun Ying

机构信息

State Key Laboratory of Oncology in South China, Guangzhou, Guangdong, 510060, P. R. China.

出版信息

Ai Zheng. 2007 Apr;26(4):398-402.

Abstract

BACKGROUND & OBJECTIVE: Concurrent chemoradiotherapy has definite effect on local-regionally advanced nasopharyngeal carcinoma (NPC). Paclitaxel is confirmed by clinical trail to be one of the most effective single drugs for NPC. This study was to define the maximal tolerant dose (MTD) of paclitaxel in weekly paclitaxel with concurrent intensity-modulated radiotherapy (IMRT) for local-regionally advanced NPC.

METHODS

Naive patients with locally advanced NPC were enrolled into this dose-escalating study. Adverse events were graded according to Common Terminology Criteria for Adverse Events version 3.0 (CTCAE v3.0). Primary end points were determined by dose-limiting toxicity (DLT). The starting dose of paclitaxel was 30 mg.(m(2).w)(-1), with a subsequent dose escalation of 10 mg.(m(2).w)(-1). IMRT was given to the nasopharynx and the upper neck; the lower neck was treated by a single anterior field irradiation. The prescription dose was 68 Gy by 30 fractions to the nasopharynx gross tumor, and 60-66 Gy by 30 fractions to the positive neck lymph nodes.

RESULTS

From Apr. 2004 to Sep. 2004, 15 patients received complete chemoradiotherapy, and all of them were eligible for toxicity evaluation. On the first two dose levels of 30 mg.(m(2).w)(-1) and 40 mg.(m(2).w)(-1), no patient experienced DLT. On the next dose level of 50 mg.(m(2).w)(-1), 1 patient experienced DLT of grade 3 mucositis for 4 weeks, and among the additional 3 patients no one developed DLT. On the forth dose level of 60 mg.(m(2).w)(-1), all the patients developed grade 3 mucositis for more than 3 weeks, and the dose-escalating trial stopped. All of the 15 patients achieved clinical complete remission (CR) in the local site; 14 (93.3%) achieved CR in the regional site, and 1 achieved partial remission (PR) and got CR 1 month later. After a median follow-up of 20 months, 1 patient developed multiple bone metastases, and 14 kept disease-free.

CONCLUSION

The MTD of paclitaxel in weekly paclitaxel with concurrent IMRT for local-regionally advanced NPC is 50 mg.(m(2).w)(-1), with mucositis as DLT.

摘要

背景与目的

同步放化疗对局部区域晚期鼻咽癌(NPC)有确切疗效。紫杉醇经临床试验证实是治疗NPC最有效的单药之一。本研究旨在确定局部区域晚期NPC患者在每周紫杉醇同步调强放疗(IMRT)中的最大耐受剂量(MTD)。

方法

将初治的局部晚期NPC患者纳入本剂量递增研究。不良事件根据《不良事件通用术语标准》第3.0版(CTCAE v3.0)进行分级。主要终点由剂量限制毒性(DLT)确定。紫杉醇起始剂量为30mg·(m²·w)⁻¹,随后每次递增10mg·(m²·w)⁻¹。对鼻咽部和上颈部进行IMRT;下颈部采用单前野照射。鼻咽部大体肿瘤的处方剂量为68Gy,分30次照射,阳性颈部淋巴结的处方剂量为60 - 66Gy,分30次照射。

结果

2004年4月至2004年9月,15例患者接受了完整的放化疗,所有患者均符合毒性评估标准。在30mg·(m²·w)⁻¹和40mg·(m²·w)⁻¹这两个初始剂量水平时,无患者发生DLT。在50mg·(m²·w)⁻¹剂量水平时,1例患者出现3级黏膜炎,持续4周,另外3例患者未发生DLT。在60mg·(m²·w)⁻¹剂量水平时,所有患者均出现3级黏膜炎,持续超过3周,剂量递增试验停止。15例患者局部均达到临床完全缓解(CR);14例(93.3%)区域达到CR,1例达到部分缓解(PR),1个月后达到CR。中位随访20个月后,1例患者发生多发骨转移,14例无疾病进展。

结论

局部区域晚期NPC患者在每周紫杉醇同步IMRT中的MTD为50mg·(m²·w)⁻¹,DLT为黏膜炎。

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