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三维调强放射治疗在鼻咽癌治疗中的应用:加利福尼亚大学旧金山分校的经验

Three-dimensional intensity-modulated radiotherapy in the treatment of nasopharyngeal carcinoma: the University of California-San Francisco experience.

作者信息

Sultanem K, Shu H K, Xia P, Akazawa C, Quivey J M, Verhey L J, Fu K K

机构信息

Department of Radiation Oncology, University of California, San Francisco, CA 94143-0226, USA.

出版信息

Int J Radiat Oncol Biol Phys. 2000 Oct 1;48(3):711-22. doi: 10.1016/s0360-3016(00)00702-1.

Abstract

PURPOSE

To review our experience with three-dimensional intensity-modulated radiotherapy (IMRT) in the treatment of nasopharyngeal carcinoma.

METHODS AND MATERIALS

We reviewed the records of 35 patients who underwent 3D IMRT for nasopharyngeal carcinoma at the University of California-San Francisco between April 1995 and March 1998. According to the 1997 American Joint Committee on Cancer staging classification, 4 (12%) patients had Stage I disease, 6 (17%) had Stage II, 11 (32%) had Stage III, and 14 (40%) had Stage IV disease. IMRT of the primary tumor was delivered using one of the following three techniques: (1) manually cut partial transmission blocks, (2) computer-controlled autosequencing static multileaf collimator (MLC), and (3) Peacock system using a dynamic multivane intensity-modulating collimator (MIMiC). A forward 3D treatment-planning system was used for the first two methods, and an inverse treatment planning system was used for the third method. The neck was irradiated with a conventional technique using lateral opposed fields to the upper neck and an anterior field to the lower neck and supraclavicular fossae. The prescribed dose was 65-70 Gy to the gross tumor volume (GTV) and positive neck nodes, 60 Gy to the clinical target volume (CTV), and 50-60 Gy to the clinically negative neck. Eleven (32%) patients had fractionated high-dose-rate intracavitary brachytherapy boost to the primary tumor 1-2 weeks following external beam radiotherapy. Thirty-two (91%) patients also received cisplatin during, and cisplatin and 5-fluorouracil after, radiotherapy. Acute and late normal tissue effects were graded according to the Radiation Therapy Oncology Group (RTOG) radiation morbidity scoring criteria. Local-regional progression-free, distant metastasis-free survival and overall survival were estimated using the Kaplan-Meier method.

RESULTS

With a median follow-up of 21.8 months (range, 5-49 months), the local-regional progression-free rate was 100%. The 4-year overall survival was 94%, and the distant metastasis-free rate was 57%. The worst acute toxicity was Grade 2 in 16 (46%) patients, Grade 3 in 18 (51%) patients and Grade 4 in 1 (3%) patient. The worst late toxicity was Grade 1 in 15 (43%), Grade 2 in 13 (37%), and Grade 3 in 5 (14%) patients. Only 1 patient had a transient Grade 4 soft-tissue necrosis. At 24 months after treatment, 50% of the evaluated patients had Grade 0, 50% had Grade 1, and none had Grade 2 xerostomia. Analysis of the dose-volume histograms (DVHs) showed that the average maximum, mean, and minimum dose delivered were 79.5 Gy, 75.8 Gy, and 56.5 Gy to the GTV, and 78.9 Gy, 71.2 Gy, and 45.4 Gy to the CTV, respectively. An average of only 3% of the GTV and 2% of the CTV received less than 95% of the prescribed dose. The average dose to 5% of the brain stem, optic chiasm, and right and left optic nerves was 48.3 Gy, 23.9 Gy, 15.0 Gy, and 14.9 Gy, respectively. The average dose to 1 cc of the cervical spinal cord was 41.7 Gy. The doses delivered were within the tolerance of these critical normal structures. The average dose to 50% of the right and left parotids, pituitary, right and left T-M joints, and ears was 43. 2 Gy, 41.0 Gy, 46.3 Gy, 60.5 Gy, 58.3 Gy, 52.0 Gy, and 52.2 Gy, respectively.

CONCLUSION

3D intensity-modulated radiotherapy provided improved target volume coverage and increased dose to the gross tumor with significant sparing of the salivary glands and other critical normal structures. Local-regional control rate with combined IMRT and chemotherapy was excellent, although distant metastasis remained unabated.

摘要

目的

回顾我们运用三维调强放射治疗(IMRT)技术治疗鼻咽癌的经验。

方法与材料

我们回顾了1995年4月至1998年3月期间在加利福尼亚大学旧金山分校接受三维IMRT治疗鼻咽癌的35例患者的记录。根据1997年美国癌症联合委员会分期分类,4例(12%)患者为I期疾病,6例(17%)为II期,11例(32%)为III期,14例(40%)为IV期疾病。原发肿瘤的IMRT采用以下三种技术之一进行:(1)手动切割部分透射挡块,(2)计算机控制的自动排序静态多叶准直器(MLC),以及(3)使用动态多叶强度调制准直器(MIMiC)的孔雀系统。前两种方法使用正向三维治疗计划系统,第三种方法使用逆向治疗计划系统。颈部采用传统技术进行照射,对上颈部使用双侧对穿野,对下颈部和锁骨上窝使用前野。处方剂量为:大体肿瘤体积(GTV)和阳性颈部淋巴结65 - 70 Gy,临床靶体积(CTV)60 Gy,临床阴性颈部50 - 60 Gy。11例(32%)患者在体外照射放疗后1 - 2周接受分次高剂量率腔内近距离放疗对原发肿瘤进行增敏。32例(91%)患者在放疗期间接受顺铂治疗,放疗后接受顺铂和5 - 氟尿嘧啶治疗。急性和晚期正常组织反应根据放射肿瘤学组(RTOG)放射发病率评分标准进行分级。采用Kaplan - Meier方法估计局部区域无进展、无远处转移生存和总生存情况。

结果

中位随访时间为21.8个月(范围5 - 49个月),局部区域无进展率为100%。4年总生存率为94%,无远处转移率为57%。最严重的急性毒性反应为:16例(46%)患者为2级,18例(51%)患者为3级,1例(3%)患者为4级。最严重的晚期毒性反应为:15例(43%)患者为1级,13例(37%)患者为2级,5例(14%)患者为3级。仅1例患者出现短暂的4级软组织坏死。治疗后24个月,50%的评估患者口干分级为0级,50%为1级,无2级口干患者。剂量体积直方图(DVH)分析显示,GTV的平均最大剂量、平均剂量和最小剂量分别为79.5 Gy、75.8 Gy和56.5 Gy,CTV的分别为78.9 Gy、71.2 Gy和45.4 Gy。平均仅有3%的GTV和2%的CTV接受的剂量低于处方剂量的95%。脑干、视交叉以及左右视神经5%体积的平均剂量分别为48.3 Gy、23.9 Gy、15.0 Gy和14.9 Gy。颈髓1 cc体积的平均剂量为41.7 Gy。所给予的剂量在这些关键正常结构的耐受范围内。左右腮腺、垂体、左右颞下颌关节和耳朵50%体积的平均剂量分别为43.2 Gy、41.0 Gy、46.3 Gy、60.5 Gy、58.3 Gy、52.0 Gy和52.2 Gy。

结论

三维调强放射治疗改善了靶体积覆盖,增加了对大体肿瘤的剂量,同时显著减少了唾液腺和其他关键正常结构所受剂量。尽管远处转移率仍未降低,但IMRT联合化疗的局部区域控制率极佳。

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