Tait D M, Nahum A E, Meyer L C, Law M, Dearnaley D P, Horwich A, Mayles W P, Yarnold J R
Department of Radiotherapy, Royal Marsden NHS Trust, Sutton, UK.
Radiother Oncol. 1997 Feb;42(2):121-36. doi: 10.1016/s0167-8140(96)01870-1.
A prospective, randomized clinical trial to assess the effect of reducing the volume of irradiated normal tissue on acute reactions in pelvic radiotherapy accured 266 evaluable patients between 1988 and 1993.
This is the definitive analysis to assess the differences between the conformal and conventional arms of the trial.
In both arms, patients were treated with 6 MV X-rays using a 3-field technique (in all but 5 cases) consisting of an anterior and two wedged lateral or posterior oblique fields; in the conventional arm, rectangular fields were employed, whereas in the conformal arm, the fields were shaped with customized blocks drawn according to the beam's-eye-view of the target volume. The most common dosage was 64 Gy in 2-Gy fractions 5 times a week, although a subgroup (of ca. bladder patients) were treated with 30-36 Gy in once-a-week 6 Gy fractions. Each patients completed a comprehensive acute toxicity scoring questionnaire concentrating on bowel and bladder problems, tiredness and nausea, before the start of treatment, weekly during and for 3 weeks after the end of treatment and then monthly for a further 2 months. compliance was excellent.
There were no differences between the patients in the two arms with respect to age, gender, tumour type (52% prostate, 41% bladder, 5% rectum, 2% other) fractionation/dosage, anterior field size, weight, or baseline symptoms. Substantial differences in normal-tissue volumes (rectum, bladder, etc.) were achieved: median high-dose volume (HDV) of 689 cm3 for the conformal technique versus 792 cm3 for the conventional. A clear pattern of an increase in symptoms during RT, followed by a decrease after RT, was observed for the patient group as a whole. However, a very extensive analysis has not revealed any (statistically) significant differences between the two arms in level of symptoms, nor in medication prescribed. The disparity between our findings and those of other, non-randomized studies is discussed.
The data on late effects must be collected and analyzed before any definite conclusions can be drawn on the benefits of conformal therapy in the pelvis.
1988年至1993年间,一项前瞻性随机临床试验对266例可评估患者进行了研究,以评估减少盆腔放疗中正常组织照射体积对急性反应的影响。
这是一项确定性分析,旨在评估该试验中适形放疗组与传统放疗组之间的差异。
两组患者均采用6兆伏X射线,使用三野技术(除5例患者外),包括一个前野和两个楔形侧野或后斜野;在传统放疗组中,采用矩形野,而在适形放疗组中,根据靶区体积的射野方向观用定制挡铅塑造射野形状。最常见的剂量是每周5次,每次2戈瑞,总量64戈瑞,不过有一小部分(约膀胱患者)采用每周1次,每次6戈瑞,总量30 - 36戈瑞的方案。每位患者在治疗开始前、治疗期间每周以及治疗结束后3周内每周填写一份综合急性毒性评分问卷,重点关注肠道和膀胱问题、疲劳和恶心,之后在接下来的2个月内每月填写一次。依从性良好。
两组患者在年龄、性别、肿瘤类型(52%为前列腺癌、41%为膀胱癌、5%为直肠癌、2%为其他)、分割/剂量、前野大小、体重或基线症状方面均无差异。正常组织体积(直肠、膀胱等)有显著差异:适形技术的中位高剂量体积(HDV)为689立方厘米,传统技术为792立方厘米。对于整个患者群体,观察到放疗期间症状增加,放疗后症状减轻的明显模式。然而,经过非常广泛的分析,未发现两组在症状水平或所开药物方面有任何(统计学)显著差异。讨论了我们的研究结果与其他非随机研究结果之间的差异。
在就适形治疗对盆腔的益处得出任何明确结论之前,必须收集和分析关于晚期效应的数据。