Preparatory clinical studies of Pi-mesons at TRIUMF.

Radiation research. Supplement Pub Date : 1985-01-01
G B Goodman, P Dixon, G K Lam, R Harrison, R O Kornelsen, C M Ludgate, A D Flores
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Abstract

Eighty patients have been treated with Pi-mesons (pions) at TRIUMF between 1979-1984. The patients had tumors rarely curable by standard methods and had no prior radiotherapy. The distribution by site included skin, metastatic nodules (13), brain, glioblastoma multiforme (32), pelvis, rectosigmoid (15), prostate (12), bladder (7), and ovary (1). The studies involve serial escalations of pion dose until maximum tissue tolerance is reached, monitoring the response at each dose increment. Sites were chosen for study where lack of local control is a significant cause of treatment failure with conventional radiation therapy. The low dose rate and the available beam access at TRIUMF limit the number of patients treated and the volume treatable. A 3-D treatment planning program is in use, and a 3-D display of the dose distribution delivered in brain tumor treatments has been developed using the PET scanner. In practice, new methods introduced for measurement of tissue response include tumor growth delay curves, fine-needle biopsy mapping, and PET scanning of brain tumors. The use of endoscopic assessment of the rectosigmoid region is emphasized. Treatment results of glioblastoma multiforme show that the median survival for patients treated to 125 pion cGy/fx is in the range of 187-198 days; for patients receiving 170 cGy per dose/fraction (fx) the range is 290-315 days, and for those receiving 200-220 cGy/fx the median survival is in excess of 290 days. For pelvic malignancies the local control obtained with doses of 2500 cGy or less was 50% in 12 assessable patients; it was 75% in 20 patients who had 3000 cGy or more.(ABSTRACT TRUNCATED AT 250 WORDS)

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π介子在TRIUMF的预备临床研究。
1979-1984年间,在TRIUMF有80名患者接受了π介子(π介子)治疗。这些患者的肿瘤很难用标准方法治愈,并且之前没有接受过放疗。按部位分布包括皮肤、转移性结节(13例)、脑、多形胶质母细胞瘤(32例)、骨盆、乙状直肠(15例)、前列腺(12例)、膀胱(7例)和卵巢(1例)。研究包括连续增加介子剂量,直到达到最大组织耐受性,监测每次剂量增加的反应。研究选择的地点缺乏局部控制是传统放射治疗失败的重要原因。低剂量率和在TRIUMF的可用光束通道限制了治疗的患者数量和可治疗的体积。3-D治疗计划程序正在使用中,并且使用PET扫描仪开发了脑肿瘤治疗中剂量分布的3-D显示。在实践中,引入了测量组织反应的新方法,包括肿瘤生长延迟曲线,细针活检绘图和脑肿瘤的PET扫描。强调使用内窥镜评估直肠乙状结肠区域。多形性胶质母细胞瘤的治疗结果显示,治疗至125介子cGy/fx的患者中位生存期为187-198天;对于每剂量/分数(fx)接受170 cGy治疗的患者,生存期为290-315天,而对于接受200-220 cGy/fx治疗的患者,中位生存期超过290天。对于盆腔恶性肿瘤,在12例可评估的患者中,2500 cGy或更低剂量获得的局部控制率为50%;在20名患者中有75%的人摄入了3000 cGy或更多。(摘要删节250字)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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