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皮奥特朗:二、II期研究中动态π介子疗法的方法和初步结果。

The Piotron: II. Methods and initial results of dynamic pion therapy in phase II studies.

作者信息

von Essen C F, Blattmann H, Bodendoerfer G, Mizoe J, Pedroni E, Walder E, Zimmermann A

出版信息

Int J Radiat Oncol Biol Phys. 1985 Feb;11(2):217-26. doi: 10.1016/0360-3016(85)90142-7.

Abstract

Negative pi-meson (pion) therapy employing dynamic scanning with a focused spot of convergent beams has been in use since 1981 at SIN. Three-dimensional conformation of the treatment volume to the target volume can thus be achieved. Following previously reported Phase I and Ib clinical trials, a Phase II trial was initiated with the goal of treating primary deep-seated tumors in a dose optimization schedule which included stepwise increase of total pion dose and of target volume. Patients with multicentric superficial bladder tumors who were cystectomy candidates were initially selected. Since then, more invasive cases have been treated. A graded scoring of acute tissue reactions was employed. Follow-up periods were from 10 to 20 months. The pion dose escalation ranged from 3000 rad (minimum) to 3600 rad (minimum) in 20 fractions over 5 weeks. The treatment volumes encompassed 190 cc for local to 1,820 cc for extended volume therapy. Treatment reactions ranged from a faint erythema and increase of bladder frequency to dry desquamation, mild nausea, moderate dysuria, and moderate proctitis or diarrhea with mucus. These reactions were closely related to treatment volume and site. One severe late cystitis has occurred in a patient treated with 2 courses of pions (4475 rad). Mild to moderate late proctitis has been seen in 4 patients. Ten of 13 bladder cancer patients had local control of disease while all 3 pancreas or biliary tract cancer patients had microscopic residual disease locally at time of death from metastasis. A total of 11 of 17 patients are thus clinically or pathologically free of local tumor to time of last observation.

摘要

自1981年起,瑞士保罗·谢尔研究所(SIN)就开始使用负π介子(π介子)疗法,采用聚焦束的动态扫描。由此可实现治疗体积与靶体积的三维构象。在先前报道的I期和Ib期临床试验之后,启动了II期试验,目标是以剂量优化方案治疗原发性深部肿瘤,该方案包括逐步增加总π介子剂量和靶体积。最初选择了适合膀胱切除术的多中心浅表性膀胱肿瘤患者。从那时起,更多侵袭性病例得到了治疗。采用了急性组织反应的分级评分。随访期为10至20个月。π介子剂量在5周内分20次递增,范围从3000拉德(最低)到3600拉德(最低)。治疗体积从局部的190立方厘米到扩展体积治疗的1820立方厘米不等。治疗反应范围从轻微红斑和膀胱频率增加到干性脱屑、轻度恶心、中度排尿困难以及中度直肠炎或伴有黏液的腹泻。这些反应与治疗体积和部位密切相关。一名接受2个疗程π介子治疗(4475拉德)的患者发生了严重的晚期膀胱炎。4名患者出现了轻度至中度的晚期直肠炎。13名膀胱癌患者中有10名实现了疾病的局部控制,而所有3名胰腺癌或胆管癌患者在因转移死亡时局部仍有微小残留病灶。因此,在最后一次观察时,17名患者中有11名在临床或病理上局部无肿瘤。

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