Ceha H M, van Tienhoven G, Gouma D J, Veenhof C H, Schneider C J, Rauws E A, Phoa S S, González González D
Department of Radiation Oncology, Academic Medical Center, Amsterdam, The Netherlands.
Cancer. 2000 Dec 1;89(11):2222-9. doi: 10.1002/1097-0142(20001201)89:11<2222::aid-cncr10>3.0.co;2-v.
The feasibility and efficacy of high dose conformal radiotherapy were examined in the treatment of patients with locally advanced, unresectable pancreatic carcinoma.
Forty-four patients with pathologically confirmed, unresectable pancreatic adenocarcinoma without distant metastases were treated in a Phase II study. The patients received three-dimensional, planned, high dose conformal radiotherapy (70-72 grays). Toxicity was scored according to the World Health Organization criteria. Follow-up time ranged from 7 months to 25 months (median, 9 months).
The treatment was feasible. Forty-one patients received the intended total dose. Treatment was never stopped because of toxicity. Acute toxicity was mainly Grade 1 and Grade 2 (in 70% and 57% of patients, respectively), whereas Grade 3 toxicity was seen in 9% of patients. One fatal event occurred that was not treatment related. Late Grade 3 and Grade 4 gastrointestinal toxicity was seen in 3 patients and 2 patients, respectively. Late (Grade 5) gastrointestinal bleeding was observed in 3 patients, 2 of whom had local tumor progression. At 3 months, reduction in tumor size was seen in 27% of patients, stable disease was seen in 20% of patients, and local disease progression was seen in 40% of patients. Ultimately, local disease progression was observed in 44% of patients. No true partial or complete responses were documented. The median survival from the time of diagnosis was 11 months (10 months from the start of radiotherapy). Seventeen of 25 patients (68%) experienced pain relief.
High dose conformal radiotherapy for the treatment of patients with locally advanced pancreatic carcinoma is feasible with acceptable toxicity. In case of pain, it can offer palliation. The efficacy of the treatment in terms of prolongation of life is not proven. Distant metastases remain the major problem.
研究高剂量适形放疗用于治疗局部晚期、不可切除胰腺癌患者的可行性及疗效。
在一项II期研究中,对44例经病理确诊、不可切除且无远处转移的胰腺腺癌患者进行治疗。患者接受三维计划的高剂量适形放疗(70 - 72格雷)。毒性按照世界卫生组织标准进行评分。随访时间为7个月至25个月(中位时间为9个月)。
该治疗方法可行。41例患者接受了预定的总剂量。治疗从未因毒性而停止。急性毒性主要为1级和2级(分别见于70%和57%的患者),而3级毒性见于9%的患者。发生了1例与治疗无关的致命事件。分别有3例和2例患者出现晚期3级和4级胃肠道毒性。观察到3例患者出现晚期(5级)胃肠道出血,其中2例有局部肿瘤进展。3个月时,27%的患者肿瘤体积缩小,20%的患者病情稳定,40%的患者局部病情进展。最终,44%的患者出现局部病情进展。未记录到真正的部分缓解或完全缓解。从诊断时起的中位生存期为11个月(从放疗开始起为10个月)。25例患者中有17例(68%)疼痛缓解。
高剂量适形放疗用于治疗局部晚期胰腺癌患者是可行的,毒性可接受。对于疼痛情况,可提供姑息治疗。该治疗方法在延长生命方面的疗效尚未得到证实。远处转移仍然是主要问题。