Chen Allen M, Chang Susan, Pouliot Jean, Sneed Penny K, Prados Michael D, Lamborn Kathleen R, Malec Mary K, McDermott Michael W, Berger Mitchell S, Larson David A
Department of Radiation Oncology, University of California, San Francisco School of Medicine, San Francisco, CA 94143-0226, USA.
Int J Radiat Oncol Biol Phys. 2007 Nov 1;69(3):825-30. doi: 10.1016/j.ijrobp.2007.03.061. Epub 2007 May 23.
To evaluate the feasibility of gross total resection and permanent I-125 brachytherapy followed by hyperfractionated radiotherapy for patients with newly diagnosed glioblastoma.
From April 1999 to May 2002, 21 patients with glioblastoma multiforme were enrolled on a Phase I protocol investigating planned gross total resection and immediate placement of permanent I-125 seeds, followed by postoperative hyperfractionated radiotherapy to a dose of 60 Gy at 100 cGy b.i.d., 5 days per week. Median age and Karnofsky performance status were 50 years (range, 32-65 years) and 90 (range, 70-100), respectively. Toxicity was assessed according to Radiation Therapy Oncology Group criteria.
Eighteen patients completed treatment according to protocol. The median preoperative tumor volume on magnetic resonance imaging was 18.6 cm(3) (range, 4.4-41.2 cm(3)). The median brachytherapy dose measured 5 mm radially outward from the resection cavity was 400 Gy (range, 200-600 Gy). Ten patients underwent 12 reoperations, with 11 of 12 reoperations demonstrating necrosis without evidence of tumor. Because of high toxicity, the study was terminated early. Median progression-free survival and overall survival were 57 and 114 weeks, respectively, but not significantly improved compared with historical patients treated at University of California, San Francisco, with gross total resection and radiotherapy without brachytherapy.
Treatment with gross total resection and permanent I-125 brachytherapy followed by hyperfractionated radiotherapy as performed in this study results in high toxicity and reoperation rates, without demonstrated improvement in survival.
评估对新诊断的胶质母细胞瘤患者进行大体肿瘤全切除及永久性碘-125近距离放疗后再进行超分割放疗的可行性。
1999年4月至2002年5月,21例多形性胶质母细胞瘤患者纳入一项I期试验方案,该方案研究计划进行大体肿瘤全切除及立即植入永久性碘-125粒子,随后进行术后超分割放疗,剂量为60 Gy,每次100 cGy,每日两次,每周5天。中位年龄和卡氏功能状态评分分别为50岁(范围32 - 65岁)和90分(范围70 - 100分)。毒性根据放射肿瘤学组标准进行评估。
18例患者按方案完成治疗。磁共振成像术前肿瘤体积中位数为18.6 cm³(范围4.4 - 41.2 cm³)。从切除腔向外径向测量5 mm处的近距离放疗剂量中位数为400 Gy(范围200 - 600 Gy)。10例患者接受了12次再次手术,12次再次手术中有11次显示为坏死,无肿瘤证据。由于毒性高,该研究提前终止。中位无进展生存期和总生存期分别为57周和114周,但与加利福尼亚大学旧金山分校接受大体肿瘤全切除及放疗但未行近距离放疗的历史患者相比,无显著改善。
本研究中所进行的大体肿瘤全切除及永久性碘-125近距离放疗后再进行超分割放疗的治疗方法导致高毒性和再手术率,且未显示出生存改善。