Bartolomei M, Mazzetta C, Handkiewicz-Junak D, Bodei L, Rocca P, Grana C, Maira G, Sturiale C, Villa G, Paganelli G
Division of Nuclear Medicine, IEO, Milan, Italy.
Q J Nucl Med Mol Imaging. 2004 Sep;48(3):220-8.
In a previous phase I-II study, the safety profile and anti-tumor efficacy of pre-targeting locoregional radioimmunotherapy (LR-RIT), based on the ''3 step'' method, was assessed in 24 high-grade glioma patients. The encouraging results in terms of low toxicity and objective response rate (25%) prompted us to continue our study.
An analysis of 73 patients with hystologically confirmed glioblastoma multiforme (GBM), treated with the ''3 step'' (90)Y-biotin based LR-RIT, is herein reported. All patients had a catheter implanted at 2(nd) surgery and underwent at least 2 cycles of LR-RIT (range 2-7) with 2 months interval. Thirty-five out of 73 patients were also treated with Temozolomide (TMZ). Two cycles of TMZ (200 mg/m(2)/day, for 5/28 days) were administered in between each course of LR-RIT. Overall survival (OS) and progression free survival (PFS) were retrospectively calculated.
Stabilization of disease was achieved in 75% of patients, while 25% progressed. In the 38 patients treated with LR-RIT alone, median OS and PFS were respectively 17.5 months (95%CI=[17-20]) and 5 months (95%CI=[4-8]), while in the 35 treated with the combined treatment (LR-RIT+TMZ) respective values were 25 months (95%CI=[23-30]) and 10 months (95%CI=[9-18] (p<0.01). The addition of TMZ to LR-RIT did not increase neurological toxicity, and no major hematological toxicity was observed.
These results confirm the safety and the efficacy of (90)Y LR-RIT in recurrent GBM patients; the addition of TMZ significantly improved the overall outcomes; a further controlled prospective, randomized study is fully justified.
在先前的一项I-II期研究中,对24例高级别胶质瘤患者评估了基于“三步”法的预靶向局部区域放射免疫疗法(LR-RIT)的安全性和抗肿瘤疗效。在低毒性和客观缓解率(25%)方面取得的令人鼓舞的结果促使我们继续开展研究。
本文报告了对73例经组织学确诊为多形性胶质母细胞瘤(GBM)的患者进行的分析,这些患者接受了基于“三步”(90)Y-生物素的LR-RIT治疗。所有患者在第二次手术时植入了导管,并接受了至少2个周期(范围为2-7个周期)的LR-RIT治疗,间隔为2个月。73例患者中有35例还接受了替莫唑胺(TMZ)治疗。在每个LR-RIT疗程之间给予两个周期的TMZ(200mg/m²/天,持续5/28天)。回顾性计算总生存期(OS)和无进展生存期(PFS)。
75%的患者病情稳定,25%的患者病情进展。在仅接受LR-RIT治疗的38例患者中,中位OS和PFS分别为17.5个月(95%CI=[17-20])和5个月(95%CI=[4-8]),而在接受联合治疗(LR-RIT+TMZ)的35例患者中,相应的值分别为25个月(95%CI=[23-30])和10个月(95%CI=[9-18])(p<0.01)。在LR-RIT中添加TMZ并未增加神经毒性,也未观察到严重的血液学毒性。
这些结果证实了(90)Y LR-RIT在复发性GBM患者中的安全性和有效性;添加TMZ显著改善了总体预后;进一步开展对照前瞻性随机研究是完全合理的。