在胶质母细胞瘤中使用亲和素-生物素预靶向系统的11年经验:毒性、疗效和生存率

C. Grana, M. Chinol, C. Cicco, M. Bartolomei, M. Cremonesi, L. Bodei, P. Rocca, M. Pacifici, Simone Tiberini, S. Baio, G. Broggi, S. Severi, G. Paganelli
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引用次数: 7

摘要

背景:在复发性胶质母细胞瘤(GBM)患者中应用三步亲和素-生物素预靶向方法,第一步使用生物素化抗tenascin单克隆抗体,然后使用亲和素和90y -生物素进行预靶向。方法:回顾我院1994年12月至2005年12月502例接受三步放射免疫治疗的胶质母细胞瘤患者的客观疗效和总生存率。患者在接受预靶向抗体引导放射性核素90 y生物素治疗(PAGRIT®)之前接受标准治疗。结果:在502例患者中,272例(54%)可评估缓解,375例(75%)可评估总生存期。174例患者(64%)在PAGRIT®后继续进展,77例(28%)获得疾病稳定,21例(8%)显示客观肿瘤消退。在第一个PAGRIT®周期后,375名可评估患者的6个月生存率为98.4%,12个月为79.2%,18个月为51.7%,24个月为30.7%。所有375例GBM复发患者均接受了3步PAGRIT治疗。诊断后的中位生存时间为19个月。结论:这项回顾性分析的结果表明,90 y -生物素PAGRIT®干扰胶质母细胞瘤的进展,延长了大量患者的生存期。我们的分析为进一步的前瞻性试验奠定了基础,在这些试验中,放射免疫疗法(已知对最小残留疾病更有效)可以在手术后立即提供。
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Eleven-year experience with the avidin-biotin pretargeting system in glioblastoma: Toxicity, efficacy and survival
Background: The 3-step avidin-biotin pretargeting approach is applied in patients with recurrent glioblastoma (GBM), using biotinylated anti-tenascin monoclonal antibody as the first step of pretargeting followed by avidin and 90 Y- biotin. Methods: The present study reviews objective response and overall survival rates in 502 glioblastoma patients treated with 3-step radioimmunotherapy in our institute from December 1994 to December 2005. Patients underwent standard treatment before receiving Pretargeted Antibody-Guided Radionuclide Therapy with 90 Y-biotin (PAGRIT ® ). Results: Of the 502 patients, 272 (54%) were evaluable for response and 375 (75%) for overall survival. 174 patients (64%) continued to progress after PAGRIT ® , 77 (28%) obtained disease stabilization, and 21 (8%) showed objective tumor regression. Survival of the 375 evaluable patients was 98.4% at 6 months, 79.2% at 12 months, 51.7% at 18 months, and 30.7% at 24 months after the first cycle of PAGRIT ® . All 375 received 3-step PAGRIT ® at recurrence of GBM. The median survival time from diagnosis was 19 months. Conclusion: The results from this retrospective analysis suggest that 90 Y-biotin PAGRIT ® interferes with the progression of glioblastoma, prolonging survival in a larger number of patients. Our analysis forms the basis for further prospective trials, where radioimmunotherapy, which is known to be more effective in minimal residual disease, could be offered immediately after surgery.
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