Boiardi A, Eoli M, Salmaggi A, Lamperti E, Botturi A, Broggi G, Bissola L, Finocchiaro G, Silvani A
Department of Neuro-Oncology, Istituto Nazionale Neurologico "Carlo Besta", Italy.
J Neurooncol. 2005 Nov;75(2):215-20. doi: 10.1007/s11060-005-3030-x.
Twenty-two recurrent GBM patients were enrolled for second tumor debulking with local positioning of a Rickam reservoir, in order to locally deliver chemotherapy with the aim of controlling local tumor recurrence. We designed a protocol using systemic temozolomide (150 mg/sqm days 1-5 every 28) in association with mitoxantrone, delivered through the reservoir (4 mg/day 1-5 every 28) positioned into the area of tumor exeresis. After re-operation a residual tumor mass no larger than 2 cm was identified in 18/22 patients. The patients were treated with monthly cycles of chemotherapy until evolution of the tumor, but in no case for more than 10 cycles. Responses were evaluated by MRI scans performed every 2 months and images assessed according to MacDonald's criteria. Response rate: no complete responses (CR), 5 partial responses (PR), 13 stable disease (SD) and 4 progressive disease (PD) occurred. The median progression-free survival (PFS) and survival time (ST) of the whole group of treated patients was 7 and 11 months, respectively and more than a quarter of the patients survived over 18 months. During the study, the patients' compliance was complete and no dropouts occurred. Hematological toxicity was mild and after repeated local injections only minor neurological side-effects occurred. Despite some bias in patients' selection not excluded in this pilot study, results are interesting: the PFS was as long as the survival of recurrent GBM reported in the literature.
22例复发性胶质母细胞瘤患者入选接受第二次肿瘤减瘤手术,并在局部放置Rickam储液囊,以便局部给予化疗,目的是控制局部肿瘤复发。我们设计了一种方案,使用全身替莫唑胺(每28天第1 - 5天150 mg/m²)联合米托蒽醌,通过放置在肿瘤切除区域的储液囊给药(每28天第1 - 5天4 mg/天)。再次手术后,18/22例患者中发现残留肿瘤块不大于2 cm。患者接受每月一次的化疗周期,直至肿瘤进展,但在任何情况下化疗周期均不超过10个周期。通过每2个月进行的MRI扫描评估反应,并根据MacDonald标准评估图像。反应率:未出现完全缓解(CR),5例部分缓解(PR),13例疾病稳定(SD),4例疾病进展(PD)。整个治疗组患者的无进展生存期(PFS)和生存时间(ST)中位数分别为7个月和11个月,超过四分之一的患者存活超过18个月。在研究期间,患者的依从性良好,未出现退出情况。血液学毒性较轻,重复局部注射后仅出现轻微的神经副作用。尽管在这项初步研究中未排除患者选择方面的一些偏差,但结果很有趣:PFS与文献报道的复发性胶质母细胞瘤的生存期一样长。