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确定用90Y或177Lu标记的单克隆抗体BR96在大鼠中的最大耐受剂量:建立同基因肿瘤模型以评估改善放射免疫疗法的方法。

Determining maximal tolerable dose of the monoclonal antibody BR96 labeled with 90Y or 177Lu in rats: establishment of a syngeneic tumor model to evaluate means to improve radioimmunotherapy.

作者信息

Mårtensson Linda, Wang Zhongmin, Nilsson Rune, Ohlsson Tomas, Senter Peter, Sjögren Hans-Olov, Strand Sven-Erik, Tennvall Jan

机构信息

Department of Oncology, Lund University, Sweden.

出版信息

Clin Cancer Res. 2005 Oct 1;11(19 Pt 2):7104s-7108s. doi: 10.1158/1078-0432.CCR-1004-0004.

Abstract

PURPOSE

To evaluate therapeutic strategies, it is essential to use biological models reflecting important aspects of the clinical situation. The aim of the present study was to compare the maximal tolerable dose of the monoclonal antibody BR96 labeled with 90Y or 177Lu in immunocompetent rats. Maximal tolerable dose was defined as the highest activity that allows 100% of the animals to survive without clinical signs, such as infections, bleeding, or diarrhea, and with <20% loss in body weight.

EXPERIMENTAL DESIGN

Increasing activity levels of BR96 labeled with 90Y or 177Lu were administered to groups of rats. Blood parameters, body weight, and general performance were monitored for 8 weeks.

RESULTS

Two days postinjection, all groups had decreased leukocyte counts down to 5% to 15% of initial values. Initiation of recovery (at 14-21 days) showed a dose-response relationship. All groups, except the group given the highest activity of 90Y, had complete resolution in their leukopenia. The decrease in platelets was delayed to days 7 to 14 postinjection with a dose-dependent response regarding both severity of the nadir (10-40% of initial value) and the start of recovery. Animals in the groups given the highest activities of both 90Y and 177Lu exhibited skin infections on day 21.

CONCLUSIONS

The results showed good reproducibility and dose-dependent toxicity for both radionuclides, indicating that the maximal tolerable dose for 177Lu-BR96 (1,000 MBq/kg) is 1.7 times that for 90Y-BR96 (600 MBq/kg) in rats. This model makes it feasible to evaluate strategies to escalate therapeutic doses to tumors without increasing normal tissue toxicity.

摘要

目的

为了评估治疗策略,使用反映临床情况重要方面的生物学模型至关重要。本研究的目的是比较用90Y或177Lu标记的单克隆抗体BR96在免疫活性大鼠中的最大耐受剂量。最大耐受剂量定义为能使100%的动物存活且无感染、出血或腹泻等临床症状,体重减轻<20%的最高活度。

实验设计

给几组大鼠注射活性不断增加的用90Y或177Lu标记的BR96。监测血液参数、体重和一般状况8周。

结果

注射后两天,所有组的白细胞计数均降至初始值的5%至15%。恢复开始(14 - 21天)呈现剂量反应关系。除给予最高活度90Y的组外,所有组的白细胞减少均完全缓解。血小板减少延迟至注射后7至14天,最低点的严重程度(初始值的10 - 40%)和恢复开始均呈剂量依赖性反应。给予最高活度90Y和177Lu的组中的动物在第21天出现皮肤感染。

结论

结果表明两种放射性核素均具有良好的可重复性和剂量依赖性毒性,表明在大鼠中177Lu - BR96的最大耐受剂量(1000 MBq/kg)是90Y - BR96(600 MBq/kg)的1.7倍。该模型使得评估在不增加正常组织毒性的情况下提高肿瘤治疗剂量的策略成为可能。

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