Röttinger Erwin M, Bartkowiak Detlef, Bunjes Donald, Wennauer Roman, Dohr Dagmar
Department of Radiotherapy, University Hospital Ulm, Germany.
Strahlenther Onkol. 2003 Oct;179(10):702-7. doi: 10.1007/s00066-003-1090-4.
Total body irradiation (TBI) with and without additional radioimmunotherapy (RIT) was examined for renal toxicity after stem cell transplantation.
Serum creatinine levels of 35 patients (15 female, 20 male, median age 40.5 years, range 17-60 years) after TBI alone and of 23 patients (eight female, 15 male, median age 47, range 16-58 years) after TBI with additional RIT were determined between 10/1997 and 11/1999. TBI was performed by external-beam radiotherapy in six fractions over 3 days with renal doses of 12 Gy in the TBI-alone group and 6 Gy in the group with additional RIT. The mean kidney dose due to the (188)Re-radiolabeled antibody was estimated to be 8.3 Gy (2.3-11.6 Gy).
Within 12 months after treatment, creatinine levels increased from 77 mmol/l (SD +/- 11) to 89 mmol/l (SD +/- 20) for TBI alone and from 78 mmol/l (SD +/- 13) to 144 mmol/l (SD +/- 52) for combined TBI and RIT.
Despite a 50% reduction of the external-beam contribution to the kidney dose, the application of approximately 10 GBq (188)Re-labeled anti-CD66 monoclonal antibody with a calculated renal dose of 8.3 Gy (range 2.3-11.5 Gy) led to renal toxicity, as reported previously. In the absence of a positive dose-response relationship for the (188)Re-labeled antibody, the observation may be explained by an underestimation of the biologically effective dose and the inaccuracy of the dose determination at the glomerular level.
研究全身照射(TBI)联合或不联合额外放射免疫疗法(RIT)在干细胞移植后的肾毒性。
测定了1997年10月至1999年11月间35例(15例女性,20例男性,中位年龄40.5岁,范围17 - 60岁)仅接受TBI治疗患者以及23例(8例女性,15例男性,中位年龄47岁,范围16 - 58岁)接受TBI联合额外RIT治疗患者的血清肌酐水平。TBI通过外照射放疗分6次在3天内完成,仅接受TBI组的肾脏剂量为12 Gy,联合RIT组为6 Gy。估计(188)Re标记抗体所致的平均肾脏剂量为8.3 Gy(2.3 - 11.6 Gy)。
治疗后12个月内,仅接受TBI治疗患者的肌酐水平从77 mmol/l(标准差±11)升至89 mmol/l(标准差±20),TBI联合RIT治疗患者的肌酐水平从78 mmol/l(标准差±13)升至144 mmol/l(标准差±52)。
尽管外照射对肾脏剂量的贡献减少了50%,但应用约10 GBq(188)Re标记的抗CD66单克隆抗体,计算得出的肾脏剂量为8.3 Gy(范围2.3 - 11.5 Gy),仍导致了肾毒性,如先前报道。由于(188)Re标记抗体不存在正剂量反应关系,这一观察结果可能是由于对生物有效剂量的低估以及肾小球水平剂量测定的不准确所致。