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首页> 外文期刊>The Journal of Nuclear Medicine >Patient-Specific Dosimetry in Predicting Renal Toxicity with 90Y-DOTATOC: Relevance of Kidney Volume and Dose Rate in Finding a Dose-Effect Relationship
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Patient-Specific Dosimetry in Predicting Renal Toxicity with 90Y-DOTATOC: Relevance of Kidney Volume and Dose Rate in Finding a Dose-Effect Relationship

机译:特定于患者的剂量测定法可预测90Y-DOTATOC的肾毒性:肾脏容量和剂量率与剂量效应关系的相关性

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id="p-1">Nephrotoxicity is the major limiting factor during therapy with the radiolabeled somatostatin analog 90Y-1,4,7,10-tetraazacyclododecane-N,Na€2,Na€3,Na€′-tetraacetic acid (DOTA)- class="sc">d-Phe1-Tyr3-octreotide (DOTATOC). Pretherapeutic assessment of kidney absorbed dose could help to minimize the risk of renal toxicity. The aim of this study was to evaluate the contribution of patient-specific adjustments to the standard dosimetric models, such as the renal volume and dose rate, for estimating renal absorbed dose during therapy with 90Y-DOTATOC. In particular, we investigated the correlation between dose estimates and effect on renal function after therapy. >Methods: Eighteen patients with neuroendocrine tumors (9 men and 9 women; median age, 59 y) underwent treatment with 90Y-DOTATOC (8.1-22.9 GBq) after pretherapeutic biodistribution study with 86Y-DOTATOC. Kidney uptake and residence times were measured and the absorbed dose (KAD) was computed using either the MIRDOSE3.1 software assuming a standard kidney volume (KADStdVol) or the MIRD Pamphlet 19 values and the actual kidney cortex volume determined by pretherapeutic CT (KADCTVol). For each patient, the biologic effective dose (BED) was calculated according to the linear quadratic model to take into account the effect of dose rate and fractionation. Renal function was evaluated every 6 mo by serum creatinine and creatinine clearance (CLR) during a median follow-up of 35.5 mo (range, 18-65 mo). The individual rate of decline of renal function was expressed as CLR loss per year. >Results: KADCTVol ranged between 19.4 and 39.6 Gy (mean, 28.9 ?± 5.34 Gy). BED, obtained from KADCTVol, ranged between 27.7 and 59.3 Gy (mean, 40.4 ?± 10.6 Gy). The CLR loss per year ranged from 0% to 56.4%. In 12 of 18 patients, CLR loss per year was 20%. No correlation was observed between CLR loss per year and the KADStdVol or the KADCTVol. In contrast, BED strongly correlated with CLR loss per year (r = 0.93; P 0.0001). All 5 patients with CLR loss per year 20% received a BED 45 Gy. Patients who were treated with low fractionation were those with the highest rate of renal function impairment. >Conclusion: Radiation nephrotoxicity after 90Y-DOTATOC therapy is dose dependent. Individual renal volume, dose rate, and fractionation play important roles in an accurate dosimetry estimation that enables prediction of risk of renal function impairment.
机译:id =“ p-1”>肾毒性是放射性标记的生长抑素类似物 90 Y-1,4,7,10-四氮杂环十二烷- N,Na€在治疗期间的主要限制因素2,Na€3,Na€'-四乙酸(DOTA)- class =“ sc”> d -Phe 1 -Tyr 3 < / sup>-奥曲肽(DOTATOC)。肾脏吸收剂量的治疗前评估可有助于最大程度地降低肾脏毒性的风险。这项研究的目的是评估特定于患者的调整对标准剂量模型(例如肾脏体积和剂量率)的贡献,以评估在使用 90 Y-DOTATOC治疗期间肾脏吸收的剂量。特别是,我们研究了剂量估计值与治疗后对肾功能的影响之间的相关性。 >方法:治疗前生物分布后,对18例神经内分泌肿瘤患者(9例男性和9例女性,中位年龄59岁)进行了 90 Y-DOTATOC(8.1-22.9 GBq)治疗用 86 Y-DOTATOC进行研究。测量肾脏摄取和停留时间,并使用MIRDOSE3.1软件(假设标准肾脏体积(KAD StdVol )或MIRD小册子19值和实际肾皮质)计算吸收剂量(KAD)体积由治疗前CT(KAD CTVol )确定。对于每个患者,根据线性二次模型计算生物学有效剂量(BED),以考虑剂量率和分馏的影响。在中位随访35.5 mo(范围18-65 mo)期间,每6个月通过血清肌酐和肌酐清除率(CLR)评估肾功能。肾功能的个体下降率表示为每年CLR丧失。 >结果:KAD CTVol 介于19.4和39.6 Gy之间(平均值为28.9?±5.34 Gy)。从KAD CTVol 获得的BED范围为27.7至59.3 Gy(平均值为40.4±±10.6 Gy)。每年的CLR损失介于0%至56.4%之间。在18位患者中的12位患者中,每年CLR丢失率<20%。每年的CLR损失与KAD StdVol 或KAD CTVol 之间没有相关性。相反,BED与每年的CLR损失密切相关( r = 0.93; P <0.0001)。每年CLR丢失> 20%的所有5名患者均接受BED> 45 Gy。低分级治疗的患者是肾功能损害率最高的患者。 >结论: 90 Y-DOTATOC治疗后的放射肾毒性是剂量依赖性的。个体肾脏的体积,剂量率和分级在精确的剂量估算中起着重要的作用,该估算可以预测肾功能损害的风险。

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