Department of Radiology and Nuclear Medicine, University Medical Center Utrecht, Huispostnummer E01.132, Postbus 85500, 3508 GA, Utrecht, The Netherlands.
Nuclear Medicine Department, Eugene Marquis Center, Rennes, France.
Eur J Nucl Med Mol Imaging. 2022 Aug;49(10):3340-3352. doi: 10.1007/s00259-022-05774-0. Epub 2022 Apr 8.
To investigate the relationships between tumor absorbed dose (TAD) or normal tissue absorbed dose (NTAD) and clinical outcomes in hepatocellular carcinoma (HCC) treated with yttrium-90 glass microspheres.
TARGET was a retrospective investigation in 13 centers across eight countries. Key inclusion criteria: liver-dominant HCC with or without portal vein thrombosis, < 10 tumors per lobe (at least one ≥ 3 cm), Child-Pugh stage A/B7, BCLC stages A-C, and no prior intra-arterial treatment. Multi-compartment pre-treatment dosimetry was performed retrospectively. Primary endpoint was the relationship between ≥ grade 3 hyperbilirubinemia (such that > 15% of patients experienced an event) without disease progression and NTAD. Secondary endpoints included relationships between (1) objective response (OR) and TAD, (2) overall survival (OS) and TAD, and (3) alpha fetoprotein (AFP) and TAD.
No relationship was found between NTAD and ≥ grade 3 hyperbilirubinemia, which occurred in 4.8% of the 209 patients. The mRECIST OR rate over all lesions was 61.7%; for the target (largest) lesion, 70.8%. Responders and non-responders had geometric mean total perfused TADs of 225.5 Gy and 188.3 Gy (p = 0.048). Probability of OR was higher with increasing TAD (p = 0.044). Higher TAD was associated with longer OS (HR per 100 Gy increase = 0.83, 95% CI: 0.71-0.95; p = 0.009). Increased TAD was associated with higher probability of AFP response (p = 0.046 for baseline AFP ≥ 200 ng/mL).
Real-world data confirmed a significant association between TAD and OR, TAD and OS, and TAD and AFP response. No association was found between ≥ grade 3 hyperbilirubinemia and NTAD.
NCT03295006.
探讨钇 90 玻璃微球治疗肝细胞癌(HCC)中肿瘤吸收剂量(TAD)或正常组织吸收剂量(NTAD)与临床结局的关系。
TARGET 是在 8 个国家的 13 个中心进行的回顾性研究。主要纳入标准:肝优势型 HCC,伴或不伴门静脉血栓形成,每个肝叶肿瘤数<10 个(至少一个肿瘤≥3cm),Child-Pugh 分级 A/B7,BCLC 分期 A-C,且无动脉内治疗史。采用多室预治疗剂量测定法进行回顾性分析。主要终点是无疾病进展的≥3 级高胆红素血症(即>15%的患者发生事件)与 NTAD 之间的关系。次要终点包括(1)客观缓解(OR)与 TAD 之间的关系,(2)总生存(OS)与 TAD 之间的关系,以及(3)甲胎蛋白(AFP)与 TAD 之间的关系。
在 209 例患者中,无 4.8%的患者发生 NTAD 与≥3 级高胆红素血症之间的关系。所有病变的 mRECIST OR 率为 61.7%;对于靶病变(最大病变),OR 率为 70.8%。应答者和无应答者的总灌注 TAD 的几何均数分别为 225.5Gy 和 188.3Gy(p=0.048)。随着 TAD 的增加,OR 的概率更高(p=0.044)。较高的 TAD 与较长的 OS 相关(每增加 100Gy,HR=0.83,95%CI:0.71-0.95;p=0.009)。TAD 升高与 AFP 反应的概率增加相关(对于基线 AFP≥200ng/mL,p=0.046)。
真实世界数据证实了 TAD 与 OR、TAD 与 OS 以及 TAD 与 AFP 反应之间存在显著关联。在≥3 级高胆红素血症与 NTAD 之间未发现相关性。
NCT03295006。