医学
肝细胞癌
肝功能
放射治疗
人口
实体瘤疗效评价标准
不利影响
临床终点
转移
肿瘤科
核医学
泌尿科
内科学
放射科
临床研究阶段
临床试验
癌症
环境卫生
作者
Marc Pracht,É. Chajon,Thierry De Baère,F. Nguyen,J.-P. Bronowicki,V. Vendrely,Anne-Sophie Baumann,V. Croisé-Laurent,E. Rio,Yan Rolland,Samuel Le Sourd,P. Gustin,Christophe Perret,F. Mornex,D. Peiffert,Philippe Merle,Éric Deutsch
标识
DOI:10.1093/annonc/mdy282.094
摘要
Background: For patients (pts) with hepatocellular carcinoma (HCC) or liver metastasis (liver mets), stereotactic body radiation therapy (SBRT) is a well-tolerated option. Yet, the risk of injury to normal tissues limits the ability to efficiently sterilize tumor cells. Thus, hafnium oxide nanoparticles, NBXTR3, were developed, which increase the interaction of radiotherapy energy dose deposition within tumor cells when activated by an ionizing energy source like SBRT. NBTXR3 innovative approach does not engage liver function, is characterized by a single injection and fits with radiotherapy standards with no change in patient treatment protocol or equipment occupancy. NBTXR3 is currently being evaluated in this population in a phase I/II clinical trial. Methods: A 3 + 3 dose-escalation design was implemented for pts with HCC with/without portal vein tumor thrombosis or liver mets, including pts who received previous liver resection or other treatments. Pts were treated with a single intralesional injection of NBTXR3 followed by SBRT (45Gy / 3 fractions / 5 to 7 days). The escalating dose levels of NBTXR3 were 10%, 15%, 22%, 33% and 45% (intraarterial injection) of the baseline tumor volume. The primary endpoints were to identify the recommended dose and observe dose-limiting toxicities (DLTs). Secondary endpoints included NBTXR3 residency/leakage and investigator assessment on target lesions by mRECIST via MRI. Results: So far, 13 pts are enrolled. Dose levels are completed at 10% (6 pts) and 15% (4 pts) and currently enrolling at 22% (3 pts). To date, no early DLTs and no adverse events related to NBTXR3 were observed. In 9 evaluable pts, the investigator mRECIST assessment on target lesions resulted with the following best observed responses: 3 complete responses, 3 partial responses, 1 stable disease and 2 progressive disease. In the same pts, NBTXR3 did not present leakage and did not affect liver function. Conclusions: NBTXR3 activated by SBRT currently reveals an encouraging safety profile with a favorable efficacy in a vulnerable population with two different liver affections. These outcomes were the result of a complex multidisciplinary cooperation of different medical expertise from different centers. Clinical trial identification: NCT02721056. Legal entity responsible for the study: Nanobiotix. Funding: Nanobiotix. Disclosure: All authors have declared no conflicts of interest.
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