Aedo-Lopez Veronica, Gérard Camille L, Boughdad Sarah, Gautron Moura Bianca, Berthod Gregoire, Digklia Antonia, Homicsko Krisztian, Schaefer Niklaus, Duran Rafael, Cuendet Michel A, Michielin Olivier
Department of Oncology, Lausanne University Hospital (CHUV), Rue du Bugnon 46, CH-1011 Lausanne, Switzerland.
Department of Oncology, Monash Medical Centre, 823-865 Centre Road, East Bentleigh, Melbourne, VIC 3165, Australia.
Cancers (Basel). 2022 Feb 24;14(5):1162. doi: 10.3390/cancers14051162.
To assess the safety and efficacy of ipilimumab plus nivolumab around selective internal radiation therapy (SIRT) in patients with metastatic uveal melanoma (mUM). We present a retrospective, single center study of 32 patients with mUM divided into two groups based on the treatment received between April 2013 and April 2021. The SIRT_IpiNivo cohort was treated with Yttrium-90 microspheres and ipilimumab plus nivolumab before or after the SIRT ( 18). The SIRT cohort underwent SIRT but did not receive combined immunotherapy with ipilimumab plus nivolumab ( 14). Twelve patients (66.7%) of the SIRT_IpiNivo arm received SIRT as first-line treatment and six patients (33.3%) received ipilimumab plus nivolumab prior to SIRT. In the SIRT group, seven patients (50.0%) received single-agent immunotherapy. One patient treated with combined immunotherapy 68 months after the SIRT was included in this group. At the start of ipilimumab plus nivolumab, 94.4% ( 17) presented hepatic metastases and 72.2% ( 13) had extra liver disease. Eight patients (44.4%) of the SIRT_IpiNivo group experienced grade 3 or 4 immune related adverse events, mainly colitis and hepatitis. Median overall survival from the diagnosis of metastases was 49.6 months (95% confidence interval (CI); 24.1-not available (NA)) in the SIRT_IpiNivo group compared with 13.6 months (95% CI; 11.5-NA) in the SIRT group (log-rank -value 0.027). The presence of extra liver metastases at the time of SIRT, largest liver lesion more than 8 cm (M1c) and liver tumor volume negatively impacted the survival. This real-world cohort suggests that a sequential treatment of ipilimumab plus nivolumab and SIRT is a well-tolerated therapeutic approach with promising survival rates.
评估伊匹单抗联合纳武单抗在转移性葡萄膜黑色素瘤(mUM)患者选择性内放射治疗(SIRT)前后的安全性和疗效。我们进行了一项回顾性单中心研究,纳入了32例mUM患者,根据2013年4月至2021年4月期间接受的治疗将其分为两组。SIRT_IpiNivo队列在SIRT之前或之后接受了钇-90微球治疗以及伊匹单抗联合纳武单抗治疗(18例)。SIRT队列接受了SIRT,但未接受伊匹单抗联合纳武单抗的联合免疫治疗(14例)。SIRT_IpiNivo组中有12例患者(66.7%)将SIRT作为一线治疗,6例患者(33.3%)在SIRT之前接受了伊匹单抗联合纳武单抗治疗。在SIRT组中,7例患者(50.0%)接受了单药免疫治疗。该组纳入了1例在SIRT后68个月接受联合免疫治疗的患者。在开始使用伊匹单抗联合纳武单抗治疗时,94.4%(17例)出现肝转移,72.2%(13例)有肝外疾病。SIRT_IpiNivo组中有8例患者(44.4%)发生3级或4级免疫相关不良事件,主要为结肠炎和肝炎。SIRT_IpiNivo组从转移诊断开始的中位总生存期为49.6个月(95%置信区间(CI);24.1 - 不可用(NA)),而SIRT组为13.6个月(95%CI;11.5 - NA)(对数秩检验P值为0.027)。SIRT时存在肝外转移、最大肝病灶超过