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首页> 外文期刊>Cancer immunology, immunotherapy : >Low-dose ipilimumab plus nivolumab combined with IL-2 and hyperthermia in cancer patients with advanced disease: exploratory findings of a case series of 131 stage IV cancers - a retrospective study of a single institution
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Low-dose ipilimumab plus nivolumab combined with IL-2 and hyperthermia in cancer patients with advanced disease: exploratory findings of a case series of 131 stage IV cancers - a retrospective study of a single institution

机译:低剂量Ipilimumab加入Nivolumab与IL-2和癌症患者的热疗联合疾病:案例系列131阶段IV癌症的探索性调查结果 - 一个机构的回顾性研究

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The 3-year overall survival (OS) rate of patients with previously treated or untreated stage III or IV melanoma has by now reached 63% using ipilimumab and nivolumab therapy. However, immune-related adverse events (irAEs) of grade 3 or 4 occurred in 59% of patients leading to discontinuation of therapy in 24.5% of patients and one death. Therapy with checkpoint inhibitors could be safer and more effective in combination with hyperthermia and fever inducing therapies. We conducted a retrospective analysis to test the safety and efficacy of a new combination immune therapy in 131 unselected stage IV solid cancer patients with 23 different histological types of cancer who exhausted all conventional treatments. Treatment consisted of locoregional- and whole-body hyperthermia, individually dose adapted interleukin 2 (IL-2) combined with low-dose ipilimumab (0.3 mg/kg) plus nivolumab (0.5 mg/kg). The objective response rate (ORR) was 31.3%, progression-free survival (PFS) was 10 months, survival probabilities at 6 months was 86.7% (95% CI, 81.0-92.8%), at 9 months was 73.5% (95% CI, 66.2-81.7%), at 12 months was 66.5% (95% CI, 58.6-75.4%), while at 24 months survival was 36.6% (95% CI:28.2%; 47.3%). irAEs of World Health Organization (WHO) Toxicity Scale grade 1, 2, 3, and 4 were observed in 23.66%, 16.03%, 6.11%, and 2.29% of patients, respectively. Our results suggest that the irAEs profile of the combined treatment is safer than that of the established protocols without compromising efficacy.
机译:使用伊普利单抗和nivolumab治疗之前治疗或未治疗的III或IV期黑色素瘤患者的3年总生存率(OS)现已达到63%。然而,59%的患者出现3级或4级免疫相关不良事件(IRAE),导致24.5%的患者停止治疗,1例死亡。与热疗和发热诱导疗法结合使用检查点抑制剂可能更安全、更有效。我们对131名未经选择的IV期实体癌患者进行了一项回顾性分析,以测试一种新的联合免疫疗法的安全性和有效性,这些患者中有23种不同的组织学类型的癌症,他们用尽了所有常规治疗。治疗包括局部和全身热疗、单独剂量适应的白细胞介素2(IL-2)联合低剂量伊普利单抗(0.3 mg/kg)加nivolumab(0.5 mg/kg)。客观有效率(ORR)为31.3%,无进展生存期(PFS)为10个月,6个月生存率为86.7%(95%CI,81.0-92.8%),9个月生存率为73.5%(95%CI,66.2-81.7%),12个月生存率为66.5%(95%CI,58.6-75.4%),24个月生存率为36.6%(95%CI:28.2%;47.3%)。在23.66%、16.03%、6.11%和2.29%的患者中观察到世界卫生组织(WHO)毒性等级1、2、3和4的IRAE。我们的结果表明,联合治疗的irAEs模式比既定方案更安全,且不会影响疗效。

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