首页> 美国卫生研究院文献>other >Whole Cell Therapeutic Vaccine Modified With Hyper-IL6 for Combinational Treatment of Nonresected Advanced Melanoma
【2h】

Whole Cell Therapeutic Vaccine Modified With Hyper-IL6 for Combinational Treatment of Nonresected Advanced Melanoma

机译:Hyper-IL6修饰的全细胞治疗疫苗可联合治疗未切除的晚期黑色素瘤

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Active specific immunotherapy of cancer requires an efficient induction and effector phase. The induction covers potent activation of anti-tumor response, whereas effector breaks the immunosuppression. We report efficacy of therapeutic melanoma vaccine (AGI-101H) used alone in advanced disease as a candidate for further combined treatment. In adjuvant setting in patients with resected metastases AGI-101H combined with surgery of recurring disease demonstrated long-term survival.Seventy-seven patients with nonresectable melanoma (8% IIIB, 21% IIIC, 71% IV) were enrolled. AGI-101H was administered 8× every 2 weeks, and then every month. At progression, maintenance was continued or induction was repeated and followed by maintenance.Median follow-up was 139.3 months. The median overall survival (OS) was 17.3 months; in patients with WHO 0-1 was 20.3 months. Complete response (CR) and partial response (PR) were observed in 19.4% and 9% of pts. Disease control rate was 54.5% of pts. The median CR+PR duration was 32 months. Reinduction was performed in 36.3% patients following disease progression with 46.6% of CR+PR. No grade 3/4 adverse events were observed.Treatment with AGI-101H of melanoma patients is safe and effective. AGI-101H is a good candidate for combinatorial treatment with immune check-points inhibitors or tumor hypoxia normalizators.Trial registration: EudraCT Number 2008–003373-40.
机译:癌症的主动特异性免疫疗法需要有效的诱导和效应期。诱导涵盖抗肿瘤反应的有效激活,而效应子破坏免疫抑制。我们报告了在晚期疾病中单独使用的治疗性黑色素瘤疫苗(AGI-101H)的疗效,作为进一步联合治疗的候选药物。在有转移灶的患者的辅助治疗中,AGI-101H结合复发性疾病的手术显示出长期生存率。纳入了47例不可切除的黑色素瘤患者(IIIB,8%IIIC,21%IIIC,71%IV)。 AGI-101H每2周一次,然后每月一次8次给药。病情进展时,继续进行维护或重复诱导,然后进行维护。中位随访时间为139.3个月。中位总生存期(OS)为17.3个月; WHO 0-1的患者为20.3个月。分别有19.4%和9%的患者出现完全缓解(CR)和部分缓解(PR)。疾病控制率为54.5%。中位CR + PR持续时间为32个月。疾病进展后,36.3%的患者进行了还原,CR + PR为46.6%。没有观察到3/4级不良事件。用AGI-101H治疗黑色素瘤患者是安全有效的。 AGI-101H是与免疫检查点抑制剂或肿瘤缺氧正常化剂联合治疗的良好选择。试验注册:EudraCT Number 2008–003373-40。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号