RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Improved Outcome in Children With Newly Diagnosed High-Risk Neuroblastoma Treated With Chemoimmunotherapy: Updated Results of a Phase II Study Using hu14.18K322A.
Improved Outcome in Children With Newly Diagnosed High-Risk Neuroblastoma Treated With Chemoimmunotherapy: Updated Results of a Phase II Study Using hu14.18K322A.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
在诱导化疗中加入 hu14.18K322A 改善了早期客观缓解,显著缩小了大多数患者的肿瘤体积,提高了诱导结束时的缓解率,并获得了令人鼓舞的 3 年 EFS。这些结果若能在更大规模的研究中得到验证,可能会改变临床实践。
我们评估了在新诊断的高危神经母细胞瘤患儿中,全程联合使用人源化抗双唾液酸神经节苷脂单克隆抗体(hu14.18K322A)是否能改善早期缓解和结局。
我们开展了一项前瞻性、单臂、三阶段、II期临床试验。6个周期的诱导化疗与hu14.18K322A、粒细胞-巨噬细胞集落刺激因子(GM-CSF)和低剂量白细胞介素-2(IL-2)联合给药。巩固方案包括白消安和美法仑。在有可用细胞时,巩固治疗期间额外给予一个周期的亲代来源NK 细胞联合hu14.18K322A(n = 31)。放疗在巩固治疗结束时进行。巩固后治疗包括hu14.18K322A、GM-CSF、IL-2和异维A酸。早期反应在最初两个周期诱导治疗后进行评估。诱导结束时的反应、无事件生存期(EFS)和总生存期(OS)进行了评估。
64例患者在接受诱导化疗的同时接受了hu14.18K322A治疗。该方案耐受良好,并使用持续输注麻醉药。在63例可评估患者中,42例(66.7%;95% CI,55.0至78.3)在最初两个化疗免疫治疗周期后达到部分缓解(PR)或更好。原发肿瘤体积中位缩小75%(范围,100%[完全消失]至增长5%)。第一个周期中hu14.18K322A血清峰值水平中位数与治疗早期缓解相关(P = .0154,单侧t检验)。62例患者中有60例(97%)在诱导结束时达到部分缓解或更好。诱导期间无患者出现疾病进展。3年EFS为73.7%(95% CI,60.0至83.4),OS为86.0%(95% CI,73.8至92.8)。
We evaluated whether combining a humanized antidisialoganglioside monoclonal antibody (hu14.18K322A) throughout therapy improves early response and outcomes in children with newly diagnosed high-risk neuroblastoma.
We conducted a prospective, single-arm, three-stage, phase II clinical trial. Six cycles of induction chemotherapy were coadministered with hu14.18K322A, granulocyte-macrophage colony-stimulating factor (GM-CSF), and low-dose interleukin-2 (IL-2). The consolidation regimen included busulfan and melphalan. When available, an additional cycle of parent-derived natural killer cells with hu14.18K322A was administered during consolidation (n = 31). Radiation therapy was administered at the end of consolidation. Postconsolidation treatment included hu14.18K322A, GM-CSF, IL-2, and isotretinoin. Early response was assessed after the first two cycles of induction therapy. End-of-induction response, event-free survival (EFS), and overall survival (OS) were evaluated.
Sixty-four patients received hu14.18K322A with induction chemotherapy. This regimen was well tolerated, with continuous infusion narcotics. Partial responses (PRs) or better after the first two chemoimmunotherapy cycles occurred in 42 of 63 evaluable patients (66.7%; 95% CI, 55.0 to 78.3). Primary tumor volume decreased by a median of 75% (range, 100% [complete disappearance]-5% growth). Median peak hu14.18K322A serum levels in cycle one correlated with early response to therapy ( P = .0154, one-sided t -test). Sixty of 62 patients (97%) had an end-of-induction partial response or better. No patients experienced progressive disease during induction. The 3-year EFS was 73.7% (95% CI, 60.0 to 83.4), and the OS was 86.0% (95% CI, 73.8 to 92.8), respectively.
Adding hu14.18K322A to induction chemotherapy improved early objective responses, significantly reduced tumor volumes in most patients, improved end-of-induction response rates, and yielded an encouraging 3-year EFS. These results, if validated in a larger study, may be practice changing.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
MEMBER ACCOUNT
登录成功会直接打开下一页。