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:Safety and Clinical Response to Combined Immunotherapy with Autologous iNKT Cells and PD-1(+)CD8(+) T Cells in Patients Failing First-line Chemotherapy in Stage IV Pancreatic Cancer.
Safety and Clinical Response to Combined Immunotherapy with Autologous iNKT Cells and PD-1(+)CD8(+) T Cells in Patients Failing First-line Chemotherapy in Stage IV Pancreatic Cancer.
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。
自体 iNKT 细胞联合 PD-1+CD8+T 细胞是治疗晚期胰腺癌的一种安全策略。患者表现出潜在有希望的延长生存时间。似乎有必要进一步研究以评估这些联合细胞输注在胰腺癌中的疗效。
一项I期临床试验旨在评估恒定自然杀伤T(iNKT)细胞联合PD-1 + CD8 + T细胞在晚期胰腺癌且一线化疗失败患者中的安全性和可行性。
共入组15例符合条件的患者,其中9例每人至少接受了三个周期的治疗。总共实施了59个疗程。
发热是最常见的不良事件,在细胞输注后约2-4小时达到高峰,所有患者均在24小时内未经治疗自行消退。还观察到流感样反应,如头痛、肌痛和关节痛,分别在4例、4例和3例患者中出现。此外,呕吐和头晕较为常见,而腹痛、胸痛、皮疹和鼻塞是罕见的不良事件,各报告于1例患者。未观察到2级以上的副作用。2例患者达到部分消退,而1例患者在第三疗程后4周评估时出现疾病进展。截至撰写时,3例患者仍存活,且无进展生存期超过12个月。9例患者中有6例的总生存时间已延长至超过12个月。除第一疗程后CD8 + T细胞升高外,未记录到CD4 + T、B和NK细胞的持续变化。
A phase I clinical trial was conducted to assess the safety and feasibility of invariant natural killer T (iNKT) cells combined with PD-1 + CD8 + T cells in patients with advanced pancreatic cancer and failing the first-line chemotherapy.
Fifteen eligible patients were enrolled, of whom 9 received at least three cycles of treatment each. In total, 59 courses were administered.
Fever was the most common adverse event, peaking at about 2-4 hours after cell infusion and reverting within 24 hours without treatment in all patients. Influenza-like reactions such as headache, myalgia, and arthralgia were also observed in 4, 4, and 3 of the patients, respectively. In addition, vomiting and dizziness were prevalent, while abdominal pain, chest pain, rash, and stuffy nose were rare adverse events, each reported in 1 patient. Side effects above grade 2 were not observed. Two patients achieved partial regression, while 1 patient experienced disease progression assessed 4 weeks after the third course. Three patients are still alive at the time of writing and have progression-free survival longer than 12 months. The overall survival time has been extended to over 12 months in 6 of the 9 patients. No constant changes of CD4 + T, B, and NK cells were recorded except for elevated CD8 + T cells after the first course.
The combination of autologous iNKT cells and PD-1 + CD8 + T cells was a safe therapeutic strategy against advanced pancreatic cancer. The patients exhibited a potentially promising prolonged survival time. Further study appears warranted to evaluate the efficacy of these combined cell infusions in pancreatic cancer. TRIAL REGISTRATION: This trial was included in the clinical trial which was registered in ClinicalTrials.gov (ID:NCT03093688) on March 15, 2017. SIGNIFICANCE: There is an unmet need for novel, more effective, and tolerable therapies for pancreatic cancer. Here we present a phase I clinical trial employing iNKT cells combined with PD-1 + CD8 + T cells in 9 patients with advanced pancreatic cancer and failing the first-line chemotherapy. The combined immunotherapy was shown to be feasible in the enrolled patients with limited side effects and optimistic clinical responses, which could bring opportunity of therapeutic advancement.
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