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自体 iNKT 细胞联合 PD-1(+)CD8(+) T 细胞过继免疫治疗在 IV 期胰腺癌一线化疗失败患者中的安全性与临床反应

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.

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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.

PubMed 2023/06/07(内容时间) Cancer Res Commun Q2 · IF 4(JCR 2025)

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。

研究概要

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。

研究思路结论见上方概要

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。

展开英文摘要原文

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.

论文信息

作者
Wang J、Cheng X、Jin Y、Xia B、Qin R、Zhang W、Hu H、Mao X
第一作者单位
Shanghai Public Health Clinical Center, Fudan University, Shanghai, P.R. China.China
通讯作者单位
Shanghai Public Health Clinical Center and Institutes of Biomedical Sciences, Shanghai Medical College, Fudan University, Shanghai, P.R. China.China
文献类型
非美国政府资助研究
期刊
Cancer research communications2023 Jun
原文标识
PubMed 37377605 · DOI 10.1158/2767-9764.CRC-23-0137