一种用于克服非小细胞肺癌治疗中抗原异质性的多靶向 CAR-T 细胞平台
A Multi-Targeting Chimeric Antigen Receptor-T Cell Platform to Overcome Antigen Heterogeneity in the Treatment of Non-Small Cell Lung Cancer.
这些发现支持采用多靶点CAR-T 策略来应对NSCLC及可能其他实体瘤中的抗原异质性。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Experience of Autologous Immunotherapy for Non-Small Cell Lung Cancer Using Zoledronate-Actived Gammadelta T Cells.
Experience of Autologous Immunotherapy for Non-Small Cell Lung Cancer Using Zoledronate-Actived Gammadelta T Cells.
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我们获得的关于自体γδT 细胞免疫治疗对非小细胞肺癌患者疗效和安全性的初步结果极为令人鼓舞,且与先前研究结果相当。
全球多个国家已将自体免疫增强疗法用于癌症治疗,并取得了初步积极结果。本研究描述了我们在越南这一发展中国家,使用自体γδ T细胞免疫疗法治疗非小细胞肺癌患者的经验。
5例III-IV期非小细胞肺癌患者纳入研究。每例患者接受6次自体γδT细胞输注,间隔两周。在治疗前、治疗期间、治疗结束时以及治疗后3个月和6个月,对该方法相关的临床、实验室、生活质量和不良事件进行了综合评估。
在培养接种时,细胞总数为2.9至18.2 x 106,γδT细胞数量为10.7至19.6 x 104。培养第14天,γδT细胞数量为3.1至8.3 x 108。关于治疗的安全性,在总共30次输注中,两例(发热)、一例(肌痛)和一例(关节痛)按CTCAE标准评为1级。疗程结束后,造血系统、肾功能或肝功能均未观察到毒性。根据RECIST 1.1标准评估患者反应:20%的患者(一例患者)达到部分缓解,80%的患者(四例患者)在治疗结束时疾病稳定。在研究随访期间,三例患者仍然存活,且疾病保持稳定。大多数功能指标(活动、认知和社交)显示患者治疗后生活质量改善,但身体和情绪评分略有下降。两例患者的疲劳症状加重,但治疗六个月后,平均值从25.3降至8.3。呼吸困难症状从治疗开始时的33.3逐渐降至六个月后的8.3。
Several nations around the world have utilized autologous immune enhancement therapy in the treatment of cancer, with initial positive outcomes. This study describes our experience with autologous gamma delta T cell immunotherapy for the treatment of non-small cell lung cancer patients in Vietnam, a developing nation.
Five patients with non-small cell lung cancer at stages III - IV were enrolled in the study. Each patient received six infusions of autologous γδT cells, separated by two weeks. Before, during, at the end of treatment, and three and six months after treatment, a comprehensive evaluation of clinical, laboratory, quality of life, and adverse events related to the method was conducted.
At the time of culture seeding, the total number of cells ranged from 2.9 to 18.2 x 106, with γδT cells ranging in number from 10.7 to 19.6 x 104. On day 14 of the culture, the number of γδT cells ranged from 3.1 to 8.3 x 108. Regarding the safety of therapy in a total of 30 infusions, two (fever), one (myalgia), and one (joint pain) were graded as 1 by CTCAE criteria. After the course, no toxicity was observed in the hematopoietic system, kidney function, or liver function. Evaluation of the patient's response in accordance with the RECIST 1.1 criteria: 20% of patients (one patient) had partial response disease, and 80% of patients (four patients) had stable disease at the end of treatment. During the follow-up period of the study, three patients were still alive, and the disease remained stable. The patient's quality of life improved after treatment in most functional measures (activity, cognitive, and social), but physical and emotional scores decreased slightly. Two patients' fatigue symptoms increased, but after six months of treatment, the average value dropped from 25.3 to 8.3. Dyspnea symptoms decreased gradually from 33.3 at the start of treatment to 8.3 six months later.
The initial results we obtained regarding the efficacy and safety of autologous γδT cell immunotherapy for patients with non-small cell lung cancer are extremely encouraging and comparable to those of previous studies.
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