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个体化新抗原脉冲树突状细胞疫苗治疗晚期肺癌。

Personalized neoantigen pulsed dendritic cell vaccine for advanced lung cancer.

机构信息

State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, and Collaborative Innovation Center for Biotherapy, Chengdu, 610041, China.

Department of Biotherapy, Cancer Center, West China Hospital, Sichuan University, Chengdu, China.

出版信息

Signal Transduct Target Ther. 2021 Jan 20;6(1):26. doi: 10.1038/s41392-020-00448-5.

Abstract

Neoantigens are considered to be ultimate target of tumor immunotherapy due to their high tumor specificity and immunogenicity. Dendritic cell (DCs) vaccines based on neoantigens have exciting effects in treatment of some malignant tumors and are a promising therapeutic modality. Lung cancer is a lethal disease with the highest morbidity and mortality rate in the world. Despite the rapid development of targeted therapy and immune checkpoint inhibitors for lung cancer in recent years, their efficacy is still unsatisfactory overall. Therefore, there is an urgent unmet clinical need for lung cancer treatment. Here, we attempted to treat lung cancer using a personalized neoantigen peptide-pulsed autologous DC vaccine and conducted a single-arm, 2 medical centers, pilot study initiated by the investigator (ChiCTR-ONC-16009100, NCT02956551). The patients enrolled were patients with heavily treated metastatic lung cancer. Candidate neoantigens were derived from whole-exome sequencing and RNA sequencing of fresh biopsy tissues as well as bioinformatics analysis. A total of 12 patients were enrolled in this study. A total of 85 vaccine treatments were administered with a median value of 5 doses/person (range: 3-14 doses/person). In total, 12-30 peptide-based neoantigens were selected for each patient. All treatment-related adverse events were grade 1-2 and there were no delays in dosing due to toxic effects. The objective effectiveness rate was 25%; the disease control rate was 75%; the median progression-free survival was 5.5 months and the median overall survival was 7.9 months. This study provides new evidence for neoantigen vaccine therapy and new therapeutic opportunities for lung cancer treatment.

摘要

新抗原被认为是肿瘤免疫治疗的终极靶点,因为它们具有高度的肿瘤特异性和免疫原性。基于新抗原的树突状细胞(DC)疫苗在治疗某些恶性肿瘤方面具有令人兴奋的效果,是一种很有前途的治疗方式。肺癌是一种致命疾病,是世界上发病率和死亡率最高的癌症。尽管近年来针对肺癌的靶向治疗和免疫检查点抑制剂发展迅速,但总体疗效仍不尽人意。因此,肺癌的治疗存在着迫切的未满足的临床需求。在这里,我们尝试使用个性化新抗原肽脉冲自体 DC 疫苗治疗肺癌,并进行了一项由研究者发起的、单臂、2 家中心的、Ⅰ期临床试验(ChiCTR-ONC-16009100,NCT02956551)。入组患者为经多线治疗的转移性肺癌患者。候选新抗原来源于新鲜活检组织的全外显子组测序和 RNA 测序以及生物信息学分析。本研究共入组 12 例患者。共进行了 85 次疫苗治疗,中位数为 5 剂/人(范围:3-14 剂/人)。总共为每位患者选择了 12-30 个基于肽的新抗原。所有治疗相关不良事件均为 1-2 级,且无因毒性作用而延迟给药。客观有效率为 25%;疾病控制率为 75%;中位无进展生存期为 5.5 个月,中位总生存期为 7.9 个月。这项研究为新抗原疫苗治疗提供了新的证据,为肺癌治疗提供了新的治疗机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80c9/7817684/71ceddc63724/41392_2020_448_Fig1_HTML.jpg

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