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:Long-term, 13-year survival after immune cell therapy combined with chemotherapy for extensive-stage small-cell lung cancer: a case report.
Long-term, 13-year survival after immune cell therapy combined with chemotherapy for extensive-stage small-cell lung cancer: a case report.
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虽然小细胞肺癌的发病率较低,但其预后较差。广泛期小细胞肺癌患者约占所有小细胞肺癌病例的70%,中位总生存期为8-13个月,5年总生存率仅为1%-5%。本文报道一例2011年经支气管镜活检诊断为小细胞肺癌的成年男性患者。该患者临床分期为cT2N2M1,IV期(即广泛期小细胞肺癌)。但通过化疗、放疗和细胞因子诱导的杀伤细胞(CIK)免疫细胞治疗联合应用,他存活了13年。通过长期随访获得了全面的肿瘤标志物、淋巴细胞亚群和肺部CT图像。在完成12个周期化疗(CE/IP方案)和5940cgy/33f放疗后,我们发现患者处于免疫抑制状态,因此给予患者CIK细胞治疗联合化疗。在免疫细胞联合化疗2年后,原发病灶或其他不良事件均无显著变化。在患者初诊后的13年中,我们监测了患者CEA、NSE、CD4/CD8比值和CD3+CD4+淋巴细胞等指标的变化,提示这些可能是值得评估患者免疫状态和联合治疗有效性的因素。在本病例中,应用CIK细胞免疫治疗联合化疗来控制肿瘤进展。结论:CIK细胞免疫治疗联合化疗可延长广泛期小细胞肺癌患者的生存期,预后良好,联合治疗的优势体现在提高机体免疫能力和增强免疫细胞的杀伤作用。
While the incidence of small-cell lung cancer is low, it has a poor prognosis. Patients with extensive small-cell lung cancer account for about 70% of all cases of small-cell lung cancer, with a median overall survival duration of 8-13 months and a 5-year overall survival rate of only 1%-5%.
Herein, we report small-cell lung cancer diagnosed by bronchoscopic biopsy in an adult male patient in 2011. The patient had a clinical stage of cT2N2M1 and stage IV disease (i. e. , extensive small-cell lung cancer). Still, he survived for 13 years through a combination of chemotherapy, radiotherapy, and cytokine-induced killer (CIK) immunocell thera. Comprehensive tumor markers, lymphocyte subsets, and lung CT images were obtained through long-term follow-up. After 12 cycles of chemotherapy (CE/IP regimen) and 5940cgy/33f radiotherapy, we found that the patient was in an immunosuppressive state, so the patient was given CIK cell therapy combined with chemotherapy. After 2 years of immunocell-combined chemotherapy, there were no significant changes in the primary lesion or other adverse events.
In the 13 years since the patient's initial diagnosis, we monitored the changes in the patient's indicators such as CEA, NSE, CD4/CD8 ratio, and CD3+CD4+ lymphocytes, suggesting that these may be the factors worth evaluating regarding the patient's immune status and the effectiveness of combination therapy.
In this case, CIK cell immunotherapy combined with chemotherapy was applied to control tumor progression. With a good prognosis, we concluded that CIK cell immunotherapy combined with chemotherapy can prolong patient survival in cases of extensive small-cell lung cancer, and the advantages of combined therapy are reflected in improving the body's immune capacity and enhancing the killing effect of immune cells.
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