γδ T 细胞调节小细胞肺癌中的抗肿瘤免疫
γδ T cells modulate anti-tumor immunity in small cell lung cancer.
我们的发现表明,活化的γδ T细胞可能是SCLC治疗的有价值靶点。
英文原题:A Single-Arm Phase II Study to Evaluate Efficacy and Safety of First-Line Treatment With DCVAC/LuCa, Standard of Care Chemotherapy and Shenqi Fuzheng Injection in Advanced (Stage IIIB/IV) Non-Small Cell Lung Cancer Patients.
DCVAC/LuCa联合标准治疗化疗和参芪扶正注射液在中国复发转移或晚期(IIIB/IV期)NSCLC患者中表现出良好获益,并显著改善气虚体质。
目的:评估肺癌树突状细胞疫苗DCVAC/LuCa联合标准化疗及参芪扶正注射液,作为晚期(IIIB/IV期)非小细胞肺癌(NSCLC)一线治疗的疗效和安全性。患者与方法:纳入组织学或细胞学确诊的复发转移或晚期NSCLC(IIIB/IV期)患者,肿瘤为表皮生长因子受体(EGFR)野生型,或所带EGFR突变不会增加肿瘤对EGFR相互作用药物的敏感性。治疗期间,白细胞分离后2至14天开始第1周期标准治疗(SoC),共进行4至6周期;自SoC第2周期起给予DCVAC/LuCa,先按每3周一个周期给药5次,随后改为每6周一个周期。每次DCVAC/LuCa给药前3天开始参芪扶正注射液治疗,每日给药,共14剂。每3个月通过CT扫描评估疾病。主要和次要终点为疗效,包括客观缓解率(ORR)和无进展生存期(PFS)。通过不良事件发生率、类型和严重程度,实验室异常(血常规、尿检及生化检查)、体能状态和生命体征评估安全性;根据中医体质分类与判定标准,通过舌诊和问卷调查评估气虚。结果:3家医院共纳入23例接受联合治疗的患者。ORR为34.8%(95% CI 16.4%–57.3%),中位缓解持续时间为5.51个月(95% CI 2.70–8.32),中位PFS为10.72个月(95% CI 4.52–16.93),1年生存率为77.8%,中位OS为21.97个月(95% CI 13.68–30.25)。发生1例与心脏病史有关的严重不良事件,未发生与DCVAC/LuCa治疗有关的不良事件。治疗后气虚评分显著改善(P<0.0001),从治疗前的41.19±14.58降至治疗后的10.52±16.58。结论:DCVAC/LuCa联合标准化疗和参芪扶正注射液对中国复发转移或晚期(IIIB/IV期)NSCLC患者显示出较好获益,并显著改善气虚体质;DCVAC/LuCa治疗未见相关不良事件。
OBJECTIVES: To evaluate the efficacy and safety of first-line treatment with a dendritic cell vaccination for lung cancer (DCVAC/LuCa), standard of care chemotherapy and Shenqi Fuzheng injection in patients with advanced (stage IIIB/IV) non-small cell lung cancer. PATIENTS AND METHODS: Patients with histologically or cytologically confirmed recurrent metastatic or advanced NSCLC (stage IIIB/IV) with wild-type epidermal growth factor receptor (EGFR) or EGFR mutation which does not confer increased tumor susceptibility to EGFR-interacting drugs were recruited. For the treatment period, the first cycle of standard of care therapy (SoC) started 2 to 14 days after the leukapheresis procedure. SoC continued 4 to 6 cycles. DCVAC/LuCa was administered from the second cycle of SoC. DCVAC/LuCa was administered in a 3-week cycle schedule (5 doses) and then in a 6-week cycle schedule. Shenqi Fuzheng injection was administered 3 days before each DCVAC/LuCa administration for a total of 14 daily doses. Patients would undergo disease evaluation by computed tomography (CT) scan every 3 months. The primary and secondary endpoint was efficacy with regard to objective response rate (ORR) and progression free survival (PFS). The safety profile was measured by: incidence, type, and severity of all adverse events (AEs), laboratory abnormalities (blood routine test, urine test, and chemical test), physical status, and vital signs. Qi insufficiency was evaluated by tongue diagnosis and questionnaire survey with "Classification and Determination of constitution in TCM." RESULTS: Twenty-three patients from 3 hospitals who received combination therapy were included. ORR was 34.8% (95% CI:16.4%-57.3%). Median duration of response was 5.51 m (95% CI:2.70-8.32). Median PFS was 10.72 m (95% CI:4.52-16.93), 1-year survival was 77.8%. mOS was 21.97 m (95% CI:13.68-30.25). There was 1 severe AE related to a history of heart disease and there were no adverse events related to DCVAC/LuCa treatment. Qi insufficiency was improved significantly ( P < .0001) from 41.19 ± 14.58 before treatment to 10.52 ± 16.58 after treatment. CONCLUSION: DCVAC/LuCa, combined with standard of care chemotherapy and Shenqi Fuzheng injection exhibited good benefit in Chinese patients with recurrent metastatic or advanced (stage IIIB/IV) NSCLC, and also significantly improved Qi insufficiency constitution. There were no related adverse events with DCVAC/LuCa treatment.
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