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:Evaluation of Microscopic Tumour Extension in Localized Stage Non-Small-Cell Lung Cancer for Stereotactic Radiotherapy Planning.
Evaluation of Microscopic Tumour Extension in Localized Stage Non-Small-Cell Lung Cancer for Stereotactic Radiotherapy Planning.
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对于无法手术或拒绝手术的局限性非小细胞肺癌(NSCLC)患者,立体定向放疗是一种替代适应证。一项研究表明,NSCLC的显微镜下肿瘤延伸(ME)因组织学类型而异,这使我们能够推断出适合临床靶区(CTV)的边缘。然而,迄今为止,尚无研究能够确定1期肿瘤患者最相关的边缘。
我们进行了一项回顾性分析,纳入接受手术的局限性T1N0或T2aN0期腺癌(ADC)或鳞状细胞癌(SCC)患者。从该边界测量ME。同时评估肿瘤播散类型的特征。
对于局限性NSCLC,以95%概率覆盖ME所需的边缘在SCC和ADC中分别为4.4 mm和2.9 mm。对于SCC,在TIL(肿瘤浸润淋巴细胞)(TILs)0−10%与50−90%之间,ME最大距离存在显著差异(p < 0.05)。对于ADC,根据患者是否患有慢性阻塞性肺疾病(COPD),最大ME距离存在显著差异(p = 0.011)。多变量分析显示,最大微延伸距离和大小与收缩系数之间存在统计学显著关系。
本研究明确证明,ME取决于NSCLC的病理亚型。根据国际辐射单位与测量委员会(ICRU)报告,应将这些结果提出的50、62和83 CTV边缘加至GTV(大体肿瘤体积)。当使用立体定向体部放疗时,该方法应结合数据集和其他需应用的边缘一并考虑。
Background: Stereotactic radiotherapy for localised stage non-small-cell lung carcinoma (NSCLC) is an alternative indication for patients who are inoperable or refuse surgery. A study showed that the microscopic tumour extension (ME) of NSCLC varied according to the histological type, which allowed us to deduce adapted margins for the clinical target volume (CTV).
However, to date, no study has been able to define the most relevant margins for patients with stage 1 tumours. Methods: We performed a retrospective analysis including patients with adenocarcinoma (ADC) or squamous cell carcinoma (SCC) of localised stage T1N0 or T2aN0 who underwent surgery. The ME was measured from this boundary. The profile of the type of tumour spread was also evaluated. Results: The margin required to cover the ME of a localised NSCLC with a 95% probability is 4. 4 mm and 2. 9 mm for SCC and ADC, respectively. A significant difference in the maximum distance of the ME between the tumour-infiltrating lymphocytes (TILs), 0−10% and 50−90% (p < 0. 05), was noted for SCC.
There was a significant difference in the maximum ME distance based on whether the patient had chronic obstructive pulmonary disease (COPD) (p = 0. 011) for ADC. Multivariate analysis showed a statistically significant relationship between the maximum microextension distance and size with the shrinkage coefficient. Conclusion: This study definitively demonstrated that the ME depends on the pathology subtype of NSCLC.
According to International Commission on Radiation Units and Measurements (ICRU) reports, 50, 62 and 83 CTV margins, proposed by these results, should be added to the GTV (Gross tumour volume). When stereotactic body radiation therapy is used, this approach should be considered in conjunction with the dataset and other margins to be applied.
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