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克唑替尼治疗重排型晚期非小细胞肺癌的肿瘤体积动态变化及肿瘤生长速率

Tumor volume dynamics and tumor growth rate in -rearranged advanced non-small-cell lung cancer treated with crizotinib.

作者信息

Nishino Mizuki, Hida Tomoyuki, Kravets Sasha, Dahlberg Suzanne E, Lydon Christine A, Hatabu Hiroto, Johnson Bruce E, Awad Mark M

机构信息

Department of Radiology, Brigham and Women's Hospital and Department of Imaging, Dana-Farber Cancer Institute, 450 Brookline Ave., Boston, MA, 02215, USA.

Department of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, 450 Brookline Ave., Boston, MA, 02215, USA.

出版信息

Eur J Radiol Open. 2020 Jan 28;7:100210. doi: 10.1016/j.ejro.2019.12.004. eCollection 2020.

Abstract

PURPOSE

The purpose of the study is to investigate volumetric tumor burden dynamics and tumor growth rates in -rearranged advanced NSCLC patients during crizotinib monotherapy.

METHODS

The study included 44 -rearranged advanced NSCLC patients treated with crizotinib monotherapy as their initial ALK-directed therapy, who had at least one measurable lung lesion and at least two follow-up CT scans, and experienced tumor volume increase while on crizotinib. The tumor volume (in mm) of the dominant lung lesion was measured on serial CT scans during therapy for analysis of tumor growth rates after the volume nadir.

RESULTS

A total of 231 volume measurements from the nadir to the end of crizotinib therapy or the last follow-up in 44 patients were analyzed in a linear mixed-effects model, fitting time (in months since baseline) as a random effect. When measured from the volume nadir, the tumor growth rate of the logarithm of tumor volume (logV) was 0.04/month (SE = 0.012, P = 0.0011) in the unadjusted model. When adjusted for the baseline volume (logV), the growth rate was again 0.04/month (SE = 0.011, P = 0.0004). When adjusted for clinical variables and logV, the growth rate was 0.045/month (SE = 0.012, P = 0.0002), indicating that the tumor growth rate after nadir in this cohort remains very close to 0.04/month regardless of logV or clinical factors.

CONCLUSIONS

Tumor volume growth rate after nadir in -rearranged NSCLC patients treated with crizotinib was obtained, providing objective reference values that can inform physicians when deciding to keep their patients on ALK directed therapy with slowly progressing lung cancer.

摘要

目的

本研究旨在调查经克唑替尼单药治疗的ALK重排晚期非小细胞肺癌(NSCLC)患者的肿瘤体积负荷动态变化及肿瘤生长速率。

方法

本研究纳入了44例接受克唑替尼单药治疗作为初始ALK靶向治疗的ALK重排晚期NSCLC患者,这些患者至少有一处可测量的肺部病变且至少进行了两次随访CT扫描,并且在接受克唑替尼治疗期间肿瘤体积增大。在治疗期间通过连续CT扫描测量主要肺部病变的肿瘤体积(单位为mm),以分析体积最低点后的肿瘤生长速率。

结果

在一个线性混合效应模型中分析了44例患者从最低点到克唑替尼治疗结束或最后一次随访的总共231次体积测量数据,将时间(自基线起的月数)作为随机效应进行拟合。从未调整的模型来看,从体积最低点开始测量时,肿瘤体积对数(logV)的肿瘤生长速率为0.04/月(标准误 = 0.012,P = 0.0011)。在对基线体积(logV)进行调整后,生长速率再次为0.04/月(标准误 = 0.011,P = 0.0004)。在对临床变量和logV进行调整后,生长速率为0.045/月(标准误 = 0.012,P = 0.0002),这表明在该队列中最低点后的肿瘤生长速率无论logV或临床因素如何,仍非常接近0.04/月。

结论

获得了接受克唑替尼治疗的ALK重排NSCLC患者最低点后的肿瘤体积生长速率,为医生在决定让缓慢进展的肺癌患者继续接受ALK靶向治疗时提供了客观参考值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0299/7569410/588d779f7720/gr1.jpg

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