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肿瘤体积分析作为预测标志物在接受克唑替尼治疗的间变性淋巴瘤激酶重排的晚期非小细胞肺癌患者中延长生存时间的应用。

Tumor Volume Analysis as a Predictive Marker for Prolonged Survival in Anaplastic Lymphoma Kinase-rearranged Advanced Non-Small Cell Lung Cancer Patients Treated With Crizotinib.

机构信息

Departments of Radiology.

Department of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, Boston MA.

出版信息

J Thorac Imaging. 2020 Mar;35(2):101-107. doi: 10.1097/RTI.0000000000000413.

DOI:10.1097/RTI.0000000000000413
PMID:30985604
Abstract

PURPOSE

Targeted inhibition of anaplastic lymphoma kinase (ALK) has been widely used for the treatment of advanced non-small cell lung cancer (NSCLC) with ALK rearrangements. We performed tumor volume analysis of ALK-rearranged advanced NSCLC treated with crizotinib to identify an early predictive marker for prolonged survival.

MATERIALS AND METHODS

Cases of 42 patients with ALK-rearranged advanced NSCLC (16 men, 26 women; median age: 55.7 y) treated with crizotinib as their first ALK-directed therapy were retrospectively studied. Tumor volume measurements of dominant lung lesions were performed on baseline computed tomography and follow-up computed tomography at 8 weeks of therapy. The relationships between the 8-week volume change (%) and overall survival (OS) were investigated.

RESULTS

The 8-week tumor volume change ranged from -99.3% to 117.5% (median: -57.7%). Using the 25th percentile of the 8-week volume change of -74%, 11 patients with >74% volume decrease at 8 weeks had a significantly longer OS compared with 31 patients with ≤74% decrease (median OS: 92.0 vs. 22.8 mo; P=0.0048). In multivariable analyses using Cox proportional hazards models, the 8-week volume decrease of >74% was significantly associated with longer OS (hazard ratio=0.14, 95% confidence interval: 0.03-0.59; Cox P=0.008) after adjusting for tumor stage (stage IV vs. recurrent NSCLC, hazard ratio=5.6, 95% confidence interval: 1.29-24.3; P=0.02).

CONCLUSIONS

The 8-week tumor volume decrease of >74% is significantly associated with longer OS in patients with ALK-rearranged NSCLC treated with crizotinib.

摘要

目的

针对间变性淋巴瘤激酶(ALK)的靶向抑制已被广泛用于治疗具有 ALK 重排的晚期非小细胞肺癌(NSCLC)。我们对接受克唑替尼治疗的 ALK 重排的晚期 NSCLC 患者进行肿瘤体积分析,以确定延长生存的早期预测标志物。

材料和方法

回顾性研究了 42 例接受克唑替尼作为一线 ALK 靶向治疗的 ALK 重排的晚期 NSCLC 患者(男性 16 例,女性 26 例;中位年龄:55.7 岁)。在基线 CT 和治疗 8 周的随访 CT 上对主要肺病变的肿瘤体积进行测量。研究了 8 周体积变化(%)与总生存期(OS)之间的关系。

结果

8 周肿瘤体积变化范围为-99.3%至 117.5%(中位数:-57.7%)。使用 8 周体积变化的第 25 百分位数-74%,8 周时体积减少>74%的 11 例患者的 OS 明显长于体积减少≤74%的 31 例患者(中位 OS:92.0 与 22.8 个月;P=0.0048)。使用 Cox 比例风险模型的多变量分析,在调整肿瘤分期(IV 期与复发性 NSCLC,风险比=5.6,95%置信区间:1.29-24.3;P=0.02)后,8 周时体积减少>74%与 OS 延长显著相关(风险比=0.14,95%置信区间:0.03-0.59;Cox P=0.008)。

结论

接受克唑替尼治疗的 ALK 重排 NSCLC 患者,8 周肿瘤体积减少>74%与 OS 延长显著相关。

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