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度伐鲁单抗作为不可切除的III期非小细胞肺癌患者同步放化疗(CCRT)后的巩固治疗:一项多中心观察性研究

Durvalumab as Consolidation Therapy in Post-Concurrent Chemoradiation (CCRT) in Unresectable Stage III Non-Small Cell Lung Cancer Patients: A Multicenter Observational Study.

作者信息

Wang Chin-Chou, Chiu Li-Chung, Ju Jia-Shiuan, Lin Yu-Ching, Fang Yueh-Fu, Yang Cheng-Ta, Hsu Ping-Chih

机构信息

Division of Pulmonary & Critical Care Medicine, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung City 83301, Taiwan.

Department of Medicine, College of Medicine, Chang Gung University, Taoyuan City 33302, Taiwan.

出版信息

Vaccines (Basel). 2021 Oct 1;9(10):1122. doi: 10.3390/vaccines9101122.

DOI:10.3390/vaccines9101122
PMID:34696229
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8541274/
Abstract

BACKGROUND

The experience of using consolidation durvalumab in post-concurrent chemoradiation (CCRT) unresectable stage III non-small cell lung cancer (NSCLC) is rare in real-world clinical practice, and the factors associated with its efficacy are also unclear. We sought to analyze the efficacy of consolidation durvalumab and the factors associated with its efficacy using a multicenter observational study.

METHODS

The data for 61 patients with post-CCR unresectable stage III NSCLC receiving consolidation durvalumab at the Chang Gung Memorial Hospitals in Linkou, Keelung, Chiayi, and Kaohsiung from November 2017 to March 2020 were analyzed. (3) Results: The median post-CCRT progression-free survival (PFS) and time to metastatic disease or death (TMDD) for consolidation durvalumab were 14.0 months and 16.7 months, respectively. In multiple variant factors analysis, we found that an epidermal growth factor receptor (EGFR) mutation was an independently unfavorable predictive factor for consolidation durvalumab therapy regarding PFS. The median post-CCRT PFS was 6.50 months for EGFR-mutated patients and 33.63 months for EGFR wild-type and unknown patients (HR = 10.47; 95% CI, 4.55-24.07; < 0.001).

CONCLUSIONS

Consolidation durvalumab is effective and safe for post-CCRT unresectable stage III NSCLC in clinical practice, but EGFR mutation is an unfavorable factor for consolidation durvalumab. Thus, searching for a better consolidation therapy for EGFR-mutated patients is warranted.

摘要

背景

在真实世界的临床实践中,同步放化疗(CCRT)后使用度伐利尤单抗巩固治疗不可切除的III期非小细胞肺癌(NSCLC)的经验很少,且与其疗效相关的因素也不清楚。我们试图通过一项多中心观察性研究分析度伐利尤单抗巩固治疗的疗效及其疗效相关因素。

方法

分析了2017年11月至2020年3月在林口、基隆、嘉义及高雄的长庚纪念医院接受度伐利尤单抗巩固治疗的61例CCRT后不可切除的III期NSCLC患者的数据。

结果

度伐利尤单抗巩固治疗的CCRT后中位无进展生存期(PFS)和至转移疾病或死亡时间(TMDD)分别为14.0个月和16.7个月。在多变量因素分析中,我们发现表皮生长因子受体(EGFR)突变是度伐利尤单抗巩固治疗PFS的独立不良预测因素。EGFR突变患者的CCRT后中位PFS为6.50个月,EGFR野生型和未知患者为33.63个月(HR = 10.47;95%CI,4.55 - 24.07;P < 0.001)。

结论

在临床实践中,度伐利尤单抗巩固治疗CCRT后不可切除的III期NSCLC是有效且安全的,但EGFR突变是度伐利尤单抗巩固治疗的不利因素。因此,有必要为EGFR突变患者寻找更好的巩固治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3da/8541274/ec9897ba112f/vaccines-09-01122-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3da/8541274/587cf058c8b3/vaccines-09-01122-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3da/8541274/9878b7c22f64/vaccines-09-01122-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3da/8541274/ec9897ba112f/vaccines-09-01122-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3da/8541274/587cf058c8b3/vaccines-09-01122-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3da/8541274/9878b7c22f64/vaccines-09-01122-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3da/8541274/ec9897ba112f/vaccines-09-01122-g003.jpg

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