A Propensity-Matched Retrospective Comparative Study with Historical Control to Determine the Real-World Effectiveness of Durvalumab after Concurrent Chemoradiotherapy in Unresectable Stage III Non-Small Cell Lung Cancer

被引:5
作者
Park, Cheol-Kyu [1 ]
Jeon, Nakyung [2 ,3 ]
Park, Hwa-Kyung [1 ]
Oh, Hyung-Joo [1 ]
Kim, Young-Chul [1 ]
Jeon, Ha-Lim [4 ]
Kim, Yong-Hyub [5 ]
Ahn, Sung-Ja [5 ]
Oh, In-Jae [1 ]
机构
[1] Chonnam Natl Univ, Chonnam Natl Univ Hwasun Hosp, Med Sch, Dept Internal Med, Hwasun 58128, South Korea
[2] Pusan Natl Univ, Coll Pharm, Pusan 46241, South Korea
[3] Pusan Natl Univ, Res Inst Drug Dev, Pusan 46241, South Korea
[4] Jeonbuk Natl Univ, Coll Pharm, Jeonju 54896, South Korea
[5] Chonnam Natl Univ, Chonnam Natl Univ Hwasun Hosp, Med Sch, Dept Radiat Oncol, Hwasun 58128, South Korea
基金
新加坡国家研究基金会;
关键词
real-world study; concurrent chemoradiotherapy; durvalumab; non-small cell lung cancer; CONSOLIDATION DURVALUMAB; THERAPY; CHEMORADIATION; NSCLC;
D O I
10.3390/cancers15051606
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary The PACIFIC trial demonstrated the survival benefits of durvalumab consolidation (DC) in patients with unresectable stage III non-small cell lung cancer (NSCLC). In this retrospective cohort study, using a propensity score-matched analysis, we investigated the effectiveness of DC after concurrent chemoradiotherapy (CCRT) and compared DC after CCRT with a historical control in this regard. DC was tolerable and consistently associated with survival benefits (compared with a lack of DC) in real-world contexts. This study suggested that the outcomes of the PACIFIC trial could be successfully translated into real practice and that DC after CCRT could be established as a new standard of care for stage III NSCLC. This study aimed to add real-world evidence to the literature regarding the effectiveness and safety of durvalumab consolidation (DC) after concurrent chemoradiotherapy (CCRT) in the treatment of unresectable stage III non-small cell lung cancer (NSCLC). Using a hospital-based NSCLC patient registry and propensity score matching in a 2:1 ratio, we conducted a retrospective cohort study of patients with unresectable stage III NSCLC who completed CCRT with and without DC. The co-primary endpoints were 2-year progression-free survival and overall survival. For the safety evaluation, we evaluated the risk of any adverse events requiring systemic antibiotics or steroids. Of 386 eligible patients, 222 patients-including 74 in the DC group-were included in the analysis after propensity score matching. Compared with CCRT alone, CCRT with DC was associated with increased progression-free survival (median: 13.3 vs. 7.6 months, hazard ratio[HR]: 0.63, 95% confidence interval[CI]: 0.42-0.96) and overall survival (HR: 0.47, 95% CI: 0.27-0.82) without an increased risk of adverse events requiring systemic antibiotics or steroids. While there were differences in patient characteristics between the present real-world study and the pivotal randomized controlled trial, we demonstrated significant survival benefits and tolerable safety with DC after the completion of CCRT.
引用
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页数:14
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