Durvalumab after chemoradiotherapy in patients with stage III non-small-cell lung cancer: real-world outcomes versus clinical trial results

被引:5
作者
Verschueren, Marjon V. [1 ,2 ]
Dijs, Talitha [1 ]
Gulikers, Judith L. [3 ,4 ]
van Veelen, Ard [2 ,4 ]
Croes, Sander [3 ,4 ]
Hendriks, Lizza E. L. [5 ]
Smit, Adrianus A. J. [6 ]
Bloem, Lourens T. [2 ]
Egberts, Antoine C. G. [2 ,7 ]
van de Garde, Ewoudt M. W. [1 ,2 ]
Peters, Bas J. M. [1 ,2 ]
机构
[1] St Antonius Hosp, Dept Clin Pharm, Utrecht, Netherlands
[2] Univ Utrecht, Utrecht Inst Pharmaceut Sci, Div Pharmacoepidemiol & Clin Pharmacol, Utrecht, Netherlands
[3] Maastricht Univ Med Ctr, Dept Clin Pharm & Toxicol, Maastricht, Netherlands
[4] Maastricht Univ Med Ctr, CARIM Sch Cardiovasc Dis, Maastricht, Netherlands
[5] Maastricht Univ Med Ctr, GROW Sch Oncol & Dev Biol, Dept Resp Med, Maastricht, Netherlands
[6] OLVG, Dept Pulm Dis, Amsterdam, Netherlands
[7] Univ Med Ctr Utrecht, Dept Clin Pharm, Utrecht, Netherlands
关键词
concurrent chemoradiotherapy; durvalumab; effectiveness-efficacy gap; NSCLC; observational study; overall survival; progression-free survival; sequential chemoradiotherapy; CHEMORADIATION; NSCLC; THERAPY;
D O I
10.2217/imt-2023-0002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Tweetable abstractReal-world stage III NSCLC patients who received durvalumab after CRT had better outcomes than those who received CRT alone. Longer PFS in real-world versus trial may be due to follow-up differences. Plain language summaryWe assessed a medicine called durvalumab on patients with non-small cell lung cancer who received chemoradiotherapy in a real-world setting. We compared their outcomes with those from a clinical trial. Patients who received two types of chemoradiotherapy with or without durvalumab were included, and their progression-free survival (PFS) and overall survival (OS) outcomes were analyzed. We found that patients treated with durvalumab had better PFS and OS than those treated without durvalumab. PFS was longer in the real-world than in the clinical trial, but OS was similar. The difference in PFS may be due to differences in measuring PFS. Aim: We investigated the effectiveness of durvalumab post-concurrent CRT (cCRT) and post-sequential CRT (sCRT) versus cCRT and sCRT alone and compared these outcomes with the PACIFIC trial. Methods: Four cohorts of stage III NSCLC patients who received CRT were included: cCRT with and without durvalumab, sCRT with and without durvalumab. PFS and OS were analyzed using Cox regression. Results: Durvalumab improved PFS (cCRT: aHR = 0.69, sCRT: aHR = 0.71) and OS (cCRT: aHR = 0.71, sCRT: aHR = 0.32), although not all results were significant. PFS was longer in the real-world than in the trial, while OS did not differ. Conclusion: Durvalumab after CRT improved the survival outcomes. The difference between PFS in our study and the trial may be due to differences in follow-up methods.
引用
收藏
页码:839 / 851
页数:13
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