Real-world overall survival after alternative dosing for pembrolizumab in the treatment of non-small cell lung cancer: A nationwide retrospective cohort study with a non-inferiority primary objective

被引:3
|
作者
Grit, Geeske F. [1 ,2 ]
van Geffen, Esmee [3 ]
Malmberg, Ruben [4 ,5 ]
van Leeuwen, Roelof [4 ,5 ]
Bohringer, Stefan [6 ,7 ]
Smit, Hans J. M. [8 ]
Brocken, Pepijn [9 ]
Eijsink, Job F. H. [10 ]
Dronkers, Esther [3 ]
Gal, Pim [3 ]
Jaarsma, Eva [3 ]
van Drie-Pierik, Regine J. H. M. [11 ]
Eldering-Heldens, Anne M. P. [12 ]
Wymenga, A. N. Machteld [13 ]
Mol, Peter G. M. [2 ]
Zwaveling, Juliette [6 ]
Hilarius, Doranne [14 ]
机构
[1] Dutch Inst Clin Auditing, Leiden, Netherlands
[2] Univ Med Ctr Groningen, Dept Clin Pharm & Pharmacol, Groningen, Netherlands
[3] LOGEX Healthcare Analyt, Amsterdam, Netherlands
[4] Erasmus MC, Dept Hosp Pharm, Rotterdam, Netherlands
[5] Erasmus MC Canc Inst, Dept Med Oncol, Rotterdam, Netherlands
[6] Leiden Univ, Med Ctr, Dept Clin Pharm & Toxicol, Leiden, Netherlands
[7] Leiden Univ, Med Ctr, Dept Biomed Data Sci, Leiden, Netherlands
[8] Rijnstate Hosp, Dept Pulm Med, Arnhem, Netherlands
[9] HAGA Teaching Hosp, Dept Pulmonol, The Hague, Netherlands
[10] Isala Klin, Dept Clin Pharm, Zwolle, Netherlands
[11] Med Spectrum Twente, Dept Clin Pharm, Enschede, Netherlands
[12] Noordwest Ziekenhuisgrp, Dept Pharm, Alkmaar, Netherlands
[13] Med Spectrum Twente, Dept Internal Med, Enschede, Netherlands
[14] Rode Kruis Ziekenhuis, Dept Pharm, Beverwijk, Netherlands
关键词
Pembrolizumab; Non-small cell lung carcinoma; Non-inferiority; ANTIBODY;
D O I
10.1016/j.lungcan.2024.107950
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: High and increasing expenses on pembrolizumab ask for more cost-effective and sustainable treatment strategies to improve affordability of healthcare. Therefore, a part of the Dutch hospitals implemented an alternative, partially lower, weight-based dosing protocol for pembrolizumab. This provided the unique opportunity to compare the overall survival (OS) of the alternative pembrolizumab dosing protocol to standard dosing using a nationwide registry in non-small cell lung cancer (NSCLC) patients. Methods: This is a retrospective cohort study with a non-inferiority primary objective. Forty hospitals in the Dutch Medication Audit and Dutch Lung Cancer Audit treated 1966 patients with NSCLC with first line pembrolizumab (mono- or combination therapy) between Jan 1st 2021, and Mar 31st, 2023. Alternative weight- based pembrolizumab dosing (100/150/200 mg Q3W or 200/300/400 mg Q6W) was administered to 604 patients, and 1362 patients received standard pembrolizumab dosing (200 mg Q3W or 400 mg Q6W). A Cox proportional hazard model with selected covariates was used to compare the OS between alternative and standard dosing protocols. The non-inferiority margin was set at a hazard ratio (HR) of 1.2 for OS. Non- inferiority is established by showing that the upper limit of the 95 % confidence interval (CI) of the HR of OS is smaller or equal to 1.2. Results: Distribution of age (66.7 years +/-9.4), sex (45 % female) and treatment combinations were similar for both groups, comorbidity score was higher in the standard group. Median daily dose in the alternative dosing group was 22 % lower compared to the standard dosing group, 7.14 mg/day (interquartile range (IQR):5.48-8.04 mg/day) vs. 9.15 mg/day (IQR:8.33-9.52 mg/day), respectively. Alternative dosing was non- inferior to standard dosing regarding overall survival (adjusted HR 0.83, 95 %CI:0.69-1.003). Conclusion: This large, retrospective real-world analysis supports the hypothesis that the alternative, partially lower pembrolizumab dosing protocol in NSCLC maintains treatment effectiveness while reducing treatment costs.
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页数:7
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