Efficacy of Lower Fixed Dose Pembrolizumab in the Treatment of Non-Small Cell Lung Cancer Patients in a Lower-Middle Income Country: Jordan Experience

Salah Abbasi, Layla S Abbasi, Adnan Almallah, Nedal F Al-Rawashdeh
{"title":"Efficacy of Lower Fixed Dose Pembrolizumab in the Treatment of Non-Small Cell Lung Cancer Patients in a Lower-Middle Income Country: Jordan Experience","authors":"Salah Abbasi, Layla S Abbasi, Adnan Almallah, Nedal F Al-Rawashdeh","doi":"10.31487/j.aco.2022.02.01","DOIUrl":null,"url":null,"abstract":"Background: Pembrolizumab was approved as first line treatment of advanced non-small cell lung cancer (NSCLC) at standard dose of 200mg every 3 weeks. We aim to assess the efficacy of a lower fixed dose of 100mg and review the Jordanian experience in first line setting. \nMethods: We conducted a retrospective study of 88 NSCLC patients, including 27 who received low fixed dose pembrolizumab (Pem100) and 61 received standard fixed dose (Pem200) from September 2016 to February 2022.\nResults: Objective response rate was (48.8%), including (5.6%) with complete response, and (43.2%) with partial response. The median progression free survival (PFS) and median overall survival (OS) for this Jordanian population were consistent with published clinical trials; 8.00 months (95% CI, 7.19 to 8.80) and 17.48 months (95 CI, 15.53 to 19.44), respectively. The PFS and OS were not statistically different between the Pem100 and Pem200 groups (8.00 vs. 8.00 months, p=0.73, and 17.02 vs 17.60 months, p=0.66, respectively). PFS and OS were significantly affected by the programmed cell death ligand (PD-L1) tumor proportion score (TPS) (12.40 vs. 8.00 vs. 5.80 months, p<0.001, and 22.70 vs. 16.47 vs. 12.71 months, p<0.001, in TPS ≥ 50% vs. TPS 1-49% vs. TPS < 1%, respectively). OS was not statistically different according to age, gender, histology, or smoking status.\nConclusion: Lower fixed dose pembrolizumab (100mg 3-weekly) appears to be effective in first line NSCLC. A randomized trial should be done to investigate this low dose with significant cost reduction potential.","PeriodicalId":320563,"journal":{"name":"Annals of Clinical Oncology","volume":"27 4","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2022-05-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annals of Clinical Oncology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.31487/j.aco.2022.02.01","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

Background: Pembrolizumab was approved as first line treatment of advanced non-small cell lung cancer (NSCLC) at standard dose of 200mg every 3 weeks. We aim to assess the efficacy of a lower fixed dose of 100mg and review the Jordanian experience in first line setting. Methods: We conducted a retrospective study of 88 NSCLC patients, including 27 who received low fixed dose pembrolizumab (Pem100) and 61 received standard fixed dose (Pem200) from September 2016 to February 2022. Results: Objective response rate was (48.8%), including (5.6%) with complete response, and (43.2%) with partial response. The median progression free survival (PFS) and median overall survival (OS) for this Jordanian population were consistent with published clinical trials; 8.00 months (95% CI, 7.19 to 8.80) and 17.48 months (95 CI, 15.53 to 19.44), respectively. The PFS and OS were not statistically different between the Pem100 and Pem200 groups (8.00 vs. 8.00 months, p=0.73, and 17.02 vs 17.60 months, p=0.66, respectively). PFS and OS were significantly affected by the programmed cell death ligand (PD-L1) tumor proportion score (TPS) (12.40 vs. 8.00 vs. 5.80 months, p<0.001, and 22.70 vs. 16.47 vs. 12.71 months, p<0.001, in TPS ≥ 50% vs. TPS 1-49% vs. TPS < 1%, respectively). OS was not statistically different according to age, gender, histology, or smoking status. Conclusion: Lower fixed dose pembrolizumab (100mg 3-weekly) appears to be effective in first line NSCLC. A randomized trial should be done to investigate this low dose with significant cost reduction potential.
低固定剂量派姆单抗治疗中低收入国家非小细胞肺癌患者的疗效:约旦经验
背景:Pembrolizumab已被批准作为晚期非小细胞肺癌(NSCLC)的一线治疗药物,标准剂量为200mg / 3周。我们的目的是评估较低固定剂量100mg的疗效,并回顾约旦在一线环境中的经验。方法:我们对2016年9月至2022年2月期间88例NSCLC患者进行回顾性研究,其中27例接受低固定剂量派姆单抗(Pem100)治疗,61例接受标准固定剂量(Pem200)治疗。结果:客观缓解率为48.8%,其中完全缓解率为5.6%,部分缓解率为43.2%。约旦人群的中位无进展生存期(PFS)和中位总生存期(OS)与已发表的临床试验一致;分别为8.00个月(95% CI, 7.19 ~ 8.80)和17.48个月(95 CI, 15.53 ~ 19.44)。Pem100组和Pem200组的PFS和OS差异无统计学意义(分别为8.00 vs 8.00个月,p=0.73, 17.02 vs 17.60个月,p=0.66)。程序性细胞死亡配体(PD-L1)肿瘤比例评分(TPS)显著影响PFS和OS (TPS≥50%、TPS 1-49%、TPS < 1%分别为12.40、8.00、5.80个月,p<0.001和22.70、16.47、12.71个月,p<0.001)。OS在年龄、性别、组织学、吸烟状况等方面无统计学差异。结论:低固定剂量派姆单抗(100mg, 3周)似乎对一线NSCLC有效。应该进行一项随机试验来调查这种具有显著降低成本潜力的低剂量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信