Pembrolizumab (Anti-PD-1) in the management of malignant pleural mesothelioma: A systematic review of the current literature

Rebaz M. Ali, F. Kakamad, Hiwa O. Abdullah, Shalaw H. Abdulla, Shaho F. Ahmed, Bnar J. Hama Amin, Marwan N. Hassan, S. J. Hasan, Hussein M. Hamasalih, Berun A. Abdalla, Rawezh Q. Salih, Hawbash M. Rahim
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Abstract

Malignant pleural mesothelioma is an infrequent and aggressive type of cancer that is difficult to treat, and standard therapies have shown limited effectiveness. There have been recent advances in the development of targeted therapies for malignant pleural mesothelioma, including immunotherapy with pembrolizumab. This is a systematic review of the current role of pembrolizumab in the treatment of this disease. A systematic search was conducted through the databases and search engines. The eligible studies to be included were those that primarily focused on the outcomes of treating this disease with pembrolizumab, regardless of study design, line of therapy, mode of therapy, and ECOG performance status. After the initial and full-text screenings, 15 studies were reviewed. The number of cases was 454 with a mean age of 68.13 years, of which males (79.7%) were the predominant gender. Most of the cases were affected by epithelioid mesothelioma (76.7%). Pembrolizumab had been used as the first line of treatment in 62 (13.7%) cases. In 92.73% of cases, the therapy mode was pembrolizumab monotherapy. A total of 68 different adverse events were recorded. The most commonly associated adverse events were fatigue (14.8%), pruritis/rash (13.7%), and diarrhea (9.7%). Two patients died due to adverse events. The overall objective response was 17.8%, stable disease was 35.7%, progression-free survival was about 47.6% with a mean of 4.73 months, and 117 cases (25.8%) could reach treatment-related survival. Pembrolizumab can serve as a viable alternative in the management of malignant pleural mesothelioma, offering satisfactory outcomes and acceptable safety profiles
Pembrolizumab(抗pd -1)治疗恶性胸膜间皮瘤:对当前文献的系统回顾
恶性胸膜间皮瘤是一种罕见且侵袭性的癌症,很难治疗,标准治疗方法的效果有限。恶性胸膜间皮瘤的靶向治疗最近取得了进展,包括派姆单抗免疫治疗。这是一篇关于派姆单抗目前在治疗这种疾病中的作用的系统综述。通过数据库和搜索引擎进行了系统的搜索。纳入的符合条件的研究是那些主要关注派姆单抗治疗这种疾病的结果的研究,而不考虑研究设计、治疗路线、治疗模式和ECOG表现状态。在初步和全文筛选后,回顾了15项研究。病例454例,平均年龄68.13岁,其中男性占79.7%。以上皮样间皮瘤居多(76.7%)。在62例(13.7%)病例中,派姆单抗被用作一线治疗。92.73%的病例采用派姆单抗单药治疗。总共记录了68个不同的不良事件。最常见的相关不良事件是疲劳(14.8%)、瘙痒/皮疹(13.7%)和腹泻(9.7%)。2例患者因不良事件死亡。总体客观缓解率为17.8%,病情稳定率为35.7%,无进展生存期约为47.6%,平均为4.73个月,117例(25.8%)达到治疗相关生存期。Pembrolizumab可以作为恶性胸膜间皮瘤治疗的可行替代方案,提供令人满意的结果和可接受的安全性
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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