Department of Medical Oncology, Dr B.R.A. Institute-Rotary Cancer Hospital., All India Institute of Medical Sciences, New Delhi, India.
DNB General Medicine, DNB resident, Department of Medical Oncology, Rajiv Gandhi Cancer Institute and Research Centre, New Delhi, India.
Curr Probl Cancer. 2020 Jun;44(3):100549. doi: 10.1016/j.currproblcancer.2020.100549. Epub 2020 Jan 23.
Immune check point inhibitors (ICIs) have changed the treatment paradigm of driver mutation negative non-small cell lung cancer (NSCLC) and they are increasingly incorporated in first-line treatment. Real-world experience of use of these drugs is limited. We aim to evaluate the real-world experience of use of ICIs in patients with advanced NSCLC.
Medical records of patients with NSCLC treated with ICIs at 4 major academic cancer centers in India between January 2016 and December 2018 were analyzed. The type of ICI taken, response rates, survival, and toxicity profiles were analyzed.
The median age at presentation was 60 years (range: 27-79 years). Nivolumab was the most commonly used ICI drug [80%, n = 70] followed by pembrolizumab [10%, n = 9], and atezolizumab [10%, n = 9]. The median number of ICIs cycles received were 4 (range 2-65). Among the evaluable responses in 74 patients, the objective response rates was 25.6% and clinical benefit rate was 46%. Immune related toxicity occurred in 39.9% of patients but, severe toxicity of Grade III and Grade IV occurred in 5 (5.6%) patients. After a median follow-up time of 8.86 months (95%CI 5.2-11.1) the progression-free survival was 4.73 months (95%CI 3.7-8.9), and overall survival was 11.6 months (95%CI 7.33-NR). ECOG PS at the time of start of ICIs was found to be significant determinant of Progression-free survival and overall survival.
Our study demonstrates the feasibility of usage of ICIs in advanced NSCLC in Indian setting with acceptable safety profile and comparable responses with the published studies.
免疫检查点抑制剂(ICIs)改变了驱动基因突变阴性非小细胞肺癌(NSCLC)的治疗模式,它们越来越多地被纳入一线治疗。这些药物的实际应用经验有限。我们旨在评估免疫检查点抑制剂在晚期 NSCLC 患者中的实际应用经验。
分析了印度 4 家主要学术癌症中心于 2016 年 1 月至 2018 年 12 月期间接受 ICIs 治疗的 NSCLC 患者的病历。分析了所使用的 ICI 类型、反应率、生存率和毒性谱。
中位发病年龄为 60 岁(范围:27-79 岁)。纳武利尤单抗是最常用的 ICI 药物[80%,n=70],其次是帕博利珠单抗[10%,n=9]和阿特珠单抗[10%,n=9]。中位接受 ICI 周期数为 4(范围 2-65)。在 74 例可评估反应的患者中,客观缓解率为 25.6%,临床获益率为 46%。39.9%的患者发生免疫相关毒性,但有 5 例(5.6%)患者发生 3 级和 4 级严重毒性。中位随访时间为 8.86 个月(95%CI 5.2-11.1),无进展生存期为 4.73 个月(95%CI 3.7-8.9),总生存期为 11.6 个月(95%CI 7.33-NR)。ICI 开始时 ECOG PS 被发现是无进展生存期和总生存期的显著决定因素。
我们的研究表明,在印度,ICIs 可用于晚期 NSCLC,具有可接受的安全性和与已发表研究相当的反应率。