Chenlin Wang, Ning Liang, Lili Qiao, Ya'nan Wu, Jiandong Zhang, Yan Zhang
{"title":"Clinical features and prognosis analysis of stage III/IV patients with lung cancer after treatment with toripalimab: A real-world retrospective.","authors":"Chenlin Wang, Ning Liang, Lili Qiao, Ya'nan Wu, Jiandong Zhang, Yan Zhang","doi":"10.4103/jcrt.jcrt_500_24","DOIUrl":null,"url":null,"abstract":"<p><strong>Aim: </strong>Toripalimab is the first antitumor programmed cell death protein 1 (PD-1) antibody approved in China. For better patient management, it is important to understand the real-world outcomes of toripalimab in treating patients with lung cancer in the real world outside of clinical trials to improve patient care.</p><p><strong>Methods: </strong>We retrospectively examined the clinical data of 80 patients with lung cancer who received the PD-1 inhibitor (toripalimab). The Chi-square test was performed to identify clinical factors associated with the advancement of the disease. Multivariate Cox regression analysis was used to screen prognostic variables linked to real-world progression-free survival (PFS) and overall survival (OS). OS and PFS were calculated using the Kaplan-Meier method, and the comparisons were determined using the log-rank test, and continuous and categorical variables were explained using median and percentage, respectively.</p><p><strong>Result: </strong>The median OS of the estimated 80 patients was 15.85 months (95% confidence interval [CI]: 14.103-17.949 months), and the estimated PFS was 5.650 months (95% CI: 7.226-11.264 months). The longer OS and PFS correlate with the patient's staging and number of treatment lines. The PD-1 drug gave stage III patients a significantly longer PFS and OS compared to stage IV patients (PFS: 14.65 vs. 6.68, P = 0.004; OS: 21.1 vs. 13.7, P = 0.003). First- or second-line immunotherapy patients have significantly longer PFS and OS than third- or fourth-line (PFS: 6.4 vs. 3.6, P = 0.009; OS: 20.0 vs. 10.5, P = 0.003). In patients with stage IV (n = 60) with extensive metastasis, the site of metastasis is mostly 1-3 sites after receiving toripalimab. The duration of PD-1 inhibitor OS in progressive patients (n = 56) was significantly prolonged (P = 0.038).</p><p><strong>Conclusion: </strong>For patients with lung cancer, toripalimab can considerably extend PFS and OS in the first or second line and in stage III. PD-1 inhibitors are administered to patients with stage IV extensively metastatic lung cancer, which indicates an oligometastatic progression pattern, primarily in 1-3 locations, who are treated with PD-1 inhibitors. Continuing toripalimab beyond disease progression significantly prolonged OS.</p>","PeriodicalId":94070,"journal":{"name":"Journal of cancer research and therapeutics","volume":"20 7","pages":"2021-2028"},"PeriodicalIF":0.0000,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of cancer research and therapeutics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/jcrt.jcrt_500_24","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/10 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Aim: Toripalimab is the first antitumor programmed cell death protein 1 (PD-1) antibody approved in China. For better patient management, it is important to understand the real-world outcomes of toripalimab in treating patients with lung cancer in the real world outside of clinical trials to improve patient care.
Methods: We retrospectively examined the clinical data of 80 patients with lung cancer who received the PD-1 inhibitor (toripalimab). The Chi-square test was performed to identify clinical factors associated with the advancement of the disease. Multivariate Cox regression analysis was used to screen prognostic variables linked to real-world progression-free survival (PFS) and overall survival (OS). OS and PFS were calculated using the Kaplan-Meier method, and the comparisons were determined using the log-rank test, and continuous and categorical variables were explained using median and percentage, respectively.
Result: The median OS of the estimated 80 patients was 15.85 months (95% confidence interval [CI]: 14.103-17.949 months), and the estimated PFS was 5.650 months (95% CI: 7.226-11.264 months). The longer OS and PFS correlate with the patient's staging and number of treatment lines. The PD-1 drug gave stage III patients a significantly longer PFS and OS compared to stage IV patients (PFS: 14.65 vs. 6.68, P = 0.004; OS: 21.1 vs. 13.7, P = 0.003). First- or second-line immunotherapy patients have significantly longer PFS and OS than third- or fourth-line (PFS: 6.4 vs. 3.6, P = 0.009; OS: 20.0 vs. 10.5, P = 0.003). In patients with stage IV (n = 60) with extensive metastasis, the site of metastasis is mostly 1-3 sites after receiving toripalimab. The duration of PD-1 inhibitor OS in progressive patients (n = 56) was significantly prolonged (P = 0.038).
Conclusion: For patients with lung cancer, toripalimab can considerably extend PFS and OS in the first or second line and in stage III. PD-1 inhibitors are administered to patients with stage IV extensively metastatic lung cancer, which indicates an oligometastatic progression pattern, primarily in 1-3 locations, who are treated with PD-1 inhibitors. Continuing toripalimab beyond disease progression significantly prolonged OS.
目的:多利帕利单抗是国内首个获批的抗肿瘤程序性细胞死亡蛋白1 (PD-1)抗体。为了更好地管理患者,重要的是要了解在临床试验之外的现实世界中,托利哌单抗治疗肺癌患者的实际结果,以改善患者护理。方法:回顾性分析80例接受PD-1抑制剂(多利帕利单抗)治疗的肺癌患者的临床资料。采用卡方检验确定与疾病进展相关的临床因素。多变量Cox回归分析用于筛选与真实世界无进展生存期(PFS)和总生存期(OS)相关的预后变量。OS和PFS采用Kaplan-Meier法计算,比较采用log-rank检验,连续变量和分类变量分别采用中位数和百分比解释。结果:估计80例患者的中位OS为15.85个月(95%可信区间[CI]: 14.103 ~ 17.949个月),估计PFS为5.650个月(95% CI: 7.226 ~ 11.264个月)。较长的OS和PFS与患者的分期和治疗线数量相关。与IV期患者相比,PD-1药物使III期患者的PFS和OS显着延长(PFS: 14.65 vs. 6.68, P = 0.004;OS: 21.1 vs. 13.7, P = 0.003)。一线或二线免疫治疗患者的PFS和OS明显长于三线或四线(PFS: 6.4 vs. 3.6, P = 0.009;OS: 20.0 vs. 10.5, P = 0.003)。在广泛转移的IV期患者(n = 60)中,托帕利单抗治疗后转移部位多为1-3个部位。进展性患者(n = 56) PD-1抑制剂OS持续时间显著延长(P = 0.038)。结论:对于肺癌患者,托帕利单抗可显著延长一线或二线及III期的PFS和OS。PD-1抑制剂用于IV期广泛转移性肺癌患者,这表明寡转移进展模式,主要在1-3个部位,使用PD-1抑制剂治疗。在疾病进展后继续使用托利单抗可显著延长OS。