Matching-adjusted indirect comparison of selpercatinib and pralsetinib in RET fusion-positive non-small cell lung cancer

被引:0
作者
Hochmair, Maximilian [1 ]
Kiiskinen, Urpo [2 ,3 ]
D'yachkova, Yulia [4 ]
Puri, Tarun [5 ]
Wang, Xuwen [6 ]
Wolowacz, Sorrel [7 ]
Vickers, Adrian [7 ]
Nadal, Ernest [8 ,9 ]
机构
[1] Klin Floridsdorf, Karl Landsteiner Inst Lung Res & Pulm Oncol, Dept Resp & Crit Care Med, Vienna, Austria
[2] Eli Lilly & Co, Indianapolis, IN USA
[3] Eli Lilly & Co, Int Value & Access, Helsinki, Finland
[4] Eli Lilly & Co, Stat, Vienna, Austria
[5] Eli Lilly & Co, Thorac Oncol Global Med Affairs, Gurgaon, Haryana, India
[6] Eli Lilly & Co, Real World Adv Anal, Indianapolis, IN USA
[7] RTI Hlth Solut, Hlth Econ, Manchester, England
[8] Inst Catala Oncol ICO, Dept Med Oncol, Avda Granvia De Lhospitalet, Lhospitalet de Llobregat 08908, Barcelona, Spain
[9] Bellvitge Biomed Res Inst IDIBELL, Oncobell Program, Preclin & Expt Res Thorac Tumors PReTT Grp, Lhospitalet de Llobregat, Barcelona, Spain
关键词
NSCLC; matching-adjusted indirect comparison; RET inhibitor; selpercatinib; pralsetinib; TYROSINE KINASE INHIBITOR; PREVIOUSLY TREATED PATIENTS; 2ND-LINE TREATMENT; NSCLC PATIENTS; RETROSPECTIVE ANALYSIS; PREDICTIVE FACTORS; PROGNOSTIC-FACTORS; TREATMENT PATTERNS; CLINICAL-OUTCOMES; PLATINUM-DOUBLET;
D O I
10.1080/14796694.2025.2508132
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
AimsSelpercatinib and pralsetinib are approved for RET-rearranged non - small cell lung cancer.Materials & methodsEfficacy and safety were compared using matching-adjusted indirect comparison.ResultsMedian progression-free survival (PFS) was 22.1 and 13.3 months for selpercatinib and pralsetinib, respectively (HR = 0.67; 95% CI, 0.53-0.85). Objective response rate was 64.5% and 65.8%, and disease control rate was 92.1% and 90.4%, respectively. Median overall survival was not reached for selpercatinib and 43.9 months for pralsetinib (HR = 0.81; 95% CI, 0.60-1.09). Grade >= 3 treatment-related adverse events (TRAEs) were reported in 39.3% and 62.6% of patients, with discontinuations due to TRAEs in 3.6% and 10.0% of patients, respectively.ConclusionOutcomes were similar; however, PFS was significantly prolonged with selpercatinib, with fewer grade >= 3 TRAEs.
引用
收藏
页码:1867 / 1878
页数:12
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