Survival with novel hormonal therapies in patients with nonmetastatic castration-resistant prostate cancer: indirect comparison of three randomized phase-III trials

被引:2
作者
Rivano, Melania [1 ]
Cancanelli, Luca [2 ]
Di Spazio, Lorenzo [3 ]
Mengato, Daniele [4 ]
Chiumente, Marco [5 ]
Messori, Andrea [6 ]
机构
[1] Binaghi Hosp, Hosp Pharm Dept, Via Guadazzonis 2, I-09126 Cagliari, Italy
[2] Azienda Ulss 2 Marca Trevigiana, Hosp Pharm Dept, Via Osped 16, I-31033 Treviso, Italy
[3] Santa Chiara Hosp, Hosp Pharm Dept, I-38122 Largo Medaglie Doro, Trento, Italy
[4] Azienda Osped Univ Padova, Hosp Pharm Dept, Via Giustiniani 2, I-35128 Padua, Italy
[5] Soc Italiana Farm Clin & Terapia SIFaCT, Direz Sci, Milan, Italy
[6] Reg Toscana, HTA Unit, Via Alderotti 26-N, I-50135 Florence, Italy
关键词
Nonmetastatic prostate cancer; Overall survival; Enzalutamide; Apalutamide; Darolutamide; METASTASIS-FREE SURVIVAL;
D O I
10.1007/s00345-022-04143-8
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Introduction In recent years, new treatments have been approved for nonmetastatic castration-resistant prostate cancer (M0CRPC). Because direct comparisons between these treatments are not available to guide treatment decisions, indirect comparisons can be of interest. Methods Our analysis evaluated second-generation hormone treatments proposed for M0CRPC. We searched multiple databases for articles published between 2010 and 2022. Phase-III clinical trials that studied these agents in M0CRPC patients were eligible. Among these, we included trials reporting overall survival (OS) through Kaplan-Meier curves. We performed the reconstruction of individual patient data from Kaplan-Meier graphs, according to the Shiny method, to indirectly compare the efficacy of the different agents. Indirect comparisons included testing for equivalence according to FDA criteria. Confidence intervals (CI) were 95% in all analyses except equivalence testing, where 90%CIs were used. Results Three studies met these inclusion criteria. Apalutamide (hazard ratio [HR]: 0.75, 95% confidence interval [CI] 0.64-0.88), darolutamide (HR 0.70, 95%CI 0.58-0.84), and enzalutamide (HR 0.77, 95%CI 0.65-0.90) were all significantly more effective than the placebo. Our results showed no difference in OS between any of these three agents, and in testing for equivalence, our estimates of HR met the 0.75-1.33 level. Conclusions While the Shiny method has confirmed its validity in reconstructing individual patient data, our indirect comparisons based on mature OS demonstrated similar efficacy and substantial equivalence among these three second-generation androgen receptor inhibitors.
引用
收藏
页码:2609 / 2615
页数:7
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