Matching-adjusted indirect comparison of talazoparib plus enzalutamide versus abiraterone acetate and docetaxel in mCRPC

被引:0
|
作者
Castro, Elena [1 ]
Wang, Di [2 ]
Walsh, Sarah [2 ]
Craigie, Samantha [2 ]
Haltner, Anja [3 ]
Nazari, Jonathan [4 ]
Niyazov, Alexander [4 ]
Samjoo, Imtiaz A. [2 ]
机构
[1] Hosp Univ 12 Octubre, Dept Med Oncol, Edif Maternidad,2a Planta Av Cordoba S-N, Madrid 28041, Spain
[2] EVERSANATM, Value & Evidence, Burlington, ON, Canada
[3] EVERSANATM, Value & Evidence, New York, NY USA
[4] Pfizer Inc, Global Value & Evidence Oncol, New York, NY USA
关键词
Metastatic castration-resistant prostate cancer; matching-adjusted indirect comparison; systematic literature review; PARP inhibitor; talazoparib; RESISTANT PROSTATE-CANCER; PREDNISONE; POPULATION; SURVIVAL; MEN;
D O I
10.1080/14796694.2025.2471200
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aims: The absence of direct comparisons between talazoparib plus enzalutamide (TALA+ENZA) and current standard of care hinders evaluating their relative efficacy for first-line (1 L) metastatic castration resistant prostate cancer (mCRPC). This study aimed to compare TALA+ENZA (TALAPRO-2) to abiraterone acetate plus prednisone (AAP) (COU-AA-302) and docetaxel (TAX 327) using a matching-adjusted indirect treatment comparison (MAIC). Methods: A systematic literature review using the Ovid (R) interface was performed to identify relevant evidence. Patient-level data from TALAPRO-2 and published data from COU-AA-302 and TAX 327 were used to match populations on clinically relevant confounders. The MAICs were conducted for radiographic progression-free survival (rPFS), overall survival (OS), objective response rate (ORR), along with additional efficacy outcomes. Results: In all-comers, TALA+ENZA statistically significantly prolonged rPFS (HR: 0.256; 95% confidence interval [CI]: 0.183, 0.359; p < 0.0001), OS (HR: 0.557; 0.405, 0.766; p = 0.0003), and improved ORR (OR: 3.924; 2.017, 7.634; p = 0001) versus AAP. In all-comers, TALA+ENZA significantly prolonged OS (HR: 0.446; 0.316, 0.631; p < 0.0001) and improved ORR (OR: 13.081; 5.757, 29.721; p < 0.0001) versus docetaxel. All other efficacy outcomes statistically favored TALA+ENZA. Conclusions: These results suggest TALA+ENZA improves clinical outcomes relative to AAP and docetaxel in the 1 L mCRPC all-comers population.
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页数:10
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