Cost-Effectiveness Analysis of Biomarker Testing to Guide First-Line PARP Inhibitor Maintenance for Patients with Advanced Ovarian Cancer After Response to First-Line Platinum Chemotherapy in the USA

被引:1
作者
Elsea, David [1 ]
Muston, Dominic [2 ]
Fan, Lin [3 ]
Mihai, Adela [4 ]
Meng, Yang [5 ]
Kasle, Adam [1 ]
Monberg, Matthew [2 ]
机构
[1] Lumanity Inc, Bethesda, MD USA
[2] Merck & Co Inc, Rahway, NJ 07065 USA
[3] Merck & Co Inc, Rahway, NJ USA
[4] AstraZeneca, Cambridge, England
[5] Lumanity Inc, Bethesda, MD USA
关键词
PLUS BEVACIZUMAB; MUTATIONS; OLAPARIB; THERAPY; TRIAL; WOMEN;
D O I
10.1007/s11523-023-00966-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundPoly(ADP-ribose) polymerase inhibitor maintenance treatments are available for platinum-sensitive advanced ovarian cancer. Olaparib (O) is available for BRCA mutation patients or in combination with bevacizumab (O+B) for patients with homologous recombination deficiency (HRD+); niraparib (N) is available for all patients.ObjectiveThis study aimed to evaluate the cost effectiveness of biomarker testing and maintenance treatments (mTx) with poly(ADP-ribose) polymerase inhibitor in platinum-sensitive advanced ovarian cancer in the USA.Patients and MethodsTen strategies were evaluated (S1-S10), representing biomarker testing (none, BRCA or HRD), and mTx (O, O+B, N or B). PAOLA-1 data were used to build a model estimating progression-free survival (PFS), second PFS (PFS2) and overall survival for O+B. PFS was modelled through mixture cure models; PFS2 and overall survival were modelled by standard parametric models. Hazard ratios of PFS for O+B versus B, N and O were obtained from the literature to estimate PFS for B, N and O. PFS2 and OS for B, N and O were informed by PFS benefits.ResultsS2 (no testing, B) had the lowest cost while S10 (HRD testing, O+B for HRD+ and B for HRD-) had the highest quality-adjusted life-years (QALYs). All niraparib strategies were dominated. S2, S4 (BRCA testing, O for BRCA+ and B for BRCA-), S6 (BRCA testing, olaparib plus bevacizumab for BRCA+ and bevacizumab for BRCA-) and S10 were the non-dominated strategies with an incremental cost-effectiveness ratio of $29,095/QALY, $33,786/QALY and $52,948/QALY for S4 versus S2, S6 versus S4 and S10 versus S6, respectively.ConclusionsHomologous recombination deficiency testing followed by O+B for HRD+ and B for HRD- is a highly cost-effective strategy for patients with platinum-sensitive advanced ovarian cancer. A HRD biomarker-guided approach provides most QALYs with good economic value.
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收藏
页码:531 / 541
页数:11
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