Financial Toxicity of Withdrawn Poly (Adenosine Diphosphate Ribose) Polymerase Inhibitor Indications for Ovarian Cancer

被引:0
作者
Dottino, Joseph A. [1 ]
Esselen, Katharine M. [1 ]
Costa, Rebecca [2 ,3 ]
Argetsinger, Stephanie [2 ,3 ]
Shahzad, Mahnum [2 ,3 ]
Ross-Degnan, Dennis [2 ,3 ]
Wagner, Anita K. [2 ,3 ]
机构
[1] Beth Israel Deaconess Med Ctr, 330 Brookline Ave,Shapiro Ctr 8th Floor, Boston, MA 02215 USA
[2] Harvard Med Sch, Dept Populat Med, Boston, MA USA
[3] Harvard Pilgrim Hlth Care Inst, Boston, MA USA
关键词
drug regulation; drug spending; indication withdrawal; oncology; ovarian cancer;
D O I
10.1016/j.jval.2024.05.022
中图分类号
F [经济];
学科分类号
02 ;
摘要
Objectives: We sought to quantify exposure to and financial impacts of poly (adenosine diphosphate ribose) polymerase inhibitor (PARPi) treatments for eventually withdrawn ovarian cancer indications. Methods: We identified in Optum's deidentified Clinformatics (R) Data Mart database 1695 patients with ovarian cancer diagnoses who received olaparib, rucaparib, or niraparib between January 2015 and September 2021. We describe PARPi use and out-of-pocket, total healthcare, and PARPi spending among patients with ovarian cancer with 3 or more previous lines of therapy. Results: Of the 1695 patients who received PARPi, 254 were estimated to have been heavily pretreated and exposed to eventually withdrawn indications. Cumulative total medical and pharmacy costs for these patients were $53 392 184; PARPi costs accounted for 34%. Median PARPi cost per patient was $43 347. Cumulative out-of-pocket costs totaled $533 281. Conclusions: Potential patient harm, including financial toxicity, might have been mitigated through more stringent drug approval requirements.
引用
收藏
页码:1175 / 1178
页数:4
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