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Cost-Effectiveness Analysis of Brentuximab Vedotin With Chemotherapy in Newly Diagnosed Stage III and IV Hodgkin Lymphoma
被引:38
作者:
Huntington, Scott F.
[1
,2
]
von Keudell, Gottfried
[5
]
Davidoff, Amy J.
[1
,2
,3
]
Gross, Cary P.
[1
,2
]
Prasad, Sapna A.
[4
]
机构:
[1] Yale Sch Med, New Haven, CT USA
[2] Yale Canc Outcomes Publ Policy & Effectiveness Re, New Haven, CT USA
[3] Yale Sch Publ Hlth, New Haven, CT USA
[4] Yale New Haven Hlth, Smilow Canc Hosp, New Haven, CT USA
[5] Weill Cornell Med Coll, Mem Sloan Kettering Canc Ctr, New York, NY USA
基金:
美国国家卫生研究院;
关键词:
STEM-CELL TRANSPLANTATION;
ECONOMIC EVALUATIONS;
FEBRILE NEUTROPENIA;
DOSE CHEMOTHERAPY;
OPEN-LABEL;
PHASE-II;
ABVD;
CANCER;
SURVIVAL;
DISEASE;
D O I:
10.1200/JCO.18.00122
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
PurposeIn a recent randomized, open-label trial (ECHELON-1), brentuximab vedotin (BV) combined with doxorubicin, vinblastine, and dacarbazine (AVD+BV) decreased the risk of progression in adults diagnosed with stage III or IV Hodgkin lymphoma (HL) compared with standard bleomycin-containing chemotherapy (doxorubicin, bleomycin, vinblastine, and dacarbazine [ABVD]). However, the cost effectiveness of incorporating BV (US$6,970 per 50-mg vial) into the first-line setting is unknown.Patients and MethodsWe constructed a Markov decision-analytic model to measure the costs and clinical outcomes for AVD+BV compared with ABVD as first-line therapy in a cohort of patients with stage III or IV HL. Transition probabilities were estimated from ECHELON-1 by fitting parametric survival distributions. Lifetime direct health care costs, quality-adjusted life-years (QALYs), and incremental cost-effectiveness ratios (ICERs) were calculated for AVD+BV compared with ABVD from a US payer perspective. Our model was also used to estimate BV price reductions that would achieve more favorable cost effectiveness under indication-specific pricing.ResultsAVD+BV was associated with an improvement of 0.56 QALYs compared with treatment with standard ABVD. However, incorporating BV into first-line therapy led to significantly higher lifetime health care costs ($361,137 v $184,291), causing the ICER for AVD+BV to be $317,254 per QALY. If indication-specific pricing were implemented, acquisition costs for BV used in the first-line setting would need to be reduced by 56% to 73% for ICERs of $150,000 to $100,000 per QALY, respectively.ConclusionSubstituting BV for bleomycin during first-line therapy for stage III or IV HL is unlikely to be cost effective under current drug pricing. Should indication-specific pricing be implemented, significant price reductions for BV used in the first-line setting would be needed to reduce ICERs to more widely acceptable values.
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页码:3307 / +
页数:9
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