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  • 1
    In: Blood, American Society of Hematology, Vol. 124, No. 21 ( 2014-12-06), p. 1281-1281
    Abstract: Background Although treatment outcomes for childhood acute lymphocytic leukemia (ALL) have dramatically improved in recent years, treatment outcomes in adolescents and young adults (AYA, ages 16-39) have remained inferior due to unfavorable cytogenetic features associated with increasing age and differences in treatment for this population. Pediatric-inspired protocols include L-asparaginase for induction and intensification phases, which are thought to be less tolerable and to lead to increased adverse events in adults. As a result, they are not widely used in the AYA population. Although non-comparative studies suggest improved survival in AYA patients treated with pediatric-inspired protocols, the long-term risk-benefit profile of treating AYAs with a pediatric-inspired ALL protocol is unknown. We utilized an exploratory decision-analytic approach to model the survival and quality-adjusted survival of a pediatric-inspired protocol versus hyper-CVAD, a widely utilized adult protocol, in AYA patients with Philadelphia negative ALL. Methods Patient outcomes were simulated using a 6-state Markov model including complete response (CR), no CR, first relapse, second CR, second relapse, and death. Hyper-CVAD protocol outcomes were modeled by fitting a Weibull distribution to the progression free survival curve of AYA patients from a single-center study of 288 patientsa; we utilized comparable patient data from a retrospective study of 85 patients treated with a pediatric-inspired regimenb to estimate a relative progression difference (HR = 0.51), and used this estimate to model survival for pediatric-inspired protocol patients. We estimated health state utilities (quality of life) based on treatment stage, and assumed the pediatric protocol had a 0.10 disutility compared to hyper-CVAD prior to the maintenance phase of treatment. Our analysis compared total life years and quality-adjusted life years (QALYs) between treatment protocols at 1 year, 5 years, and 10 years. Figure 1 Figure 1. Results Treatment with the pediatric-inspired protocol led to a 0.04 increase in life years but a 0.01 decrease in QALYs at 1 year. By years 5 and 10, the pediatric-inspired protocol resulted in 0.18 and 0.24 increases in life years and 0.25 and 0.32 increases in QALYs, respectively, relative to hyper-CVAD. The lower quality of life associated with the induction and intensification phases of pediatric treatment was largely offset by more favorable progression-free survival and overall survival in comparison to hyper-CVAD. Table Outcome Pediatric Hyper-CVAD Difference 1 Year Life Years 0.815 0.774 0.041 QALYs 0.507 0.513 -0.006 5 Years Life Years 1.882 1.633 0.250 QALYs 1.362 1.179 0.182 10 Years Life Years 2.120 1.802 0.318 QALYs 1.564 1.324 0.241 Conclusions Our exploratory analysis suggests Philadelphia negative AYA patients treated with a pediatric-inspired protocol experience a decrease in QALYs versus hyper-CVAD during the initial stages of treatment for ALL. However, the pediatric protocol leads to an increase in life years throughout all treatment stages and an increase in QALYs in the long-term following the initial stages of treatment. Ongoing work will incorporate treatment and adverse event costs to estimate the cost-effectiveness of pediatric-inspired versus hyper-CVAD protocols. a Kantarjian H. et al. Cancer 2004; 2788-801. b Storring JM, et al. BJH 2009; 76-85. Analysis support: This analysis was supported by Jazz Pharmaceuticals. Disclosures Guzauskas: Jazz Pharmaceuticals: Consultancy. Villa:Jazz Pharmaceuticals: Employment, Equity Ownership. Off Label Use: Defibrotide is an investigational treatment for hepatic veno-occlusive disease in the United States.. Vanhove:Jazz Pharmaceuticals: Employment, Equity Ownership. Veenstra:Jazz Pharmaceuticals: Consultancy.
    Type of Medium: Online Resource
    ISSN: 0006-4971 , 1528-0020
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    RVK:
    Language: English
    Publisher: American Society of Hematology
    Publication Date: 2014
    detail.hit.zdb_id: 1468538-3
    detail.hit.zdb_id: 80069-7
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  • 2
    Online Resource
    Online Resource
    Ovid Technologies (Wolters Kluwer Health) ; 2012
    In:  Stroke Vol. 43, No. 6 ( 2012-06), p. 1617-1623
    In: Stroke, Ovid Technologies (Wolters Kluwer Health), Vol. 43, No. 6 ( 2012-06), p. 1617-1623
    Abstract: Primary stroke centers (PSC) have demonstrated improved survival in patients with acute ischemic stroke (AIS). The objective of this study was to evaluate the cost-effectiveness of treating AIS patients in a PSC compared with a nonPSC hospital setting. Methods— We developed a decision analytic model to project the lifetime outcomes and costs of 2 hypothetical cohorts of 75 AIS patients. Clinical data were derived from a recent observational study comparing PSC- and nonPSC-admitted patients, clinical trials, longitudinal cohort studies, and health state preference studies. Cost data were based on Medicare reimbursement and other published sources. We used a healthcare payer perspective, and the primary outcomes were incremental life expectancy, quality-adjusted life years, and healthcare costs. We performed sensitivity and scenario analyses to evaluate uncertainty in the results. Results— Admission to a PSC resulted in a gain of 0.22 years of life (95% credible range [CR], 0.12–0.33) and 0.15 quality-adjusted life years (95% CR, 0.08–0.23) per patient, at a cost of $3600 (95% CR, $2400–$5000) per patient, compared wit h admission to a nonPSC hospital. The incremental cost/quality-adjusted life year gained was $24 000, and all probabilistic simulation results were below the $100 000/quality-adjusted life year threshold. In scenario analyses accounting for as few as 7 and as many as 500 AIS patients/year per PSC, cost-effectiveness improved as the number of AIS patients admitted per year increased. Conclusions— Our study indicates that care at a PSC for patients with AIS is cost-effective and improves outcomes across a wide range of possible scenarios.
    Type of Medium: Online Resource
    ISSN: 0039-2499 , 1524-4628
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    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2012
    detail.hit.zdb_id: 1467823-8
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  • 3
    In: American Journal of Medical Genetics Part A, Wiley, Vol. 155, No. 9 ( 2011-09), p. 2146-2153
    Type of Medium: Online Resource
    ISSN: 1552-4825
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2011
    detail.hit.zdb_id: 1493479-6
    SSG: 12
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  • 4
    In: Stroke, Ovid Technologies (Wolters Kluwer Health), Vol. 45, No. suppl_1 ( 2014-02)
    Abstract: Background: A recently completed meta-analysis by Wardlaw and colleagues, including the results of the IST-3 trial, provides more precise estimates of the efficacy and safety of r-tPA in the treatment of acute ischemic stroke (AIS) within 3 hours of symptom onset. No economic analyses have been conducted for r-tPA in the 0-3 hour treatment timeframe since 1998, and changing healthcare costs and better estimates of long-term disposition offer an opportunity to reassess the value of r-tPA in AIS. Objective: To evaluate the cost-effectiveness of r-tPA within 3 hours of symptom onset compared to no r-tPA among patients with AIS using updated efficacy, safety, and healthcare cost data. Methods: A Markov decision model compared r-tPA treatment within 3 hours of symptom onset vs. no treatment in a hypothetical cohort of r-tPA-eligible AIS patients. Key model inputs (efficacy, safety, and mortality associated with each health state parameter) were varied based on the NINDS and ECASS III clinical trials and a recent meta-analysis of all trials, including the newly published IST-3 trial. Patients with modified Rankin scores of 0-1, 2-5, and 6 were classified into health states of non-disabled, disabled, or dead, respectively. Costs and utilities (patient preferences) associated with each health state were derived from the literature. The primary outcomes were incremental quality-adjusted life years (QALYs) gained and lifetime healthcare costs from a payer perspective. Results: Treatment with r-tPA was associated with increased QALYs between 0.14 and 0.46. The cost-effectiveness results ranged from a cost savings of $2700 to $25,000 per QALY gained in a worst-case scenario. Major drivers of results were efficacy, cost of r-tPA, disabled patient mortality, disabled patient quality of life, and risk of recurrent stroke. Conclusion: Economic analyses based on current clinical and cost data suggest that r-tPA is highly cost effective in the treatment of AIS across numerous efficacy, safety, and mortality estimates. Further research on differences in long-term mortality in disabled and non-disabled patients will refine these estimates.
    Type of Medium: Online Resource
    ISSN: 0039-2499 , 1524-4628
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    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2014
    detail.hit.zdb_id: 1467823-8
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  • 5
    In: Stroke, Ovid Technologies (Wolters Kluwer Health), Vol. 45, No. 10 ( 2014-10), p. 3032-3039
    Abstract: Despite the availability of results from multiple newer clinical trials and changing healthcare costs, the cost-effectiveness of recombinant tissue-type plasminogen activator (r-tPA) for treatment of acute ischemic stroke within 0 to 3 hours of symptom onset was last evaluated in 1998 for the United States Using current evidence, we evaluate the long-term cost-effectiveness of r-tPA administered 0 to 3 hours after acute ischemic stroke onset versus no r-tPA. Methods— A disease-based decision model to project lifetime outcomes of patients after acute ischemic stroke by r-tPA treatment status from the US payer perspective was developed. Model inputs were derived from a recent meta-analysis of r-tPA trials, cohort studies, and health state preference studies. Cost data, inflated to 2013 dollars, were based on drug wholesale acquisition cost and the literature. To compare r-tPA to no r-tPA, we calculated incremental total direct costs, incremental quality-adjusted life years, and incremental cost-effectiveness ratios. We performed 1-way and probabilistic sensitivity analyses to evaluate uncertainty in the results. Results— r-tPA resulted in a gain of 0.39 quality-adjusted life years (95% confidence range, 0.16–0.66) on average per patient and a lifetime cost-saving of $25 000 (95% confidence range, −$42 500 to −$11 000) compared with no r-tPA. In probabilistic sensitivity analyses, r-tPA was dominant compared with no r-tPA in ≈100% of simulations. The model was sensitive to inputs for r-tPA efficacy, healthcare costs for disabled patients, mortality rates for disabled and nondisabled patients, and quality of life estimates. Conclusions— Our analysis supports earlier economic evaluations that r-tPA is a cost-effective method to treat stroke. Appropriate use of r-tPA should be prioritized nationally.
    Type of Medium: Online Resource
    ISSN: 0039-2499 , 1524-4628
    RVK:
    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2014
    detail.hit.zdb_id: 1467823-8
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  • 6
    In: Genetics in Medicine, Elsevier BV, Vol. 15, No. 1 ( 2013-01), p. 84-87
    Type of Medium: Online Resource
    ISSN: 1098-3600
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2013
    detail.hit.zdb_id: 2063504-7
    SSG: 12
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  • 7
    Online Resource
    Online Resource
    Ovid Technologies (Wolters Kluwer Health) ; 2014
    In:  Stroke Vol. 45, No. suppl_1 ( 2014-02)
    In: Stroke, Ovid Technologies (Wolters Kluwer Health), Vol. 45, No. suppl_1 ( 2014-02)
    Abstract: Background: The use of r-tPA in patients with moderate to severe stroke has been shown to be efficacious and cost-effective. However, nearly half of all ischemic strokes present with mild deficits (i.e. either persistently mild or rapidly improving stroke), and a third of untreated mild strokes result in significant disability. Small studies and post-hoc analyses of the recently completed IST-3 trial suggested r-tPA may reduce disability for mild stroke. If these preliminary clinical findings are verified, r-tPA in mild stroke patients may provide good economic value to healthcare systems. Objective: To model the potential cost-effectiveness of r-tPA in the treatment of mild stroke in the US. Methods: We developed a decision analytic model to simulate the outcomes of mild stroke patients treated vs. not treated with r-tPA. We modeled stroke severity health states based on modified Rankin scale (mRS) and Oxford handicap scale (OHS) scores using Markov techniques. Preliminary estimates of r-tPa effectiveness in patients suffering mild strokes were derived from a subset of IST-3 patients. Non-disabled patients were defined as having baseline NIHSS 0-15 who otherwise met all other standard three-hour r-tPA eligibility criteria. Healthcare costs, quality-adjusted life-years, and incremental cost-effectiveness were calculated, and scenario analyses were conducted to assess uncertainty. Results: Treatment with r-tPA was estimated to lead to a 0.36 (range, 0.34 to 0.76) increase in quality-adjusted life years per patient treated, and cost-savings ranging from $871 to $5500. In widely varying scenario analyses, as long as r-tPA treatment resulted in a 2% absolute increase in the proportion of non-disabled patients, r-tPA was highly cost effective. The main drivers in the results were r-tPA effectiveness, healthcare costs for disabled patients, and quality-of-life for non-disabled patients. Conclusion: Economic analyses based on preliminary clinical data suggest that r-tPA could be cost-saving or highly cost-effective in the treatment of mild patients. Controlled clinical trials will be valuable in definitively establishing the clinical and economic value of r-tPA in this patient population.
    Type of Medium: Online Resource
    ISSN: 0039-2499 , 1524-4628
    RVK:
    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2014
    detail.hit.zdb_id: 1467823-8
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