Frontline Rituximab Monotherapy Induction Versus a Watch and Wait Approach For Asymptomatic Advanced Stage Follicular Lymphoma: A Cost-Effectiveness Analysis

Blood ◽  
2013 ◽  
Vol 122 (21) ◽  
pp. 2941-2941 ◽  
Author(s):  
Anca Prica ◽  
Kelvin KW Chan ◽  
Matthew C Cheung

Abstract Background Follicular lymphoma is the most common indolent lymphoma, with median survival over 10 years. A large proportion of patients present with advanced, but asymptomatic disease. Three randomized controlled trials in the last 25 years have confirmed there is no detriment to deferred chemotherapy vs. upfront treatment with respect to overall survival in such patients. However, these studies were all comparing upfront toxic regimens. Single agent rituximab (R) is associated with less side-effects, thus there are advantages to giving it upfront and significantly delaying further more toxic and expensive treatments. Recently, Ardeshna et al. (2010) compared upfront rituximab to watchful waiting in asymptomatic stage II-IV follicular lymphoma, and demonstrated significant improvement in time to initiation of next treatment (TTINT). We performed a cost-effectiveness analysis comparing the two strategies. Methods We developed a Markov decision-analytic model to compare upfront R-induction (RI) X 4 weekly doses vs. a watch and wait (WW) strategy for a hypothetical cohort of 60 year old patients newly-diagnosed with asymptomatic low burden advanced stage follicular lymphoma. The model simulates the clinical course of patients over a lifetime horizon, with the end-points of quality-adjusted life years (QALYs) and incremental cost effectiveness ratio (ICER). The baseline probabilities used in the model were derived from a systematic review of published studies. Key health states include PF1 (progression-free 1), PD1 (1st progressive disease needing treatment), R-maintenance (2-year state progression-free post-PD1 receiving R q3mo), PF2 (post 2 years of R-maintenance), PD2/3/4 (subsequent progressions requiring salvage), PF3/4/5 (subsequent PF states post-salvage), palliation and death. The probabilities of transitioning from one state to another were evaluated on a 6-month cycle. The model incorporated data on health state utilities, which were derived from the literature. Direct costs were collected from a Canadian public health payer's perspective. Resource utilization was based on guidelines, literature and expert opinion. Cost information was obtained from hospital, provincial and national costing sources, as well as the literature, and presented in 2012 Canadian dollars. Costs and effects were discounted at 5%. All patients were assumed to be treated with bendamustine and rituximab (BR) upon PD1, followed by 2 years of R-maintenance. Patients were treated with a maximum of 3 lines of salvage therapy, after which they entered palliation for maximum of 2 cycles. Results The quality-adjusted life expectancy was 6.70 QALYs for the RI strategy vs. 6.66 QALYs for the WW strategy, yielding an expected benefit from RI of 0.04 QALYs. Over a lifetime horizon, the total cost of the RI arm is $59061 and $74531 for the WW arm. The RI strategy dominates, as it is $15469 cheaper than the WW approach (Table 1). In one-way sensitivity analyses of key variables, effectiveness was sensitive to probability of PD2, PF4, age and time horizon. The model particularly favours RI in people under the age of 65. However, even at extreme end values for these variables that remain reasonable from the literature, the largest effectiveness difference in favour of WW is 0.06 QALYs (22 days) over the lifetime horizon. Thus overall the difference in either direction is minimal, demonstrating that the quality-adjusted life expectancy is essentially equivalent between the two strategies. Probabilistic sensitivity analyses (10 000 simulations) were performed. For the commonly accepted willingness to pay threshold of $50000, RI is the more cost-effective strategy 82% of the time (figure 1). Conclusions In conclusion, rituximab monotherapy as an induction strategy for asymptomatic advanced stage follicular lymphoma is the dominant strategy from a cost-utility perspective over the standard watch and wait strategy, with neutral overall effectiveness, but significant cost minimization of fifteen thousand dollars per patient over the lifetime horizon. Particularly, it is the optimal strategy in patients under the age of 65 and should be recommended. Disclosures: No relevant conflicts of interest to declare.

2017 ◽  
Vol 35 (15_suppl) ◽  
pp. 6619-6619 ◽  
Author(s):  
Joanna C. Yang ◽  
Elena B. Elkin ◽  
Rahul Parikh ◽  
Joachim Yahalom

6619 Background: Low-grade follicular lymphoma (FL) can present as localized stage I to II disease in up to one-third of patients. Upfront involved-site radiation therapy (RT) to 24-30Gy is the preferred first-line management strategy for these patients. However, the National LymphoCare Study found that less than one quarter of patients with early-stage, low-grade FL received upfront RT, while more than half received either chemoimmunotherapy or observation. Methods: We performed a cost-effectiveness analysis using a Markov state-transition model to simulate the progression of early-stage, low-grade FL in a cohort of 60-year-old men. The following first-line treatments were compared: RT, observation, rituximab induction (RI), rituximab and bendamustine (BR), and rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone (RCHOP). Patients who relapsed received second-line therapies that were dependent on their first-line treatment: RT for RI and observation, RCHOP for RT and BR, and BR for RCHOP. Disease-progression probabilities and other model inputs were from published trials. Results: First-line RT followed by RCHOP for relapses had a quality-adjusted life expectancy (QALE) of 11.4 years, superior to first-line observation, RI, BR, and RCHOP strategies. First-line RT strongly dominated observation, BR, and RCHOP. Compared with RI, first-line RT resulted in an incremental cost-effectiveness ratio of $2,740 per quality-adjusted life year. The probability of dying from other causes, the probability of a complete response to RT, and the probability of relapse had the greatest impact on both cost and effectiveness expected values. Conclusions: In contrast to current practice patterns, first-line RT is the most effective upfront treatment for patients with early-stage, low-grade FL. Further, first-line RT paired with RCHOP for relapses is a cost-effective treatment paradigm, relative to other strategies. [Table: see text]


2020 ◽  
pp. 112070002095277
Author(s):  
Philip J Rosinsky ◽  
Cammille C Go ◽  
Rishika Bheem ◽  
Jacob Shapira ◽  
David R Maldonado ◽  
...  

Purpose: The purpose of this study was to perform a cost-effectiveness analysis of outpatient versus inpatient total hip arthroplasty (THA) in the USA, considering complication probability and the potential cost of such complications. Methods: A cost-effectiveness analysis was conducted from the societal perspective to evaluate the incremental cost and effectiveness of inpatient THA compared to outpatient THA over a lifetime horizon. Effectiveness was expressed in quality-adjusted life years (QALYs). Costs, expressed in 2019 US dollars, transition probabilities, and health utilities were derived from the literature. The primary outcome was the incremental cost-effectiveness ratio (ICER), with a willingness to pay (WTP) threshold set at $50,000/QALY. 1-way and probabilistic sensitivity analyses was performed to evaluate the effect of the various variables on the model. Results: In the base case, inpatient THA was more effective in terms of total utility (10.36 vs. 10.30 QALY), but also more costly ($48,155 ± 1673 vs. $43,288 ± 1, 606 for Medicare) than outpatient THA. Even with a lifetime horizon, the ICER was $81,116 per QALY and $140,917 per QALY for Medicare and private payer insurance, respectively, which is higher than the willingness to pay threshold. 1-way sensitivity analyses indicated that the variables having the most influence on the model were the utility of inpatient and outpatient THA and cost of inpatient and outpatient THA. Conclusions: This model determined that for a WTP threshold set at $50,000/QALY, outpatient THA is more cost-effective than inpatient THA from a societal perspective. Despite this, surgeons must weigh clinical factors first and foremost in determining if an individual patient can be safely operated on in the outpatient setting.


2021 ◽  
Vol 39 (15_suppl) ◽  
pp. 8043-8043
Author(s):  
Mavis Obeng-Kusi ◽  
Daniel Arku ◽  
Neda Alrawashdh ◽  
Briana Choi ◽  
Nimer S. Alkhatib ◽  
...  

8043 Background: IXA, CAR, ELO and DARin combination with LEN+DEXhave been found superior in efficacy compared to LEN+DEX in the management of R/R MM. Applying indirect treatment comparisons from a network meta-analysis (NMA), this economic evaluation aimed to estimate the comparative cost-effectiveness and cost-utility of these four triplet regimens in terms of progression-free survival (PFS). Methods: In the absence of direct treatment comparison from a single clinical trial, NMA was used to indirectly estimate the comparative PFS benefit of each regimen. A 2-state Markov model simulating the health outcomes and costs was used to evaluate PFS life years (LY) and quality-adjusted life years (QALY) with the triplet regimens over LEN+DEX and expressed as the incremental cost-effectiveness (ICER) and cost-utility ratios (ICUR). Probability sensitivity analyses were conducted to assess the influence of parameter uncertainty on the model. Results: The NMA revealed that DAR+LEN+DEX was superior to the other triplet therapies, which did not differ statistically amongst them. As detailed in the Table, in our cost-effectiveness analysis, all 4 triplet regimens were associated with increased PFSLY and PFSQALY gained (g) over LEN+DEX at an additional cost. DAR+LEN+DEX emerged the most cost-effective with ICER and ICUR of $667,652/PFSLYg and $813,322/PFSQALYg, respectively. The highest probability of cost-effectiveness occurred at a willingness-to-pay threshold of $1,040,000/QALYg. Conclusions: Our economic analysis shows that all the triplet regimens were more expensive than LEN +DEX only but were also more effective with respect to PFSLY and PFSQALY gained. Relative to the other regimens, the daratumumab regimen was the most cost-effective.[Table: see text]


2021 ◽  
Vol 39 (6_suppl) ◽  
pp. 419-419
Author(s):  
Ali Raza Khaki ◽  
Yong Shan ◽  
Richard Nelson ◽  
Sapna Kaul ◽  
John L. Gore ◽  
...  

419 Background: Multiple single-arm clinical trials have shown promising pathologic complete response (pCR) rates with neoadjuvant ICIs in MIBC. However, ICIs remain costly. We conducted a cost-effectiveness analysis comparing neoadjuvant ICIs with CBC. Methods: We applied a decision analytic simulation model with a health care payer perspective and two-year time horizon to compare neoadjuvant ICIs vs CBC. For the primary analysis we compared pembrolizumab with dose dense methotrexate, vinblastine, doxorubicin, and cisplatin (ddMVAC). We performed a secondary analysis with gemcitabine/cisplatin (GC) as CBC and exploratory analyses with atezolizumab or nivolumab/ipilimumab as ICIs (vs both ddMVAC and GC). We input pCR rates from trials (ICIs) or a weighted average of prior studies (CBC) and costs from average sales price. Outcomes of interest included costs, 2-year recurrence-free survival (RFS), and incremental cost-effectiveness ratio (ICER) of cost per 2-year RFS. A threshold analysis estimated a pCR rate or price reduction for ICI to be cost-effective and one-way and probabilistic sensitivity analyses were performed. Results: Results of the cost effectiveness analysis are shown in the table. The incremental cost of pembrolizumab compared with ddMVAC was $8,042 resulting in an incremental improvement of 0.66% in 2-year RFS for an ICER of $1,218,485 per 2-year RFS. A pCR of 71% or a 26% reduction in cost of pembrolizumab would render it more cost-effective with an ICER of $100,000 per 2-year RFS. GC required a 96% pembrolizumab cost reduction to achieve an ICER of $100,000 per 2-year RFS. Atezolizumab appeared to be more cost-effective than ddMVAC, even though the 2yr RFS was 0.66% worse. Conclusions: ICIs were not cost-effective as neoadjuvant therapies, except when atezolizumab was compared with ddMVAC. Pembrolizumab would approach cost-effective thresholds with 26% or 96% reduction in cost when compared to ddMVAC and GC, respectively. Randomized clinical trials, larger sample sizes and longer follow-up are required to better understand the value of ICIs as neoadjuvant treatments. [Table: see text]


2020 ◽  
Vol 13 (4) ◽  
pp. S44-S45
Author(s):  
Luis Augusto Dallan ◽  
Natali Giannetti ◽  
Thatiane Facholi Polastri ◽  
Antonio Baruzzi ◽  
Gisele Sampaio ◽  
...  

Blood ◽  
2016 ◽  
Vol 128 (22) ◽  
pp. 1183-1183 ◽  
Author(s):  
Abi Vijenthira ◽  
Matthew C Cheung ◽  
Chai Wye Phua ◽  
Kelvin Chan ◽  
Joanna Graczyk ◽  
...  

Abstract Background: The past 30 years has heralded significant improvements in the treatment and outcomes of patients with advanced-stage Hodgkin lymphoma, with the introduction of ABVD (doxorubicin, bleomycin, vinblastine, and dacarbazine) and various combinations of BEACOPPbaseline and BEACOPPescalated (bleomycin,etoposide, doxorubicin, cyclophosphamide, vincristine,procarbazine, and prednisone). Initially, BEACOPP-containing regimens demonstrated superior progression-free survival (PFS) and overall survival (OS) compared to ABVD, despite higher rates of hematologic toxicity, infections, and infertility. However, the superiority of this regimen was tempered by concerns of increased toxicity and long-term complications including secondary malignancy and infertility. Furthermore, quality-adjusted measures and patient preferences have not been factored into analyses of the evidence. We performed a decision analysis to explore the trade-off that occurs when initial improvements in progression-free survival and overall survival are balanced with increased morbidity and mortality associated with infections, secondary malignancies, and infertility in the BEACOPP-containing strategy. Methods: We developed a Markov decision-analytic model to compare ABVD versus BEACOPPbaseline and BEACOPPescalated (hereinafter referred to as BEACOPP) for a hypothetical cohort of transplant-eligible patients withnewly-diagnosed, advanced-stage Hodgkin lymphoma. The model simulates the clinical course of patients over a 20-year time horizon, with the end-points of life expectancy and quality-adjusted life expectancy. The baseline probabilities used in the model were derived from a systematic review of published randomized controlled trials. Key variables included response, relapse and survival rates comparing ABVD versus BEACOPP, risk of developing complications such as infection, infertility, or secondary malignancy with each strategy, and the estimated survival once secondary malignancy develops. We also incorporated therapies for relapsed disease including autologous stem cell transplantation, and post-transplant strategies, based on available data. Efficacy was discounted by 3%. The model incorporated data on health state utilities, which were derived from a review of the literature. Sensitivity analyses were performed for key variables. Results: Based on a 20-year model with 100,000 trials, life expectancy was 10.9 years with ABVD and 12.3 years with BEACOPP, resulting in a net benefit of 1.4 years for the BEACOPP strategy. The quality-adjusted life expectancies for the two strategies, respectively, were 9.1 and 10.5 years, with an expected benefit of 1.4 QALYs with BEACOPP. Sensitivity analyses demonstrated that the model was robust to the key variables of probability of death from secondary malignancy, probability of relapse, and probability of infertility secondary to BEACOPP. A range of relapse probabilities post-ABVD and BEACOPP were tested in sensitivity analyses, and BEACOPP was consistently superior, with the lowest difference between QALYs found to be 0.5 QALYs. In sensitivity analysis of treatment-related mortality secondary to BEACOPP, the threshold value was found to be 8% mortality over the6 monthtreatment period, a value much greater than that reported in the literature (see Figure 1). The threshold utility of infertility was found to be 0.60 in sensitivity analysis (see Figure 2), a value lower than the utility derived from a systemic review of the literature (0.87). Onmicrosimulation(100,000 trials), 88% of the simulations showed that BEACOPP was the preferred strategy compared to ABVD. Conclusion: The preferred treatment strategy for patients with newly diagnosed advanced-stage Hodgkin lymphoma is a combination BEACOPP regimen. This strategy maximizes life expectancy and quality-adjusted life years, accounting for the increased rates of hematologic toxicity, secondary malignancy, and infertility in patients receiving the BEACOPP strategy. The model was robust to sensitivity analyses of key variables tested through plausible ranges obtained from the published literature. Disclosures Buckstein: Novartis: Honoraria; Celgene: Honoraria, Research Funding. Prica:Celgene: Honoraria; Janssen: Honoraria.


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