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Advantages of the net benefit regression framework for trialbased economic evaluations of cancer treatments: an example from the Canadian Cancer Trials Group CO.17 trial
BMC Cancer volume 19, Article number: 552 (2019)
Abstract
Background
Economic evaluations commonly accompany trials of new treatments or interventions; however, regression methods and their corresponding advantages for the analysis of costeffectiveness data are not widely appreciated.
Methods
To illustrate regressionbased economic evaluation, we review a costeffectiveness analysis conducted by the Canadian Cancer Trials Group’s Committee on Economic Analysis and implement net benefit regression.
Results
Net benefit regression offers a simple option for costeffectiveness analyses of personlevel data. By placing economic evaluation in a regression framework, regressionbased techniques can facilitate the analysis and provide simple solutions to commonly encountered challenges (e.g., the need to adjust for potential confounders, identify key patient subgroups, and/or summarize “challenging” findings, like when a more effective regimen has the potential to be costsaving).
Conclusions
Economic evaluations of patientlevel data (e.g., from a clinical trial) can use net benefit regression to facilitate analysis and enhance results.
Background
We must deal with the escalating price of cancer therapy now… We cannot ignore the cumulative costs of the tests and treatments we recommend and prescribe. As the agents of change, professional societies, including their academic and practicing oncologist members, must lead the way. The time to start is now [1].
Cancer is a costly disease; there are huge costs physically, mentally and financially. A major component of many treatment regimens is pharmaceuticals. Fiscal toxicity of cancer treatment is not unique to patients and their families; healthcare payers also experience financial distress. Without the resources to pay for all treatments for all diseases for all patients, most healthcare payers have embraced an evidence informed decisionmaking process involving recommendation committees. Frequently, these recommendation committees embrace other types of evidence in addition to clinical evidence. For example, in Canada, the panCanadian Oncology Drug Review (pCODR), a national recommendation committee for oncology drugs, uses a deliberative framework that includes clinical evidence, patient values, system feasibility as well as economic evidence [2]. In the United States, the Institute for Clinical and Economic Review considers both net clinical benefit as well as value (i.e., costeffectiveness and budget impact). Usually, the economic evidence used by recommendation committees is in the form of a costeffectiveness model with inputs, based in part, on patientlevel trial data.
In advance of formal drug reimbursement dossier submissions trial data are often presented at national conferences and published in scientific journals, providing an initial (and often impactful) preview of the clinical and economic evidence. Thus, costeffectiveness analyses based entirely on patientlevel trial data have the potential to play a major role in influencing clinical and decision maker perceptions of whether a drug provides value (e.g., is economically attractive). The analysis of a costeffectiveness dataset provides insight into the value of the clinical benefit, over the same time horizon as the clinical study. In this way, the extra costs of the extra patient benefits accruing in the trial can be appreciated concurrently. However, there are some challenges that attend the analysis of patientlevel costeffectiveness data. For example, in cancer studies, these can involve the need to i) adjust for potential confounders, ii) identify key patient subgroups (e.g., with biomarkers), and iii) summarize the economic evidence when there is a negative costeffectiveness ratio (e.g., when more effective treatment regimens are also potentially cost saving).
This article illustrates a regressionbased method for analyzing patientlevel costeffectiveness data called net benefit regression. It has a variety of benefits that address shortcomings in conventional costeffectiveness analysis methods. These benefits are illustrated using the Canadian Cancer Trials Group CO.17 study showing that patients with advanced colorectal cancer had improved overall survival and greater costs when cetuximab, an epidermal growth factor receptortargeting antibody, was given in addition to best supportive care. Although the concepts of net benefit and net benefit regression have been applied in other healthcare areas, their application in oncology has not been widespread [3,4,5]. It is the goal of this article to clarify how to use and interpret the net benefit regression method, so that more authors and readers can appreciate what it offers.
Methods
Case study description
Mittmann and colleagues [6] conducted an economic evaluation of cetuximab plus best supportive care versus best supportive care alone in unselected advanced colorectal cancer patients. The initial clinical trial was conducted by the Canadian Cancer Trials Group as a multicenter, openlabel, randomized phase III trial of cetuximab plus best supportive care versus best supportive care alone in patients with chemotherapyrefractory metastatic EGFRpositive colorectal cancer (ClinicalTrials.gov number NCT00079066). Survival times for the entire study population and for patients whose tumors harbored wildtype KRAS were calculated over an 18 to 19month period [6], and the trial (hereafter referred to as CO.17) found a statistically significant overall survival advantage for cetuximab with a 1.5 month difference in median survival for cetuximab versus best supportive care [7]. In patients with wildtype KRAS tumors, there was a larger survival advantage (i.e., 4.7 months additional median survival for cetuximab) [8].
Mittmann and colleagues conducted a costeffectiveness analysis using prospectively collected cost and quality adjusted life year (QALY) data for patients in the CO.17 [6]. For patients in the trial, cetuximab showed unattractively high incremental costeffectiveness ratios. The incremental costeffectiveness ratios (ICERs) were more favorable for patients whose tumors harbored wildtype KRAS but were still more than $186,000 per qualityadjusted lifeyear gained. Since there is no universally agreed upon costeffectiveness threshold or willingness to pay (WTP) value, jurisdictions often adopt fuzzy thresholds that are guided by several factors [9,10,11]. Nevertheless, the likelihood of a positive funding recommendation appears inversely related to the incremental costeffectiveness ratio (i.e., higher ICERs have a lower probability of being funded). [12, 13] This suggest that costeffectiveness methods that explicitly allow the WTP threshold to vary may be helpful.
In the following section, we describe net benefit regression before applying the technique to analyze the costeffectiveness data for patients in the CO.17 study.
Net benefit regression framework
We briefly review below the key components of net benefit regression and offer additional references for the interested reader [14,15,16]. With the net benefit regression approach, analysts can use regressionbased techniques to analyze costeffectiveness data; some advantages of the net benefit regression approach include facilitating solutions to challenging statistical situations (e.g., negative costeffectiveness ratios or when Fieller’s theorem will not yield a confidence interval) [14]. The net benefit regression framework was proposed a decade ago to marry regression and costeffectiveness methods [17]. At that time, the conventional statistic reported in most costeffectiveness studies was the ICER.
Building from the ICER
Mathematically, the ICER estimate is defined as Extra Cost ÷ Extra Effect, where Extra Cost is defined as ΔC = Expected Cost with New Treatment  Expected Cost with Usual Care and Extra Effect is defined as ΔE = Expected Effect with New Treatment  Expected Effect with Usual Care. With a costeffectiveness dataset, it is common to use the Average Cost and Average Effect to represent Expected values. The ICER is troublesome to estimate because it is a ratio; however, its parts—the numerator and denominator—can be estimated easily by regression.
If one defines a binary treatment indicator variable as TX = 1 for a study participant receiving the new treatment, and TX = 0 for a study participant receiving usual care, then one can use ordinary least squares (OLS) to estimate linear regressions for cost (c_{i}) and effect (e_{i}). By adding an interaction term (say, between the KRAS status and TX indicator variables), it is possible to explore hypothesisgenerating questions about subgroups for whom the new intervention may be more (or less) costeffective. For example, is a drug more costeffective for patients with wildtype KRAS tumors?
Willingness to pay (WTP)
When a new treatment costs more (ΔC > 0) and is more effective (ΔE > 0), the ICER > 0. For decisions, an ICER must be compared with a WTP threshold value. Unfortunately, a decision maker’s WTP is unknown, so methods that treat WTP as unknown are best (e.g., varying WTP and exploring how a recommendation based on the estimated ICER may change). Net benefit regression addresses the unknown nature of the “correct” WTP value within the incremental net benefit.
Incremental net benefit regression
By computing each patient’s net benefit (NB) as WTP × e_{i} − c_{i} and using it for a dependent variable, one can run a simple or multiple linear regression of the form
If b_{TX} > 0, the new treatment is costeffective since b_{TX} equals the incremental net benefit (INB); the INB conveys by how much the value of the extra effect outweighs the extra cost (i.e., INB = WTP × ΔE − ΔC) [17]. Another way to view the INB is as the difference in the average net benefits between the new treatment and usual care: new treatment is more costeffective if it has higher net benefits than usual care. The linearity of the dependent variable NB means the estimate of b_{TX} = WTP × ΔE − ΔC. While the 95% confidence interval (CI) for the ICER cannot be made from the separate CIs for the estimates of ΔC and ΔE (because this process ignores the correlation between the cost and effect data) [18], the 95% CI for b_{TX} is the 95% CI for the INB. If there is concern about using a parametric method for the 95% CI, one can use a nonparametric method like bootstrapping [19].
By estimating net benefit regression equations with various WTP values, one can gauge the sensitivity of costeffectiveness findings in relation to WTP assumptions. One WTP value that should always be checked in a net benefit regression is WTP = $ΔC/ΔE since this should yield an INB estimate of zero (i.e., b_{TX} = 0). By setting WTP = $0, the INB should become − 1 × ΔC. One can characterize uncertainty using CIs or pvalues to create costeffectiveness acceptability curves (e.g., see [20] for a step by step tutorial on using pvalues this way). Because the INB and the ICER are related through WTP, both their estimates and uncertainty are closely connected. A graph of INB by WTP has a yintercept equal to ΔC, a slope of ΔE and an xintercept of the ICER. The addition to the graph of 95% CIs for the INB illustrates, at their xintercepts, the lower and upper 95% CIs (from Fieller’s Theorem) for the ICER (see Results section for examples). We illustrate these points next using net benefit regression results.
Results
Table 1 reports the results of simple linear regressions with dependent variables Effect, Cost and NB regressed on the cetuximab treatment indicator (i.e., the TX variable in the METHODS section). The estimates in Table 1 represent ΔE, ΔC and ΔNB (i.e., INB), respectively. Results when WTP = $0 are reported in the NB ($0) column; results for WTP = $500,000 are reported in the NB ($500 k) column. In this economic analysis, cetuximab showed extra cost of $22,210 and extra effect of 0.0771 QALYs (see the row labeled “ALL” in Table 1) when compared with best supportive care for all patients in the CO.17 trial. This corresponds to an ICER over $288,000 (i.e., 22,210/0.0771), not generally considered economically attractive. However, the results differ by KRAS status. While the extra cost estimate appears larger for patients with wildtype KRAS tumors (ΔC = $30,843, pvalue < 0.001) than patients whose tumors do not express wildtype KRAS (ΔC = $13,787, pvalue < 0.001), the extra effect estimates tell a much different story. Cetuximab appears more effective than best supportive care for patients with wildtype KRAS tumors (ΔE = 0.1769 QALYs, pvalue < 0.001) but less effective than best supportive care for patients whose tumors do not express wildtype KRAS (ΔE = − 0.0172 QALYs, pvalue > 0.40).
Table 2 shows the estimates for multiple linear regression; these results further support analyzing the data stratified by KRAS status. The coefficient on the cetuximab treatment indicator, which represents INB for patients with mutant status, is negative for WTP values from $0 to $500,000. However, the interaction term between cetuximab treatment and wildtype KRAS status, which represents difference of INBs between patients with KRAS wildtype and mutant statuses, switches from a negative value (− 738) to a positive value (14,762) as WTP increases from $100,000 to $200,000. This coincides with the INB estimate transitioning from a negative value (− 14,637) to a positive value (1149) over the same WTP range for patients whose tumors express wildtype KRAS (KRASWT). For the lowest value of WTP ($0), the interaction term between the cetuximab treatment and KRASWT indicator variables is statistically significantly negative (− 16,238, pvalue < 0.001). This implies that ΔC is significantly higher for patients with wildtype KRAS than those with mutant KRAS. Conversely, for the highest value of WTP ($500,000), the interaction term is statistically significantly positive (61,262, pvalue < 0.05); this suggests INB with this WTP is significantly higher for patients with wildtype KRAS than those with mutant KRAS.
Figure 1 plots the incremental net benefit estimate (as a solid line) and the pointwise 95% CIs (as dashed lines) in relation to WTP values varying from $0 to $500,000. Vertical values greater than zero indicate when INB is positive and cetuximab is costeffective. The graphs for the overall sample and the KRASWT subgroup (the top and middle graphs in Fig. 1) show a positively sloped INB line that intersects the horizontal axis; for the overall sample this occurs near the WTP value of $300,000 and near $200,000 for the KRASWT subgroup. For the patients whose tumors do not express wildtype KRAS (i.e., the KRASMUT group), the negatively sloped INB line does not intersect any positive WTP value (on the horizontal axis). Figure 2 communicates the probability that cetuximab is costeffective as WTP varies. There are three curves: one for KRASWT patients (upper solid line), one for all patients (middle dashed line) and one for KRASMUT patients (lower hashed line).
Discussion
Typically, ICERs are the metrics reported in economic evaluations; However, in this case study, the ICER for the patients whose tumors do not express wildtype KRAS (KRASMUT) is negative. Based on expert recommendations, this means the ICER should not be calculated [21]. This makes it challenging to report the conventional costeffectiveness statistic (which is negative in this case) and to report its 95% CI (where at least one limit will be negative as well). In contrast, Table 1’s negative INB estimates, reported for all WTP values, indicate that cetuximab for KRASMUT patients is not economically attractive (at least for WTP values from $0 to $500,000). For KRASWT patients, the INB estimate becomes positive (switching from − 13,154 to 4536) as WTP increases from $100,000 to $200,000. This indicates that the ICER falls within this range (ΔC/ΔE = 30,843/0.1769 ≈ 174,350 per QALY). The overall sample demonstrates a similar pattern, switching from − 6805 to 898 as the WTP increases from $200,000 to $300,000 due to the overall ICER being ΔC/ΔE = 22,210/0.0771 ≈ $288,000 per QALY. As noted earlier, when WTP = $0, the INB estimate reduces to −ΔC; this explains the similarity between the coefficients in the Cost Column and those in the NB($0) column in Table 1.
As noted earlier, the findings in Table 2 support stratifying the analysis by KRAS status. Either simple linear or multiple linear regression can be run separately stratifying on a patient’s tumor’s KRAS status. In this case study, we simplified matters by focusing on simple linear regressions (except for Table 2). The findings of the simple linear regression models were similar to those of the multiple linear regression models for small WTP values; they diverged more for larger WTP values. This suggests that there is important variability in the patient outcome related to the independent variables; however, the variability in cost is not as strongly associated with the independent variables since adjusting for the patient covariates (i.e., all of the X_{p}’s) does not affect the INB estimate for small WTP values. In passing, we note that investigators interested in studying a patient subgroup, defined by a continuous variable (e.g., age, disease severity, etc.), would not be able to stratify and run separate models; a model with a treatment interaction term would be better suited to exploring this type of hypothesis generating question (involving a continuous covariate).
Figure 1 demonstrates the usefulness of an INB by WTP graph. The different shapes of the curves suggest different findings. The upper graph (for the overall sample) and the middle graph (for the KRASWT group) show INB lines with negative yintercepts, positive slopes and xintercepts at WTP values of approximately $300,000 (for the overall sample) and approximately $200,000 (for the KRASWT group). As noted in the Methods section, an INB by WTP graph has a yintercept equal to ΔC, a slope of ΔE and an xintercept of the ICER. Thus, a negative yintercept means cetuximab is more costly, a positive slope means that cetuximab is more effective, and the WTP value where the INB estimate line intersects is the ICER. Of the three graphs in Fig. 1, the KRASWT group has the steepest INB estimate line; therefore, that group enjoys the largest gain from treatment (i.e., has the biggest ΔE). For the KRASMUT group, the negative yintercept means cetuximab is more costly, the slightly negative slope means that cetuximab is slightly less effective than best supportive care, and the WTP value where the INB estimate line looks to intersect indicates a negative ICER.
Figure 1 can also be used to characterize the uncertainty associated with both the INB and the ICER. For the KRASWT group (in the middle graph), the upper and lower 95% confidence limits for the INB intersect the horizontal axis over the illustrated WTP range of $0 to $500,000. The two intersection points mark the Fieller’s Theorem 95% CI for the ICER. This 95% CI corresponds very closely to the 95% CI of $130,326 to 334,940 reported in the original economic analysis. For the overall sample, Mittmann and colleagues reported a 95% CI of $187,440 to 898,201. This is congruent with the upper graph in Fig. 1; one confidence limit intersects the horizontal axis near a WTP = $200,000 and the other intersection point appears greater than $500,000. The lower graph (for the KRASMUT group) suggests a negative ICER with one 95% confidence limit that will be negative.
The costeffectiveness acceptability curve (CEAC) in Fig. 2 combines parts of the regression results and Fig. 1 to characterize uncertainty [20]. The CEAC shows the probability that cetuximab plus best supportive care is costeffective compared to best supportive care alone. WTP varies along the horizontal axis reflecting its unknown nature (to the analyst). The vertical axis communicates the portion of the INB distribution that is positive (indicating the probability that cetuximab is costeffective). The three curves—one for KRASWT patients (upper solid line), one for all patients (middle dashed line) and one for KRASMUT patients (lower solid line)—support the general conclusions that have been offered. While the CEACs presented in Fig. 2 were made using parametric pvalues from Table 1, it is possible to create them using nonparametric bootstrapping methods [20].
Limitations
We conclude our discussion by reviewing some key limitations in our example involving the analysis of personlevel costeffectiveness data. The usefulness of personlevel costeffectiveness data is diminished when either a relevant outcome is not included in the original study or when the trial is too short in duration to see activity in the outcome of interest. The original clinical trial in our example used overall survival as its primary end point with secondary outcomes that included progressionfree survival as well as quality adjusted life years (QALYs). Even with the strength of the trial’s design, there is still the critical question of whether “enough” study participants contributed outcome data. Of the randomly assigned 572 patients, a total of 456 deaths occurred by the date of analysis. The median survival was 6.1 months in the cetuximab group and 4.6 months in the supportivecare group. The proportions of patients surviving at 6 and 12 months were 50 and 21%, respectively, in the cetuximab group and 33 and 16%, respectively, in the supportive care group.
Typically, when timetoevent data (e.g., survival) are incomplete, methods for censored data are employed. In contrast to the original economic evaluation which employed two methods to calculate overall survival: the restricted mean survival method (which restricts calculation of mean survival to the longest observed survival time) and the Kaplan – Meier method (which takes into account censoring), we used only the restricted mean survival method. Our simplifications (e.g., ordinary least squares to estimate a simple linear regression without specific methods for censoring) did not appear to make any qualitative difference in this case study; the original economic evaluation reported ICERs of $186,761 (KRASWT) and $299,613 (entire study population) compared to ICERs of $174,353 and $288,067 calculated using estimates from our Table 1, respectively. While our simple illustration of net benefit regression is meant to facilitate understanding, there are situations where more advanced methods for the analysis of censored costeffectiveness data may be desired. Advanced papers by Bang and Tsiatis [22] as well as Chen et al. [23] provide excellent direction in this area. More advanced methods for simultaneous estimation of cost and effect equations are also available [24].
Finally, often analysts do not report INB results for all willingness to pay (WTP) values. When a reader is interested in a WTP value occurring within the range of WTP values that are used (e.g., WTP = $123,456) or a WTP value outside the range (e.g. WTP = $600,000), this may appear to be a concern. This concern can be addressed easily because the formula for INB is linear (i.e., INB = WTP × ΔE − ΔC). For each $1 change in WTP, the INB changes by ΔE. Thus, the INB when WTP = $123,456 is $23,456 × ΔE more than the INB when WTP = $100,000. Using Table 1 and KRASWT as an example, INB($123,456) = INB($100,000) + ($23,456 × ΔE) = − 13,154 + ($23,456 × 0.1769) = −$9005. This matches the result from a direct calculation of INB($123,456) = $123,456 × ΔE − ΔC = $123,456 × 0.1769 − $30,843 ≈ −$9005. This method can also be used for WTP values outside of the WTP ranges reported. For example, using the values in Table 1 for KRASWT, INB($600,000) = INB($500,000) + ($100,000 × ΔE) = 57,606 + ($100,000 × 0.1769) = $75,296.
Direct calculation verifies this result for KRASWT, INB($600,000) = $600,000 × 0.1769 − $30,843 ≈ $75,297.
Conclusion
This article showcases the advantages of the net benefit regression framework [17]. The framework allows incremental cost and incremental effect to be estimated either separately (i.e., using cost or effect as a dependent variable) or together (i.e., using net benefit as a dependent variable). In this paper’s case study, there was a straightforward application of OLS. However, more ambitious analytical strategies with more sophisticated techniques can be used (e.g., using regression diagnostics, employing interaction terms and/or using advanced methods for nonrandomized data). We were able to adjust our costeffectiveness analysis for covariates using multiple linear regression and to explore clinically relevant patient subgroups. The incremental net benefit by WTP curve illustrated both our estimate of costeffectiveness and the associated uncertainty. The INB by WTP graph allows the costeffectiveness results to reflect the unknown WTP’s impact on policy implications. When analyzing a costeffectiveness dataset, net benefit regression can be a useful starting point for exploring one’s data and communicating a new treatment’s value.
Availability of data and materials
The datasets analysed during the current study are not publicly available due to the Canadian Cancer Trials Group’s policy. However, the results can verified based on this analysis and the separate publication of the original costeffectiveness article.
Abbreviations
 CEAC:

Costeffectiveness acceptability curve
 CI:

Confidence interval
 ICER:

Incremental costeffectiveness ratio
 INB:

Incremental net benefit
 MLR:

Multiple linear regression
 MUT:

Mutant
 NB:

Net benefit
 OLS:

Ordinary least squares
 QALY:

Qualityadjusted lifeyear
 SLR:

Simple linear regression
 WT:

Wild type
 WTP:

Willingness to pay
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Funding
This work was supported by funding from the Canadian Centre for Applied Research in Cancer Control (ARCC). ARCC is funded by a grant from the Canadian Cancer Society Research Institute (CCSRI). The Canadian Cancer Trials Group is supported in part by the CCSRI. Funding for this trial used in the examples was provided by Eli Lilly Canada, HoffmanLa Roche Limited, BristolMyers Squibb, and ImClone Systems Incorporated. The authors take responsibility for all aspects of the study including design, data acquisition, analysis, interpretation, and drafting of the article. The study funders played no role in the design, analysis, or interpretation of the study.
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AH, NBL, DT, CO’C, JP, DJ, BEC, NM designed and conducted the randomized trial that served as the case study for this analysis. JSH, KT and WI led the net benefit regression analysis. JSH, AH, LT, CD and WI collaborated on drafting the manuscript. All authors provided feedback on the manuscript. All authors approved the manuscript for submission.
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This was a reanalysis of the data from a published paper, so ethics approval was not sought by the research ethics boards of participating institutions.
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The authors declare that they have no competing interests. The authors take responsibility for all aspects of the study including design, data acquisition, analysis, interpretation, and drafting of the article.
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Hoch, J.S., Hay, A., Isaranuwatchai, W. et al. Advantages of the net benefit regression framework for trialbased economic evaluations of cancer treatments: an example from the Canadian Cancer Trials Group CO.17 trial. BMC Cancer 19, 552 (2019). https://doi.org/10.1186/s128850195779x
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DOI: https://doi.org/10.1186/s128850195779x