Skip to main content
  • Research article
  • Open access
  • Published:

Cost-effectiveness analysis of fruquintinib for metastatic colorectal cancer third-line treatment in China



In this study, we analyze the cost-effectiveness of fruquintinib as third-line treatment for patients with metastatic colorectal cancer in China, especially after a recent price drop suggested by the National Healthcare Security Administration.


A Markov model was developed to investigate the cost-effectiveness of fruquintinib compared to placebo among patients with metastatic colorectal cancer. Effectiveness was measured in quality-adjusted life years (QALY). The Chinese healthcare payer’s perspective was considered with a lifetime horizon, including direct medical cost (2019 US dollars [USD]). A willing-to-pay threshold was set at USD 27,130/QALY, which is three times the gross domestic product (GDP) per capita. We examined the robustness of the model in one-way and probabilistic sensitivity analysis.


Fruquintinib was associated with better health outcomes than placebo (0.640 vs 0.478 QALYs) with a higher cost (USD 20750.9 vs USD 12042.2), resulting in an incremental cost-effectiveness ratio (ICER) of USD 53508.7 per QALY. This ICER is 25% lower than the one calculated before the price drop (USD 70952.6 per QALY).


After the price negotiation, the drug becomes cheaper and the ICER is lower, but the drug is still not cost effective under the standard of 3 times GDP willing-to-pay threshold. For patients with metastatic colorectal cancer in China, fruquintinib is not a cost-effective option under the current circumstances in China.

Peer Review reports


With increasing incidence and mortality, colorectal cancer is a major public health problem, and has brought constantly heavy economic burden. Over 1.8 million new colorectal cancer cases and 881,000 deaths were estimated to occur in 2018, ranking third in incidence and second in mortality all over the world [1]. The statistics from China not only showed a high prevalence of colorectal cancer in this country with 376,300 new cases and 191,000 deaths in 2015, but a steadily increasing trend of incidence and mortality rates over the years which added great stress on Chinese public health [2,3,4].

Systematic antineoplastic agents represent the main approach in the management of metastatic colorectal cancer (mCRC). Fluorouracil, oxaliplatin, irinotecan, bevacizumab, cetuximab, and panitumumab are widely used alone or in combination for the treatment [5,6,7,8,9,10]. However, progression was still common after the initial and subsequent palliative care [11]. Effective third line or later line treatment is urgently needed to release the medical and economic pressure in China.

Fruquintinib is an effective small molecular vascular endothelial growth factor receptor (VEGFR) inhibitor. In the absence of a randomized clinical trial (RCT) comparing fruquintinib with any of the two other agents approved in this setting, TAS-102 and regorafenib, indirectly demonstrated little differences in efficacy, if any, among the three drugs [12]. In a phase III multicenter RCT, the FRESCO (fruquintinib efficacy and safety in 3+ line colorectal cancer patients) trial, fruquintinib demonstrated the effectiveness in prolonging the progression-free survival (PFS) (3.7 versus 1.8 months; HR 0.26, 95% CI, 0.21–0.34) and overall survival (OS) (9.3 vs 6.6 months; HR 0.65, 95% CI, 0.51–0.83) in metastatic colorectal cancer patients compared with placebo. Moreover, fruquintinib was subsequently approved by Chinese National Medical Products Administration for metastatic colorectal cancer refractory to standard regimen. However, according to the trial data, 61.2% of the patients experienced grade 3 or grade 4 adverse effects (AEs) in the fruquintinib arm comparing with 19.7% in the placebo arm. The most frequently reported grade 3 or grade 4 adverse effects with fruquintinib were hypertension (21.2%), hand-foot skin reaction (10.8%), and proteinuria (3.2%) [13].

Unlike regorafenib, TAS-102 or other imported anti-angiogenesis drugs, fruquintinib is produced in China, which might lead to lower pricing and higher accessibility in mCRC patients in China. In the end of 2019, China started a price negotiation process, and decided to include fruquintinib in the medical insurance by 2020, in the hope of decreasing out-of-pocket payment for patients, as well as supporting domestic origin drugs. As a result, the price for fruquintinib has decreased by over 60%, and the out-of-pocket payment has decreased from over CNY (Chinese yuan) 20,000 to CNY 2381 per month after medical insurance. However, whether fruquintinib earns incremental benefit is unknown. There is no previously reported cost-effectiveness data on fruquintinib. Therefore, in this study based on the survival benefits reported in the FRESCO trial, we built a Markov model to investigate the cost-effectiveness of fruquintinib, compared to supportive care among patients with metastatic colorectal cancer who had previously progressed after at least 2 lines of chemotherapy in China.


Model structure

The Markov is a commonly used approach in health economics evaluation. It comprises a finite set of health states in which an individual can be found and analyzes uncertain disease process over time through cycles consisting of short time intervals, in which individuals can move between states or remain in the same state. In this study, a Markov model was constructed using the TreeAge Pro 2011 software ( to simulate the mCRC disease process. Statistical analyses were performed in R software (

As shown in Fig. 1, all patients initially entered the model in one of the two initial states, which included treatment with fruquintinib or best supportive care (BSC). At the end of each model cycle, patients could remain in the original state or move to other states. Treatment with fruquintinib was discontinued in patients who experienced disease progression, grade 3/4 adverse events (AE) or intolerance to treatment. Patients discontinuing treatment were assigned to receive BSC. All patients in each state could experience progression to death.

Fig. 1
figure 1

Markov model. mCRC, metastatic colorectal cancer

Mortality rates of each group were calculated based on the survival data derived from the FRESCO trial [11]. Weibull model was used to fit the OS curves published in the FRESCO trial. The mortality rates were calculated based on the equation \( {P}_{(t)}=1-\frac{S\left(t+1\right)}{S(t)} \), where P(t) and S(t) represented mortality rates and survival rates at cycle t, respectively. Based on the median treatment duration published in the FRESCO trial, treatment discontinuation probabilities in the fruquintinib group were estimated supposing they were exponentially distributed. For the mortality and treatment discontinuation risk beyond the follow-up time in the trials, we estimated them based on the fitted survival models. In order to prove that the OS curve generated by the Markov model simulation had a close approximation comparing with those shown in the FRESCO trial, we performed internal model verification.

A lifetime horizon was used in the Markov model. Each cycle in the model lasts for 4 weeks, which includes a 3-week daily fruquintinib treatment routine and a 1-week break. The outputs of the model are cost and QALY. QALY is a composite measure of quality of life and quantity of life, which typically assigns to each period of time a weight corresponding to the health-related quality of life during that period. The incremental cost-effectiveness ratio (ICER) was calculated as the difference in cost between the two treatments arms divided by the difference in QALYs.

Cost estimates

In the study, we considered direct medical costs, which related to costs for drugs, BSC, as well as treatments for grade 3/4 AEs. Societal costs like travel fees and time costs were not taken into consideration. All the parameters were stated in 2019 US dollars.

In order to estimate drug price for each unit, we considered two different situations. Fruquintinib was newly added into the drug lists of Chinese medical insurance in 2020 with a lower price after the negotiation by the National Healthcare Security Administration. After the negotiation, the price of two types of fruquintinib are USD 384.7 / box (5 mg / capsule), and USD 288.5/ box (1 mg / capsule). The recommended dose for fruquintinib is 5 mg per day with a unit cost of USD 53.8/5 mg.

We also calculated the cost-effectiveness before the price negotiation, which refers to the price of fruquintinib in the Chinese drug market which takes drug donation activities from the fruquintinib manufacturers. Before the negotiation, the prices of fruquintinib were USD 1064.3/box (5 mg/capsule) and USD 892/box (1 mg/capsule). The unit cost was USD 162.3. Considering the drug donation activities, in the first, second and fifth cycles of fruquintinib treatment, patients payed for the drug themselves; in other cycles of treatment, the drug was handed to the patients free of charge.

Some grade 3/4 AEs were included in the model, whose incidence was significantly different between two groups in the FRESCO trial, including hand-foot syndrome, hypertension, diarrhea, proteinuria and platelet count decreased. Costs for treatments for grade 3/4 AEs and best supportive care were estimated based on guidelines and articles recently published [14,15,16,17].

Utility estimates

To calculate QALYs in the model, we adjusted survival time by utility. There was no quality-of-life data collected in the FRESCO trial, therefore, each health state was assigned with a health utility score based on literature [14]. Referring to the trial, the value assigned to the basic utility for all patients was 0.66, and we used 0.735 and 0.59 as the upper and lower boundaries of utility in the sensitivity analysis.

In addition, the duration-adjusted decreases in utility caused by grade 3/4 AEs were subtracted from the baseline utility. The disutility of AEs was estimated based on published manuscripts [14, 15]. The unmeasured decreases for the same health states in the FRESCO study were expected to be similar. Duration of AEs was estimated based on clinical experience. Hand-foot syndrome was assumed to be with a disutility of − 0.116 and a duration of 14 days, diarrhea was assumed to be with a disutility of − 0.103 and a duration of 5 days, platelet count decreased and hypertension were assumed to be with a disutility of 0. The annual discounting of the costs and utility in this analysis was set at a rate of 3%.

Sensitivity analysis

Internal model validations were performed, to demonstrate that the OS curves generated by the Markov model simulation closely approximated those presented in the FRESCO trial.

We performed one-way sensitivity analysis and probabilistic sensitivity analysis in order to quantify uncertainty and evaluate the robustness of the model. In one-way sensitivity analysis, the parameters analyzed were varied within ±20% of their baseline values. The baseline values, ranges, and distributions used in the analysis are listed in Table 1. In probabilistic sensitivity analysis, a Monte Carlo simulation was performed for 1000 times, each time randomly sampling from all the parameters of their distributions. Cost-effectiveness acceptability curves were used to demonstrate the uncertainty on the result in relation to possible values of the willingness-to-pay (WTP) thresholds.

Table 1 Baseline values, ranges, and distributions for sensitivity analysis

According to the World Health Organization (WHO) Guide to Generalized Cost-Effectiveness Analysis [18], the WTP threshold in the cost-effectiveness acceptability curves was set at USD 27,130/QALY, which is three times the per capita Chinese GDP of China in 2018.

Scenario analysis

In order to compare the effect of medical insurance, we made a scenario analysis with the total price before price negotiation to see how medical insurance affects the overall cost effectiveness of fruquintinib.


Base case results

As shown in Table 2, after price negotiation, the estimated cost for the fruquintinib group is USD 20750.9, which is higher than the USD 12042.2 estimated for the placebo group, resulting an incremental cost (IC) of USD 8708.7. Compared with the placebo group, the fruquintinib group gains 0.163 QALYs. The ICER of the study is USD 53508.7 per QALY.

Table 2 Base case model results after price negotiation

Sensitivity analyses

Tornado diagrams are used to present the results of one-way sensitivity analysis (Fig. 2). The cost of best supportive care, the cost of fruquintinib, and the baseline utility value have the largest impact on the ICER. The parameters with less influence on the ICER are the duration and disutility for AEs. In the range of variation of each parameter, the ICER remains >USD 27,130/QALY.

Fig. 2
figure 2

Invariable sensitivity analyses after price negotiation

The cost-effectiveness acceptability curves are shown as Fig. 3. As the value of WTP, the curves demonstrate the probability of fruquintinib to be cost-effective. These curves show that, after price negotiation, the cost-effective possibility of fruquintinib is close to 0% at a WTP value < USD 49,000 per QALY. When the WTP value is about USD 54000 per QALY, There is a 50% probability that fruquintinib is cost-effective.

Fig. 3
figure 3

Cost-effectiveness Acceptability Curve after price negotiation

Scenario analysis

As shown in Table 3, before the price negotiation, the estimated cost for the fruquintinib group increases into USD 23590.0, the ICER of the study is USD 70952.6 per QALY.

Table 3 Base case model results before price negotiation


This study primarily investigated the cost-effectiveness of fruquintinib as third-line treatment for mCRC. Fruquintinib, as a potent and highly selective small molecular inhibitor targeting VEGFR-1, VEGFR-2 and VEGFR-3, significantly prolonged the PFS and OS in a phase III RCT [13]. In our study, fruquintinib was associated with relatively longer QALYs (0.64, vs 0.48 with BSC). However, the cost of fruquintinib is expensive, and the ICER remained nearing USD 53508.7 per QALY after adjusting sensitive variables, which was far higher than the acceptance threshold set at three-fold the per capita Chinese GDP. Thus, the results suggested an unlikelihood of incremental benefit of fruquintinib in the mCRC third-line treatment in China.

Standard regimens containing fluorouracil, oxaliplatin, irinotecan, and targeted agents interfering with the epidermal growth factor receptor (EGFR), vascular endothelial growth factor (VEGF) pathways are widely used in the first-line and second-line treatment for mCRC [5,6,7]. However, few drugs except regorafenib and TAS-102 were approved in the mCRC third-line settings by Food and Drug Administration (FDA) [19, 20]. In addition, the drugs are not without great cost. Considering the survival benefit, the quality of life and the expensive price, the cost-effectiveness of mCRC third-line treatment drugs is uncertain.

Recently, the Chinese government has included fruquintinib in the medical insurance, in the hope of decreasing the drug price, as well as supporting domestic origin drugs. After the price negotiation, both the total price of the drug, and the ICER decreased. Before being included in the medical insurance, the cost of fruquintinib was a heavy burden for most cancer patients’ families. After entering the medical insurance, the official announced price reduced more than 60%, with a reimbursement proportion of 70%. This greatly reduces the financial burden on the patient’s family, allowing more patients to fruquintinib for a long time, thereby extending survival. However, our results indicated that fruquintinib is still unlikely to be cost-effective.

This is similar with the cost-effectiveness study on TAS-102 and regorafenib in the United States, where both were not cost-effective at standard WTP thresholds (ie, USD 150,000 per QALY) relative to BSC, and showed no clear evidence for better relative value [21]. These findings were not surprising, since many researchers have argued that the price for cancer drugs was independent of novelty, that the pricing models were not rational but simply reflected what the market will bear [22, 23]. Researchers have suggested that policy makers should evaluate the effects of pricing policies on both affordability and access to anticancer drugs, as well as on the anticancer drug-development pipeline [23]. However, in the case of China, the non-cost-effectiveness of fruquintinib might also be related to the thresholds commonly used in cost-effectiveness studies, where the limited GDP owing to the developing status of China might result in lower thresholds. Several researchers suggested that the use of conventional cost-effectiveness analysis thresholds recommended by World Health Organization might cause misleading conclusions, especially for low- and middle-income countries with low GDP [24, 25]. Patients WTP and pricing policy from government should find a new benchmark for cost-effective care.

Based on data from the CORRECT trial, Goldstein et al. reported an additional 0.04 QALYs (0.13 life years) at a cost of USD 40,000 and ICER of USD 900,000 per QALY for regorafenib. Regorafenib was demonstrated to be of minimal incremental benefit at high costs per QALY in the United States [14]. Additionally, Cho et al. revealed similar results, showing that BSC was more cost-effective than regorafenib at standard WTP [26]. On the other hand, although TAS-102 provided an additional 0.041 QALY compared with regorafenib, it showed the same negative result of TAS-102 for cost-effectiveness analysis in the United States [26]. Another comparative cost-effectiveness study conducted in England and Wales, showed that TAS-102 was associated with longer life year (LY) (0.92 versus 0.82) and QALY (0.82 versus 0.51) when compared with regorafenib, which was consistent with the United States showing the TAS-102 superiority. The ICER for TAS-102 was £51,194 per QALY. After the probabilistic analysis, TAS-102 showed an > 60% probability to achieve a 3-months OS gain [27]. Similar to regorafenib, fruquintinib failed to show cost-effectiveness in our study. And although TAS-102 luckily achieved potential benefit in England and Wales, the worldwide cost-effectiveness of the drug is controversial. The results jointly provided useful references to assess the cost of mCRC third-line treatment, however, due to the policy and price variations, it is challenging to compare the cost-effectiveness of the drugs across different countries. The most cost-effective choice of mCRC third-line treatment in China needs further investigation.

Anti-angiogenesis agents play a pivotal role in the mCRC treatment. Aside from regorafenib and fruquintinib, adding biochemical targeting VEGF pathway, like bevacizumab, aflibercept and ramucirumab, also significantly prolonged the PFS and OS in the first-line and second-line mCRC treatment [28,29,30,31]. By pooling data from six RCTs, Hurwitz et al. demonstrated the prolongation of PFS (9.1 versus 6.9 months; HR, 0.58; 95% CI, 0.46–0.73; p < 0.0001) and OS (19.8 versus 17.6 months; HR, 0.81; 95% CI, 0.70–0.93; p = 0.0034) by adding bevacizumab to chemotherapy backbone in the mCRC first-line treatment. However, the cost-effectiveness study revealed that bevacizumab gained minimal survival benefit at USD 571,240 per QALY in the first-line treatment. Moreover, in the second-line treatment, bevacizumab failed to show cost-effectiveness, with ICER USD 364,083 per QALY. Aflibercept combined with FOLFIRI regimen (folinic acid, luorouracil and irinotecan) on the other hand, prolonged 2.23 months PFS and 1.44 months OS in a phase III RCT, after model adjustment the ICER turned out to be > £62,000 per QALY (USD 95,000 per QALY), which was thought to be not cost-effective in the United Kingdom either [32]. To date, all the three anti-angiogenesis drugs were thought to have similar efficacy and survival benefit in the second-line mCRC treatment when added to FOLFIRI. However, ramucirumab was far more expensive than the other two agents [33]. Although no studies have demonstrated the cost-effectiveness of ramucirumab to date, the results may probably be negative too. So far, all of the approved anti-angiogenesis drugs in the mCRC treatment failed to show cost-effectiveness, no matter in which line. However, owing to the lack of anti-angiogenesis drugs cost-effectiveness study in China, adding these drugs to mCRC patients’ treatment plan may need a careful discussion between physicians and the patients.

On the other hand, adding cetuximab, an anti-EGFR monoclonal antibody, to chemotherapy also showed prolongation of survival, with an ICER of USD 2.9 million per LY. Interestingly, by testing KRAS mutation status as a stratification strategy, the ICER was reduced to USD 2.8 million per LY [34]. Using biomarker to select patients that may benefit can be an effective way to improve the cost-effectiveness of fruquintinib. However, as there are no currently validated biomarkers for anti-angiogenesis agents efficacy in mCRC, further studies in this field are urgently needed.

There are several limitations in our study. First, this study was not prospective, and drug price and costs were assumed as static. AEs were given pre-defined durations, which may not fully reflect the real world. Secondly, we used conventional WHO’s cost-effectiveness thresholds, however, the threshold might not be the best option for oncology drugs, thus the conclusion of not cost-effectiveness should be drawn with caution [35, 36]. Lastly, all the results were based on the FRESCO study, a multicenter RCT conducted only in China, which might not be the case for other countries.


In conclusion, this is the first study to investigate the cost-effectiveness of fruquintinib in the mCRC third-line treatment. With the ICER far exceeding the three-fold Chinese per capita GDP, fruquintinib seems unable to be cost-effective in China under current standard. Finding dependable biomarkers for fruquintinib, establishing new value-based pricing and payment system are needed in the future.

Availability of data and materials

All data analysed during this study are included in published article.



Quality-adjusted life years


US dollars


Incremental results effectiveness ratio


Gross domestic product


Metastatic colorectal cancer


Vascular endothelial growth factor receptor


Progression-free survival


Randomized controlled trial


Overall survival


Adverse effect


Chinese yuan


Fruquintinib efficacy and safety in 3+ line colorectal cancer patients


Best supportive care




World Health Organization


Incremental cost


Incremental effectiveness


Epidermal growth factor receptor


Vascular endothelial growth factor


Food and Drug Administration


Colorectal cancer treated with regorafenibor placebo after failure of standard therapy


Life year


Folinic acid, luorouracil and irinotecan


  1. Bray F, Ferlay J, Soerjomataram I, Siegel RL, Torre LA, Jemal A. Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. 2018;68(6):394–424.

    Article  Google Scholar 

  2. Zhu J, Tan Z, Hollis-Hansen K, Zhang Y, Yu C, Li Y. Epidemiological trends in colorectal cancer in China: an ecological study. Dig Dis Sci. 2017;62(1):235–43.

    Article  Google Scholar 

  3. Arnold M, Sierra MS, Laversanne M, Soerjomataram I, Jemal A, Bray F. Global patterns and trends in colorectal cancer incidence and mortality. Gut. 2017;66(4):683–91.

    Article  Google Scholar 

  4. Chen W, Zheng R, Baade PD, Zhang S, Zeng H, Bray F, et al. Cancer statistics in China, 2015. CA Cancer J Clin. 2016;66(2):115–32.

    Article  Google Scholar 

  5. Ciardiello F, Normanno N, Martinelli E, Troiani T, Pisconti S, Cardone C, et al. Cetuximab continuation after first progression in metastatic colorectal cancer (CAPRI-GOIM): a randomized phase II trial of FOLFOX plus cetuximab versus FOLFOX. Ann Oncol. 2016;27(6):1055–61.

    Article  CAS  Google Scholar 

  6. Hurwitz HI, Tebbutt NC, Kabbinavar F, Giantonio BJ, Guan ZZ, Mitchell L, et al. Efficacy and safety of bevacizumab in metastatic colorectal cancer: pooled analysis from seven randomized controlled trials. Oncologist. 2013;18(9):1004–12.

    Article  Google Scholar 

  7. Heinemann V, von Weikersthal LF, Decker T, Kiani A, Vehling-Kaiser U, Al-Batran SE, et al. FOLFIRI plus cetuximab versus FOLFIRI plus bevacizumab as first-line treatment for patients with metastatic colorectal cancer (FIRE-3): a randomised, open-label, phase 3 trial. Lancet Oncol. 2014;15(10):1065–75.

    Article  CAS  Google Scholar 

  8. Seymour MT, Maughan TS, Ledermann JA, Topham C, James R, Gwyther SJ, et al. Different strategies of sequential and combination chemotherapy for patients with poor prognosis advanced colorectal cancer (MRC FOCUS): a randomised controlled trial. Lancet. 2007;370(9582):143–52.

    Article  CAS  Google Scholar 

  9. Van Cutsem E, Peeters M, Siena S, Humblet Y, Hendlisz A, Neyns B, et al. Open-label phase III trial of panitumumab plus best supportive care compared with best supportive care alone in patients with chemotherapy-refractory metastatic colorectal cancer. J Clin Oncol. 2007;25(13):1658–64.

    Article  Google Scholar 

  10. Jonker DJ, O'Callaghan CJ, Karapetis CS, Zalcberg JR, Tu D, Au HJ, Berry SR, Krahn M, Price T, Simes RJ, Tebbutt NC, et al. Cetuximab for the treatment of colorectal cancer. N Engl J Med. 2007;357(20):2040-8. PMID: 18003960.

  11. Bekaii-Saab T, Kim R, Kim TW, O'Connor JM, Strickler JH, Malka D, et al. Third- or later-line therapy for metastatic colorectal cancer: reviewing best practice. Clin Colorectal Cancer. 2019;18(1):e117–e29.

    Article  Google Scholar 

  12. Zhang Q, Wang Q, Wang X, Li J, Shen L, Peng Z. Regorafenib, TAS-102, or fruquintinib for metastatic colorectal cancer: any difference in randomized trials?[J]. Int J Color Dis. 2019;35(2):295–306.

    Article  Google Scholar 

  13. Li J, Qin S, Xu RH, Shen L, Xu J, Bai Y, et al. Effect of fruquintinib vs placebo on overall survival in patients with previously treated metastatic colorectal cancer: the FRESCO randomized clinical trial. JAMA. 2018;319(24):2486–96.

    Article  CAS  Google Scholar 

  14. Goldstein DA, Ahmad BB, Chen Q, et al. Cost-effectiveness analysis of regorafenib for metastatic colorectal cancer.[J]. J Clin Oncol. 2011;33(32):3727–32.

    Article  Google Scholar 

  15. Lloyd A, Nafees B, Narewska J, Dewilde S, Watkins J. Health state utilities for metastatic breast cancer. Br J Cancer. 2006;95(6):683–90. PubMed PMID: PMC2360509. PMID: 16967055.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  16. Ju-Xiang C, Hong-Xuan Z, Lan MA, et al. Comparison between gemcitabine plus oxaliplatin or S-1 and singleagent gemcitabine in the treatment of advanced pancreatic cancer[J]. Anhui Med Pharm J. 2015;19(02):359-62.

  17. Chong-Qing T. Build pharmacoeconomics evaluation model of gastric cancer fitted China based on Markov model [D]. Changsha: Central South University; 2014.

    Google Scholar 

  18. WHO guide to generalized cost-effectiveness analysis. 2016. Accessed 7 Oct 2016.

  19. Grothey A, Van Cutsem E, Sobrero A, Siena S, Falcone A, Ychou M, et al. Regorafenib monotherapy for previously treated metastatic colorectal cancer (CORRECT): an international, multicentre, randomised, placebo-controlled, phase 3 trial. Lancet. 2013;381(9863):303–12.

    Article  CAS  Google Scholar 

  20. Mayer RJ, Van Cutsem E, Falcone A, Yoshino T, Garcia-Carbonero R, Mizunuma N, et al. Randomized trial of TAS-102 for refractory metastatic colorectal cancer. N Engl J Med. 2015;372(20):1909–19.

    Article  Google Scholar 

  21. Cho SK, Hay JW, Barzi A. Cost-effectiveness analysis of regorafenib and TAS-102 in refractory metastatic colorectal cancer in the United States.[J]. Clin Colorectal Cancer. 2018;17(4):e751–61.

    Article  Google Scholar 

  22. Mailankody S, Prasad V. Five years of cancer drug approvals: innovation, efficacy, and costs.[J]. JAMA Oncol. 2015;1(4):539–40.

    Article  Google Scholar 

  23. Prasad V, De Jesús K, Mailankody S. The high price of anticancer drugs: origins, implications, barriers, solutions[J]. Nat Rev Clin Oncol. 2017;14(6):381.

    Article  Google Scholar 

  24. Leech AA, Kim DD, Cohen JT, et al. Use and misuse of cost-effectiveness analysis thresholds in low- and middle-income countries: trends in cost-per-DALY studies[J]. Value Health. 2018;21(7):759–61 S1098301518300160.

    Article  Google Scholar 

  25. Cameron D, Ubels J, et al. On what basis are medical cost-effectiveness thresholds set? Clashing opinions and an absence of data: a systematic review.[J]. Glob Health Action. 2018;11(1):1447828.

    Article  Google Scholar 

  26. Cho SK, Hay JW, Barzi A. Cost-effectiveness analysis of regorafenib and TAS-102 in refractory metastatic colorectal cancer in the United States. Clin Colorectal Cancer. 2018;17(4):e751–e61.

    Article  Google Scholar 

  27. Bullement A, Underhill S, Fougeray R, Hatswell AJ. Cost-effectiveness of trifluridine/tipiracil for previously treated metastatic colorectal cancer in England and Wales. Clin Colorectal Cancer. 2018;17(1):e143–e51.

    Article  Google Scholar 

  28. Hurwitz H, Fehrenbacher L, Novotny W, Cartwright T, Hainsworth J, Heim W, et al. Bevacizumab plus irinotecan, fluorouracil, and leucovorin for metastatic colorectal cancer. N Engl J Med. 2004;350(23):2335–42.

    Article  CAS  Google Scholar 

  29. Bennouna J, Sastre J, Arnold D, Osterlund P, Greil R, Van Cutsem E, et al. Continuation of bevacizumab after first progression in metastatic colorectal cancer (ML18147): a randomised phase 3 trial. Lancet Oncol. 2013;14(1):29–37.

    Article  CAS  Google Scholar 

  30. Tabernero J, Yoshino T, Cohn AL, Obermannova R, Bodoky G, Garcia-Carbonero R, et al. Ramucirumab versus placebo in combination with second-line FOLFIRI in patients with metastatic colorectal carcinoma that progressed during or after first-line therapy with bevacizumab, oxaliplatin, and a fluoropyrimidine (RAISE): a randomised, double-blind, multicentre, phase 3 study. Lancet Oncol. 2015;16(5):499–508.

    Article  CAS  Google Scholar 

  31. Van Cutsem E, Tabernero J, Lakomy R, Prenen H, Prausova J, Macarulla T, et al. Addition of aflibercept to fluorouracil, leucovorin, and irinotecan improves survival in a phase III randomized trial in patients with metastatic colorectal cancer previously treated with an oxaliplatin-based regimen. J Clin Oncol. 2012;30(28):3499–506.

    Article  Google Scholar 

  32. Wade R, Duarte A, Simmonds M, Rodriguez-Lopez R, Duffy S, Woolacott N, et al. The clinical and cost effectiveness of aflibercept in combination with Irinotecan and fluorouracil-based therapy (FOLFIRI) for the treatment of metastatic colorectal cancer which has progressed following prior oxaliplatin-based chemotherapy: a critique of the evidence. PharmacoEconomics. 2015;33(5):457–66.

    Article  Google Scholar 

  33. Goldstein DA, El-Rayes BF. Considering efficacy and cost, where does ramucirumab fit in the management of metastatic colorectal cancer? Oncologist. 2015;20(9):981–2.

    Article  CAS  Google Scholar 

  34. Behl AS, Goddard KA, Flottemesch TJ, Veenstra D, Meenan RT, Lin JS, et al. Cost-effectiveness analysis of screening for KRAS and BRAF mutations in metastatic colorectal cancer. J Natl Cancer Inst. 2012;104(23):1785–95.

    Article  Google Scholar 

  35. Jung BYH, Daniel MC. Do value thresholds for oncology drugs differ from nononcology drugs?[J]. J Manag Care Pharm. 2014;20(11):1086–92.

    Google Scholar 

  36. Aguiar PN, Roitberg F, Noia Barreto CM, et al. Back to the future: in the era of cost-effectiveness analysis, affordability is a limiting factor for patients’ access to innovative cancer treatments[J]. Value Health Reg Issues. 2019;20:47–50.

    Article  Google Scholar 

Download references


Not applicable.


This work was supported by Clinical Medicine Plus X - Young Scholars Project of Peking University [grant numbers PKU2019LCXQ020, PKU2018LCXQ018]; and Beijing Municipal Administration of Hospital’s Youth Program [grant number 20171102]. The two funders supported the establishment of the research group and the successful publishing process.

Author information

Authors and Affiliations



ZP conceived the study, designed the study, supervised the study, interpreted the results, collected the data and revised the manuscript. XH1 analyzed the data, interpreted the results, and drafted the manuscript. YH and XH2 designed the study, supervised the study, searched the literature, collected the data and revised the manuscript. TX searched the literature, and drafted the manuscript. ZP and XH1 made same contribution to this paper. All authors contributed to the writing of the manuscript.

Corresponding author

Correspondence to Yangmu Huang.

Ethics declarations

Ethics approval and consent to participate

Not applicable.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Peng, Z., Hou, X., Huang, Y. et al. Cost-effectiveness analysis of fruquintinib for metastatic colorectal cancer third-line treatment in China. BMC Cancer 20, 990 (2020).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: