Literature DB >> 29743945

Evidence on the cost of breast cancer drugs is required for rational decision making.

Anne Margreet Sofie Berghuis1, Hendrik Koffijberg1, Leonardus Wendelinus Mathias Marie Terstappen2, Stefan Sleijfer3, Maarten Joost IJzerman1.   

Abstract

BACKGROUND: For rational decision making, assessing the cost-effectiveness and budget impact of new drugs and comparing the costs of drugs already on the market is required. In addition to value frameworks, such as the American Society of Clinical Oncology Value Framework and the European Society of Medical Oncology-Magnitude of Clinical benefit Scale, this also requires a transparent overview of actual drug prices. While list prices are available, evidence on treatment cost is not. This paper aims to synthesise evidence on the reimbursement and costs of high-cost breast cancer drugs in The Netherlands (NL).
METHODS: A literature review was performed to identify currently reimbursed breast cancer drugs in the NL. Treatment costs were determined by multiplying list prices with the average length of treatment and dosing schedule.
RESULTS: Comparing list prices to the estimated treatment cost resulted in substantial differences in the ranking of costliness of the drugs. The average mean treatment length was unknown for 11/31 breast cancer drugs (26.2%). The differences in the 15 highest-cost drugs were largest for Bevacizumab, Lapatinib and everolimus, with list prices of €541, €158, €1,168 and estimated treatment cost of €174,400, €18,682 and €31,207, respectively. The lowest-cost (patented) targeted drug is €1,818 more expensive than the highest-cost (off-patent) generic drug according to the estimated drug treatment cost.
CONCLUSIONS: A lack of evidence on the reimbursement and cost of high-cost breast cancer drugs complicates rapid and transparent evidence synthesis, necessary to focus strategies aiming to limit the increasing healthcare costs. Interestingly, the findings show that off-patent generics (such as paclitaxel or doxorubicin), although substantially cheaper than patented drugs, are still relatively costly. Extending standardisation and increasing European and national regulations on presenting information on costs per cancer drug is highly recommended.

Entities:  

Keywords:  breast cancer; cost; drug; health economics; medication; treatment

Year:  2018        PMID: 29743945      PMCID: PMC5931813          DOI: 10.3332/ecancer.2018.825

Source DB:  PubMed          Journal:  Ecancermedicalscience        ISSN: 1754-6605


Background

Globally, breast cancer is the most common form of cancer among women. In the past decades, several new treatments that improve clinical outcome became available on the market [1]. Systemic treatment with e.g. Trastuzumab, for which specific biomarkers are employed, is one of these survival improving new treatments [2]. When trials have shown the effectiveness or clinical benefit of a specific treatment, the treatment needs to be approved before it can be implemented and used in clinical practice. Several international regulatory agencies are responsible for these drug approval processes, such as the European Medicines Agency (EMA) and the Food and Drug Administration [3]. In addition, national bodies typically apply country specific regulations concerning drug approval. A major challenge in oncology today is the swift increase in healthcare costs [4]. Currently, the costs of cancer treatment can even account for up to 30% of the total hospital expenditures [5]. As more and more new cancer treatments are being developed, it is important to anticipate on the increasing cancer costs in hospitals already during early development stages. To be able to compare future treatment cost of upcoming new drugs to the prices that are currently paid, and to put the costs of new drugs into perspective, an overview of the current drug treatment cost should be available. However, such an overview of the actual cost of breast cancer treatments in European countries is lacking [5]. List prices are available and of interest but are not truly reflecting the actual drug treatment cost, as these prices only show the maximum purchase costs for a particular drug [5]. Furthermore, these list prices are not suitable for the comparison of treatment cost, as drugs may be prescribed in different dosages, have different administration forms and can have different toxicities, thereby impacting the total drug treatment cost for each drug. In addition, these costs should have been determined for currently reimbursed drugs but are even more important for new drugs that are currently investigated in trials. As there is currently no overview of the actual cost of currently used breast cancer drugs, there is no reference towards what we are currently able to afford cancer drugs [6]. To anticipate on future treatment costs and to strive towards maintaining good affordability of cancer care, it is important that such a framework will be established. A preliminary step would be to gain insight in the actual treatment costs for high-cost breast cancer drugs by using European and national assessment reports. In addition, there is increasing attention being given to the lack of transparency in drug pricing. Both the American Society of Clinical Oncology (ASCO) and the European Society for Medical Oncology (ESMO) have already developed value frameworks, which aim to guide decisions by comparing costs and net health benefits. The recent update of the ASCO Value Framework (ASCO-VF) shows that costs included in this framework are based on monthly drug acquisition cost and patient co-payments [7]. Comparisons between the ASCO-VF and the ESMO Magnitude of Clinical benefit Scale (ESMO-MCBS) frameworks have shown that there are substantial differences in estimated costs depending on whether drugs meet the criteria from the ESMO-MCBS or the ASCO-VF [8]. Therefore, this study aims to estimate the total drug treatment costs based on list prices and by using guidance from official approval and reimbursement documents. As this analysis is preliminary, no breast cancer subtypes (based on stage, receptor, and/or metastatic status) were distinguished.

Methods

The EMA is the first agency to give market approval for newly developed drugs. Individual countries can decide themselves whether or not these drugs will be approved and/or reimbursed based on the evaluation of the cost-effectiveness of the new drug. Cost-effectiveness thresholds and approval and/or reimbursement mechanisms differ between countries [5, 6]. This study focusses on The Netherlands (NL), as this is one of the countries which has an open-access, reliable database containing list prices for all drugs, hosted by the Dutch Administrative Health Authority (ZINL). To extract all information that is necessary to calculate the average drug treatment cost for all approved breast cancer drugs in the NL, information from multiple databases was aggregated. Information was extracted using a stepwise approach of four steps. First, an overview of all currently approved breast cancer drugs or therapies in the NL was created. Documents of ZINL were investigated for all drugs or therapies that are approved for use in any part of the whole care pathway in breast cancer treatment. Second, data on the approval and costs of all drugs was retrieved via ZINL. As ZINL frequently updates their cost data, the cost data used were last extracted on 1 June 2017 [9, 10]. For some drugs, different forms and strengths of the active drug substance exist. For each of these forms of the particular drug, the list price of the high-volume, high-dose package was used in the analysis as it was assumed that total cost for a particular quantity of a drug would then be less costly compared to using low-volume, low-dose packages. High-volume, high-dose packages were chosen because producing, packaging and shipping larger (aggregated) products is generally cheaper than doing the same for multiple smaller products when the overall quantity remains fixed. For each of the forms of these drugs (e.g. 100 mL infusion fluid of 2 mg/mL), the lowest and highest list prices are presented by ZINL [9]. It was assumed that hospitals buying these drugs would pick the lowest-price option when multiple drug manufacturers produce similar drugs (same dose, same form, other manufacturer and/or brand name). Therefore, use of the currently available lower list price was deemed the most realistic approach. Furthermore, due to collaborations between hospitals, potential purchase benefits may arise resulting in lower purchase prices paid for particular drugs [9]. Third, further evidence on the effective dosage and average (if available) or median (if an average was lacking) duration of treatment was used in the calculations. This evidence was identified by using the European Public Assessment Reports (EPARs) when these were available for drugs that are approved in the NL. EPARs are the full scientific assessment reports that are published for every medicine for which authorisation was applied at the EMA. When no EPAR was available concerning the particular drug, the official reports of the national health regulating agency ZINL were used. When both, EPARs and ZINL reports, did not present any information on the average or median duration of treatment with that particular drug, corresponding trials were searched for estimates of progression-free survival (PFS) or disease-free survival (DFS). When these were available, the PFS or DFS were used in the further estimation of treatment costs, as for most, drugs treatment continues until progression is reported. When EPARs, ZINL assessment reports or the corresponding trials did not provide any of this information, the treatment duration for that particular drug was set equal to the average treatment length of all other drugs for which this information was available. Fourth, all information was accumulated in the estimation of the drug treatment costs for all of the breast cancer drugs that are approved in the NL. The price per milligram of the specific form of the drug was calculated from the list prices per package of the drug. Following, dosing information was used to calculate the total number of milligrams of the drug necessary per treatment cycle. Dosing information in the EPARs and ZINL documents is presented in milligram per square meter or per kilogram of the patient. The average Dutch female has been used as a reference here, with a body surface of 1.6 square meters and a weight of 71.3 kilograms. This dosage per treatment cycle, corresponding list prices and the average length of treatment were used to determine the total estimated drug treatment cost.

Results

According to ZINL, 31 drugs are approved for breast cancer treatment in the NL. In Table 1, the list prices for a single package of the specific drug packages are presented for the 15 highest-cost approved breast cancer drugs in the NL. Several drugs are available in multiple forms and concentrations of that particular drug. In Table 1, the lowest list prices are presented for one package of the highest volume and highest dose substance available for each specific form of every drug. Besides, the reimbursement status of that particular form and strength of the drug was reported. A further extension of Table 1 presenting all approved breast cancer drugs in all available forms and strengths of the drug substance and their reimbursement status is presented in Appendix 1. Appendix 1 shows that only one of all approved breast cancer drugs is not reimbursed in any form or strength of the drug substance, which is pamidronate disodium. For doxorubicin and Bevacizumab, only one of the forms or strengths of the drug substance is not reimbursed. Pertuzumab, Trastuzumab Emtansine and Trastuzumab are the three breast cancer drugs with the highest list prices.
Table 1.

Average list prices and reimbursement for the 15 highest-cost breast cancer drugs.

List price rankActive substanceForm and strength of drug substanceReimbursedList Price
1PertuzumabConcentrate for solution infusion 30mg/ml 14 mlYes€3,030.12
2Trastuzumab emtansinePowder for solution infusion 160 mgYes€2,984.96
3TrastuzumabInjection fluid 120mg/ml 5 mlYes€1,751.19
4PaclitaxelConcentrate for solution infusion 6 mg/ml 100 mlYes€1,584.70
5BevacizumabConcentrate for solution infusion 25mg/ml 16 mlYes€1,310.65
6DoxorubicinConcentrate for solution infusion 2mg/ml 25 mlYes€1,079.75
7ThiotepaPowder for solution infusion 100 mgYes€1,028.20
8DocetaxelConcentrate for solution infusion 10mg/ml 16 mlYes€889.68
9DocetaxelConcentrate for solution infusion 20mg/ml 8 mlYes€877.47
10DoxorubicinPowder for solution infusion 50 mgNo€689.49
11EribulinInjection fluid 0,44mg/ml 3 mlYes€614.32
12TrastuzumabPowder for solution infusion 150 mgYes€589.99
13EPIRUBICINInjection fluid 2mg/ml 100 mlYes€362.45
14PaclitaxelPowder for solution infusion 100 mgYes€344.44
15Goserelin acetateImplantation stick 10.8 mgYes€341.56
If for a particular form of a drug, multiple list price were presented by ZINL (n = 9), the highest list prices were on average 86.3 % higher than the lowest prices. However, this high percentage was caused by two outliers (ibandronic acid–difference of 717.2 % and capecitabin—difference of 47.0%). The median of the difference between the highest cost and the lowest cost was only 0.5%. To convert these list prices to the estimated average treatment cost, evidence on the effective dosage and length of treatment was used. In Table 2, the estimated average treatment costs are presented and ranked for the 15 highest-cost drugs. In the column for treatment duration is shown which type of treatment length (mean/median actual treatment length or mean/median PFS) for each drug has been identified from the EPAR or ZINL assessment reports. For thiotepa and vinblastin, an assumption on treatment length was made as there was no information on treatment length available within these reports for these drugs. These assumptions were based on the average length of treatment for all other drugs for which the treatment lengths were available in EPARs or ZINL assessment reports (n = 31, 73.8%), and was calculated to be 7.6 cycles or 22.8 weeks.
Table 2.

Total estimated drug treatment cost and rankings.

List price rankEstimated treatment cost rankActive substanceForm and strength of drug substanceNumber of cycles (3 weeks)Treatment durationEstimated treatment cost
311BevacizumabInjection fluid 25mg/ml 0.15 ml15.1Mean TL€174,399.68
52BevacizumabConcentrate for solution infusion 25mg/ml 16 ml15.1Mean TL€51,836.10
23Trastuzumab emtansinePowder for solution infusion 160 mg9.5Median TL€44,505.75
284EverolimusDispersible tablet 5 mg8.0Mean TL€31,207.25
125TrastuzumabPowder for solution infusion 150 mg13.0Mean TL€21,947.45
256EverolimusTablet 10 mg8.0Mean TL€21,254.31
367LapatinibTablet 250 mg15.0Median TL€18,682.30
18PertuzumabConcentrate for solution infusion 30mg/ml 14 ml4.5Mean TL€16,665.64
39TrastuzumabInjection fluid 120mg/ml 5 ml13.0Mean TL€16,286.10
710Thiotepa*Powder for solution infusion 100 mg7.6Assumption€14,467.30
3211Vinblastin*Injection fluid 1mg/ml 10 ml7.6Assumption€10,175.00
612Doxorubicin*Concentrate for solution infusion 2mg/ml 25 ml4.3Median PFS€9,950.96
1113Eribulin*Injection fluid 0,44mg/ml 3 ml4.8Mean TL€8,551.01
1414Paclitaxel*Powder for solution infusion 100 mg5.6Mean TL€8,024.00
1015Doxorubicin*Powder for solution infusion 50 mg4.3Median PFS€6,354.32

generic drugs

If an assumption was used to estimate the average treatment length, this assumption was based on the average treatment length of all other drugs for which a treatment length was available in the EPARs or ZINL assessment reports. Mean TL = Mean treatment length. median PFS = Median progression-free survival

Furthermore, Table 2 shows that the highest factorial differences between list prices and estimated treatment cost are found for Bevacizumab (list price: €541.08––treatment cost: €174,399.68––factorial difference: 322.3 times more costly), Lapatinib (list price €158.37––treatment cost €18,682.30––factorial difference: 118.0 times more costly) and everolimus (list price €1,168.65––treatment cost €31,207.25––factorial difference: 26.7 times more costly). The full overview of the ranking and prices of all drugs is presented in Appendix 1. Table A1 in Appendix 1 shows that similar differences can be found for all approved breast cancer drugs according to their estimated treatment cost.
Table A1.

Total estimated drug treatment cost and rankings.

List price rankEstimated treatment cost rankActive substanceForm and strength of drug substanceNumber of cycles (3 weeks)Treatment durationEstimated treatment price
311BevacizumabInjection fluid 25mg/ml 0.15 ml15.1Mean TL€174,399.68
52BevacizumabConcentrate for solution infusion 25mg/ml 16 ml15.1Mean TL€51,836.10
23Trastuzumab emtansinePowder for solution infusion 160 mg9.5Median TL€44,505.75
284EverolimusDispersible tablet 5 mg8.0Mean TL€31,207.25
125TrastuzumabPowder for solution infusion 150 mg13.0Mean TL€21,947.45
256EverolimusTablet 10 mg8.0Mean TL€21,254.31
367LapatinibTablet 250 mg15.0Median TL€18,682.30
18PertuzumabConcentrate for solution infusion 30mg/ml 14 ml4.5Mean TL€16,665.64
39TrastuzumabInjection fluid 120mg/ml 5 ml13.0Mean TL€16,286.10
710ThiotepaPowder for solution infusion 100 mg7.6Assumption€14,467.30
3211VinblastinInjection fluid 1mg/ml 10 ml7.6Assumption€10,175.00
612DoxorubicinConcentrate for solution infusion 2mg/ml 25 ml4.3Median PFS€9,950.96
1113EribulinInjection fluid 0,44mg/ml 3 ml4.8Mean TL€8,551.01
1414PaclitaxelPowder for solution infusion 100 mg5.6Mean TL€8,024.00
1015DoxorubicinPowder for solution infusion 50 mg4.3Median PFS€6,354.32
416PaclitaxelConcentrate for solution infusion 6 mg/ml 100 ml5.6Mean TL€6,152.86
1617FulvestrantInjection fluid 50 mg/ml 5 ml8.7Median PFS€5,490.16
818DocetaxelConcentrate for solution infusion 10mg/ml 16 ml6.0Mean TL€5,338.08
919DocetaxelConcentrate for solution infusion 20mg/ml 8 ml6.0Mean TL€5,264.81
3820FluorouracilCrème 50mg/g 15 g6.0Mean TL€4,136.00
2121GemcitabinPowder for solution infusion 2000 mg8.2Mean DFS€2,418.96
2022GemcitabinInfusion fluid 10mg/ml 220 ml8.2Mean DFS€2,277.94
1323EpirubicinInjection fluid 2mg/ml 100 ml7.6Assumption€1,841.13
2224GemcitabinConcentrate for solution infusion 100mg/ml 20 ml8.2Mean DFS€1,824.52
1725EpirubicinInfusion fluid 2mg/ml 100 ml7.6Assumption€1,561.51
1926Mitoxantrone hydrochlorideConcentrate for solution infusion 2mg/ml 15 ml7.6Assumption€1,486.01
2927VinorelbinCapsule 30 mg4.0TTP€1,371.22
2728VinorelbinConcentrate for solution infusion 10mg/ml 5 ml4.0TTP€1,272.71
2429PamidronatedisodiumConcentrate for solution infusion 9mg/ml 10 ml7.6Assumption€1,109.25
3930MegestrolTablet 160 mg7.6Assumption€1,025.81
2631MelphalanPowder for solution infusion 50 mg7.6Assumption€985.34
1532Goserelin AcetateImplantation stick 10.8 mg7.6Assumption€865.92
1833DoxorubicinInjection fluid 2mg/ml 100 ml4.3Median PFS€641.65
3034Ibandronic acidInjection fluid 1mg/ml 3ml7.6Assumption€554.99
3535VincristineInjection fluid 1mg/ml 2 ml7.6Assumption€517.39
4036Melphalan*Tablet 2 mg7.6Assumption€500.85
4237CapecitabinTablet 500 mg4.4TTP€339.55
3338CyclophosphamidePowder injection fluid 2000 mg6.0Mean TL€227.25
2339Mitomycin CPowder for injection fluid 40 mg7.6Assumption€207.01
3740PamidronatedisodiumInfusion fluid 0,18mg/ml 500 ml7.6Assumption€131.09

If an assumption was used to estimate the average treatment length, this assumption was based on the average treatment length of all other drugs for which a treatment length was available in the EPARs or ZINL assessment reports. Mean TL = Mean treatment length. median PFS = Median progression-free survival. TTP = Time to progression

Absolute differences between low-cost targeted drugs (which are all drugs in rank 1–9) and the high-cost generic drugs (which are all drugs in rank 10–15) are relatively small. Of these generic drugs, doxorubicin, paclitaxel, vinblastine and thiotepa are already off-patent. The difference in estimated drug treatment cost between the relatively low-cost targeted drug Trastuzumab (rank 9) and the relatively high-cost generic drug thiotepa (rank 10) is €1,818.81. In the estimation of the estimated drug treatment cost, list prices of high-volume, high-dose packages were used as these were assumed to be less costly than low-volume, low-dose packages. A comparison of the estimated drug treatment cost using high-volume, high-dose packages with the estimated drug treatment cost using low-dose, low-volume packages is presented in Appendix 2.

Discussion

This study aimed to give an estimation of the total drug treatment cost in breast cancer based on list prices and official approval and reimbursement documents. However, there are still several difficulties encountered in the process of estimating drug treatment costs. The first difficulty concerns the identification of the average length of treatment from EPARs or ZINL assessment reports. For some drugs, the average or median length of treatment is not reported standardised in these reports. By extending the search to the clinical trials reports on which the EPAR and ZINL assessment reports were based, for most drugs, the duration of treatment could be defined based on the PFS or DFS. However, there are still some drugs for which this evidence is lacking in these reports or the trials on which these reports are based. The second difficulty concerned the lack of evidence stating which particular form or strength of the drugs is most likely to be used in clinical practice. For multiple drugs, there are several forms and strengths available. In this study, high-volume, high-dose packages were used to calculate the drug treatment cost. However, there are several options in combining different package sizes to different doses. This prohibits accurate cost estimations as well as estimations on the amount of waste arising when packages are not fully used. As an increasing number of cancer drugs keep being developed and the cost of cancer care continues to increase, it is important to take the estimated total treatment costs of new drugs into account from early development stages onwards. One of the most important means to manage cancer drug prices and to further ensure the affordability of cancer care, is the targeting of those patients who are most likely to respond to particular treatments. One of the ways to identify those patients is the use of biomarkers, which are biological characteristics that can be identified from tissue or body fluids. Biomarkers enable the identification of patients who are highly likely or unlikely to benefit from a particular treatment or can be used as response markers to establish treatment effectiveness very rapidly after treatment initiation. Several studies have been focusing on the use of liquid biopsies, which are tests for biomarkers traceable in body fluids such as blood and urine, to be able to further target and personalise treatment [11]. One of the advantages of using these liquid biopsies is that tests can be cheaper, less invasive, and might even be more sensitive in targeting the treatment population than expensive imaging diagnostics [12-15]. However, as new drug development and cost-effectiveness studies (focusing on the personalised prescription of high-cost drugs based on liquid biopsies) should refer to the prices that we should be able to pay currently, it is important that we are able to create an overview of the actual treatment prices that are currently being reimbursed. As it is hard to find evidence on especially the average length of treatment, it would be valuable to further extend standardisation of reporting this evidence in national or international drug assessment reports. An extended standardisation in which all treatment measures (such as the treatment duration, dosage and forms and strengths of the active substance on which the results are based) are presented in the same format in the same sections of these reports will improve the availability and transparency of such evidence, and thereby also the accuracy of cost estimations. Even though these standardised measures are currently unavailable for such cost estimations, the results of this review have already shown that there are substantial differences in the ranking of costliness of drugs according to their list prices or their estimated treatment costs. However, even though drugs are costly and have substantial influence on the budget impact, when developing new drugs and referring to such frameworks, it is important to not solely focus on potential budget impact constraints. Cost-effectiveness, that is, the balance between the additional costs and the associated improvement in health outcomes should also be taken into account. Furthermore, in such cost-effectiveness analyses, the (higher) full patient treatment costs should also be taken into account, as the drug treatment costs identified in this study do not include further patient treatment costs (e.g. the drug treatment costs do not include costs for differences in the administration such as hospitalisation or home medication of different treatments). Although only one drug was identified which was approved but not reimbursed in the NL, other countries have other reimbursement regulations and might, therefore, have different drugs (not) reimbursed [6, 16]. The cost calculations that were performed in this study provide a stepwise approach to establishing a reference framework of drug treatment costs (necessary for rational decision making) when there is limited open-access to cost information. Even though list prices are not the prices that are actually paid, these are currently the only drug prices which are openly available. Furthermore, though these list prices exist for all drugs in most countries, in some countries these list prices are only openly available in a standardised way for generic drugs and not for the typically more costly targeted drugs. When more countries aim for a transparent costing system, this would enable faster, easier and a more realistic collection of drug treatment costs.

Conclusions

This study presented an initial estimation of drug treatment cost based on list prices. An important finding was that off-patent generics, such as paclitaxel and doxorubicin, are still relatively costly. Although most generics are substantially cheaper than (patented) targeted drugs, the estimated drug treatment costs for the highest-cost generics were higher than expected for off-patent drugs. Furthermore, it was shown that there are still several barriers which prohibit accurate estimations of drug treatment cost. List prices are available for all breast cancer drugs in the NL. However, in other European countries, this availability is less standardised. In addition, substantial differences can exist between the list prices of drugs and the associated average actual treatment costs which further complicate accurate estimations of drug treatment cost. To improve on cost estimations and increase the relevance of such estimates for research on the development of new drugs, it is important to further extend standardisation and increase European and national regulations on the presentation of treatment or drug costs, dosage and further treatment specifications. Furthermore, such calculations give average estimates of probable drug treatment costs and would improve if real world data can be collected.

Conflicts of interest

The authors declare that they have no conflicts of interest.

Financial disclosure

This study was not funded.

Disclosure of results at meeting

Preliminary results of this study were presented as a poster during ESMO 2017, Madrid.

Institutional review

All authors have read and approved the final manuscript.
Table B1.

Estimated drug treatment costs based on different package forms of the active substances

Active substanceLarge package form and strength of drugEstimated treatment cost (large package)Small package form and strength of drugEstimated treatment cost (small package)
BevacizumabConcentrate for solution infusion 25mg/ml 16 ml€51,836.10Concentrate for solution infusion 25mg/ml 4 ml€51,835.28
BevacizumabInjection fluid 25mg/ml 0.15 ml€174,399.68Injection fluid 25mg/ml 0.05 ml€603,691.20
CapecitabinTablet 500 mg€339.55Tablet 150 mg€1,131.84
CyclophosphamidePowder injection fluid 2000 mg€227.25Powder injection fluid 500 mg€251.90
DocetaxelConcentrate for solution infusion 10mg/ml 16 ml€5,338.08Concentrate for solution infusion 20mg/ml 1 ml€2,865.98
DocetaxelConcentrate for solution infusion 20mg/ml 8 ml€5,264.81Concentrate for solution infusion 10mg/ml 2 ml€2,643.38
DoxorubicinConcentrate for solution infusion 2mg/ml 25 ml€641.65Powder for solution infusion 50 mg€6,354.32
DoxorubicinPowder for solution infusion 50 mg€6,354.32Concentrate for solution infusion 2mg/ml 10 ml€9,950.91
DoxorubicinInjection fluid 2mg/ml 100 ml€9,950.96Injection fluid 2mg/ml 5 ml€637.44
EpirubicinInjection fluid 2mg/ml 100 ml€1,561.51Infusion fluid 2mg/ml 5 ml€7,250.40
EpirubicinInfusion fluid 2mg/ml 100 ml€1,841.13Injection fluid 2mg/ml 5 ml€7,178.40
EribulinInjection fluid 0,44mg/ml 3 ml€8,551.01Injection fluid 0,44mg/ml 2ml€8,550.85
EverolimusTablet 10 mg€31,207.25Tablet 0.25 mg€16,888.38
EverolimusDispersible tablet 5 mg€21,254.31Dispersible tablet 0.25 mg€14,217.53
FluorouracilInjection fluid 50mg/ml 100 ml€4,136.00Crème 50mg/g 15 g€52.09
fluorouracilCrème 50mg/g 15 g€33.04Injection fluid 50mg/ml 5 ml€177.12
FulvestrantInjection fluid 50 mg/ml 5 ml€5,490.16Injection fluid 50 mg/ml 5 ml€5,490.16
GemcitabinPowder for solution infusion 2000 mg€1,824.52Powder for solution infusion 200 mg€2,603.36
GemcitabinConcentrate for solution infusion 100mg/ml 20 ml€2,418.96Concentrate for solution infusion 38 mg/ml 5.26 ml€1,411.00
GemcitabinInfusion fluid 10mg/ml 220 ml€2,277.94Infusion fluid 10mg/ml 120 ml€2,277.94
Goserelin AcetateImplantation stick 10.8 mg€865.92Implantation stick 3,6 mg€880.71
Ibandronic acidInjection fluid 1mg/ml 3ml€554.99Injection fluid 1mg/ml 3ml€851.38
Ibandronic acidTablet 150 mg€0.26Tablet 50 mg€2.40
LapatinibTablet 250 mg€18,682.30Tablet 250 mg€28,023.45
MegestrolTablet 160 mg€1,025.81Tablet 160 mg€1,025.81
MelphalanPowder for solution infusion 50 mg€985.34Powder for solution infusion 50 mg€4,138.43
MelphalanTablet 2 mg€500.85Tablet 2 mg€2,103.58
Mitomycin CPowder for injection fluid 40 mg€207.01Powder for injection fluid 2 mg€451.49
Mitoxantrone HydrochlorideConcentrate for solution infusion 2mg/ml 15 ml€1,486.01Concentrate for solution infusion 2mg/ml 5 ml€1,434.06
PaclitaxelConcentrate for solution infusion 6 mg/ml 100 ml€6,152.86Powder for solution infusion 100 mg€4,629.23
PaclitaxelPowder for solution infusion 100 mg€8,024.00Concentrate for solution infusion 6 mg/ml 5 ml€2,849.28
Pamidronate disodiumConcentrate for solution infusion 9mg/ml 10 ml€1,109.25Concentrate for solution infusion 3mg/ml 5 ml€1,384.41
Pamidronate disodiumInfusion fluid 0,18mg/ml 500 ml€131.09Infusion fluid 0,18mg/ml 500 ml€131.09
PertuzumabConcentrate for solution infusion 30mg/ml 14 ml€16,665.64Concentrate for solution infusion 30mg/ml 14 ml€16,665.64
ThiotepaPowder for solution infusion 100 mg€14,467.30Powder for solution infusion 15 mg€16,207.35
TrastuzumabInjection fluid 120mg/ml 5 ml€16,286.10Injection fluid 120mg/ml 5 ml€16,286.10
TrastuzumabPowder for solution infusion 150 mg€21,947.45Powder for solution infusion 150 mg€21,947.45
Trastuzumab emtansinePowder for solution infusion 160 mg€44,505.75Powder for solution infusion 100 mg€44,505.75
VinblastinInjection fluid 1mg/ml 10 ml€10,175.00Injection fluid 1mg/ml 10 ml€3,092.64
VincristineInjection fluid 1mg/ml 2 ml€517.39Injection fluid 1mg/ml 1 ml€517.41
  13 in total

1.  International variability in the reimbursement of cancer drugs by publically funded drug programs.

Authors:  P K Cheema; S Gavura; M Migus; B Godman; L Yeung; M E Trudeau
Journal:  Curr Oncol       Date:  2012-06       Impact factor: 3.677

2.  Actual costs of cancer drugs in 15 European countries.

Authors:  Wim H van Harten; Anke Wind; Paolo de Paoli; Mahasti Saghatchian; Simon Oberst
Journal:  Lancet Oncol       Date:  2015-12-04       Impact factor: 41.316

3.  Delivery of meaningful cancer care: a retrospective cohort study assessing cost and benefit with the ASCO and ESMO frameworks.

Authors:  Joseph C Del Paggio; Richard Sullivan; Deborah Schrag; Wilma M Hopman; Biju Azariah; C S Pramesh; Ian F Tannock; Christopher M Booth
Journal:  Lancet Oncol       Date:  2017-06-02       Impact factor: 41.316

4.  Cross-comparison of cancer drug approvals at three international regulatory agencies.

Authors:  N Samuel; S Verma
Journal:  Curr Oncol       Date:  2016-10-25       Impact factor: 3.677

5.  Updating the American Society of Clinical Oncology Value Framework: Revisions and Reflections in Response to Comments Received.

Authors:  Lowell E Schnipper; Nancy E Davidson; Dana S Wollins; Douglas W Blayney; Adam P Dicker; Patricia A Ganz; J Russell Hoverman; Robert Langdon; Gary H Lyman; Neal J Meropol; Therese Mulvey; Lee Newcomer; Jeffrey Peppercorn; Blase Polite; Derek Raghavan; Gregory Rossi; Leonard Saltz; Deborah Schrag; Thomas J Smith; Peter P Yu; Clifford A Hudis; Julie M Vose; Richard L Schilsky
Journal:  J Clin Oncol       Date:  2016-05-31       Impact factor: 44.544

6.  Cancer statistics, 2016.

Authors:  Rebecca L Siegel; Kimberly D Miller; Ahmedin Jemal
Journal:  CA Cancer J Clin       Date:  2016-01-07       Impact factor: 508.702

7.  Circulating tumor cells as prognostic and predictive markers in metastatic breast cancer patients receiving first-line systemic treatment.

Authors:  Mario Giuliano; Antonio Giordano; Summer Jackson; Kenneth R Hess; Ugo De Giorgi; Michal Mego; Beverly C Handy; Naoto T Ueno; Ricardo H Alvarez; Michelino De Laurentiis; Sabino De Placido; Vicente Valero; Gabriel N Hortobagyi; James M Reuben; Massimo Cristofanilli
Journal:  Breast Cancer Res       Date:  2011-06-15       Impact factor: 6.466

8.  A multiplexed marker-based algorithm for diagnosis of carcinoma of unknown primary using circulating tumor cells.

Authors:  Elizabeth M Matthew; Lanlan Zhou; Zhaohai Yang; David T Dicker; Sheldon L Holder; Bora Lim; Ramdane Harouaka; Si-Yang Zheng; Joseph J Drabick; Nicholas E Lamparella; Cristina I Truica; Wafik S El-Deiry
Journal:  Oncotarget       Date:  2016-01-26

9.  Responsible pricing in value-based assessment of cancer drugs: real-world data are an inevitable addition to select meaningful new cancer treatments.

Authors:  Wim van Harten; Maarten J IJzerman
Journal:  Ecancermedicalscience       Date:  2017-09-11

Review 10.  Detecting Blood-Based Biomarkers in Metastatic Breast Cancer: A Systematic Review of Their Current Status and Clinical Utility.

Authors:  A M Sofie Berghuis; Hendrik Koffijberg; Jai Prakash; Leon W M M Terstappen; Maarten J IJzerman
Journal:  Int J Mol Sci       Date:  2017-02-09       Impact factor: 5.923

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