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COSIMO – patients with active cancer changing to rivaroxaban for the treatment and prevention of recurrent venous thromboembolism: a non-interventional study

Abstract

Background

Around 20% of venous thromboembolism (VTE) cases occur in patients with cancer. Current guidelines recommend low molecular weight heparin (LMWH) as the preferred anticoagulant for VTE treatment. However, some guidelines state that vitamin K antagonists (VKAs) and direct oral anticoagulants (DOACs) are acceptable alternatives for long-term therapy in some patients if LMWHs are not available. LMWHs and VKAs have a number of drawbacks that can increase the burden on patients. DOACs, such as rivaroxaban, can ameliorate some burdens and may offer an opportunity to increase patient satisfaction and health-related quality of life (HRQoL). The Cancer-associated thrOmboSIs – patient-reported outcoMes with rivarOxaban (COSIMO) study is designed to provide real-world information on treatment satisfaction in patients with active cancer who switch from LMWH or VKA to rivaroxaban for the treatment of acute VTE or to prevent recurrent VTE.

Methods

COSIMO is a prospective, non-interventional, single-arm cohort study that aims to recruit 500 patients in Europe, Canada and Australia. Adults with active cancer who are switching to rivaroxaban having received LMWH/VKA for the treatment and secondary prevention of recurrent VTE for at least the previous 4 weeks are eligible. Patients will be followed for 6 months. The primary outcome is treatment satisfaction assessed as change in the Anti-Clot Treatment Scale (ACTS) Burdens score at week 4 after enrolment compared with baseline. Secondary outcomes include treatment preferences, measured using a discrete choice experiment, change in ACTS Burdens score at months 3 and 6, and change in HRQoL (assessed using the Functional Assessment of Chronic Illness Therapy – Fatigue questionnaire). COSIMO will collect data on patients’ medical history, patterns of anticoagulant use and incidence of bleeding and thromboembolic events. Study recruitment started in autumn 2016.

Conclusions

COSIMO will provide information on outcomes associated with switching from LMWH or VKA therapy to rivaroxaban for the treatment or secondary prevention of cancer-associated thrombosis in a real-life setting. The key goal is to assess whether there is a change in patient-reported treatment satisfaction. In addition, COSIMO will facilitate the evaluation of the safety and effectiveness of rivaroxaban in preventing recurrent VTE in this patient population.

Trial registration

NCT02742623. Registered 19 April 2016.

Background

Cancer and its treatments (e.g. chemotherapeutic or anti-angiogenic agents) are well-established risk factors for venous thromboembolism (VTE) [1], and up to 20% of patients with active cancer will develop VTE, depending on the cancer type, stage and treatment [2, 3]. Cancer-associated thrombosis (CAT) has a significant impact on prognosis and patients’ quality of life (QoL). CAT is a leading cause of death among patients with cancer [4]; survivors of an initial event are at higher risk of recurrent events and bleeding during anticoagulation therapy compared with patients with VTE without malignancy [3, 5]. In the CLOT, CATCH and DALTECAN studies evaluating low molecular weight heparin (LMWH) therapy for the treatment of CAT, the residual risk of a recurrent event with 6 months’ LMWH therapy was ~7–9%, and that for major bleeding was ~2–6% [6,7,8]. CAT not only adds to the symptomatic burden of cancer but also to the treatment burden and emotional trauma caused by cancer and its treatment [9]. The risk of CAT is at its highest in the first few months after cancer diagnosis [10], and patients may already require multiple concurrent anti-neoplastic and supportive therapies during this time. Furthermore, the occurrence of CAT may delay critical treatments for cancer, including chemotherapy and surgery [11].

Current guidelines for the treatment of CAT recommend LMWH for initial and long-term (at least 3–6 months) therapy [12,13,14,15]. The American Society of Clinical Oncology (ASCO) guidelines also consider vitamin K antagonists (VKAs) as an acceptable alternative for long-term therapy if LMWHs are not available [16]. Although efficacious, both LMWH and VKAs have drawbacks that impose significant challenges in the care of patients with CAT: daily injections and a risk of heparin-induced thrombocytopenia with LMWHs, and frequent international normalised ratio monitoring and numerous food and drug interactions with VKAs [17].

Direct oral anticoagulants (DOACs; apixaban, dabigatran, edoxaban and rivaroxaban) were developed to overcome some of the limitations associated with traditional anticoagulants, and are now recommended over [15] or as an alternative [18] to LMWH/VKA therapy for long-term VTE treatment in patients without cancer. They have the potential benefits of fixed-dosing, no requirement for routine coagulation tests and few drug or food interactions, in addition to oral administration [17]. The phase III Hokusai-VTE-Cancer and select-d pilot trials provided the first randomised comparisons of edoxaban and rivaroxaban, respectively, versus dalteparin for the treatment of CAT, supporting their use in some patients [19, 20]. Recently published international guidance suggests that DOACs can be considered for treatment of CAT in patients with stable cancer not receiving systemic anti-cancer therapy, and in cases where a VKA is an acceptable treatment choice [21]; this is also reflected in the most recent American College of Chest Physicians guidelines update [15].

The burden of care associated with traditional anticoagulation therapies for CAT may explain the high levels of non-adherence to current guidelines and frequent switching between anticoagulation therapies in clinical practice. In Europe, over 90% of patients receiving treatment for active cancer and first VTE are initially prescribed LMWH for the prevention of VTE recurrence; approximately 30% are subsequently switched to VKAs for long-term therapy (Fig. 1) [22]. In a retrospective analysis of 52,911 patients with CAT from the US MarketScan Treatment Pathways database, 50% of patients were initially prescribed warfarin [23] despite guidelines recommending LMWH [16]. Furthermore, of the 40% of patients initially prescribed LMWH, 44% switched to another anticoagulant within 1 month [23]. Patient involvement and treatment satisfaction are increasingly emphasised as key to improving adherence with long-term therapy [24, 25]. Unfortunately, there is only limited real-world information on patient satisfaction with or preferences for different anticoagulants for CAT treatment [25].

Fig. 1
figure 1

Initial and long-term anticoagulant therapy in patients with cancerb and a first episode of VTE – data from the RIETE registry [22]. aIncludes unfractionated heparin and thrombolytic agents. bDefined as newly diagnosed cancer, metastatic cancer or cancer undergoing treatment. LMWH, low molecular weight heparin; PE, pulmonary embolism; VKA, vitamin K antagonist; VTE, venous thromboembolism

This paper presents the study design and rationale for the Cancer-associated thrOmboSIs – patient-reported outcoMes with rivarOxaban (COSIMO) study, which aims to collect prospective real-world data on patient satisfaction with anticoagulation treatment after a switch from LMWH or VKA to rivaroxaban in patients with cancer. In addition, COSIMO will facilitate the evaluation of adverse events (AEs) and the recurrence of VTE with rivaroxaban in this patient population. COSIMO is part of the Cancer Associated thrombosis – expLoring soLutions for patients through Treatment and Prevention with RivarOxaban (CALLISTO) programme (Table 1) [20].

Table 1 Studies included in the CALLISTO programmea

Methods

Study design and patient population

COSIMO is a prospective, non-interventional, single-arm cohort study that is recruiting patients at approximately 70 sites across Australia, Belgium, Canada, Denmark, France, Germany, Italy, Netherlands, Spain and the UK.

Adults with active cancer and acute deep vein thrombosis (DVT) and/or pulmonary embolism (PE), or with recurrent VTE, who are scheduled to be switched to rivaroxaban after having received standard of care (SOC) anticoagulation therapy (either LMWH or a VKA) for CAT for ≥4 weeks are eligible. Patients with an Eastern Cooperative Oncology Group (ECOG) performance status score of 0, 1 or 2 will be included. ‘Active cancer’ includes cancer (other than fully treated basal cell or squamous cell carcinoma of the skin) that has been diagnosed or treated within the previous 6 months, or recurrent or metastatic cancer. Inclusion and exclusion criteria are shown in Table 2.

Patients enrolled into the study will be observed for 6 months. Treatment duration is at the physician’s discretion and is not dependent on the initially scheduled treatment duration. In addition to contact at enrolment and the end of the 6-month observational period, patients should undergo two follow-up visits (at approximately week 4 and month 3; timepoints of interest for data collection) (Fig. 2). Owing to the observational nature of the study, the protocol does not define the exact dates for the two follow-up visits, and investigators are advised to schedule these to coincide with regular physician appointments.

Fig. 2
figure 2

COSIMO – study design and data collection. aDCE per telephone interview 4–12 weeks after starting rivaroxaban treatment. bPatients treated for at least 4 weeks of SOC anticoagulation therapy with LMWH or VKA therapy. cFor previous anticoagulation therapy. dFor rivaroxaban treatment. eIncluding anti-cancer medication. fHaemoglobin, haematocrit, white blood cells, platelets, electrolytes, C-reactive protein, serum creatinine, CrCl, liver enzymes and haemoccult test. ACTS, Anti-Clot Treatment Scale; CrCl, creatinine clearance; DCE, discrete choice experiment; DVT, deep vein thrombosis; FACIT, Functional Assessment of Chronic Illness Therapy – Fatigue questionnaire; LMWH, low molecular weight heparin; PE, pulmonary embolism; SOC, standard of care; VKA, vitamin K antagonist

Study outcomes

The primary outcome of the COSIMO study is treatment satisfaction, assessed as change in the Anti-Clot Treatment Scale (ACTS) Burdens score [26] from enrolment to week 4. Secondary outcomes include patient preferences with regard to convenience attributes; the change in ACTS Burdens score at month 3 and month 6; change in health-related QoL (HRQoL); patterns of anticoagulant use and incidence of bleeding, thromboembolic events and other AEs and serious AEs.

Data collection and management

Data collection is illustrated in Fig. 2. Treatment-related data will be collected at baseline and during visits that take place in routine clinical practice. Data will be recorded in an electronic case report form. The information collected at enrolment will include prior medical history and current co-morbidities, current and previous medication, a description of the index venous thromboembolic event and its treatment, and the results of routine laboratory tests. The reasons for switching to rivaroxaban, planned treatment duration and dose will also be recorded.

Treatment satisfaction will be measured using the self-administered ACTS questionnaire. Patients will be asked to complete the questionnaire at enrolment and, after the initiation of rivaroxaban therapy, at approximately week 4, month 3 and month 6 (end of the observation period). During this time, the investigator may decide to change anticoagulation therapy; in these circumstances, the patient would remain in the study until the end of the 6-month follow-up period but would not need to complete any further ACTS questionnaires. The Functional Assessment of Chronic Illness Therapy (FACIT) Fatigue questionnaire will be used to assess HRQoL and will be completed alongside the ACTS questionnaire at enrolment, during the two follow-up visits and at the end of the observation period. Information on convenience-related patient preferences in anticoagulation treatment will be collected by means of a discrete choice experiment (DCE) in a semi-structured telephone interview. Patients will be asked to volunteer to take part in the DCE, which will be conducted by telephone at 4–12 weeks after enrolment.

AEs and serious AEs will be documented up to the completion of the 6-month observation period or up to 30 days after rivaroxaban discontinuation, whichever occurs earlier. Bleeding events (collected as serious AEs or non-serious AEs) will be adjudicated and categorised as major or non-major bleeding. Thromboembolic events, including incidental thromboembolic events documented in routine imaging (e.g. incidental PE from staging computed tomography; collected as serious AEs or non-serious AEs) will be adjudicated and categorised (symptomatic or incidental). An independent Central Adjudication Committee of four expert physicians will adjudicate major bleeding and thromboembolic events (recurrent VTE, other thromboembolic events, major adverse cardiovascular events). All events resulting in death (as reported by the investigator) will be adjudicated. Causes of death will be categorised as being related to cancer, thrombosis, bleeding, infectious diseases or other.

In cases of rivaroxaban discontinuation, the reason for permanent cessation and potential switch to another anticoagulant will be documented.

Study questionnaires

The ACTS questionnaire uses a five-point Likert scale, ranging from ‘5 = not at all’ to ‘1 = extremely’, to assess patient response [26] (Additional file 1). It is a self-administered instrument that includes 13 items about the burden of anticoagulant therapy (bleeding, bruising, limitation of activities, food and drink limitations, need to avoid other medications, daily inconveniences, occasional inconveniences, adherence issues, time spent on regimen, anxiety, frustration and overall burden), and four items about the benefits of anticoagulant therapy (confidence, reassurance, satisfaction and overall benefit) [26]. The use of separate subscales for ACTS Burdens and Benefits means that it will be possible to focus specifically on the burdens of anticoagulant therapy as the primary outcome [26]. Because the ACTS questionnaire has a recall period of 4 weeks, data should be collected between -2 to +4 weeks around each visit. Further information is given in Additional file 1.

During the DCE, participants will be asked to make a choice between options ‘A’ and ‘B’ across nine treatment scenarios (plus a control scenario) on pictorial charts, considering differing combinations of utility-increasing and utility-decreasing attribute levels (trade-off type of choice) [27]. The aim of the DCE is to define the ideal anticoagulant treatment from the perspective of patients with CAT (Additional file 2).

FACIT Fatigue is a 13-item questionnaire that assesses feelings of tiredness, weakness, listlessness, frustration, energy levels, ability to perform daily tasks (including eating) and need for help to complete tasks [28]. Patients will score each item on a five-point (0 to 4) scale; a higher score indicates better HRQoL (Additional file 3).

Sample size calculation

The sample size calculation was based on the primary outcome, a change in ACTS Burdens score at week 4 after enrolment compared with baseline. Based on data from the XALIA cancer subgroup analysis (data on file) [29], the mean difference in ACTS Burdens score between enrolment and week 4 was assumed to be 1.3, with a standard deviation of 8.0 considered reasonable. Based on these assumptions, 300 patients will be needed to reach a power of 80% for the primary analyses. Considering high drop-out rates in this patient population [6], 375 patients should be included to ensure sufficient numbers for the primary analyses. Given the heterogeneous nature of the cancer population and expected high drop-out rates after week 4, the COSIMO study aims to enrol 500 patients overall to have sufficient numbers for the secondary analyses.

Statistical analyses

Analyses will generally include all patients who received at least one dose of rivaroxaban, and who completed the ACTS questionnaire at the particular time point being assessed (e.g. week 4, month 3 or month 6). The questionnaire responses are multiple measurements on patient-reported treatment satisfaction over time; therefore, a mixed model repeated measures analysis will be used to analyse the data. The null hypothesis is no change in ACTS Burdens score between enrolment and week 4; hypothesis testing will be at a 5% significance level. The change in the ACTS Burdens score is assumed to be normally distributed and will be analysed using a paired t-test. The assumption of normality will be tested using the Shapiro–Wilk test at the 0.10 level of significance. If the test shows significance, the Wilcoxon signed-rank test will be used. For missing items, imputation to the mean will be used where there are >50% of the questions (>6 items for ACTS Burdens) completed. Otherwise, the item will be regarded as a missing value. Subgroup analyses, by type and duration of SOC therapy and by reason for switching from SOC, will be provided. Sensitivity analyses will be conducted to investigate the potential impact of patients discontinuing the study earlier than week 4 on the outcome.

Discussion

For some patients undergoing treatment for cancer, the necessity for anticoagulant therapy may be regarded as an added burden [30]. LMWHs are recommended as first-line therapy for acute and long-term treatment of CAT in clinical guidelines; nevertheless, many patients with CAT are switched to, or even initiated on, a VKA [22, 23], possibly because of a preference for oral over injectable therapies [25] or for cost reasons. DOACs such as rivaroxaban are considered more convenient than VKAs because of their simple dosing regimens and lack of the need for routine coagulation monitoring [31, 32]. A subgroup analysis of pooled results from EINSTEIN DVT and EINSTEIN PE demonstrated that the rate of recurrent VTE was similarly reduced in patients treated with rivaroxaban or enoxaparin/VKA therapy, and that the number of major bleeding events was reduced with rivaroxaban therapy in patients with or without active cancer [33]. More recently, the efficacy and safety of edoxaban and rivaroxaban for the treatment of CAT have been demonstrated in the first randomised head-to-head comparisons with a LMWH (dalteparin) in the phase III Hokusai-VTE-Cancer study [34] and the phase III pilot study select-d [20], respectively. Several studies on the use of rivaroxaban for the treatment of CAT in clinical practice have also been published; these results provide some reassurance that rivaroxaban is safe and effective in this clinical setting [29, 35,36,37]. Furthermore, in the EINSTEIN studies, patients treated with rivaroxaban reported greater treatment satisfaction than patients treated with enoxaparin/VKA, as measured by the ACTS questionnaire [32, 38]. The role of DOACs in the treatment and secondary prevention of CAT is being investigated in ongoing studies [39,40,41,42,43].

The COSIMO study aims to collect real-world data in consecutive patients with cancer switching from SOC therapy (LMWH or VKA) to rivaroxaban in circumstances where SOC therapy cannot be continued [44]. The study began recruiting patients in October 2016. The primary outcome is a change in patient-reported treatment satisfaction (specifically, the ACTS Burdens score) between baseline (the point of switching) and week 4. Treatment satisfaction will also be measured at month 3 and at the end of the 6-month observation period, so that changes in ACTS Burdens and Benefits scores can be compared over time. Effectiveness and safety data will be gathered through AE reporting by study investigators. To improve the current understanding of treatment needs, comprehensive data on cancer type and stage, treatment patterns and clinical management will be collected. In this regard, COSIMO will provide prospective real-world data on the effectiveness and safety of rivaroxaban according to cancer type and stage, as well as on overlapping toxicities and interactions between rivaroxaban and anti-cancer therapies. COSIMO will also contribute important information on the management of challenging patient populations with CAT, such as patients in whom AEs occur because of chemotherapeutic agents (e.g. thrombocytopenia) or patients who require surgery or other interventions (biopsies, etc.).

Table 2 Inclusion and exclusion criteria for the COSIMO study

COSIMO is a non-interventional study; therefore, the inclusion and exclusion criteria are deliberately minimal, to mirror real-world practice. However, there are some restrictions to enrolment to ensure the following: the welfare of the population under study (e.g. inclusion is restricted to patients with an ECOG performance status score of ≤2) and alignment with current guideline recommendations (e.g. exclusion of patients pre-treated with anticoagulants other than SOC). These criteria will also ensure a level of study homogeneity for the facilitation of data analyses.

The choice of instruments for evaluating HRQoL is critical for accurate interpretation of patient self-reporting. The COSIMO study will use the ACTS and a DCE to record patient treatment satisfaction and preferences, respectively, and FACIT Fatigue instruments to measure changes in HRQoL relating to the cancer itself.

The ACTS questionnaire is specific for anticoagulation and, therefore, the score should not be affected by the patient’s cancer stage and/or cancer treatment. It is a modified form of the Duke Anticoagulation Satisfaction Scale, a 25-item, single scale, which is used to assess limitations, inconveniences and/or discomforts, as well as positive impacts, related to anticoagulant treatment [45]. ACTS was validated using data from the EINSTEIN DVT study [31], which included patients with acute symptomatic DVT treated with rivaroxaban or enoxaparin/VKAs [46]. A rigorous development process was used to ensure that it was appropriate for patients with atrial fibrillation and VTE globally [31]. The DCE is a validated tool for assessing patient preference for anticoagulation therapy [47,48,49].

Fatigue is one of the most common side effects in patients with cancer who are receiving cancer therapy [28, 50], and it may have a pervasive effect on treatment satisfaction. The FACIT Measurement System offers several benefits for measuring HRQoL in people with cancer and other chronic diseases and has proven utility for measuring change in HRQoL in observational studies [51, 52]. The content was developed jointly by experts and patients, and the scales have been validated in patients with different forms of cancer [52].

One of the limitations of this study is that it was not designed to examine the impact of cancer subtypes, or other potential confounding factors that vary over time, on outcomes. An additional limitation, which applies to all studies enrolling patients with cancer, is the high discontinuation rates over time. Nonetheless, this should have minimal impact on the primary outcome, which is measured at week 4 after initiation of treatment with rivaroxaban; there would likely be minimum impact on other outcomes. There might also be the potential to overestimate treatment satisfaction with rivaroxaban due to selection bias, because the patients eligible for COSIMO (or their physicians) had chosen not to continue with SOC treatment. Finally, the lack of a control patient cohort might make it difficult to put the results into perspective, but finding a matched comparator group of patients with CAT would have been a major challenge.

Conclusions

The ongoing COSIMO study is designed to evaluate satisfaction with anticoagulation treatment in patients with active cancer who are at risk of recurrent VTE or have switched from LMWH/VKA to rivaroxaban. It will also evaluate the safety and effectiveness of rivaroxaban in preventing recurrent VTE in this important patient population. The evaluation tools in this study – the ACTS and FACIT Fatigue questionnaires and a DCE focused on treatment preferences – have been specifically chosen to provide information that might help guide the future management and treatment of patients coping with serious concurrent illnesses.

Abbreviations

ACTS:

Anti-Clot Treatment Scale

AE:

Adverse event

CALLISTO:

Cancer Associated thrombosis – expLoring soLutions for patients through Treatment and Prevention with RivarOxaban

CAT:

Cancer-associated thrombosis

COSIMO:

Cancer-associated thrOmboSIs – patient-reported outcoMes with rivarOxaban

DCE:

Discrete choice experiment

DOAC:

Direct oral anticoagulant

DVT:

Deep vein thrombosis

ECOG:

Eastern Cooperative Oncology Group

FACIT:

Functional Assessment of Chronic Illness Therapy

HRQoL:

Health-related quality of life

LMWH:

Low molecular weight heparin

PE:

Pulmonary embolism

QoL:

Quality of life

SOC:

Standard of care

VKA:

Vitamin K antagonist

VTE:

Venous thromboembolism

References

  1. Ay C, Pabinger I, Cohen AT. Cancer-associated venous thromboembolism: burden, mechanisms, and management. Thromb Haemost. 2017;117:219–30.

    Article  PubMed  Google Scholar 

  2. Horsted F, West J, Grainge MJ. Risk of venous thromboembolism in patients with cancer: a systematic review and meta-analysis. PLoS Med. 2012;9:e1001275.

    Article  PubMed  PubMed Central  Google Scholar 

  3. Cohen AT, Katholing A, Rietbrock S, Bamber L, Martinez C. Epidemiology of first and recurrent venous thromboembolism in patients with active cancer. A population-based cohort study. Thromb Haemost. 2017;117:57–65.

    Article  PubMed  Google Scholar 

  4. Khorana AA, Francis CW, Culakova E, Kuderer NM, Lyman GH. Thromboembolism is a leading cause of death in cancer patients receiving outpatient chemotherapy. J Thromb Haemost. 2007;5:632–4.

    Article  PubMed  CAS  Google Scholar 

  5. Prandoni P, Lensing AWA, Piccioli A, Bernardi E, Simioni P, Girolami B, et al. Recurrent venous thromboembolism and bleeding complications during anticoagulant treatment in patients with cancer and venous thrombosis. Blood. 2002;100:3484–8.

    Article  PubMed  CAS  Google Scholar 

  6. Lee AY, Levine MN, Baker RI, Bowden C, Kakkar AK, Prins M, et al. Low-molecular-weight heparin versus a coumarin for the prevention of recurrent venous thromboembolism in patients with cancer. N Engl J Med. 2003;349:146–53.

    Article  PubMed  CAS  Google Scholar 

  7. Lee AY, Kamphuisen PW, Meyer G, Bauersachs R, Janas MS, Jarner MF, et al. Tinzaparin vs warfarin for treatment of acute venous thromboembolism in patients with active cancer: a randomized clinical trial. JAMA. 2015;314:677–86.

    Article  PubMed  CAS  Google Scholar 

  8. Francis CW, Kessler CM, Goldhaber SZ, Kovacs MJ, Monreal M, Huisman MV, et al. Treatment of venous thromboembolism in cancer patients with dalteparin for up to 12 months: the DALTECAN Study. J Thromb Haemost. 2015;13:1028–35.

    Article  PubMed  CAS  Google Scholar 

  9. Noble S, Prout H, Nelson A. Patients' Experiences of LIving with CANcer-associated thrombosis: the PELICAN study. Patient Prefer Adherence. 2015;9:337–45.

    Article  PubMed  PubMed Central  Google Scholar 

  10. Blom JW, Doggen CJ, Osanto S, Rosendaal FR. Malignancies, prothrombotic mutations, and the risk of venous thrombosis. JAMA. 2005;293:715–22.

    Article  PubMed  CAS  Google Scholar 

  11. Qureshi W, Ali Z, Amjad W, Alirhayim Z, Farooq H, Qadir S, et al. Venous thromboembolism in cancer: an update of treatment and prevention in the era of newer anticoagulants. Front Cardiovasc Med. 2016;3:24.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  12. Mandala M, Falanga A, Roila F. Management of venous thromboembolism (VTE) in cancer patients: ESMO Clinical Practice Guidelines. Ann Oncol. 2011;22(Suppl 6):vi85–92.

    PubMed  Google Scholar 

  13. Lyman GH, Bohlke K, Khorana AA, Kuderer NM, Lee AY, Arcelus JI, et al. Venous thromboembolism prophylaxis and treatment in patients with cancer: American Society of Clinical Oncology clinical practice guideline update 2014. J Clin Oncol. 2015;33:654–6.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  14. National Comprehensive Cancer Network. Cancer-associated venous thromboembolic disease, version 1.2016. National Comprehensive Cancer Network, Inc. 2016. http://excellence.acforum.org/Resource-Center/resource_files/1119-2017-12-13-101157.pdf. Accessed 27 October 2017.

  15. Kearon C, Akl EA, Ornelas J, Blaivas A, Jimenez D, Bounameaux H, et al. Antithrombotic therapy for VTE disease: CHEST guideline and expert panel report. Chest. 2016;149:315–52.

    Article  PubMed  Google Scholar 

  16. Lyman GH, Khorana AA, Kuderer NM, Lee AY, Arcelus JI, Balaban EP, et al. Venous thromboembolism prophylaxis and treatment in patients with cancer: American Society of Clinical Oncology clinical practice guideline update. J Clin Oncol. 2013;31:2189–204.

    Article  PubMed  CAS  Google Scholar 

  17. Wharin C, Tagalakis V. Management of venous thromboembolism in cancer patients and the role of the new oral anticoagulants. Blood Rev. 2014;28:1–8.

    Article  PubMed  CAS  Google Scholar 

  18. Konstantinides SV, Torbicki A, Agnelli G, Danchin N, Fitzmaurice D, Galiè N, et al. 2014 ESC Guidelines on the diagnosis and management of acute pulmonary embolism. Eur Heart J. 2014;35:3033–69.

    Article  PubMed  CAS  Google Scholar 

  19. Raskob GE, van Es N, Verhamme P, Carrier M, Di Nisio M, Garcia D, et al. Edoxaban for the treatment of cancer-associated venous thromboembolism. N Engl J Med. 2018;378:615–24.

    Article  PubMed  CAS  Google Scholar 

  20. Young AM, Marshall A, Thirlwall J, Chapman O, Lokare A, Hill C, et al. Comparison of an oral factor Xa inhibitor with low molecular weight heparin in patients with cancer with venous thromboembolism: results of a randomized trial (select-d). J Clin Oncol. 2018 https://doi.org/10.1200/jco.2018.78.8034. Jco2018788034

  21. Farge D, Bounameaux H, Brenner B, Cajfinger F, Debourdeau P, Khorana AA, et al. International clinical practice guidelines including guidance for direct oral anticoagulants in the treatment and prophylaxis of venous thromboembolism in patients with cancer. Lancet Oncol. 2016;17:e452–66.

    Article  PubMed  CAS  Google Scholar 

  22. Ageno W, Samperiz A, Caballero R, Dentali F, Di Micco P, Prandoni P, et al. Duration of anticoagulation after venous thromboembolism in real world clinical practice. Thromb Res. 2015;135:666–72.

    Article  PubMed  CAS  Google Scholar 

  23. Khorana AA, Yannicelli D, McCrae KR, Milentijevic D, Crivera C, Nelson WW, et al. Evaluation of US prescription patterns: Are treatment guidelines for cancer-associated venous thromboembolism being followed? Thromb Res. 2016;145:51–3.

    Article  PubMed  CAS  Google Scholar 

  24. Kirchhof P, Benussi S, Kotecha D, Ahlsson A, Atar D, Casadei B, et al. 2016 ESC Guidelines for the management of atrial fibrillation developed in collaboration with EACTS. Eur Heart J. 2016;37:2893–962.

    Article  PubMed  Google Scholar 

  25. Noble S, Matzdorff A, Maraveyas A, Holm MV, Pisa G. Assessing patients' anticoagulation preferences for the treatment of cancer-associated thrombosis using conjoint methodology. Haematologica. 2015;100:1486–92.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  26. Cano SJ, Lamping DL, Bamber L, Smith S. The Anti-Clot Treatment Scale (ACTS) in clinical trials: cross-cultural validation in venous thromboembolism patients. Health Qual Life Outcomes. 2012;10:120.

    Article  PubMed  PubMed Central  Google Scholar 

  27. Böttger B, Thate-Waschke IM, Bauersachs R, Kohlmann T, Wilke T. Preferences for anticoagulation therapy in atrial fibrillation: the patients' view. J Thromb Thrombolysis. 2015;40:406–15.

    Article  PubMed  CAS  Google Scholar 

  28. Kapoor A, Singhal MK, Bagri PK, Narayan S, Beniwal S, Kumar HS. Cancer related fatigue: A ubiquitous problem yet so under reported under recognized and under treated. South Asian J Cancer. 2015;4:21–3.

    Article  PubMed  PubMed Central  Google Scholar 

  29. Ageno W, Mantovani LG, Haas S, Kreutz R, Monje D, Schneider J, et al. Subgroup analysis of patients with cancer in XALIA: a noninterventional study of rivaroxaban versus standard anticoagulation for VTE. TH Open. 2017;1:e33–42.

    Article  Google Scholar 

  30. Lee AY, Bauersachs R, Janas MS, Jarner MF, Kamphuisen PW, Meyer G, et al. CATCH: a randomised clinical trial comparing long-term tinzaparin versus warfarin for treatment of acute venous thromboembolism in cancer patients. BMC Cancer. 2013;13:284.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  31. Bamber L, Wang MY, Prins MH, Ciniglio C, Bauersachs R, Lensing AWA, et al. Patient-reported treatment satisfaction with oral rivaroxaban versus standard therapy in the treatment of acute symptomatic deep-vein thrombosis. Thromb Haemost. 2013;110:732–41.

    Article  PubMed  CAS  Google Scholar 

  32. Prins MH, Bamber L, Cano SJ, Wang MY, Erkens PM, Bauersachs R, et al. Patient-reported treatment satisfaction with oral rivaroxaban versus standard therapy in the treatment of pulmonary embolism; results from the EINSTEIN PE trial. Thromb Res. 2015;135:281–8.

    Article  PubMed  CAS  Google Scholar 

  33. Prins MH, Lensing AWA, Brighton TA, Lyons RM, Rehm J, Trajanovic M, et al. Oral rivaroxaban versus enoxaparin with vitamin K antagonist for the treatment of symptomatic venous thromboembolism in patients with cancer (EINSTEIN-DVT and EINSTEIN-PE): a pooled subgroup analysis of two randomised controlled trials. Lancet Haematol. 2014;1:e37–46.

    Article  PubMed  Google Scholar 

  34. Raskob GE, Van Es N, Verhamme P, Carrier M, Di Nisio M, Garcia DA, et al. Randomized, open-label, blinded outcome assessment trial evaluating the efficacy and safety of LMWH/edoxaban versus dalteparin for venous thromboembolism associated with cancer: Hokusai VTE-Cancer study. American Society of Hematology 59th Annual Meeting and Exposition. Atlanta, USA, 9–12 December 2017, Abstract LBA-6 A.

  35. Bott-Kitslaar DM, Saadiq RA, McBane RD, Loprinzi CL, Ashrani AA, Ransone TR, et al. Efficacy and safety of rivaroxaban in patients with venous thromboembolism and active malignancy: a single-center registry. Am J Med. 2016;129:615–9.

    Article  PubMed  CAS  Google Scholar 

  36. Mantha S, Laube E, Miao Y, Sarasohn DM, Parameswaran R, Stefanik S, et al. Safe and effective use of rivaroxaban for treatment of cancer-associated venous thromboembolic disease: a prospective cohort study. J Thromb Thrombolysis. 2017;43:166–71.

    Article  PubMed  CAS  Google Scholar 

  37. Hummert SE, Gilreath J, Rodgers GM, Wilson N, Stenehjem DD. Comparative evaluation of the safety and effectiveness of rivaroxaban (riva) and enoxaparin (enox) for treatment of venous thromboembolism (VTE) in cancer patients. J Clin Oncol. 2017;35:suppl.e18268.

  38. Bamber L, Cano SJ, Lamping DL, Wang MY, Prins MH, Bauersachs R, et al. Patient-reported treatment satisfaction with oral rivaroxaban versus standard therapy in the treatment of symptomatic deep vein thrombosis (DVT). J Thromb Haemost. 2011;9:859. Abstract P-TH-284

    Article  CAS  Google Scholar 

  39. Fadoi Foundation, University of Perugia. Apixaban for the treatment of venous thromboembolism in patients with cancer (CARAVAGGIO). 2018. https://clinicaltrials.gov/ct2/show/study/NCT03045406. Accessed 19 June 2018.

  40. McBane RD, Loprinzi CL, Ashrani A, Perez-Botero J, Leon Ferre RA, Henkin S, et al. Apixaban and dalteparin in active malignancy associated venous thromboembolism. The ADAM VTE Trial. Thromb Haemost. 2017;117:1952–61.

    Article  Google Scholar 

  41. Assistance Publique Hopitaux de Paris. Cancer associated thrombosis, a pilot treatment study using rivaroxaban (CASTA-DIVA). 2017. https://clinicaltrials.gov/ct2/show/NCT02746185. Accessed 19 June 2018.

  42. Riess H, Sinn M, Kreher S, für den Arbeitskreis Hämostaseologie der Deutschen Gesellschaft für Hämatologie und Medizinische Onkologie (DGHO). [CONKO-011: Evaluation of patient satisfaction with the treatment of acute venous thromboembolism with rivaroxaban or low molecular weight heparin in cancer patients. A randomized phase III study]. Dtsch Med Wochenschr. 2015;140(Suppl 1):S22–S3.

  43. Alliance Foundation Trials LLC, Patient-Centered Outcomes Research Institute. Direct oral anticoagulants versus LMWH +/- warfarin for VTE in cancer (CANVAS). 2017. https://clinicaltrials.gov/ct2/show/study/NCT02744092. Accessed 19 June 2018.

  44. Bach M, Bauersachs R. Spotlight on advances in VTE management: CALLISTO and EINSTEIN CHOICE. Thromb Haemost. 2016;116:S24–32.

    Article  PubMed  Google Scholar 

  45. Samsa G, Matchar DB, Dolor RJ, Wiklund I, Hedner E, Wygant G, et al. A new instrument for measuring anticoagulation-related quality of life: development and preliminary validation. Health Qual Life Outcomes. 2004;2:22.

    Article  PubMed  PubMed Central  Google Scholar 

  46. The EINSTEIN Investigators. Oral rivaroxaban for symptomatic venous thromboembolism. N Engl J Med. 2010;363:2499–510.

    Article  Google Scholar 

  47. Moia M, Mantovani LG, Carpenedo M, Scalone L, Monzini MS, Cesana G, et al. Patient preferences and willingness to pay for different options of anticoagulant therapy. Intern Emerg Med. 2013;8:237–43.

    Article  PubMed  Google Scholar 

  48. Reed Johnson F, Lancsar E, Marshall D, Kilambi V, Muhlbacher A, Regier DA, et al. Constructing experimental designs for discrete-choice experiments: report of the ISPOR Conjoint Analysis Experimental Design Good Research Practices Task Force. Value Health. 2013;16:3–13.

    Article  PubMed  CAS  Google Scholar 

  49. Ryan M. Discrete choice experiments in health care. BMJ. 2004;328:360–1.

    Article  PubMed  PubMed Central  Google Scholar 

  50. Cella D, Peterman A, Passik S, Jacobsen P, Breitbart W. Progress toward guidelines for the management of fatigue. Oncology (Williston Park ). 1998;12:369–77.

    PubMed  CAS  Google Scholar 

  51. Acaster S, Dickerhoof R, DeBusk K, Bernard K, Strauss W, Allen LF. Qualitative and quantitative validation of the FACIT-fatigue scale in iron deficiency anemia. Health Qual Life Outcomes. 2015;13:60.

    Article  PubMed  PubMed Central  Google Scholar 

  52. Webster K, Cella D, Yost K. The functional assessment of chronic illness therapy (FACIT) measurement system: properties, applications. and interpretation. Health Qual Life Outcomes. 2003;1:79.

    Article  PubMed  Google Scholar 

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Acknowledgements

The authors would like to acknowledge Hayley Dawson, who provided medical writing assistance, with funding from Bayer AG and Janssen Scientific Affairs, LLC.

Funding

The COSIMO study is funded by Bayer AG and Janssen Pharmaceuticals. MB is an employee of Bayer AG.

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Contributions

The authors are solely responsible for the design and conduct of this study; all study analyses, the drafting and editing of the manuscript, and its final contents. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Alexander T. Cohen.

Ethics declarations

Ethics approval and consent to participate

Documented approval from appropriate independent ethics committees/institutional review boards will be obtained for all participating centres prior to study start. Patients will be asked to provide signed informed consent forms before joining the study. Few patients have yet completed the study, and so no data are available to share.

Consent for publication

Not applicable.

Competing interests

ATC reports grants and personal fees from Bayer during the conduct of the study; personal fees from Boehringer Ingelheim, grants and personal fees from Bristol-Myers Squibb, grants and personal fees from Daiichi Sankyo Europe, personal fees from Johnson & Johnson, grants and personal fees from Pfizer, personal fees from Portola, personal fees from Sanofi, personal fees from XO1, personal fees from Janssen, personal fees from ONO Pharmaceuticals, outside the submitted work; AM reports personal fees and non-financial support from Bayer, during the conduct of the study; personal fees and non-financial support from Bayer, grants from Bristol-Myers Squibb, other from Pfizer, outside the submitted work; JB-W reports grants and personal fees from Bayer, grants and personal fees from Boehringer Ingelheim, grants and personal fees from Daiichi Sankyo, grants and personal fees from Pfizer, outside the submitted work; AYYL reports other from Bayer, during the conduct of the study; LGM reports personal fees from Bayer, during the conduct of the study; grants and personal fees from Boehringer Ingelheim, personal fees from Pfizer, grants from Daiichi Sankyo, outside the submitted work; MB is an employee of Bayer AG.

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Additional files

Additional file 1:

Anti-Clot Treatment Scale (ACTS). (DOCX 30 kb)

Additional file 2:

Discrete Choice Experiment (DCE). (DOCX 26 kb)

Additional file 3:

Functional Assessment of Chronic Illness Therapy (FACIT) Fatigue score. (DOCX 27 kb)

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Cohen, A.T., Maraveyas, A., Beyer-Westendorf, J. et al. COSIMO – patients with active cancer changing to rivaroxaban for the treatment and prevention of recurrent venous thromboembolism: a non-interventional study. Thrombosis J 16, 21 (2018). https://doi.org/10.1186/s12959-018-0176-2

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