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Psychometric properties of the FACT-M questionnaire in patients with Merkel cell carcinoma

The Correction to this article has been published in Health and Quality of Life Outcomes 2019 17:52

Abstract

Background

No validated disease-specific questionnaires exist to capture health-related quality of life (HRQoL) in patients with Merkel cell carcinoma (MCC). The Functional Assessment of Cancer Therapy – Melanoma (FACT-M) is validated in patients with melanoma, which shares many similarities with MCC. This paper reports the psychometric properties of the FACT-M in the metastatic MCC population.

Methods

Data were collected as part of a single-arm, open-label, multicenter trial involving patients with metastatic MCC who had failed at least one previous line of chemotherapy. FACT-M and EQ-5D were administered at baseline, Week 7, Week 13, and Week 25. An optional interview was administered at the same time points. MCC-specific FACT-M scores were derived following a combined quantitative and qualitative approach. Reliability and construct validity of original and additional MCC-specific FACT-M scores were assessed at baseline. Capacity to detect change in tumor size was assessed from baseline to Week 7. Minimally important differences (MIDs) were computed using distribution and anchor-based methods.

Results

Baseline assessments were available in 70 patients (mean age: 70 years; 74.3% male); 19 patients were interviewed at baseline. Additional MCC-specific scores were as follows: Physical Function score (six items), Psychological Impact score (six items), and MCC summary score (12 items). FACT-M original and additional MCC-specific scores both demonstrated acceptable psychometric properties: high reliability (Cronbach’s alpha: 0.81–0.96), good convergent validity (correlations above 0.4 observed for 88% of items of the Melanoma surgery scale, 75% of items of the Melanoma scale, and 100% of items of the other FACT-M domains). Some evidence of floor/ceiling effects and poor discriminant ability was found. Higher scores (better HRQoL) on all FACT-M domains were observed in patients with better functioning (assessed by ECOG performance score), supporting clinical validity. Despite the small sample for responsiveness analysis (n = 37), the majority of FACT-M scores showed sensitivity to changes in tumor size at Week 7 with small to moderate effect sizes. MIDs were consistent with previously reported values in the literature for FACT-M domains.

Conclusions

FACT-M is suitable to capture HRQoL in patients with metastatic MCC, thus making it a potential candidate for assessing HRQoL in MCC trials.

Trial registration

This study is a post-hoc analysis conducted on data collected in Part A of the JAVELIN Merkel 200 trial. This trial was registered on 2 June 2014 with ClinicalTrials.gov as NCT02155647.

Background

Merkel cell carcinoma (MCC) is a rare and aggressive skin cancer associated with Merkel cell polyomavirus, exposure to ultraviolet irradiation, immunosuppression, and old age [1, 2]. MCC occurs with an incidence of 0.2–0.4 cases per 100,000 people per year in Europe, 0.8 cases per 100,000 people per year in the United States of America, and 1.6 cases per 100,000 people per year in Australia [3,4,5]. The 5-year overall survival rate with metastatic MCC ranges from 0% to 18% based on retrospective analyses [6,7,8,9].

MCC is challenging to treat in metastatic stages due to limited treatment options and lack of standard therapeutic procedures. Avelumab is an anti-PD-L1 monoclonal antibody recently approved by the Food and Drug Administration (FDA) to treat patients 12 years and older with metastatic MCC (mMCC). Approval was based on data from an open-label, single-arm, multicenter clinical trial (JAVELIN Merkel 200 trial) including a cohort of patients who had previously progressed after chemotherapy for distant metastatic disease (Part A) as well as early data from patients naïve to systemic therapy in the metastatic setting (Part B) demonstrating a clinically meaningful and durable overall response rate [10,11,12].

The relevance of the assessment of how patients function and feel from their direct perspective is an important clinical endpoint in the literature. It has also been highlighted by both the FDA and the European Medicines Agency [13, 14]. Recently, the FDA emphasized the importance of patient-reported evaluation of disease-related symptoms, treatment-related symptoms, and physical functioning [15]. Questionnaires available to collect patient-reported outcomes (PROs) in patients with non-melanoma skin cancer and malignant melanoma were identified in a systematic literature review conducted in 2012 [16]. Nine cancer and skin cancer-specific PRO measures were identified for which adequate evidence of psychometric properties were available. Of these, the Functional Assessment of Cancer Therapy – General (FACT-G) and Functional Assessment of Cancer Therapy – Melanoma (FACT-M) provided evidence of acceptable psychometric properties. The FACT-G was only evaluated in patients with non-melanoma skin cancers. The FACT-M had more promising characteristics for patients with malignant melanomas, especially those with advanced disease, with good internal consistency of all scales, high reproducibility, and good sensitivity [17, 18]. In addition, significant correlations were reported between the FACT-M and other questionnaires measuring similar constructs (European Organisation for Research and Treatment of Cancer Quality of Life questionnaire [EORTC-QLQ] Melanoma; Profile of Mood States). Finally, the FACT-M was shown to distinguish between disease stages with significantly lower scores in patients with advanced (stages III or IV) melanoma than in patients with early-stage melanoma [19].

No validated disease-specific tools exist to capture health-related quality of life (HRQoL) in patients with MCC. The FDA encourages the use of adapted questionnaires in oncology, provided that the adaptation and validation follow a rigorous, scientific and sound approach [20]. As melanoma and MCC share many similarities, both being aggressive skin cancers, the FACT-M was considered as a potentially adequate tool to assess HRQoL in the MCC population. However, FACT-M psychometric properties have yet to be confirmed in patients with MCC.

This study was conducted to assess the reliability and validity of the FACT-M questionnaire in patients with mMCC.

Methods

Study design

A specific statistical analysis investigating psychometric properties of the FACT-M questionnaire in patients with mMCC was conducted on data collected in the avelumab clinical trial JAVELIN Merkel 200 (NCT02155647, [10]). This single-arm, open-label, multicenter trial was conducted in the United States of America, Europe, Australia, and Japan. Enrolled patients were male and female adults with histologically proven mMCC and an Eastern Cooperative Oncology Group performance status (ECOG PS) of 0 or 1 at trial entry, who had failed at least one line of chemotherapy. During the trial, patients received avelumab at a dose of 10 mg/kg as a 1-h intravenous infusion once every 2 weeks until significant clinical deterioration, unacceptable toxicity, or any criterion for withdrawal from the trial or trial drug was fulfilled. The primary analysis of the trial was performed in patients with a minimum of 6 months follow-up (date of data cutoff March 3, 2016), and the results have been published in Kaufman et al. (2016) [10, 11].

Data collected

HRQoL was assessed during the JAVELIN Merkel 200 trial using a generic questionnaire (EuroQol-5 Dimensions [EQ-5D), a melanoma-specific questionnaire (FACT-M), and optional subject qualitative interviews. FACT-M and EQ-5D were collected at sites using electronic tablets at baseline, throughout the treatment period (at Week 7 and then every 6 weeks) and at the End-of-Treatment visit. Optional qualitative patient interviews were conducted via telephone at baseline, Week 13, and Week 25.

Data used to assess the FACT-M psychometric properties were cut when all patients had at least 6 months of treatment follow up, and, as such, PRO data were available up to Week 25. Data collected during the baseline qualitative patient interviews were used to explore the content validity of the FACT-M in the MCC population.

FACT-M questionnaire

The FACT-M includes 51 items grouped into nine multi-item scores [17, 18]: six subscale scores and three summary scores. The six subscales consist of four subscales from the FACT-G (physical well-being [PWB], social well-being [SWB], emotional well-being [EWB], functional well-being [FWB]), one Melanoma scale, and one Melanoma surgery scale. The three summary scores include the FACT-M Trial Outcome Index (TOI), the FACT-G total score, and the FACT-M total score. The FACT-M administration guideline instructed patients to answer all items and select “Not at all” if they felt that the item was not applicable to them.

EQ-5D questionnaire

The EQ-5D is a self-administered, generic, utility questionnaire developed by the EuroQoL Group in 1990 [21]. It includes five single-item dimensions (mobility, self-care, usual activities, pain/discomfort, and anxiety/depression) and a vertical visual analogue scale (VAS) for the patients to rate their current health state. Patients must choose between five levels of difficulty in accomplishing tasks in each dimension (EQ-5D-5L). The responses to the five dimensions are used to create a utility index. In this study, utility values were calculated using country-specific value sets from the United States of America [22]. The VAS ranges from 0 (worst imaginable health state) to 100 (best imaginable health state).

Patient interviews

Interviews with patients were conducted to gather information regarding the impact of MCC and its treatments (radiotherapy or chemotherapy) on patients’ everyday lives, to assess patients’ experience of avelumab during the trial and to document the evolution of these experiences along the trial. Qualitative data obtained from these interviews were used to understand HRQoL concepts and symptoms in the MCC population, and these were compared to the concepts covered in the FACT-M in order to identify those most relevant items for mMCC patients.

Statistical analyses

Statistical analyses were conducted on the PRO analysis set (PAS), which included all patients from the trial intent-to-treat population (i.e. all patients who received at least one dose of trial treatment) who completed at least one item of each PRO (FACT-M and EQ-5D) at baseline.

Identified concepts of interest in the MCC population included Physical Function, Visual Lesion Impact, and Psychological Impact. These concepts were identified following qualitative research in MCC and regulatory guidance.

MCC-specific FACT-M scores were derived by first selecting only those FACT-M items that matched to at least some extent concepts identified from the qualitative interviews, then by selecting FACT-M items that matched concepts of interest, and finally by conducting a statistical analysis assessing psychometric properties, including a data-reduction technique (principal component analysis).

Reliability and validity of scores for both original and additional MCC-specific FACT-M scores were assessed. Reliability is the degree to which an instrument is free from measurement error. Internal consistency reliability (the extent to which items within a domain are consistent with each other and measure a single underlying concept) was assessed at baseline using Cronbach’s alpha [23]. Validity is defined as the accuracy with which a measurement tool measures the concept it is intended to measure. Construct validity, i.e. confirmation of the scaling structure, clinical validity, and concurrent validity, were assessed at baseline. Scaling structure was confirmed using multitrait analysis assessing item convergent and discriminant validity. Clinical validity was assessed by comparing the FACT-M mean scale scores between groups of patients categorized by ECOG PS [24]; the hypothesis put forward being that patients with a better level of functioning should have better HRQoL. Concurrent validity was assessed at baseline by calculating the Pearson coefficient between the FACT-M scores and the EQ-5D VAS and Index score; the hypothesis was that domains measuring related concepts should have high correlation levels while domains measuring different concepts should have low correlations. Ability of the FACT-M scale to detect change over time was assessed from baseline to Week 7 by comparing change in FACT-M scale scores according to percentage change in tumor size (classified into three groups: reduction ≥30%, reduction between 0% and 30%, increase >0%) using paired t-test, effect size (ES), Standardized Response Mean (SRM), and Guyatt’s statistics [25, 26]. Tumor size reduction greater than 30% is consistent with RECIST 1.1 criteria for determining partial response, a commonly used clinical criteria in the evaluation of tumor burden [27]. Finally, minimally important differences (MIDs), defined as the smallest difference in score in the PRO domain that is perceived as meaningful and beneficial for the patient [28] were computed using distribution-based and anchor-based methods. Anchor-based MID thresholds were explored using the percentage change in tumor size at Week 7. The responder threshold was defined for each FACT-M score as the mean change from baseline to Week 7 in patients whose percentage change in tumor size decreased over 30%. The distribution-based method included the use of ES and standard error of measurement (SEM). Two responder thresholds were calculated as 0.2 x SDBL and as 0.5 x SDBL, with SDBL being the standard deviation of the score at baseline. The MID threshold using SEM was calculated as \( {\mathrm{SD}}_{\mathrm{BL}}\mathrm{x}\sqrt{1-r} \) where r is the reliability coefficient. Recommended MID range for FACT-M scores in the mMCC population were identified based on maximum and minimum MID thresholds obtained using the different methods.

Comparison of quantitative variables between groups of patients was assessed using t-test when comparing two groups of patients or ANOVA when comparing three groups of patients or more. Statistical significance threshold was set to 5% for each two-sided test and is provided to aid interpretation. No adjustments were made to account for multiplicity. Statistical analyses were performed using SAS software for Windows (Version 9.4, SAS Institute Inc., Cary, NC, USA).

Results

Patient population

Among the 88 enrolled patients who received at least one dose of trial treatment, 70 patients completed at least one item of both EQ-5D and FACT-M questionnaires at baseline and were included in the PAS. The number of patients in the PAS was 49 at Week 7, 38 at Week 13, and 27 at Week 25. The optional interview was conducted with 19 patients.

Socio-demographics and clinical characteristics of patients in the PAS and interviewed patients are presented in Table 1 Overall, patients were mostly males (74.3%), with a mean age of 70.2 years. Patients were mainly from the USA (40 patients, 57.1%), followed by Europe (22 patients; 31.4%), and the rest of the world, i.e. Japan and Australia (8 patients; 11.4%). Socio-demographic and clinical characteristics of interviewed patients were very similar to those from the PAS, except that interviewed patients were mainly from the United States of America and none were from Asia.

Table 1 Patients’ socio-demographic and clinical characteristics at baseline

Development of the additional MCC-specific FACT-M scores

Additional MCC-specific FACT-M scores were developed to obtain constructs of interest specific to the mMCC population with specific focus items. Forty-three items from the FACT-M questionnaire were initially selected, corresponding to the core FACT-G and the Melanoma Subscale; the Melanoma surgery scale was not deemed relevant to the disease and objective of the trial. The iterative and combined qualitative and quantitative process allowed to derive three additional MCC-specific scores: Physical Function score (six items), Psychological Impact score (six items), and MCC summary score (sum of Physical Function and Psychological Impact scores; 12 items) (Table 2).

Table 2 Original and additional MCC-specific FACT-M scores

Description of original FACT-M scale and additional MCC-specific scale scores over time

Original FACT-M scores and additional MCC-specific scores were rather steady over time, with a slight tendency to increase (better HRQoL) (Table 3).

Table 3 FACT-M scores and MCC-specific scores from baseline to each measurement time point

Psychometric validation in the mMCC population of both original and additional MCC-specific FACT-M scores

Internal consistency reliability

FACT-M original and additional MCC-specific scores demonstrated very good internal consistency, with Cronbach’s alpha coefficient varying from 0.81 to 0.96 for the original FACT-M scores and from 0.85 to 0.91 for the additional MCC-specific scores (Table 4).

Table 4 Internal consistency reliability and clinical and concurrent validity of the FACT-M and MCC-specific scores in the mMCC population

Construct validity

Convergent validity criterion, i.e. Pearson’s correlation above 0.4, was met for 75% of the items of the Melanoma Subscale, 88% of the items of the Melanoma surgery scale, and 100% of the items of the 4 subscales of the FACT-G scale (PWB, SWB, EWB, and FWB) (Table 4). Discriminant validity criterion, met when correlation of an item with its own dimension is higher than the correlation of this item with all other dimensions, was met for 57% to 71% of the items of the subscales PWB, SWB, EWB, FWB, and Melanoma surgery scale but only 31% of the items in the Melanoma Subscale, suggesting poor discriminant validity of this subscale. Both original and additional MCC-specific FACT-M scores demonstrated clinical validity, with higher scores (better HRQoL) observed in patients with better functioning (assessed by ECOG PS) (Table 4). A significant difference was even observed for the PWB subscale (p = 0.0221). Similarly, a lower score in all domains of the FACT-M, except the Melanoma Subscale and the Melanoma surgery scale, was observed among patients with visceral metastases at baseline compared to those without visceral metastases (p > 0.05). The FACT-M questionnaire presented good concurrent validity, as high correlation coefficients were observed between the FACT-M scores and EQ-5D for items that represented the same underlying concept, and lower coefficients were observed when different concepts were assessed by the two instruments. In particular, higher coefficients were found between the EQ-5D index score and the FACT-M physical well-being dimension score and the Melanoma Subscale score (Table 5).

Table 5 Ability of the FACT-M to detect change and MIDs in the mMCC population

Ability to detect change and MID

Measurable tumor shrinkage greater than 30% (i.e. indicating partial/complete response) was associated with an improvement in HRQoL scores, whereas tumor growth was associated with a decrease in HRQoL scores. The magnitude of these change scores were in the region of small to moderate effect sizes for both tumor shrinkage and tumor increase groups (Table 5). Clear differentiation of change scores between groups was observed for FWB (p = 0.005), Melanoma surgery scale (p = 0.036), and TOI (p = 0.038). A similar trend was observed for the other scales and subscales with the exception of EWB, where a decrease was observed for the tumor shrinkage group.

Anchor-based calculations of the MIDs were generally consistent with distribution based calculations; MID ranges (min – max) based on the different calculation methods was generally in the range of 0.2 x SDBL (lowest) to 0.5 x SDBL (highest) (Table 5). Percentage of responders varied from 18% to 39% when response was defined as a change in score above SEM calculated MIDs and from 22% to 53% when response was defined as a change in score above anchor calculated MIDs (Table 6).

Table 6 Responder analysis based on various MID methods

Discussion

The FACT-M is a validated questionnaire to assess HRQoL in patients with melanoma, a disease sharing similarities with MCC. As there is currently no existing validated disease-specific PRO questionnaire to capture HRQoL in patients with MCC, the FACT-M questionnaire was a candidate questionnaire to capture disease-specific HRQoL outcomes in mMCC.

Overall, psychometric properties of the FACT-M questionnaire in the mMCC population was acceptable, as the questionnaire demonstrated good item convergent validity, very good internal consistency reliability, clinical validity, and notable ability to detect change in tumor size, given the small sample size. Very good internal consistency ensured that items within a domain reflect a single underlying concept and responses to these items are consistent with each other. However, the FACT-M questionnaire demonstrated insufficient discriminant validity, especially for items of the Melanoma Subscale. A similar finding has been previously reported in the original FACT-M validation work [17] and is likely due to the addition disease-specific module items that correlate highly with core items but not necessarily together. Therefore, results from the Melanoma Subscale should be interpreted cautiously not only in patients with melanoma but also in patients with MCC. Altogether, these results showed a good construct validity of both original and additional MCC-specific FACT-M scores.

In an attempt to create scores with better psychometric properties for the mMCC population, additional scores were derived from concepts arising from patient interviews. In contrary to our expectation, these additional scores did not perform markedly better than the original FACT-M scores, suggesting that the original scores are sufficient for future studies in the mMCC population.

Trends in change scores were observed in both tumor shrinkage and tumor increase groups. MID values were consistent in magnitude with previously reported values in the literature for FACT-M domains [29, 30] as expected considering the similarities between the two diseases. The magnitude of these change scores were consistent with distribution based methods of MID calculation, which supports the choice of anchor for detecting differences in HRQoL domains. One unexplained finding was the small reduction in social/family well-being in the tumor shrinkage group, which requires further investigation. Ranges of MIDs for future studies involving the FACT-M in the mMCC population exclude this observed negative association and are as follows: PWB (1–3), SWB (1–3), EWB (1–3), FWB (2–4), MS (2–5), MSS (2–3), TOI (4–9), FACT-G total (4–8), and FACT-M total (5–12).

Limitations and future directions

Data used in this study were collected in a clinical trial setting, which may have biased the study results: e.g. restrictive patient eligibility criteria may result in a study population not entirely representative of the mMCC population. Another limitation to the study results may be the small sample sizes. However, adequate quantity of analyzable data was retrieved from the PRO administered during the trial. This was likely due to protocol specific procedures such as training and reminders, electronic administration of PRO data (missing items were not permitted by the electronic questionnaires), and instructions provided by the FACT-M questionnaire. Indeed, patients were required to answer all items and select “Not at all” if they felt that the item is not applicable to them.

Further work could include performing specific cognitive debriefing interviews (i.e. an in-depth item per item review of the questionnaire by patients) that could provide additional insights on the relevance of the item selected for the study-specific scores.

Conclusion

In conclusion, assessment of FACT-M psychometric properties demonstrated that FACT-M is suitable to capture HRQoL in patients with mMCC, thus making it a potential candidate for assessing HRQoL in mMCC trials. HRQoL improvements were observed in patients with relevant tumor shrinkage after 7 weeks of avelumab treatment for the majority of FACT-M scores, except the Social/Family well-being domain. This link between HRQoL and clinically relevant endpoints will be valuable to assess benefits of novel treatments for mMCC. Furthermore, as psychometric properties of the additional MCC-specific FACT-M scores were similar to the original ones with no evidence of superior measurement properties, the original FACT-M scores are the ones recommended to capture HRQoL in patients with mMCC.

Change history

  • 27 March 2019

    .

Abbreviations

ECOG PS:

Eastern Cooperative Oncology Group performance status

EORTC-QLQ:

European Organisation for Research and Treatment of Cancer Quality of Life questionnaire

EQ-5D:

EuroQol-5 Dimensions

ES:

Effect size

EWB:

Emotional well-being

FACT-M:

Functional Assessment of Cancer Therapy – Melanoma

FDA:

Food and Drug Administration

FWB:

Functional well-being

HRQoL:

Health-related quality of life

MCC:

Merkel cell carcinoma

MID:

Minimally important differences

PF:

Physical Function

PI:

Psychological Impact

PRO:

Patient-reported outcomes

PWB:

Physical well-being

SDBL :

Standard deviation of the score at baseline

SEM:

Standard error of measurement

SRM:

Standardized Response Mean

SWB:

Social well-being

TOI:

Trial Outcome Index

References

  1. 1.

    Agelli M, Clegg LX. Epidemiology of primary Merkel cell carcinoma in the United States. J Am Acad Dermatol. 2003;49:832–41.

  2. 2.

    Feng H, Shuda M, Chang Y, Moore PS. Clonal integration of a polyomavirus in human Merkel cell carcinoma. Science. 2008;319:1096–100.

  3. 3.

    Lebbe C, Becker JC, Grob JJ, Malvehy J, Del Marmol V, Pehamberger H, Peris K, Saiag P, Middleton MR, Bastholt L, et al. Diagnosis and treatment of Merkel cell carcinoma. European consensus-based interdisciplinary guideline. Eur J Cancer. 2015;51:2396–403.

  4. 4.

    Fitzgerald TL, Dennis S, Kachare SD, Vohra NA, Wong JH, Zervos EE. Dramatic increase in the incidence and mortality from Merkel cell carcinoma in the United States. Am Surg. 2015;81:802–6.

  5. 5.

    Youlden DR, Soyer HP, Youl PH, Fritschi L, Baade PD. Incidence and survival for Merkel cell carcinoma in Queensland, Australia, 1993-2010. JAMA Dermatol. 2014;150:864–72.

  6. 6.

    Allen PJ, Bowne WB, Jaques DP, Brennan MF, Busam K, Coit DG. Merkel cell carcinoma: prognosis and treatment of patients from a single institution. J Clin Oncol. 2005;23:2300–9.

  7. 7.

    Tai PT, Yu E, Winquist E, Hammond A, Stitt L, Tonita J, Gilchrist J. Chemotherapy in neuroendocrine/Merkel cell carcinoma of the skin: case series and review of 204 cases. J Clin Oncol. 2000;18:2493–9.

  8. 8.

    Santamaria-Barria JA, Boland GM, Yeap BY, Nardi V, Dias-Santagata D, Cusack JC Jr. Merkel cell carcinoma: 30-year experience from a single institution. Ann Surg Oncol. 2013;20:1365–73.

  9. 9.

    Voog E, Biron P, Martin JP, Blay JY. Chemotherapy for patients with locally advanced or metastatic Merkel cell carcinoma. Cancer. 1999;85:2589–95.

  10. 10.

    Kaufman HL, Russell J, Hamid O, Bhatia S, Terheyden P, D'Angelo SP, Shih KC, Lebbe C, Linette GP, Milella M, et al. Avelumab in patients with chemotherapy-refractory metastatic Merkel cell carcinoma: a multicentre, single-group, open-label, phase 2 trial. Lancet Oncol. 2016;17:1374–85.

  11. 11.

    Kaufman HL, Russell JS, Hamid O, Bhatia S, Terheyden P, D'Angelo SP, Shih KC, Lebbé C, Milella M, Brownell I, et al. Durable responses to avelumab (anti-PD-L1) in patients with Merkel cell carcinoma progressed after chemotherapy: 1-year efficacy update. Washington, DC: In 2017 AACR Annual Meeting; 2017.

  12. 12.

    D'Angelo SP, Russell J, Hassel JC, Lebbe C, Chmielowski B, Rabinowits G, Terheyden P, Brownell I, Zwiener V, Bajars M, et al. First-line (1L) avelumab treatment in patients (pts) with metastatic Merkel cell carcinoma (mMCC): Preliminary data from an ongoing study. Chicago: In 2017 ASCO Annual Meeting; 2017.

  13. 13.

    Gnanasakthy A, Mordin M, Clark M, DeMuro C, Fehnel S, Copley-Merriman C. A review of patient-reported outcome labels in the United States: 2006 to 2010. Value Health. 2012;15:437–42.

  14. 14.

    US Department of Health and Human Services. Guidance for Industry Clinical Trial Endpoints for the Approval of Cancer Drugs and Biologics. 2007. https://www.fda.gov/downloads/drugsGuidanceComplianceRegulatoyInformation/Guidance/UCM071590.pdf.

  15. 15.

    FDA: Patient-Reported Outcome Measures in U.S. Regulatory Review of Cancer Products. In Workshop on Clinical Outcome Assessments (COAs) in Cancer Clinical Trials; Silver Spring, MD. 2016.

  16. 16.

    Gibbons E, Casanas i Comabella C, Fitzpatrick R. A structured review of patient-reported outcome measures for patients with skin cancer, 2013. Br J Dermatol. 2013;168:1176–86.

  17. 17.

    Cormier JN, Ross MI, Gershenwald JE, Lee JE, Mansfield PF, Camacho LH, Kim K, Webster K, Cella D, Palmer JL. Prospective assessment of the reliability, validity, and sensitivity to change of the functional assessment of cancer therapy-melanoma questionnaire. Cancer. 2008;112:2249–57.

  18. 18.

    Cormier JN, Davidson L, Xing Y, Webster K, Cella D. Measuring quality of life in patients with melanoma: development of the FACT-melanoma subscale. J Support Oncol. 2005;3:139–45.

  19. 19.

    Cormier JN, Cromwell KD, Ross MI. Health-related quality of life in patients with melanoma: overview of instruments and outcomes. Dermatol Clin. 2012;30:245–54. viii.

  20. 20.

    Shields AL, Hao Y, Krohe M, Yaworsky A, Mazar I, Foley C, Mehmed F, Globe D. Patient-reported outcomes in oncology drug labeling in the United States: a framework for navigating early challenges. Am Health Drug Benefits. 2016;9:188–97.

  21. 21.

    EuroQol G. EuroQol--a new facility for the measurement of health-related quality of life. Health Policy. 1990;16:199–208.

  22. 22.

    van Hout B, Janssen MF, Feng YS, Kohlmann T, Busschbach J, Golicki D, Lloyd A, Scalone L, Kind P, Pickard AS. Interim scoring for the EQ-5D-5L: mapping the EQ-5D-5L to EQ-5D-3L value sets. Value Health. 2012;15:708–15.

  23. 23.

    Cronbach LJ. Coefficient alpha and the internal structure of tests. Psychometrika. 1951;16:297–334.

  24. 24.

    Chassany O, Sagnier P, Marquis P, Fullerton S, Aaronson N. Patient-reported outcomes: the example of health-related quality of life: a European guidance document for the improved integration of health-related quality of life assessment in the drug regulatory process. Drug Inf J. 2002;36:209–38.

  25. 25.

    Guyatt G, Walter S, Norman G. Measuring change over time: assessing the usefulness of evaluative instruments. J Chronic Dis. 1987;40:171–8.

  26. 26.

    Kazis LE, Anderson JJ, Meenan RF. Effect sizes for interpreting changes in health status. Med Care. 1989;27:178–89.

  27. 27.

    Eisenhauer EA, Therasse P, Bogaerts J, Schwartz LH, Sargent D, Ford R, Dancey J, Arbuck S, Gwyther S, Mooney M, et al. New response evaluation criteria in solid tumours: revised RECIST guideline (version 1.1). Eur J Cancer. 2009;45:228–47.

  28. 28.

    Coon CD, Cappelleri JC. Interpreting change in scores on patient-reported outcome instruments. Therapeutic Innov Regul Sci. 2016;50(1):22–9.

  29. 29.

    Askew RL, Xing Y, Palmer JL, Cella D, Moye LA, Cormier JN. Evaluating minimal important differences for the FACT-Melanoma quality of life questionnaire. Value Health. 2009;12:1144–50.

  30. 30.

    Pickard AS, Neary MP, Cella D. Estimation of minimally important differences in EQ-5D utility and VAS scores in cancer. Health Qual Life Outcomes. 2007;5:70.

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Acknowledgements

The authors thank the patients and their families, investigators, co-investigators, and the study teams at each of the participating centers and at Merck KGaA, Darmstadt, Germany, and EMD Serono, Billerica, MA, USA (a business of Merck KGaA, Darmstadt, Germany). Céline Faure, Mapi, provided support for scientific writing.

Funding

This trial was sponsored by Merck KGaA, Darmstadt, Germany, and is part of an alliance between Merck KGaA, Darmstadt, Germany and Pfizer Inc., New York, NY, USA.

Availability of data and materials

The datasets generated and/or analyzed during the current study are not publicly available (clinical trial still ongoing) but are available from the corresponding author on reasonable request.

Author’s contributions

MB participated in the study design, analysis plan, and data interpretation and reviewed the manuscript; FF developed the analysis plan and performed the analyses; PW conducted complementary analyses and data interpretation; CD participated in the study design and data interpretation and reviewed the manuscript; AM and LM participated in the development and review of the manuscript; and MS reviewed the analysis plan and the manuscript. All authors read and approved the final manuscript.

Author information

Correspondence to Murtuza Bharmal.

Ethics declarations

Ethics approval and consent to participate

This study was performed in compliance with the ethical principles arising from the Declaration of Helsinki and all current local regulations. The study protocol was approved by an Independent Ethics Committee or Institutional Review Board prior to the study launch at each site. All patients gave written informed consent.

Consent for publication

Not applicable.

Competing interests

MB and MS are employees of Merck KGaA, Darmstadt, Germany. FF, CDB, PW, and AM are employees of Mapi and paid consultants to Merck KGaA, Darmstadt, Germany. LM is an employee of EMD Serono, Boston, MA, USA. Authors did not receive payment for authorship.

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Keywords

  • Quality of life
  • Merkel cell carcinoma
  • FACT-M questionnaire
  • Psychometric validation
  • Patient-reported outcomes