Psychometric Evaluation Of Health-Related Quality Of Life Assessments From The Along and Blong Hemophilia Clinical Trials

Blood ◽  
2013 ◽  
Vol 122 (21) ◽  
pp. 423-423 ◽  
Author(s):  
Kathleen W Wyrwich ◽  
Priscilla Auguste ◽  
Robyn von Maltzahn ◽  
Ren Yu ◽  
Sangeeta Krishnan ◽  
...  

Abstract Hemophilia patients on prophylactic treatment can experience an improvement in health-related quality of life (HRQoL) through better protection from breakthrough bleeds and the reduction in long-term joint damage complications compared to episodic treatment. In two recent Phase 3 clinical trials with new, longer lasting factor concentrates (ALONG: rFVIIIFc; BLONG: rFIXFc), the benefit of HRQoL was assessed as a secondary endpoint in addition to primary objectives of safety, tolerability, and efficacy in adolescents and adults with severe hemophilia A and B, respectively, who received prophylactic or episodic regimens. HRQoL was assessed in the adult population via the EuroQoL-5 Dimension (EQ-5D) and the 46-item Haem-A-QoL questionnaire, yielding 10 domain scores and a total score ranging from 0 (best HRQoL) to 100 (worst HRQoL). Incorporating the hypothesis of improved HRQoL for patients receiving prophylaxis treatment, the goal of this analysis was to use these trials’ data to understand the Haem-A-QoL’s reliability, validity, and sensitivity to change over time in an adult male hemophilia population from six continents. In ALONG, 133 adult patients (mean age: 36.0 years) had at least one Haem-A-QoL domain score at baseline, with the highest HRQoL mean impairments at baseline in the ‘Sport & Leisure’ (52.4) and ‘Physical Health’ (41.9) domains. In BLONG, the 73 adult patients (mean age: 33.6 years) with at least one baseline domain score also had their highest baseline mean scores in these two domains (56.2 and 42.8, respectively). Internal consistency reliability as assessed by Cronbach’s alpha (α) was generally adequate (α > 0.70) for all 10 Haem-A-QoL domains and for the total score in both trials. Comparisons of mean Haem-A-QoL baseline domain and total scores for each of the EQ-5D item’s Level 1 responders (no problem) to those at Levels 2 or 3 (some problems or unable) in ALONG demonstrated the validity of most scores (p <0.05). Comparisons between subjects with and without bleeds in the past 12 months also showed important differences (p <0.05) in most Haem-A-QoL baseline domain and the total scores. Convergent validity was tested correlating baseline scores of the Haem-A-QoL with the EQ-5D utility index and the modified Hemophilia Joint Health Score (HJHS). These analyses revealed a strong negative correlation between the two instruments’ total scores (r = -0.63), and between the EQ-5D index and the ‘Physical Health’ (r = -0.63) and ‘Feeling’ (r = -0.62) domains of the Haem-A-QoL. Moderate negative relationships were observed between the EQ-5D scores and the ‘View,’ ‘Sports & Leisure,’ ‘Work & School,’ ‘Treatment,’ ‘Future,’ and ‘Relationships & Sexuality’ domains. The moderate correlations between the ‘Physical Health,’ ‘Feelings,’ ‘Sports & Leisure,’ ‘Work & School,’ and ‘Future’ domain scores and the Haem-A-QoL total score when compared to the HJHS at baseline in the ALONG trial further support the instrument’s construct validity (p <0.001 for all reported correlations). Change score correlations (baseline to 28 weeks) with the EQ-5D were moderate in magnitude for the Haem-A-QoL total score, and ‘Physical Health’ and ‘Feeling’ domains, demonstrating the sensitivity to change for these outcome measures in the ALONG data (p <0.02). Although differences were not statistically significant (p >0.05), mean change score comparisons between the ALONG treatment arms demonstrated a trend supporting the expectation that improved mean change in the HRQoL total scores (-3.2 and -3.4) were similar for the tailored prophylaxis and weekly dosing arms, respectively, compared to very limited change in the on-demand group (-1.1). This pattern was also observed for the BLONG treatment arms at 26 weeks, where the individualized treatment arm had improved mean change total scores (-4.0) similar to the fixed weekly interval treatment arm (-6.5). The use of rFVIIIFc and rFIXFc during study was associated with an overall HRQoL improvement from baseline, in addition to demonstrating differences between patients receiving prophylactic or episodic treatment. These psychometric analyses using the ALONG and BLONG clinical trial data underscores this finding by providing a substantial body of evidence that is pertinent to the reliability, validity, and ability to detect change of this instrument, and provide further evidence to support the usefulness of the Haem-A-QoL in an adult multinational population. Disclosures: Wyrwich: Biogen Idec Inc.: Research Funding. Auguste:Biogen Idec Inc.: Research Funding. von Maltzahn:Biogen Idec Inc.: Research Funding. Yu:Biogen Idec Inc.: Research Funding. Krishnan:Biogen Idec Inc.: Employment. Dodd:Biogen Idec Inc.: Employment. von Mackensen:Evidera: Consultancy.

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Kayo Togawa ◽  
Huiyan Ma ◽  
Ashley Wilder Smith ◽  
Marian L. Neuhouser ◽  
Stephanie M. George ◽  
...  

AbstractWe examined cross-sectional associations between arm lymphedema symptoms and health-related quality of life (HRQoL) in the Health, Eating, Activity and Lifestyle (HEAL) Study. 499 women diagnosed with localized or regional breast cancer at ages 35–64 years completed a survey, on average 40 months after diagnosis, querying presence of lymphedema, nine lymphedema-related symptoms, e.g., tension, burning pain, mobility loss, and warmth/redness, and HRQoL. Analysis of covariance models were used to assess HRQoL scores in relation to presence of lymphedema and lymphedema-related symptoms. Lymphedema was self-reported by 137 women, of whom 98 were experiencing lymphedema at the time of the assessment. The most common symptoms were heaviness (52%), numbness (47%), and tightness (45%). Perceived physical health was worse for women reporting past or current lymphedema than those reporting no lymphedema (P-value < 0.0001). No difference was observed for perceived mental health (P-value = 0.31). Perceived physical health, stress, and lymphedema-specific HRQoL scores worsened as number of symptoms increased (P-values ≤ 0.01). Women reporting tension in the arm had lower physical health (P-value = 0.01), and those experiencing burning pain, tension, heaviness, or warmth/redness in the arm had lower lymphedema-specific HRQoL (P-values < 0.05). Treatment targeting specific lymphedema-related symptoms in addition to size/volume reduction may improve some aspects of HRQoL among affected women.


2004 ◽  
Vol 15 (5) ◽  
pp. 491-499
Author(s):  
Sati Mazumdar ◽  
Mary Amanda Dew ◽  
Patricia R. Houck ◽  
Charles F. Reynolds

2013 ◽  
Vol 122 (1) ◽  
pp. 70-77 ◽  
Author(s):  
Melanie Wickert ◽  
Mike T. John ◽  
Oliver Schierz ◽  
Christian Hirsch ◽  
Ghazal Aarabi ◽  
...  

2017 ◽  
Vol 15 (9) ◽  
pp. 1435-1443.e2 ◽  
Author(s):  
Jorge D. Machicado ◽  
Amir Gougol ◽  
Kimberly Stello ◽  
Gong Tang ◽  
Yongseok Park ◽  
...  

Blood ◽  
2018 ◽  
Vol 132 (Supplement 1) ◽  
pp. 4260-4260
Author(s):  
Henrik Hjorth-Hansen ◽  
Satu Mustjoki ◽  
Ulla Olsson-Strömberg ◽  
Jesper Stentoft ◽  
Fabio Efficace ◽  
...  

Abstract Background: Tyrosine kinase inhibitors (TKI) have revolutionized CML treatment but only a minority of patients are candidates to discontinue their TKI treatment, i.e. achieve treatment-free remission (TFR). Therefore, for the majority of patients TKI treatments are lifelong and it becomes critical to understand impact of therapy on patients' health-related quality of life (HRQoL).To obtain a maximal response for TFR, second generation TKIs like Dasatinib (DAS) induce deeper and faster responses than imatinib,and combination with pegylated forms of interferon-α2 have shown promising effect in several studies. Aims: To prospectively examine HRQoL outcomes in CML patients treated with DAS plus low-dose pegylated interferon- α2b (PegIFN). Methods: We have performed a single armed study (NordCML007) using DAS 100 mg OD from inclusion through the study including 40 patients, of these 31 were male. From month 3 (M3) low-dose PegIFN was added for one year until M15. We chose, based on previous experience, a dose of only 15 µg/week for 3 months and if tolerated, the dose was increased to 25 µg/week from M6. At M12, 80% of patients still took PegIFN and the mean administered dose was 18 µg/week. Side effects were moderate and fewer patients than expected developed pleural effusions in the combination period. Efficacy of the combination measured by BCR-ABL1 RQ-PCR was superior to the historical control DASISION, exemplified by M12 achievement of MMR, 46% vs 86% and MR4, 12% vs 46%. Before starting this project, concern was raised regarding tolerability of PegIFN. An acceptable tolerability of combined TKI+PegIFN is key for inclusion of combination treatment as standard of caretreatment. We did expect moderate negative effect of PegIFN treatment on HRQoL parameters. We assessed HRQoL with the well validated and widely used EORTC-QLQC30 questionnaire combined with the disease-specific CML module EORTC-CML24 at study inclusion and thereafter at 3, 6, 12 and at 18 months. Patient scoring was also compared with sex- and age-matched normative data. Results: Patients completed HRQOL questionnaires at baseline, M3 (DAS only), M6 and M12 (on combination) and finally at M18 (DAS only). About 80% of HRQOL forms were completed, withh 31-33 respondents at each time point. Most of these patients completed all forms. CML patients at baseline had statistically and clinically significant poorer scores for "Overall quality of life" (65 vs 77 points), "Role functioning" (72 vs 87 points), "Emotional functioning" (73 vs 82 points,) "Social functioning" (79 vs 91 points), "Fatigue" (32 vs 19 points) and "Insomnia" (25 vs 16 points) compared to matched normal populations (a difference of >5 pts is estimated to representa difference of clinically significance) During treatment, scoring of all modalities approached the normative (i.e. no statistical difference), except for "Fatigue". Most of the improvement occurred during the first 3 months, i.e on DAS alone. Of note, HRQOL scores remained stable or improved further also with combination treatment, hence we observed no negative effect of low dose PegIFN treatment. Conclusions: These preliminary results suggest that low-dose PegIFN in combination with DAS has no detrimental effects on HRQOL over time. Rather we observed improvement with regard to CML disease specific HRQOL domains. The efficacy, safety and HRQoL data encourages further study of PegIFN in combination with 2nd generation TKIs. Disclosures Hjorth-Hansen: Bristol-Myers Squibb: Research Funding; Merck Sharp&Dohme: Research Funding. Mustjoki:Bristol-Myers Squibb: Honoraria, Research Funding; Pfizer: Honoraria, Research Funding; Novartis: Honoraria, Research Funding; Ariad: Research Funding; Celgene: Honoraria. Olsson-Strömberg:Merck Sharp and Dohme: Research Funding; Bristol-Myers-Squibb: Research Funding. Stentoft:Bristol-Myers Squibb: Research Funding; Merck Sharp&Dohme: Research Funding. Efficace:Orsenix: Consultancy; Incyte: Consultancy; Lundbeck: Research Funding; TEVA: Research Funding; AMGEN: Research Funding; Amgen: Consultancy; TEVA: Consultancy; Bristol Meyers Squibb: Consultancy; Seattle Genetics: Consultancy.


1993 ◽  
Vol 53 (2) ◽  
pp. 75-77 ◽  
Author(s):  
Gail A. Greendale ◽  
Stuart L. Silverman ◽  
Ron D. Hays ◽  
Cyrus Cooper ◽  
Timothy Spector ◽  
...  

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