Abstract:Background: Considering the worldwide incidence of breast cancer (BC) and the importance of health-related quality of life (HRQoL) assessment, there is a growing need to have accurate and up-to-date reference values (RVs). RVs are useful for the design of randomised controlled trials (RCTs) and as benchmarks for comparison of cancer RCTs and health care interventions. This study aimed to provide RVs for the QLQ-C30 in early BC (EBC) and metastatic BC (MBC). General patterns of main results from the EORTC datas… Show more
“…Our results attest that more than half of the survivors had a mean GHQ (57.2 ± 25.4), which is similar to the mean score of metastatic breast cancer (57.6 ± 23.1) and lower than the mean score of early breast cancer (76.9 ± 19.2) [33]. In addition, the survivors had physical (72.6 ± 28.0), social (84.5 ± 29.3), and emotional (51.2 ± 31.3) functioning that [33]. In the same perspective, the physical role and emotional functional scales in the study survivors are worse than the functional scales in the Härtl et al study [34].…”
Section: Discussionsupporting
confidence: 74%
“…For early breast cancer, RV EORTC revealed high functioning and low prevalence of symptoms, while RV from metastatic breast cancer had lower baseline Health-Related Quality of Life (HRQoL) values than those from early breast cancer, and cognitive functioning presents the highest mean scores, while role functioning presents the lowest mean score. In addition, in the symptom scales, metastatic breast cancer presents a low prevalence of nausea/vomiting and diarrhea and a high prevalence of fatigue and pain, while HRQoL was more impaired in patients with metastatic breast cancer than in the general healthy population [ 33 ].…”
Introduction. The objective of this study was to investigate the impact of socioeconomic determinants on the quality of life of Moroccan women with breast cancer two years after their diagnosis who are followed up at the National Institute of Oncology (INO) in Rabat. Methods. This is a cross-sectional study that was conducted between May 2019 and September 2020. The sample size was 304 women. Data were collected using the EORTC QLQ-C30 and EORTC QLQ-BR 23 questionnaires in the Moroccan dialect. Results. The mean age of participants was 53.5 ± 12.4 years, where the majority resided in urban areas and more than half were illiterate. Moreover, three-quarters of the survivors were not working, and almost all have basic medical coverage. Nearly one-third of the respondents had experienced discrimination from those around them, and nearly half attributed the decrease in income to their state of health. In addition, 38.2 percent of participants stated that they had great difficulty living on their monthly income after the illness, whereas more than half of the survivors had a good quality of life in terms of overall health (GHS/QOL). Besides, social function obtained the highest score, while emotional function obtained the lowest score. Furthermore, financial difficulty was the most distressing symptom. Indeed, income adjustment after the disease, discrimination, distance between home and treatment center, professional status, and medical coverage were correlated with GHS/QOL. Regression analysis revealed that income adjustment after illness and discrimination were significant predictors of GHS/QOL. Conclusion. The data suggest establishing a financial support program and the development of education and awareness-raising policies to combat discrimination.
“…Our results attest that more than half of the survivors had a mean GHQ (57.2 ± 25.4), which is similar to the mean score of metastatic breast cancer (57.6 ± 23.1) and lower than the mean score of early breast cancer (76.9 ± 19.2) [33]. In addition, the survivors had physical (72.6 ± 28.0), social (84.5 ± 29.3), and emotional (51.2 ± 31.3) functioning that [33]. In the same perspective, the physical role and emotional functional scales in the study survivors are worse than the functional scales in the Härtl et al study [34].…”
Section: Discussionsupporting
confidence: 74%
“…For early breast cancer, RV EORTC revealed high functioning and low prevalence of symptoms, while RV from metastatic breast cancer had lower baseline Health-Related Quality of Life (HRQoL) values than those from early breast cancer, and cognitive functioning presents the highest mean scores, while role functioning presents the lowest mean score. In addition, in the symptom scales, metastatic breast cancer presents a low prevalence of nausea/vomiting and diarrhea and a high prevalence of fatigue and pain, while HRQoL was more impaired in patients with metastatic breast cancer than in the general healthy population [ 33 ].…”
Introduction. The objective of this study was to investigate the impact of socioeconomic determinants on the quality of life of Moroccan women with breast cancer two years after their diagnosis who are followed up at the National Institute of Oncology (INO) in Rabat. Methods. This is a cross-sectional study that was conducted between May 2019 and September 2020. The sample size was 304 women. Data were collected using the EORTC QLQ-C30 and EORTC QLQ-BR 23 questionnaires in the Moroccan dialect. Results. The mean age of participants was 53.5 ± 12.4 years, where the majority resided in urban areas and more than half were illiterate. Moreover, three-quarters of the survivors were not working, and almost all have basic medical coverage. Nearly one-third of the respondents had experienced discrimination from those around them, and nearly half attributed the decrease in income to their state of health. In addition, 38.2 percent of participants stated that they had great difficulty living on their monthly income after the illness, whereas more than half of the survivors had a good quality of life in terms of overall health (GHS/QOL). Besides, social function obtained the highest score, while emotional function obtained the lowest score. Furthermore, financial difficulty was the most distressing symptom. Indeed, income adjustment after the disease, discrimination, distance between home and treatment center, professional status, and medical coverage were correlated with GHS/QOL. Regression analysis revealed that income adjustment after illness and discrimination were significant predictors of GHS/QOL. Conclusion. The data suggest establishing a financial support program and the development of education and awareness-raising policies to combat discrimination.
“…To overcome the aforementioned barriers, creating dashboards that visually present the scores of a specific patient in simplified pictures, graphics or tables can be more informative than only abstractive numbers. Additionally, individual patient scores can be compared with scores of breast cancer patients with the same biological or treatment-related characteristics also known as reference scores [ 64 ]. Normative data reflect outcomes of a population unencumbered by a disease or specific condition, and can be used by both clinicians and patients to provide more context when interpreting PROs.…”
Metastatic breast cancer (MBC) patients are almost always treated to minimize the symptom burden, and to prolong life without a curative intent. Although the prognosis of MBC patients has improved in recent years, the median survival after diagnosis is still only 3 years. Therefore, the health-related quality of life (HRQoL) should play a leading role in making treatment decisions. Heterogeneity in questionnaires used to evaluate the HRQoL in MBC patients complicates the interpretability and comparability of patient-reported outcomes (PROs) globally. In this review, we aimed to provide an overview of PRO instruments used in real-world MBC patients and to discuss important issues in measuring HRQoL. Routinely collecting symptom information using PROs could enhance treatment evaluation and shared decision-making. Standardizing these measures might help to improve the implementation of PROs, and facilitates collecting and sharing data to establish valid comparisons in research. This is a prerequisite to learn about how they could impact the clinical care pathway. In addition, the prognostic value of intensified PRO collection throughout therapy on survival and disease progression is promising. Future perspectives in the field of PROs and MBC are described.
“…(4) Quality of life was much more commonly used as an end-point in the phase III TOSs initiated before 2007 (n Z 74) than in the industry-sponsored phase III cancer studies entered into the ClinicalTrials.gov registry before August 2006 (41.9% vs. 6.9% [42]). This highlights the prominent role that the EORTC has played and continues to play in the establishment of healthrelated quality of life as a key outcome measure of efficacy in oncology and the development of associated tools [43e47], which have been widely adopted across the areas of breast [48,49], lung [50] and colorectal [51,52] cancer. (5) Consistent with EORTC policy, the results of completed TOSs were nearly always published, leading to a publication rate that was markedly higher than those found by authors in the field for both clinical studies as a whole (97.9% vs. 46.0% [53], 66.4% [54], 66.…”
Background: Treatment optimisation studies (TOSs) are clinical trials which aim to tackle research questions that are often left unaddressed within the current drug development paradigm due to a lack of financial and regulatory incentives to undertake them. Examples include comparative effectiveness, therapeutic sequencing and dose de-escalation studies. Trials of this nature have historically been primarily carried out by academic institutions and notfor-profit organisations such as the European Organisation for Research and Treatment of Cancer (EORTC). Objectives: Our objective was to conduct an in-depth analysis of the breast, lung and colorectal cancer TOSs that have been performed by the EORTC in the past four decades. Methods: We searched the EORTC clinical trials database for relevant studies and subsequently analysed them based on a number of predefined criteria relating to their design, organisation and scientific impact. Results: The 113 EORTC TOSs examined in this analysis were mainly standard-sized, international, multicentre phase III trials using a relatively simple, randomised, open-label design and comparing pharmacological combination regimens against standard-of-care treatments in terms of their potential to improve overall survival of patients with cancer. Although they were typically financially and/or materially supported by the industry, their legal sponsor was nearly always an independent party that did not benefit monetarily from their outcomes. If meaningful findings were obtained, their results, regardless of whether positive or negative, were published in high-impact journals, and the corresponding articles usually received a
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