835 results on '"Husson, Olga"'
Search Results
2. Health-related conditions among long-term cancer survivors diagnosed in adolescence and young adulthood (AYA): results of the SURVAYA study
3. The impact of electronic versus paper-based data capture on data collection logistics and on missing scores in thyroid cancer patients
4. ‘There is still a part of me that would love to be the old me again’, how do adolescents and young adults (AYA) experience cancer-related bodily changes: a phenomenological interview study
5. The association of cognitive coping style with patient preferences in a patient-led follow-up study among colorectal cancer survivors
6. Acceptability and usefulness of the EORTC ‘Write In three Symptoms/Problems’ (WISP): a brief open-ended instrument for symptom assessment in cancer patients
7. Protocol for the development of a Core Outcome Set (COS) for Adolescents and Young Adults (AYAs) with cancer
8. Pre-treatment fertility preservation and post-treatment reproduction in long-term survivors of adolescent and young adult (AYA) cancer
9. Adherence to the World Cancer Research Fund/American Institute for Cancer Research recommendations for cancer prevention in adolescent and young adult (AYA) cancer survivors: results from the SURVAYA study
10. Financial difficulties experienced by patients with gastrointestinal stromal tumours (GIST) in the Netherlands: data from a cross-sectional multicentre study
11. Patient-physician agreement on function and pain is associated with long-term outcomes in sarcoma: findings from a longitudinal study
12. Assessing patients’ needs in the follow-up after treatment for colorectal cancer—a mixed-method study
13. Exploring the interconnectedness between health-related quality of life factors among long-term adolescent and young adult cancer survivors (AYAs): a network analysis
14. Phase III study of the European Organisation for Research and Treatment of Cancer Quality of Life cancer survivorship core questionnaire
15. Patient-reported outcomes in randomized clinical trials of systemic therapy for advanced soft tissue sarcomas in adults: A systematic review
16. A qualitative study on the healthcare experiences of adolescents and young adults (AYA) with an uncertain or poor cancer prognosis
17. Health-related quality of life of Adolescent and Young Adult Cancer Survivors before and during the COVID-19 pandemic: longitudinal improvements on social functioning and fatigue
18. Determinants and mediating mechanisms of quality of life and disease-specific symptoms among thyroid cancer patients: the design of the WaTCh study
19. The views of cancer patients of Turkish, Moroccan, Surinamese, and Dutch-Caribbean descent on diagnosis, treatment and prognosis: A systematic literature review
20. Fear, anxiety and depression in gastrointestinal stromal tumor (GIST) patients in the Netherlands: Data from a cross-sectional multicenter study
21. Measuring health-related quality of life in solid rare cancer patients: A study protocol
22. Self-reported causes of cancer among 6881 survivors with 6 tumour types: results from the PROFILES registry
23. Health-related quality of life of children with neurofibromatosis type 1: Analysis of proxy-rated PedsQL and CHQ questionnaires
24. Psychological and social challenges of patients with locally advanced and metastatic gastrointestinal stromal tumours (GIST) on long-term treatment with tyrosine kinase inhibitors: a qualitative study with patients and medical oncologists
25. Quality of Life in Adolescents and Young Adults with Cancer
26. Identifying health-related quality of life cut-off scores that indicate the need for supportive care in young adults with cancer
27. Internal Responsiveness of EQ-5D-5L and EORTC QLQ-C30 in Dutch Breast Cancer Patients during the First Year Post-Surgery: A Longitudinal Cohort Study
28. Symptoms reported by gastrointestinal stromal tumour (GIST) patients on imatinib treatment: combining questionnaire and forum data
29. Self-perceived cognitive functioning and quality of life among cancer survivors: results from the PROFILES registry
30. Health-related Quality of Life of Patients With Non–Intra-abdominal Desmoid-Type Fibromatosis During Active Surveillance: Results of a Prospective Observational Study
31. Assessing measurement invariance in the EORTC QLQ-C30
32. A qualitative study on the involvement of adolescents and young adults (AYAs) with cancer during multiple research phases: “plan, structure, and discuss”
33. ‘I thought I had fibroids, and now I don’t’: a mixed method study on health-related quality of life in uterine sarcoma patients
34. Assessing the collection and reporting of patient-reported outcome data in interventional cancer trials: a single institution, retrospective systematic evaluation
35. Health-related quality of life after isolated limb perfusion compared to extended resection, or amputation for locally advanced extremity sarcoma: Is a limb salvage strategy worth the effort?
36. The prediagnostic general practitioner care of sarcoma patients: A real‐world data study.
37. Feasibility, reliability and satisfaction of (automated) capillary carcinoembryonic antigen measurements for future home‐based blood sampling: the prospective CASA‐I study.
38. Current Management of Desmoid Tumors: A Review.
39. Employment outcomes of adolescent and young adult cancer survivors and their partners: A Dutch population‐based study.
40. The complexity of assessing health-related quality of life among sarcoma patients
41. The association of Cognitive Coping Style with Patient Preferences in a Patient- Led Follow-Up Study among Colorectal Cancer Survivors
42. Actionability of Synthetic Data in a Heterogeneous and Rare Healthcare Demographic; Adolescents and Young Adults (AYAs) with Cancer
43. Employment outcomes of adolescent and young adult (AYA) cancer survivors and their partners: A Dutch population‐based study
44. Author response to: Comment on: Oncological surgery follow-up and quality of life: meta-analysis
45. Assessing health-related quality of life in cancer survivors : factors impacting on EORTC QLU-C10D-derived utility values
46. Improving Diagnosis and Care for Patients With Sarcoma: Do Real-World General Practitioners Data and Prospective Data Collections Have a Place Next to Clinical Trials?
47. Patient-Reported Outcomes of Accelerated Aging: A Novel Approach to Investigate Second Cancer Risk in Adolescent and Young Adult (18−39 Years) Cancer Survivors.
48. The sarcoma diagnostic interval: a systematic review on length, contributing factors and patient outcomes
49. Unravelling the heterogeneity of soft tissue and bone sarcoma patients’ health-related quality of life: a systematic literature review with focus on tumour location
50. Same Journey, Different Paths: Caregiver Burden among Informal Caregivers of Adolescent and Young Adult Patients with an Uncertain or Poor Cancer Prognosis (UPCP)
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