9 results on '"Van de Werf E"'
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2. EP-1612 FEASIBILITY OF A PAIN ASSESSMENT PROCEDURE FOR BRACHYTHERAPY IN BREAST CANCER PATIENTS: A PILOT STUDY
- Author
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Vandezande, L., primary, Raeymaekers, B., additional, Luyten, K., additional, Janssen, H., additional, Van de Werf, E., additional, and Van Limbergen, E., additional
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- 2012
- Full Text
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3. Vaginal mucositis in patients with gynaecological cancer undergoing (chemo-)radiotherapy: a retrospective analysis.
- Author
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Robijns J, Censabella S, Bollen H, Claes S, Van Bever L, Becker J, Pannekoeke L, Bulens P, and Van de Werf E
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- Chemoradiotherapy adverse effects, Constriction, Pathologic etiology, Female, Humans, Retrospective Studies, Vagina, Genital Neoplasms, Female drug therapy, Genital Neoplasms, Female radiotherapy, Head and Neck Neoplasms, Mucositis complications, Mucositis etiology, Radiation Injuries epidemiology, Radiation Injuries etiology
- Abstract
The objective of this retrospective analysis was to determine the incidence and extent of vaginal mucositis (VM) in women with gynaecological cancer undergoing external (chemo)radiation therapy (CRT). A retrospective analysis was set up to collect data on the incidence and severity of VM in women treated with external pelvic RT for gynaecological cancer at the Jessa Hospital, Hasselt and ZOL, Genk, BE between January 2017 and June 2018. At the start and end of their external (C)RT, they rated the frequency and intensity of five common symptoms of VM. Thirty-three patients treated with RT for gynaecological cancer met the inclusion criteria. A non-negligible proportion of patients already experienced at least one VM symptom to any degree before the start of RT, a proportion that further increased towards the end of the RT (73%). At the end of RT, on average, about 25% of these patients reported moderate-to-severe symptoms (against about 7% before the (C)RT). These results suggest that VM is a rather frequent side effect in gynaecological cancer patients that aggravates during treatment up to a moderate severity level. Although the small sample size, these data highlight the need for attention to VM.Impact Statement What is already known about this topic? Radiotherapy plays an important role in the treatment of gynaecological malignancies. A debilitating complication in patients undergoing pelvic radiotherapy is vaginal mucositis, an inflammation of the vaginal mucosal lining. To date, the incidence of vaginal mucositis is still not well documented. What this paper adds? A non-negligible proportion of patients already experienced at least one symptom related to vaginal mucositis before the start of radiotherapy. Most patients presented mild to moderate vaginal mucositis symptoms at the end of external pelvic radiotherapy. Burning sensation, pruritus, and pain were the most frequently documented radiotherapy-induced complications. The implications of this paper: Vaginal mucositis is an underrated side effect of pelvic radiotherapy that needs to be tackled multidisciplinary by a team of nurses, radiotherapists, oncologists, and gynaecologists. The team should tackle the complication from the start of radiotherapy by using the most appropriate measures. Due to a possible link between acute vaginal mucositis and late vaginal toxicity, the team needs to follow-up patient's post-radiotherapy to support patients in late complications and advise/encourage patients in performing vaginal dilatation to prevent vaginal stenosis.
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- 2022
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- View/download PDF
4. The Effectiveness of a Novel Skin Barrier Protectant in the Management of Acute Radiation Dermatitis: A Case Series.
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Robijns J, Van Bever L, Claes S, Censabella S, Pannekoeke L, Maes A, Van de Werf E, and Bulens P
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- Female, Humans, Skin Care, Breast Neoplasms, Radiodermatitis drug therapy, Radiodermatitis prevention & control
- Abstract
Objective: Acute radiation dermatitis (ARD) is a frequent adverse effect in patients with cancer undergoing radiotherapy (RT). The aim of this case series is to evaluate the effect of a novel skin barrier protectant in patients with ARD., Methods: The skin barrier protectant was used in four patients with different cancer types undergoing RT at two clinical sites. All patients received the standard institutional skincare alongside the novel skin barrier protectant. The skin reactions were evaluated by an RT nurse using the modified version of the Radiation Therapy Oncology Group criteria., Results: At the final RT session, three of four patients developed erythema with or without dry desquamation. One patient presented only a minor patchy moist wound. Overall, the pain and pruritus due to ARD was low or nonexistent. No adverse events related to the skin barrier protectant were reported., Conclusions: This case series demonstrates the beneficial effects and safety of the novel skin barrier protectant in the management of ARD in patients with cancer of different etiologies. These results lay the foundation for future studies with larger, more homogeneous patient populations; a well-defined application scheme; and a stricter study design., (Copyright © 2022 Wolters Kluwer Health, Inc. All rights reserved.)
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- 2022
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5. Photobiomodulation therapy for the prevention of acute radiation dermatitis in breast cancer patients undergoing hypofractioned whole-breast irradiation (LABRA trial).
- Author
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Robijns J, Lodewijckx J, Puts S, Vanmechelen S, Van Bever L, Claes S, Pannekoeke L, Timmermans A, Noé L, Govers M, Van de Werf E, Maes A, Bulens P, and Mebis J
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- Breast, Female, Humans, Breast Neoplasms radiotherapy, Breast Neoplasms surgery, Low-Level Light Therapy methods, Radiodermatitis etiology, Radiodermatitis prevention & control, Radiodermatitis radiotherapy
- Abstract
Objectives: To evaluate the efficacy of photobiomodulation therapy in breast cancer patients post-lumpectomy undergoing hypofractionated whole-breast irradiation (HF-WBI) for the prevention and management of acute radiodermatitis (ARD)., Materials and Methods: A randomized, multicentric clinical trial (LABRA trial, NCT03924011) was set up at the Limburg Oncology Center, including the Jessa Hospital (Hasselt, BE) and Ziekenhuis Oost-Limburg (Genk, BE). A total of 71 breast cancer patients planned to undergo HF-WBI were randomized to one of the two study arms: the control group (n = 32) or the PBM group (n = 39). The PBM group received the standard institutional skincare combined with PBM (2×/week) during the complete radiotherapy (RT) course. Patients in the control group received the standard skincare combined with placebo treatment (2x/week). Patients' skin reactions were evaluated weekly during the RT treatment by using the modified version of the Radiation Therapy Oncology Group (RTOG) criteria., Results: At week 3 of RT, one patient presented a grade 2 and one patient a grade 3 skin reaction in the control group, while in the PBM group, all patients still presented grade 1 ARD. At the final RT session 28% of the patients presenting grade 2-3 ARD, while in the PBM group 10% presented grade 2 and no grade 3 ARD. PBM reduced the incidence of severe ARD by 18%. However, the difference was not significant (p = 0.053)., Conclusion: Based on the LABRA trial results, PBM seems not able to reduce the incidence of severe ARD in breast cancer patients undergoing HF-WBI. Research in a larger patient population is recommended., (© 2021 Wiley Periodicals LLC.)
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- 2022
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6. Evaluating the Effectiveness of a Novel Skin Barrier Protectant in a Patient with Acute Radiodermatitis of the Vulva: A Case Report.
- Author
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Van Bever L, Claes S, Robijns J, Censabella S, Pannekoeke L, Van de Werf E, and Bulens P
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- Aged, Aged, 80 and over, Architectural Accessibility statistics & numerical data, Belgium, Female, Humans, Skin Care methods, Skin Care statistics & numerical data, Vulva drug effects, Vulva physiopathology, Architectural Accessibility standards, Radiodermatitis drug therapy, Skin Care standards, Vulvar Neoplasms drug therapy
- Abstract
Objective: To evaluate the use of a novel skin barrier protectant in a patient treated with radiotherapy for vulvar cancer., Methods: This case report was conducted in a radiotherapy department with two women undergoing radiotherapy for vulvar carcinoma. A novel skin barrier protectant was evaluated in one patient; the other underwent the institutional standard skin care protocol. Skin reactions and pain were evaluated using the Radiotherapy Oncology Group Criteria., Main Results: The patient who was treated with the skin protectant showed accelerated healing toward the end of radiotherapy, and this was accompanied with a decrease in pain (maximum pain score 6/10). In comparison, the patient treated with the standard skin care protocol had an extended healing process, experienced a higher pain level (maximum pain score 9/10), and required more nursing care., Conclusions: This case report is the first to suggest that this novel skin barrier protectant could effectively manage acute radiodermatitis in patients with cancer. This case report hopes to lay the foundation for future randomized controlled trials with a larger and broader patient population.
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- 2021
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7. The cost of radiotherapy in a decade of technology evolution.
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Van de Werf E, Verstraete J, and Lievens Y
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- Accounting methods, Algorithms, Benchmarking, Cost Allocation methods, Costs and Cost Analysis, Diffusion of Innovation, Humans, Radiation Oncology economics, Radiation Oncology trends, Radiotherapy trends, Models, Economic, Radiotherapy economics
- Abstract
Purpose: To quantify changes in radiotherapy costs occurring in a decade of medical-technological evolution., Materials and Methods: The activity-based costing (ABC) model of the University Hospitals Leuven (UHL) radiotherapy (RT) department was adapted to current RT standards. It allocated actual resource costs to the treatments based on the departmental work-flow and patient mix in 2009. A benchmark with the former model analyzed the cost increases related to changes in RT infrastructure and practice over 10 years., Results: A considerable increase in total RT costs was observed, resulting from higher capital investments (96%) and personnel cost (103%), the latter dominating the total picture. Treatment delivery remains the most costly activity, boosted by the cost of improved quality assurance (QA), 23% of total product costs, coming along with more advanced RT techniques. Hence, cost increases at the product level are most obvious for complex treatments, such as intensity-modulated radiotherapy (IMRT), representing cost increases ranging between 38% and 88% compared to conformal approaches., Conclusions: The ABC model provides insight into the financial consequences of evolving technology and practice. Such data are a mandatory first step in our strive to prove RT cost-effectiveness and thus support optimal reimbursement and provision of radiotherapy departments., (Copyright © 2011 Elsevier Ireland Ltd. All rights reserved.)
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- 2012
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8. Time and motion study of radiotherapy delivery: Economic burden of increased quality assurance and IMRT.
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Van de Werf E, Lievens Y, Verstraete J, Pauwels K, and Van den Bogaert W
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- Cost-Benefit Analysis, Equipment Failure Analysis economics, Female, Humans, Male, Quality Control, Radiation Oncology economics, Radiation Oncology methods, Radiotherapy Planning, Computer-Assisted methods, Radiotherapy, Intensity-Modulated methods, Risk Assessment, Health Care Costs, Quality Assurance, Health Care, Radiotherapy Planning, Computer-Assisted economics, Radiotherapy, Intensity-Modulated economics, Time and Motion Studies
- Abstract
Time measurements were performed on daily treatment delivery with the aim to quantify the impact of quality assurance (QA) using an electronic portal imaging device (EPID) on RT delivery time and to validate the time burden of intensity modulated radiation therapy (IMRT) as an example of advanced technology. Both increased QA and the delivery of IMRT were found to be significant parameters determining daily treatment time (TT), which in turn translates in increased treatment costs.
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- 2009
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9. Reproduction rates after cytotoxic therapy.
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Mispelaere B, Van de Werf E, D'Hooghe T, Dieudonné AS, Amant F, Van Mieghem T, Neven P, Paridaens R, and Wildiers H
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- Adolescent, Adult, Female, Fertility drug effects, Humans, Infertility, Female psychology, Menstrual Cycle, Norway, Pregnancy psychology, Surveys and Questionnaires, Young Adult, Antineoplastic Agents adverse effects, Breast Neoplasms drug therapy, Infertility, Female chemically induced, Lymphoma drug therapy, Pregnancy Rate
- Published
- 2009
- Full Text
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