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http://hdl.handle.net/11434/1132
Title: | Variations of surveillance practice for patients with bone sarcoma: a survey of Australian sarcoma clinicians. |
Epworth Authors: | Bae, Susan Desai, Jayesh |
Other Authors: | Lewin, Jeremy Thompson, Kate Strong, Robyn Caruso, Denise Howell, Deborah Herschtal, Alan Sullivan, Michael Orme, Lisa |
Keywords: | Neoplasms Cancer Bone Sarcoma Multimodal Therapy Pediatric Medical Oncology PO Nonpediatric Medical Oncology NP Paediatric Medical Oncology Nonpaediatric Medical Oncology Relapse Surveillance Practice Radiologic Surveillance Strategies RS Late Toxicity Assessment Psychosocial Interventions Local Disease Metastatic Disease Cancer Services Clinical Institute, Epworth HealthCare, Victoria, Australia |
Issue Date: | 2017 |
Publisher: | Hindawi |
Citation: | Sarcoma. 2017;2017:1837475 |
Abstract: | INTRODUCTION: After treatment, bone sarcoma patients carry a high chance of relapse and late effects from multimodal therapy. We hypothesize that significant variation in surveillance practice exists between pediatric medical oncology (PO) and nonpediatric medical oncology (NP) sarcoma disciplines. METHODS Australian sarcoma clinicians were approached to do a web based survey that assessed radiologic surveillance (RS) strategies, late toxicity assessment, and posttreatment psychosocial interventions. RESULTS: In total, 51 clinicians responded. No differences were identified in local disease RS. In metastatic disease response assessment, 100% of POs (23/23) and 93% of NPs (24/26) conducted CT chest. However, this was more likely to occur for NPs in the context of a CT chest/abdomen/pelvis (NP: 10/26; PO: 1/23; p = 0.006). POs were more likely to use CXR for RS (p = 0.006). POs showed more prescriptive intensity in assessment of heart function (p = 0.001), hearing (p < 0.001), and fertility (p = 0.02). POs were more likely to deliver written information for health maintenance/treatment summary (p = 0.04). The majority of respondents described enquiring about psychosocial aspects of health (n = 33/37, 89%), but a routine formal psychosocial screen was only used by 23% (n = 6/26). CONCLUSION: There is high variability in bone sarcoma surveillance between PO and NP clinicians. Efforts to harmonize approaches would allow early and late effects recognition/intervention and facilitate improved patient care/transition and research. |
URI: | http://hdl.handle.net/11434/1132 |
DOI: | 10.1155/2017/1837475 |
URL: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5350324/pdf/SARCOMA2017-1837475.pdf |
PubMed URL: | https://www.ncbi.nlm.nih.gov/pubmed/28348507 |
ISSN: | 1357-714X 1369-1643 |
Journal Title: | Sarcoma |
Type: | Journal Article |
Affiliated Organisations: | Victorian Adolescent & Young Adult Cancer Service, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia. Adolescent and Young Adult Oncology, Princess Margaret Cancer Centre, Toronto, ON, Canada. Australasian Sarcoma Study Group, Melbourne, VIC, Australia. Australian and New Zealand Children's Hematology/Oncology Group, Melbourne, VIC, Australia. Centre for Biostatistics and Clinical Trials, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia. Children's Cancer Centre, Royal Children's Hospital, Melbourne, VIC, Australia. Department of Paediatrics, University of Melbourne, Melbourne, VIC, Australia. |
Type of Clinical Study or Trial: | Cross-Sectional Study |
Appears in Collections: | Cancer Services |
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