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Variations of Surveillance Practice for Patients with Bone Sarcoma: A Survey of Australian Sarcoma Clinicians

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....

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Autores principales: Lewin, Jeremy, Thompson, Kate, Bae, Susie, Desai, Jayesh, Strong, Robyn, Caruso, Denise, Howell, Deborah, Herschtal, Alan, Sullivan, Michael, Orme, Lisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5350324/
https://www.ncbi.nlm.nih.gov/pubmed/28348507
http://dx.doi.org/10.1155/2017/1837475
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author Lewin, Jeremy
Thompson, Kate
Bae, Susie
Desai, Jayesh
Strong, Robyn
Caruso, Denise
Howell, Deborah
Herschtal, Alan
Sullivan, Michael
Orme, Lisa
author_facet Lewin, Jeremy
Thompson, Kate
Bae, Susie
Desai, Jayesh
Strong, Robyn
Caruso, Denise
Howell, Deborah
Herschtal, Alan
Sullivan, Michael
Orme, Lisa
author_sort Lewin, Jeremy
collection PubMed
description 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.
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spelling pubmed-53503242017-03-27 Variations of Surveillance Practice for Patients with Bone Sarcoma: A Survey of Australian Sarcoma Clinicians Lewin, Jeremy Thompson, Kate Bae, Susie Desai, Jayesh Strong, Robyn Caruso, Denise Howell, Deborah Herschtal, Alan Sullivan, Michael Orme, Lisa Sarcoma Research Article 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. Hindawi Publishing Corporation 2017 2017-02-28 /pmc/articles/PMC5350324/ /pubmed/28348507 http://dx.doi.org/10.1155/2017/1837475 Text en Copyright © 2017 Jeremy Lewin et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Lewin, Jeremy
Thompson, Kate
Bae, Susie
Desai, Jayesh
Strong, Robyn
Caruso, Denise
Howell, Deborah
Herschtal, Alan
Sullivan, Michael
Orme, Lisa
Variations of Surveillance Practice for Patients with Bone Sarcoma: A Survey of Australian Sarcoma Clinicians
title Variations of Surveillance Practice for Patients with Bone Sarcoma: A Survey of Australian Sarcoma Clinicians
title_full Variations of Surveillance Practice for Patients with Bone Sarcoma: A Survey of Australian Sarcoma Clinicians
title_fullStr Variations of Surveillance Practice for Patients with Bone Sarcoma: A Survey of Australian Sarcoma Clinicians
title_full_unstemmed Variations of Surveillance Practice for Patients with Bone Sarcoma: A Survey of Australian Sarcoma Clinicians
title_short Variations of Surveillance Practice for Patients with Bone Sarcoma: A Survey of Australian Sarcoma Clinicians
title_sort variations of surveillance practice for patients with bone sarcoma: a survey of australian sarcoma clinicians
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5350324/
https://www.ncbi.nlm.nih.gov/pubmed/28348507
http://dx.doi.org/10.1155/2017/1837475
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