TY - JOUR
T1 - The cost-saving effect of centralized histological reviews with soft tissue and visceral sarcomas, GIST, and desmoid tumors
T2 - The experiences of the pathologists of the French Sarcoma Group
AU - Perrier, Lionel
AU - Rascle, Pauline
AU - Morelle, Magali
AU - Toulmonde, Maud
AU - Vince, Dominique Ranchere
AU - Le Cesne, Axel
AU - Terrier, Philippe
AU - Neuville, Agnès
AU - Meeus, Pierre
AU - Farsi, Fadila
AU - Ducimetière, Françoise
AU - Blay, Jean Yves
AU - Coquard, Isabelle Ray
AU - Coindre, Jean Michel
N1 - Publisher Copyright:
© 2018 Perrier et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
PY - 2018/4/1
Y1 - 2018/4/1
N2 - Objective This study examined the types of discordance occurring in the diagnosis of soft tissue and visceral sarcomas, gastrointestinal stromal tumors (GIST), and desmoid tumors, as well as the economic impact of diagnostic discrepancies. Methods We carried out a retrospective, multicenter analysis using prospectively implemented databases performed on a cohort of patients within the French RRePS network in 2010. Diagnoses were deemed to be discordant based on the 2013 World Health Organization (WHO) classification. Predictive factors of discordant diagnoses were explored. A decision tree was used to assess the expected costs of two strategies of disease management: one based on revised diagnoses after centralized histological review (option 1), the other on diagnoses without centralized review (option 2). Both were defined based on the patient and the disease characteristics, according to national or international guidelines. The time horizon was 12 months and the perspective of the French National Health Insurance (NHI) was retained. Costs were expressed in Euros for 2013. Sensitivity analyses were performed using low and high scenarios that included ± 20% estimates for cost. Results A total of 2, 425 patients were included. Three hundred forty-one patients (14%) had received discordant diagnoses. These discordances were determined to mainly be benign tumors diagnosed as sarcomas (n = 124), or non-sarcoma malignant tumors diagnosed as sarcomas (n = 77). The probability of discordance was higher for a final diagnosis of desmoid tumors when compared to liposarcomas (odds ratio = 5.1; 95%CI [2.6±10.4]). The expected costs per patient for the base-case analysis (low- and high-case scenarios) amounted to €8, 791 (€7, 033 and €10, 549, respectively) for option 1 and €8, 904 (€7, 057 and €10, 750, respectively) for option 2.
AB - Objective This study examined the types of discordance occurring in the diagnosis of soft tissue and visceral sarcomas, gastrointestinal stromal tumors (GIST), and desmoid tumors, as well as the economic impact of diagnostic discrepancies. Methods We carried out a retrospective, multicenter analysis using prospectively implemented databases performed on a cohort of patients within the French RRePS network in 2010. Diagnoses were deemed to be discordant based on the 2013 World Health Organization (WHO) classification. Predictive factors of discordant diagnoses were explored. A decision tree was used to assess the expected costs of two strategies of disease management: one based on revised diagnoses after centralized histological review (option 1), the other on diagnoses without centralized review (option 2). Both were defined based on the patient and the disease characteristics, according to national or international guidelines. The time horizon was 12 months and the perspective of the French National Health Insurance (NHI) was retained. Costs were expressed in Euros for 2013. Sensitivity analyses were performed using low and high scenarios that included ± 20% estimates for cost. Results A total of 2, 425 patients were included. Three hundred forty-one patients (14%) had received discordant diagnoses. These discordances were determined to mainly be benign tumors diagnosed as sarcomas (n = 124), or non-sarcoma malignant tumors diagnosed as sarcomas (n = 77). The probability of discordance was higher for a final diagnosis of desmoid tumors when compared to liposarcomas (odds ratio = 5.1; 95%CI [2.6±10.4]). The expected costs per patient for the base-case analysis (low- and high-case scenarios) amounted to €8, 791 (€7, 033 and €10, 549, respectively) for option 1 and €8, 904 (€7, 057 and €10, 750, respectively) for option 2.
UR - http://www.scopus.com/inward/record.url?scp=85045132196&partnerID=8YFLogxK
U2 - 10.1371/journal.pone.0193330
DO - 10.1371/journal.pone.0193330
M3 - Article
C2 - 29621244
AN - SCOPUS:85045132196
SN - 1932-6203
VL - 13
JO - PLoS ONE
JF - PLoS ONE
IS - 4
M1 - e0193330
ER -