5 results on '"Aston, Will"'
Search Results
2. High Subcortical Sacral Resection {Hiss] for Locally Advanced & Recurrent Rectal Cancer Extending onto L5/S1/2.
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Pring, Edward, Gould, Laura, Fletcher, Jordan, Claire, Taylor, Hona, Therese, Corr, Alison, Burling, David, Holloway, Ian, Aston, Will, and Antoniou, Anthony
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RECTAL cancer - Abstract
B Background: b In locally advanced and recurrent rectal cancer disease extension onto the lower lumbar spine and sacrum at L5/S1/2 is regarded as surgically unsalvageable, en-bloc bony cortex excision, High Subcortical Sacral resection [HiSS], may offer the chance of salvage in patients regarded as unsuitable or at high risk of incomplete resection with conventional surgical approaches. Consecutive National Health Service (NHS) patients undergoing exenterative surgical procedures at a single centre were assessed and those with disease extension onto L5/S1/2 assessed for suitability for HiSS. [Extracted from the article]
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- 2020
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3. Surgical outcomes of patients with diffuse-type tenosynovial giant-cell tumours: an international, retrospective, cohort study.
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Mastboom, Monique J L, Palmerini, Emanuela, Verspoor, Floortje G M, Rueten-Budde, Anja J, Stacchiotti, Silvia, Staals, Eric L, Schaap, Gerard R, Jutte, Paul C, Aston, Will, Gelderblom, Hans, Leithner, Andreas, Dammerer, Dietmar, Takeuchi, Akihiko, Thio, Quirina, Niu, Xiaohui, Wunder, Jay S, van de Sande, Michiel A J, and TGCT Study Group
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GIANT cell tumors , *DISEASE risk factors , *COHORT analysis , *KNEE diseases , *CANCER , *SURGICAL complications - Abstract
Background: Diffuse-type tenosynovial giant-cell tumour is a rare, locally aggressive, and difficult-to-treat soft tissue tumour. Clinical and surgical outcomes depend on multiple factors, including preoperative diagnostic assessment, the localisation and extent of disease, and possibly the choice of treatment modalities by orthopaedic surgeons. We did a retrospective cohort study to characterise global surgical treatment protocols, and assess surgical outcomes, complications, and functional results in patients with diffuse-type tenosynovial giant-cell tumours.Methods: In this international, multicentre, retrospective cohort study, we included consecutive patients treated in 31 sarcoma reference centres between Jan 1, 1990, and Dec 31, 2017. Eligible patients were of any age and had histologically proven diffuse-type tenosynovial giant-cell tumour of large joints. Patient data were retrieved from the local databases of participating centres. Patients with localised-type tenosynovial giant-cell tumour were excluded. In the analysis, we only included patients with complete core criteria data regarding admission status, date of treatment, type of treatment at participating centre, and first local recurrence after treatment. We used a non-parametric method to estimate recurrence-free survival at 3, 5, and 10 years after initial surgical resection in a tertiary centre. We used a multivariate Cox regression model to estimate the effect of risk factors. We also present subgroup analyses of disease status at presentation (primary vs recurrent disease) and recurrence-free survival by surgery type (open surgery vs arthroscopic synovectomy), and prespecified risk factors were tested in a univariate and multivariable analyses, with an endpoint of first local recurrence after treatment in a tertiary centre.Findings: Data collection for these analyses occurred between January, 2016, and May, 2018. We received the records of 1192 patients, of which 966 (81%) were surgically treated and had complete information on core criteria. 445 patients were admitted with therapy-naive disease of the knee and were primarily treated in a tertiary centre. Since patients with wait and see treatment do not have a starting date of treatment, these patients were excluded in the calculation of median follow-up time for all patients. For this calculation we used time of surgery as a starting date. 758 (64%) of 1192 patients had knee involvement and 628 (54%) of 1163 patients with complete data on type of surgery had one-staged open synovectomy. At a median follow-up of 54 months (IQR 27-97), recurrent disease developed in 425 (44%) of all 966 surgically treated cases, and recurrence-free survival was 62% (95% CI 59-65) at 3 years, 55% (51-58) at 5 years, and 40% (35-45) at 10 years. Surgical complications were reported in 105 (12%) of 906 patients who had complete data on surgical complications. Pain improved after surgical treatment in 255 (59%) of 434 patients and swelling improved in 328 (72%) of 453 patients who had complete data.Interpretation: This study of patients with diffuse-type tenosynovial giant-cell tumour provides a comprehensive and up-to-date disease overview, assessing the clinical profile and management of the disease in multiple specialised referral centres. Surgical treatment of diffuse-type tenosynovial giant cell tumours is not a definitive treatment for every patient because it involves a high risk for local recurrent disease and a relatively high risk for postoperative complications. After surgical treatment in treatment-naive patients, risk factors for recurrent disease in individual patients were not identified in what we believe is the largest cohort to date.Funding: Daiichi Sankyo. [ABSTRACT FROM AUTHOR]- Published
- 2019
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4. Dynamic prediction of overall survival for patients with high-grade extremity soft tissue sarcoma.
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Rueten-Budde, A. J., van Praag, V. M., Jeys, Lee M., Laitinen, Minna K., Pollock, Rob, Aston, Will, van der Hage, Jos A., Dijkstra, PD Sander, Ferguson, Peter C., Griffin, Anthony M., Willeumier, Julie J., Wunder, Jay S., Styring, Emelie, Posch, Florian, Zaikova, Olga, Maretty-Kongstad, Katja, Keller, Johnny, Leithner, Andreas, Smolle, Maria A., and Haas, Rick L.
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SOFT tissue injuries , *SARCOMA , *PREDICTION models , *METASTASIS , *PROGNOSIS - Abstract
Purpose There is increasing interest in personalized prediction of disease progression for soft tissue sarcoma patients. Currently, available prediction models are limited to predictions from time of surgery or diagnosis. This study updates predictions of overall survival at different times during follow-up by using the concept of dynamic prediction. Patients and methods Information from 2232 patients with high-grade extremity soft tissue sarcoma, who underwent surgery at 14 specialized sarcoma centers, was used to develop a dynamic prediction model. The model provides updated 5-year survival probabilities from different prediction time points during follow-up. Baseline covariates as well as time-dependent covariates, such as status of local recurrence and distant metastases, were included in the model. In addition, the effect of covariates over time was investigated and modelled accordingly in the prediction model. Results Surgical margin and tumor histology show a significant time-varying effect on overall survival. The effect of margin is strongest shortly after surgery and diminishes slightly over time. Development of local recurrence and distant metastases during follow-up have a strong effect on overall survival and updated predictions must account for their occurrence. Conclusion The presence of time-varying effects, as well as the effect of local recurrence and distant metastases on survival, suggest the importance of updating predictions during follow-up. This newly developed dynamic prediction model which updates survival probabilities over time can be used to make better individualized treatment decisions based on a dynamic assessment of a patient's prognosis. [ABSTRACT FROM AUTHOR]
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- 2018
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5. A prediction model for treatment decisions in high-grade extremity soft-tissue sarcomas: Personalised sarcoma care (PERSARC).
- Author
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van Praag, Veroniek M., Rueten-Budde, Anja J., Jeys, Lee M., Laitinen, Minna K., Pollock, Rob, Aston, Will, van der Hage, Jos A., Dijkstra, P.D. Sander, Ferguson, Peter C., Griffin, Anthony M., Willeumier, Julie J., Wunder, Jay S., van de Sande, Michiel A.J., and Fiocco, Marta
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AGE distribution , *CANCER relapse , *DECISION making , *EXTREMITIES (Anatomy) , *MATHEMATICAL models , *HEALTH outcome assessment , *SARCOMA , *SOFT tissue tumors , *SURVIVAL , *THEORY , *PROPORTIONAL hazards models , *PROGNOSIS ,RESEARCH evaluation - Abstract
Background To support shared decision-making, we developed the first prediction model for patients with primary soft-tissue sarcomas of the extremities (ESTS) which takes into account treatment modalities, including applied radiotherapy (RT) and achieved surgical margins. The PERsonalised SARcoma Care (PERSARC) model, predicts overall survival (OS) and the probability of local recurrence (LR) at 3, 5 and 10 years. Aim Development and validation, by internal validation, of the PERSARC prediction model. Methods The cohort used to develop the model consists of 766 ESTS patients who underwent surgery, between 2000 and 2014, at five specialised international sarcoma centres. To assess the effect of prognostic factors on OS and on the cumulative incidence of LR (CILR), a multivariate Cox proportional hazard regression and the Fine and Gray model were estimated. Predictive performance was investigated by using internal cross validation (CV) and calibration. The discriminative ability of the model was determined with the C-index. Results Multivariate Cox regression revealed that age and tumour size had a significant effect on OS. More importantly, patients who received RT showed better outcomes, in terms of OS and CILR, than those treated with surgery alone. Internal validation of the model showed good calibration and discrimination, with a C-index of 0.677 and 0.696 for OS and CILR, respectively. Conclusions The PERSARC model is the first to incorporate known clinical risk factors with the use of different treatments and surgical outcome measures. The developed model is internally validated to provide a reliable prediction of post-operative OS and CILR for patients with primary high-grade ESTS. Level of significance level III. [ABSTRACT FROM AUTHOR]
- Published
- 2017
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