Philip Robert Debruyne

Prof. Dr. Philip Robert Debruyne

OECI-designated Kortrijk Cancer Centre, AZ Groeninge, Kortrijk, Belgium
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orcid

Research Focus & Metrics

Academic Career Length

28Years (1999-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 September 2001 in Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis
Verified
Journal Article
Closed access
Philip Robert DebruynePhilip Robert Debruyne
Philip Robert Debruyne
EBErik A. Bruyneel
Erik A. Bruyneel
XLXuedong Li
Xuedong Li
AZAmazia Zimber
Amazia Zimber
CGChristian Gespach
Christian Gespach
MMMarc M. Mareel
Marc M. Mareel

6 November 2012 in British Journal of Cancer
Verified
Journal Article
Open access
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BBBenoit Beuselinck
Benoit Beuselinck
PWP Wolter
P Wolter
AKA Karadimou
A Karadimou
RER Elaidi
R Elaidi
HDH Dumez
H Dumez
PSP Schöffski
P Schöffski
The presence of bone metastases in patients with metastatic renal cell carcinoma treated with oral tyrosine kinase inhibitors (TKIs) is associated with poorer outcome as compared with patients without bone involvement. Concomitant bisphosphonates could probably improve outcomes but also induce osteonecrosis of the jaw (ONJ). Retrospective study on all the renal cell carcinoma patients with bone metastases treated with sunitinib or sorafenib between November 2005 and June 2012 at the University Hospitals Leuven and AZ Groeninge in Kortrijk. Seventy-six patients were included in the outcome analysis: 49 treated with concomitant bisphosphonates, 27 with TKI alone. Both groups were well balanced in terms of prognostic and predictive markers. Response rate (38% vs 16% partial responses, P=0.028), median progression-free survival (7.0 vs 4.0 months, P=0.0011) and median overall survival (17.0 vs 7.0 months, P=0.022) were significantly better in patients receiving bisphosphonates. The incidence of ONJ was 10% in patients treated with TKI and bisphosphonates. Concomitant use of bisphosphonates and TKI in renal cell carcinoma patients with bone involvement probably improves treatment efficacy, to be confirmed by prospective studies, but is associated with a high incidence of ONJ.

1 April 2006 in Gastroenterology
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Journal Article
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Philip Robert DebruynePhilip Robert Debruyne
Philip Robert Debruyne
MWMatthew Witek
Matthew Witek
LGLi Gong
Li Gong
RBRuth Birbe
Ruth Birbe
ICInna Chervoneva
Inna Chervoneva
Scott WaldmanScott Waldman
Scott Waldman

9 November 2015 in BMC Cancer
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Journal Article
Open access
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LPLies Pottel
Lies Pottel
MLMichelle Lycke
Michelle Lycke
TBTom Boterberg
Tom Boterberg
HPHans Pottel
Hans Pottel
LGLaurence Goethals
Laurence Goethals
Philip Robert DebruynePhilip Robert Debruyne
Philip Robert Debruyne
Evidence-based guidelines concerning the older head and neck cancer (HNCA) patient are lacking. Accurate patient selection for optimal care management is therefore challenging. We examined if geriatric assessment is indicative of long-term health-related quality of life (HRQOL) and overall survival in this unique population. All HNCA patients, aged ≥65 years, eligible for curative radio(chemo)therapy were evaluated with the Geriatric-8 (G-8) questionnaire and a comprehensive geriatric assessment (CGA). Euroqol-5 dimensions (EQ-5D) and survival were collected until 36 months post treatment start. Repeated measures ANOVA was applied to analyse HRQOL evolution in ‘fit’ and ‘vulnerable’ patients, defined by G-8. Kaplan-Meier curves and cox proportional hazard analysis were established for determination of the prognostic value of geriatric assessments. Quality-adjusted survival was calculated in both patient subgroups. One hundred patients were recruited. Seventy-two percent of patients were considered vulnerable according to CGA (≥2 abnormal tests). Fit patients maintained a relatively acceptable long-term HRQOL, whilst vulnerable patients showed significantly lower median health states. The difference remained apparent at 36 months. Vulnerability, as classified by G-8 or CGA, came forward as independent predictor for lower EQ-5D index scores. After consideration of confounders, a significantly lower survival was observed in patients defined vulnerable according to G-8, compared to fit patients. A similar trend was seen based on CGA. Calculation of quality-adjusted survival showed significantly less remaining life months in perfect health in vulnerable patients, compared to fit ones. G-8 is indicative of quality-adjusted survival, and should be considered at time of treatment decisions for the older HNCA patient.

28 January 2014 in European Journal of Cancer Care
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Journal Article
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LPL. Pottel
L. Pottel
MLM. Lycke
M. Lycke
TBT. Boterberg
T. Boterberg
HPH. Pottel
H. Pottel
LGL. Goethals
L. Goethals
Philip Robert DebruynePhilip Robert Debruyne
Philip Robert Debruyne
Head and neck (H&N) cancer is mainly a cancer of the elderly; however, the implementation of comprehensive geriatric assessment (CGA) to quantify functional age in these patients has not yet been studied. We evaluated the diagnostic performance of screening tools [Vulnerable Elders Survey‐13 (VES‐13), G8 and the Combined Screening Tool ‘VES‐13 + (17‐G8)’ or CST], the feasibility of serial CGA, and correlations with health‐related quality of life evolution [HRQOL; European Organisation for Research and Treatment of Cancer Quality of Life Questionnaires (EORTC QLQ)‐C30 and ‐HN35] during therapy in hundred patients, aged ≥65 years, with primary H&N cancer undergoing curative radio(chemo)therapy. Respectively 36.8%, 69.0%, 62.1% and 71.3% were defined vulnerable according to VES‐13, G8, CST and CGA at week 0, mostly due to presence of severe grade co‐morbidities, difficulties in community functioning and nutritional problems. At week 4, significantly more patients were identified vulnerable due to nutritional, functional and emotional deterioration. The CST did not achieve the predefined proportion necessary for validation. Vulnerable patients reported lower function and higher symptom HRQOL scores as compared with fit patients. A comparable deterioration in HRQOL was observed in both groups through therapy. In conclusion, G8 remains the screening tool of choice. Serial CGA identifies the evolution of multidimensional health problems and HRQOL conditions during therapy with potential to guide individualised supportive care.

1 June 2019 in The Lancet Oncology
Verified
Journal Article
Closed access
IVIgnace Vergote
Ignace Vergote
GSGiovanni Scambia
Giovanni Scambia
DODavid M O'MAlley
David M O'MAlley
BCBen Van Calster
Ben Van Calster
JCJosep M del Campo
Josep M del Campo
MEMark Einstein
Mark Einstein