David Bowen

Dr. David Bowen


Research Focus & Metrics

Academic Career Length

32Years (1995-Present)

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

Representative Publications

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3 July 2008 in Leukemia
Verified
Journal Article
Open access
PDF file
DBDavid Bowen
David Bowen
MGM J Groves
M J Groves
ABA K Burnett
A K Burnett
YPY Patel
Y Patel
CAC Allen
C Allen
DLD C Linch
D C Linch
TP53 gene mutation is frequent in patients with acute myeloid leukemia and complex karyotype, and is associated with very poor prognosis

10 June 2022 in Transfusion
Verified
Journal Article
Closed access
AVAbi Vijenthira
Abi Vijenthira
RSRebecca Starkman
Rebecca Starkman
YLYulia Lin
Yulia Lin
SSSimon J. Stanworth
Simon J. Stanworth
DBDavid Bowen
David Bowen
RBRena Buckstein
Rena Buckstein

1 November 2015 in European Journal of Cancer
Verified
Journal Article
Open access
DSDan Stark
Dan Stark
DBDavid Bowen
David Bowen
EDElaine Dunwoodie
Elaine Dunwoodie
RFRichard Feltbower
Richard Feltbower
RJRod Johnson
Rod Johnson
COCatherine O’hAra
Catherine O’hAra
We aimed to describe and compare survival in teenagers and young adults (TYAs) with cancer to that of younger children and older adults, to identify sub-populations at greater or lesser risk of death. We compared survival in cancer patients diagnosed in the United Kingdom aged 13-24 years (TYAs) to those aged 0-12 (children) and 25-49 years (adults) using the National Cancer Data Repository. All cases had a first cancer diagnosis between 1st January 2001 and 31st December 2005 with censor date 31st December 2010 or death if earlier. We found six distinct statistically significant survival patterns. In pattern 1, the younger the age-group the better the 1- and 5-year survival (acute lymphoid leukaemia, carcinoma of ovary and melanoma). In pattern 2, TYAs had a worse 5-year survival than both children and young adults (bone and soft tissues sarcomas). In pattern 3, TYAs had a worse 1-year survival but no difference at 5-years (carcinoma of cervix and female breast). In pattern 4, TYAs had better 1-year survival than adults, but no difference at 5 years (carcinoma of liver and intrahepatic bile ducts, germ cell tumours of extra-gonadal sites). In pattern 5, the younger the age-group the better the 5-year survival, but the difference developed after 1-year (acute myeloid leukaemia, carcinoma of colon and rectum). In pattern 6, there was no difference in 1- and 5-year survival between TYAs and adults (testicular germ cell tumours, ovarian germ cell tumours and carcinoma of thyroid). TYAs with specific cancer diagnoses can be grouped according to 1- and 5-year survival patterns compared to children and young adults. To further improve survival for TYAs, age-specific biology, pharmacology, proteomics, genomics, clinician and patient behaviour studies embedded within clinical trials are required.

25 August 2020 in Blood Advances
Verified
Journal Article
Open access
PDF file
KSKristina Stojkov
Kristina Stojkov
TSTobias Silzle
Tobias Silzle
GSGeorg Stüssi
Georg Stüssi
DSDavid Schwappach
David Schwappach
JBJuerg Bernhard
Juerg Bernhard
Nicolas BonadiesNicolas Bonadies
Nicolas Bonadies
Myelodysplastic syndromes (MDSs) represent a heterogeneous group of hematological stem cell disorders with an increasing burden on health care systems. Evidence-based MDS guidelines and recommendations (G/Rs) are published but do not necessarily translate into better quality of care if adherence is not maintained in daily clinical practice. Guideline-based indicators (GBIs) are measurable elements for the standardized assessment of quality of care and, thus far, have not been developed for adult MDS patients. To this end, we screened relevant G/Rs published between 1999 and 2018 and aggregated all available information as candidate GBIs into a formalized handbook as the basis for the subsequent consensus rating procedure. An international multidisciplinary expert panel group (EPG) of acknowledged MDS experts (n = 17), health professionals (n = 7), and patient advocates (n = 5) was appointed. The EPG feedback rates for the first and second round were 82% (23 of 28) and 96% (26 of 27), respectively. A final set of 29 GBIs for the 3 domains of diagnosis (n = 14), therapy (n = 8), and provider/infrastructural characteristics (n = 7) achieved the predefined agreement score for selection (>70%). We identified shortcomings in standardization of patient-reported outcomes, toxicity, and geriatric assessments that need to be optimized in the future. Our GBIs represent the first comprehensive consensus on measurable elements addressing best practice performance, outcomes, and structural resources. They can be used as a standardized instrument with the goal of assessing, comparing, and fostering good quality of care within clinical development cycles in the daily care of adult MDS patients.

1 December 2013 in Best Practice & Research Clinical Haematology
Verified
Journal Article
Closed access
DBDavid Bowen
David Bowen

1 March 1995 in British Journal of Haematology
Verified
Journal Article
Closed access
PDF file
DCDominic J. Culligan
Dominic J. Culligan
DBDavid Bowen
David Bowen
AMAlison May
Alison May
DWDenise White
Denise White
RPRose Ann Padua
Rose Ann Padua
ABAlan K. Burnett
Alan K. Burnett