TY - JOUR
T1 - Evaluation of the current knowledge limitations in breast cancer research
T2 - A gap analysis
AU - Thompson, Alastair
AU - Brennan, Keith
AU - Cox, Angela
AU - Gee, Julia
AU - Harcourt, Diana
AU - Harris, Adrian
AU - Harvie, Michelle
AU - Holen, Ingunn
AU - Howell, Anthony
AU - Nicholson, Robert
AU - Steel, Michael
AU - Streuli, Charles
N1 - Funding Information:
The following individuals participated in the gap analysis meeting (*denotes recipient of current or previous Breast Cancer Campaign funding, +denotes current or previous Breast Cancer Campaign Scientific Advisory Board membership): Dr Liz Anderson, Dr John Bartlett, Dr Shelia Bingham, Dr Jeremy Blaydes*, Dr Simon Boulton*, Professor Nigel Bundred* +, Dr Robert Clarke* +, Professor Robert Coleman*, Professor Charles Coombes, Professor Jessica Corner*, Professor Jack Cuzick, Professor Trevor Dale*, Dr Amanda Daley, Dr Isabel dos Santos Silva*, Dr Alison Dunning*, Dr Suzanne Eccles* +, Dr Paul Edwards*, Professor Dylan Edwards*, Professor Ian Ellis*, Dr Olivia Fletcher*, Dr Thomas Friedberg*, Professor William Gullick*, Professor Ian Hart* +, Dr Penelope Hopwood+, Professor Wen Jiang*, Dr Stephen Johnston* +, Professor Louise Jones*+, Professor William Miller* +, Dr Sotiris Missai- lidis*, Ms Barbara Parry, Professor Julian Peto, Dr Sarah Pinder+, Dr Colin Purdie, Dr Erik Sahai*, Dr Andrew Schofield*, Dr Matthew Smalley, Dr Valerie Speirs* +, Professor Joyce Taylor-Papadimitriou*, Professor Gerry Thomas, Professor Ashok Venkitaraman*, Professor Rosemary Walker* +, Dr Andrew Wardley+, Dr Ruth Warren* + and Dr Christine Watson*. Rachel Wheeler acted as scientific editor and was funded by Breast Cancer Campaign. Breast Cancer Campaign staff Arlene Wilkie and Dr Lisa Wilde assisted in the design and implementation of the meeting format and acted as facilitators throughout the process. Dr Annabelle Ballsdon was responsible for the meeting logistics and acted as a facilitator at the meeting. Amy Caldwell, Pamela Goldberg, Claire Learner and Tanya Sadhwani acted as facilitators at the meeting. The gap analysis meeting was held at The Novartis Foundation a registered charity in England and Wales, which has no commercial ties.
PY - 2008/3/27
Y1 - 2008/3/27
N2 - Background: A gap analysis was conducted to determine which areas of breast cancer research, if targeted by researchers and funding bodies, could produce the greatest impact on patients.Methods: Fifty-six Breast Cancer Campaign grant holders and prominent UK breast cancer researchers participated in a gap analysis of current breast cancer research. Before, during and following the meeting, groups in seven key research areas participated in cycles of presentation, literature review and discussion. Summary papers were prepared by each group and collated into this position paper highlighting the research gaps, with recommendations for action.Results: Gaps were identified in all seven themes. General barriers to progress were lack of financial and practical resources, and poor collaboration between disciplines. Critical gaps in each theme included: (1) genetics (knowledge of genetic changes, their effects and interactions); (2) initiation of breast cancer (how developmental signalling pathways cause ductal elongation and branching at the cellular level and influence stem cell dynamics, and how their disruption initiates tumour formation); (3) progression of breast cancer (deciphering the intracellular and extracellular regulators of early progression, tumour growth, angiogenesis and metastasis); (4) therapies and targets (understanding who develops advanced disease); (5) disease markers (incorporating intelligent trial design into all studies to ensure new treatments are tested in patient groups stratified using biomarkers); (6) prevention (strategies to prevent oestrogen-receptor negative tumours and the long-term effects of chemoprevention for oestrogen-receptor positive tumours); (7) psychosocial aspects of cancer (the use of appropriate psychosocial interventions, and the personal impact of all stages of the disease among patients from a range of ethnic and demographic backgrounds).Conclusion: Through recommendations to address these gaps with future research, the long-term benefits to patients will include: better estimation of risk in families with breast cancer and strategies to reduce risk; better prediction of drug response and patient prognosis; improved tailoring of treatments to patient subgroups and development of new therapeutic approaches; earlier initiation of treatment; more effective use of resources for screening populations; and an enhanced experience for people with or at risk of breast cancer and their families. The challenge to funding bodies and researchers in all disciplines is to focus on these gaps and to drive advances in knowledge into improvements in patient care.
AB - Background: A gap analysis was conducted to determine which areas of breast cancer research, if targeted by researchers and funding bodies, could produce the greatest impact on patients.Methods: Fifty-six Breast Cancer Campaign grant holders and prominent UK breast cancer researchers participated in a gap analysis of current breast cancer research. Before, during and following the meeting, groups in seven key research areas participated in cycles of presentation, literature review and discussion. Summary papers were prepared by each group and collated into this position paper highlighting the research gaps, with recommendations for action.Results: Gaps were identified in all seven themes. General barriers to progress were lack of financial and practical resources, and poor collaboration between disciplines. Critical gaps in each theme included: (1) genetics (knowledge of genetic changes, their effects and interactions); (2) initiation of breast cancer (how developmental signalling pathways cause ductal elongation and branching at the cellular level and influence stem cell dynamics, and how their disruption initiates tumour formation); (3) progression of breast cancer (deciphering the intracellular and extracellular regulators of early progression, tumour growth, angiogenesis and metastasis); (4) therapies and targets (understanding who develops advanced disease); (5) disease markers (incorporating intelligent trial design into all studies to ensure new treatments are tested in patient groups stratified using biomarkers); (6) prevention (strategies to prevent oestrogen-receptor negative tumours and the long-term effects of chemoprevention for oestrogen-receptor positive tumours); (7) psychosocial aspects of cancer (the use of appropriate psychosocial interventions, and the personal impact of all stages of the disease among patients from a range of ethnic and demographic backgrounds).Conclusion: Through recommendations to address these gaps with future research, the long-term benefits to patients will include: better estimation of risk in families with breast cancer and strategies to reduce risk; better prediction of drug response and patient prognosis; improved tailoring of treatments to patient subgroups and development of new therapeutic approaches; earlier initiation of treatment; more effective use of resources for screening populations; and an enhanced experience for people with or at risk of breast cancer and their families. The challenge to funding bodies and researchers in all disciplines is to focus on these gaps and to drive advances in knowledge into improvements in patient care.
UR - https://www.scopus.com/pages/publications/48949119487
UR - https://www.scopus.com/pages/publications/48949119487#tab=citedBy
U2 - 10.1186/bcr1983
DO - 10.1186/bcr1983
M3 - Article
C2 - 18371194
AN - SCOPUS:48949119487
SN - 1465-5411
VL - 10
JO - Breast Cancer Research
JF - Breast Cancer Research
IS - 2
M1 - R26
ER -