A comprehensive resource available via ESMO OncologyPRO

 

A comprehensive resource developed by experts Prof. Simon Boulton, Prof. Charlie Gourley, Dr. Judith Balmaña and Dr. Violeta Serra, available via ESMO OncologyPRO portal, covering the following areas in detail:

  • Mechanism of Action (MoA) targeting DDR

  • MoA of PARP inhibitors (being the proof of concept for targeting DDR)

  • Clinical efficacy and safety/tolerability profile of PARP inhibitors and their benefit in various tumour types, now and in the future

  • Patient selection for PARP inhibition: diagnostics involved in DDR

  • Potential combination strategies with PARP inhibitors

  • Potential future applications for DDR

The information is primarily directed at healthcare professionals and contains information regarding the rationale for targeting DDR, including PARP inhibition as the proof of concept, the current role of PARP inhibition in clinical practice, and the potential future application of targeting DDR in clinical practice.

 

However, there is also a helpful section for patients and caregivers on the two novel types of targeted cancer drugs known as DDR (DNA damage response)-targeting agents and PARP (poly-ADP ribose polymerase) inhibitors with information on how these drugs work and how patients can work with their healthcare professional to manage any changes that may occur during treatment.

 

COR2ED have donated this content to ESMO to ensure that this comprehensive guide reflects today's best clinical practice in PARP inhibition and DNA Damage Response.

Prof. Simon Boulton has received financial support/sponsorship for research support, consultation, or speaker fees from the following companies:

Artios Pharma Ltd.

Dr Violeta Serra has received financial support/sponsorship for research support, consultation, or speaker fees from the following companies:

AstraZeneca and Tesaro. 

Dr Judith Balmaña has received financial support/sponsorship for research support, consultation, or speaker fees from the following companies:

AstraZeneca. 

Professor of Medical Oncology and Honorary Consultant in Medical Oncology; Clinical Director, CRUK Scotland Centre; Director, Nicola Murray Centre for Ovarian Cancer Research

Charlie graduated in Genetics and Medicine from Glasgow University in 1991 and 1994 respectively. From 1998 to 2005, he trained in medical oncology in Edinburgh, during which time he was awarded a PhD in ovarian cancer genetics from the University of Edinburgh and an NHS Education for Scotland Clinician Scientist Award. He was appointed as Senior Lecturer in Medical Oncology at the University of Edinburgh in 2005, Reader in Medical Oncology in 2011 and Professor of Medical Oncology (Personal Chair) in 2012. He received a Scottish Senior Clinical Fellowship Award in 2010. He became Director of the Nicola Murray Centre for Ovarian Cancer Research in 2016, Clinical Director of the Cancer Research UK Edinburgh Centre in 2019 and Clinical Director of the Cancer Research UK Scotland Centre in 2022.

Charlie’s clinical research focus is ovarian cancer clinical trials. He was UK Lead for the SOLO1 trial, which led to the first-line licence for olaparib in BRCA-mutant ovarian cancer, and for the GOG281/LOGS trial of trametinib, which is the first positive randomised controlled trial in low-grade serous ovarian cancer.

Charlie’s translational research focuses on molecular characterisation of ovarian cancer in order to improve understanding of drug sensitivity and resistance. His current priorities include targeting the molecular subgroups revealed by whole genome sequencing of high grade serous ovarian cancer and discovering new therapeutic strategies for treatment of low grade serous ovarian cancer.

Prof. Charlie Gourley has received financial support/sponsorship for research support, consultation, or speaker fees from the following companies:

AstraZeneca, Apera, Clovis, MSD, Nucana, Novartis, Roche, Sierra Oncology and Tesaro. 

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This educational programme is supported by an Independent Educational Grant from AstraZeneca
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