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J Med Oncl Ther 2017 | Volume 2 Issue 3

Breast Cancer

November 01-02, 2017 | Toronto, Canada

7

th

World Congress on

Novel therapeutic drug combinations with CDK4/6 inhibitors, beyond ER+ve breast cancer

Uzma Saddia Asghar

1,2

1

University College London Hospital, UK

2

Institute of Cancer Research, London

T

he CDK4/6 – RB1 axis controls transition through the

restriction point in the G1 phase of the cell cycle, and

cancers frequently subvert the regulation of this axis

to promote proliferation. CDK4/6 inhibition is a proven

therapeutic strategy for estrogen receptor positive (ER+ve)

breast cancers, with selective CDK4/6 inhibitors (palbociclib

and ribociclib) demonstrating substantial improvements in

progression free survival in phase two and three clinical trials

(PALOMA1, PALOMA2, PALOMA3 and MONALEESA-2). There

is considerable interest in exploring the role CDK4/6 inhibitors

in drug combinations for patients with HER2 amplified breast

groups and the TNBC subtypes. Triple negative breast cancer

(TNBC) is an aggressive subtype of breast cancer associated

with poor prognosis. Although TNBC may be sensitive to

chemotherapy there is a substantial need to identify novel

targeted therapeutic strategies. TNBC are a heterogeneous

group of tumours with gene expression profiling identifying

distinct subgroups, including luminal androgen receptor

(LAR), mesenchymal stem like (MSL), mesenchymal (MES),

and basal-like.

In vitro

data and

in vivo

data have shown that

the LAR subtypes of breast cancer are highly sensitive to

CDK4/6 inhibition and this is currently being tested in clinical

trials. There is now growing amount of data suggesting that

CDK4/6 inhibitor drug combinations, may have a role in

breast cancer subtypes, beyond ER receptor positivity.

Speaker Biography

Uzma Saddia Asghar was awarded her MBBS (2004) and intercalated BSc in

Neurosciences (2001) from University College London (UCL). She was awarded her

MRCP in 2008 (London) and did her PhD at Breast Cancer now, Institute of Cancer,

London as an Avon Clinical Research Fellow (2017). Her interests includes novel

targeted therapeutic agents for breast cancer, inhibitors of cell cycle and PI3 kinase

signaling pathway, immunotherapy and drug development and currently setting up

these breast translational clinical trials at UCL.

e:

uzmaasg@yahoo.co.uk